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The State of Theragnostics in BRICS Nations: A Data-Driven Multicentre Report
*Corresponding author: Masha Maharaj, Department of Nuclear Medicine, Umhlanga Molecular Imaging and Therapy Centres of Excellence, Netcare Umhlanga & Hibiscus Hospitals, KwaZulu-Natal, South Africa. drmasha@yahoo.co.uk
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Received: ,
Accepted: ,
How to cite this article: Maharaj M, Mansurov O, Rangarajan V, Tuti Y, Mbakaza O, Duarte PS, et al. The State of Theragnostics in BRICS Nations: A Data-Driven Multicentre Report. Indian J Nucl Med. 2026;41:327-39. doi: 10.25259/IJNM_95_2026
Abstract
Objectives:
Theragnostic integrates diagnostic imaging with targeted radionuclide therapy, offering a precision approach in oncology. The BRICS Multicentre Theragnostic Survey (2025–2026) aimed to evaluate current clinical practices in radionuclide therapy across participating centres within BRICS member and partner countries. The survey aimed to assess clinical activity, patterns of therapeutic radionuclide utilisation, implementation of patient-specific dosimetry, and to identify key logistical, regulatory, infrastructural, and workforce-related challenges. It also sought to define institutional training needs and opportunities for collaborative development in theragnostic applications across the BRICS network.
Material and Methods:
A multicentre, cross-sectional survey was conducted using a structured questionnaire distributed to nuclear medicine and theragnostic centres across BRICS countries and affiliated partner nations. Aggregated, non-identifiable institutional-level data were collected on clinical workload, radiopharmaceutical targets, therapeutic radionuclides used, clinical indications, dosimetry practices (including SPECT, SPECT/CT, and PET/CT), operational challenges, proposed solutions, and training needs. Data were analysed descriptively.
Results:
A total of 137 centres from 14 countries participated in the BRICS Multicentre Theragnostic Survey 2026, with the largest contributions from India (n=72, 52.6%) and Indonesia (n=21, 15.3%), followed by South Africa (n=11, 8.0%), Brazil (n=10, 7.3%), China (n=5, 3.6%), Iran (n=4, 2.9%), and Republic of Belarus (n=4, 2.9%). The majority of institutions were private hospitals or clinics (51.1%), followed by academic/university hospitals (26.3%) and government/public hospitals (19.0%). Dedicated theragnostic services were established in 71.3% of centres. Procedure volumes varied widely, with 34.3% of centres performing fewer than 50 procedures per year and only 13.1% exceeding 500 annually. Prostate-specific membrane antigen (PSMA) based theragnostics were offered by 82.3%, and DOTATATE-based therapies by 70.8% of centres. 131I was the most widely used therapeutic radionuclide (86.1%), followed by 177Lu (73.7%). The leading clinical indications were thyroid cancer (90.8%), prostate cancer (82.4%), neuroendocrine tumours (70.2%), and bone metastases (60.3%). Patient-specific dosimetry was performed routinely in 8.0% and selectively in 35.8% of centres, while 51.1% reported not performing it at all. SPECT/CT was the predominant imaging modality among those performing dosimetry. Key challenges included limited radionuclide availability (82.4%), reimbursement and funding issues (77.4%), lack of harmonised regulations (72.5%), insufficient trained personnel (67.0%), import/export delays (56.3%), and licensing and authorisation delays (55.9%).
Conclusion:
This survey reveals substantial heterogeneity in theragnostic implementation across BRICS centres and highlights persistent gaps in radionuclide supply, reimbursement, regulatory harmonisation, infrastructure, and workforce capacity. Without coordinated intervention, current disparities in infrastructure, workforce, and radionuclide supply are likely to widen, limiting equitable access to theragnostic therapies across BRICS nations. Strengthening collaboration through the BRICS network offers a strategic pathway to expand equitable access to safe and effective theragnostic therapies across all disease stages.
Keywords
BRICS
Dosimetry
Nuclear medicine
Radioligand therapy
Radionuclide therapy
Theragnostic
INTRODUCTION
BRICS is an intergovernmental organisation established in 2009 by Brazil, Russia, India, and China, with South Africa joining in 2011. It has since expanded to include eleven full member countries—Brazil, Russia, India, China, South Africa, Saudi Arabia, Egypt, the United Arab Emirates, Ethiopia, Indonesia, and Iran—along with a network of partner nations. Collectively, these countries represent approximately 4.0 billion people, accounting for nearly 48% of the global population based on recent 2026 estimates. This substantial demographic and economic footprint positions BRICS as a major platform for political coordination and multilateral collaboration across key sectors, including economic development, health, science, and technology.[1–3]Its broad geographic and socioeconomic diversity further underscores its role as a critical driver of capacity building and shared development priorities, particularly within healthcare systems.
Nuclear medicine originated in the 1940s with the pioneering work of Saul Hertz, who administered the first therapeutic doses of radioactive iodine (131I) for hyperthyroidism in 1941, marking the birth of targeted radionuclide therapy.[4] Since then, the field has evolved from a primarily diagnostic discipline focused on organ function and disease detection into an integral component of modern medicine, spanning oncology, cardiology, neurology, endocrinology, and other specialities. By integrating functional and molecular imaging with targeted radionuclide therapy, nuclear medicine enables the non-invasive characterisation of disease at the cellular and molecular level. The emergence of theragnostic — the coupling of diagnostic radiopharmaceuticals with their therapeutic counterparts — represents a major paradigm shift, allowing clinicians to “see, treat, and monitor” disease within a single molecular framework.[5,6]
Theragnostic has become a cornerstone of precision oncology, leveraging radiolabelled ligands that target tumour-specific biomarkers such as prostate-specific membrane antigen (PSMA) and somatostatin receptors. This “see-and-treat” approach utilises positron- or gamma-emitting tracers (e.g., 99mTc, 68Ga, and 18F) for disease characterisation and patient selection through PET or SPECT imaging. The same ligands can then be labelled with therapeutic radionuclides, including beta-emitters such as 177Lu or alpha-emitters such as 225Ac, enabling precise delivery of cytotoxic radiation while minimising damage to surrounding normal tissues. Landmark trials, including NETTER-1, NETTER-2, and VISION, have demonstrated not only significant survival benefits but also sustained preservation of quality of life, often exceeding that achieved with conventional chemotherapy or external beam radiotherapy.[7–9] With the development of novel radioligands, theragnostic applications are rapidly expanding into a broader range of malignancies, including breast, pancreatic, hepatocellular, and colorectal cancers. This combination of targeted efficacy, favourable safety profile, and patient-centred outcomes positions theragnostic as a major advancement in contemporary oncology.[10–14]
Recognising the growing clinical significance of nuclear medicine, the BRICS Nuclear Medicine Working Group (NMWG) was established in 2024 to strengthen collaboration and advance the delivery of theragnostic services across member and partner nations. Despite rapid progress in theragnostic, considerable heterogeneity persists among BRICS countries in terms of infrastructure, radionuclide availability, implementation of standardised protocols, regulatory frameworks, and workforce capacity. These disparities contribute to variability in clinical practice and hinder the widespread adoption of theragnostic approaches.[15-17]
To address these challenges, a systematic multicentre evaluation was undertaken to characterise current practices, identify critical gaps, and inform strategies for harmonisation and capacity building. Accordingly, this study conducted a cross-sectional survey across BRICS institutions to evaluate theragnostic practices, radionuclide utilisation, dosimetry implementation, and operational constraints. The findings provide a basis for coordinated efforts to strengthen nuclear medicine services and promote equitable access to advanced theragnostic care across the BRICS network.
MATERIAL AND METHODS
Study design
This was a multicentre, cross-sectional, descriptive survey designed to assess the current status of theragnostic practices, infrastructure, and challenges across nuclear medicine centres in BRICS member and partner countries. The study was conducted over a three-month period from 06 January to 02 April 2026. A structured, self-administered, web-based questionnaire was used to collect aggregated institutional-level data.
Study population and sampling
The target population consisted of nuclear medicine departments and theragnostic centres actively involved in or preparing to provide radionuclide therapy services in BRICS member countries (Brazil, Russia, India, China, South Africa, Egypt, Ethiopia, Iran, Saudi Arabia, the United Arab Emirates, and Indonesia) and affiliated partner nations (including Belarus, Bolivia, Cuba, Kazakhstan, Malaysia, Nigeria, Thailand, Uganda, Uzbekistan, and Vietnam). Both established and developing theragnostic programs were eligible for inclusion. Centres were recruited through professional networks, national nuclear medicine societies, BRICS nuclear medicine forums, and direct invitations to known theragnostic centres. Purposive and snowball sampling techniques were employed to ensure broad geographic representation in the absence of a centralised registry. A total of 137 centres from 14 countries participated in the final analysis.
Questionnaire development and domains
The questionnaire was developed by a core team of nuclear medicine physicians and researchers with expertise in theragnostic. It underwent content validation by senior experts before distribution. The instrument comprised both closed-ended (multiple-choice and select-all-that-apply) and limited open-ended questions organised into the following major domains [Table 1].
| Domain/section | Description/content covered | Question type |
|---|---|---|
| Institutional profile | Country, type of centre (private, academic, government/public), name of the responsible person | Open/categorical |
| Dedicated theragnostic service status | Established, developing, not available | Single choice |
| Annual theragnostic procedure volume | Approximate number of procedures per year (<50, 50–200, 201–500, >500) | Categorical |
| Radiopharmaceutical targets used | DOTATATE-based theragnostic, PSMA-based theragnostic, other (specify) | Multi-select |
| Therapeutic radionuclides administered | 177Lu, 131I, 225Ac, 161Tb, and 188Re, other (specify) with approximate annual dose ranges | Multi-select + categories |
| Clinical indications treated | Neuroendocrine tumours, prostate cancer, thyroid cancer, bone metastases, hepatocellular carcinoma, others | Multi-select |
| Patient-specific dosimetry practices | Performed? (routinely, selectively, no) | Single choice |
| Dosimetry imaging modalities used | SPECT/CT, PET/CT, planar imaging | Multi-select |
| Indications for which dosimetry is applied | Specific clinical indications where dosimetry is performed | Multi-select |
| Main barriers to implementing dosimetry | Time constraints, limited software/hardware, lack of expertise, not reimbursed, etc. | Multi-select |
| Major challenges – logistics and supply chain | Limited radionuclide availability, import/export delays, short half-life, transportation issues | Multi-select |
| Major challenges – regulatory and policy | Licensing delays, lack of harmonised regulations, and restrictions on alpha- emitters | Multi-select |
| Major challenges – clinical and operational | Reimbursement/funding issues, insufficiently trained personnel, infrastructure limitations, and patient referral pathways | Multi-select |
| Preferred solutions | Structured training programs, hands-on dosimetry workshops, multicentre protocols, regional supply coordination, fellowships, guideline development | Multi-select |
| Willingness to participate in BRICS collaboration | Multicentre research studies, training & capacity-building initiatives, guideline development projects | Multi-select |
| Additional comments/suggestions | Open field for further relevant suggestions (limited to 100 words) | Open-ended |
BRICS: BRICS member and associate member states; SPECT/CT: Single photon emission computed tomography/computed tomography; PET/CT: Positron emission tomography/computed tomography; DOTATATE: DOTA-(Tyr3)-octreotate
Institutional profile and type of centre
Dedicated theragnostic service status (Established /Developing / Not available)
Approximate annual theragnostic procedure volume
Radiopharmaceutical targets used (DOTATATE-based, PSMA-based, and others)
Therapeutic radionuclides administered (177Lu, 131I, 225Ac, 161Tb, and 188Re, and others) with approximate annual dose ranges
Clinical indications treated with radionuclide therapy
Implementation of patient-specific dosimetry and imaging modalities used (SPECT, SPECT/CT, PET/CT, planar imaging)
Main barriers to implementing patient-specific dosimetry
Major challenges categorised into logistics/supply chain, regulatory/policy, and clinical/operational domains
Preferred solutions and support required (training workshops, multicentre protocols, regional supply coordination, guideline development, fellowships)
Willingness to participate in BRICS collaborative initiatives (multicentre research studies, training programs, guideline development)
Additional open-ended comments and suggestions (limited to 100 words)
Data collection
The questionnaire was distributed electronically through a secure online platform. Responses were collected anonymously at the institutional level. No patient-level or identifiable data were gathered. Participating centres were encouraged to provide approximate figures based on institutional records and standard practices.
Data management and statistical analysis
Raw data were exported and cleaned using Microsoft Excel. Country names and categorical responses with minor spelling, capitalisation, or spacing variations were standardised and consolidated. Multi-select questions were analysed, allowing cumulative percentages to exceed 100%. All quantitative variables were summarised using descriptive statistics – frequencies and percentages rounded to one decimal place. No inferential statistical analysis was performed, as the primary aim was to provide a descriptive overview of current practices and challenges.
Data limitations
This study has several limitations. First, the use of purposive and snowball sampling may introduce selection bias, potentially overrepresenting centres with established theragnostic capabilities. Second, data were self-reported and not independently validated, which may introduce reporting bias. Third, variability in response completeness across domains may affect the precision of some estimates. Finally, the cross-sectional design captures practices at a single time point and may not fully reflect the rapidly evolving landscape of theragnostic services.
Ethical considerations
As the survey collected only aggregated, de-identified institutional data and posed no risk to patients or participants, formal ethical approval was not required by most participating institutions. Completion of the questionnaire was considered implied consent. The study was conducted in accordance with the ethical principles of the Declaration of Helsinki.
RESULTS
A total of 137 institutional responses from 14 countries were received between 6 January and 2 April 2026. The highest representation was from India (n = 72, 52.6%), followed by Indonesia (n = 21, 15.3%), South Africa (n = 11, 8.0%), and Brazil (n = 10, 7.3%). Other contributing countries included China (n = 5, 3.6%), Iran (n = 4, 2.9%), the Republic of Belarus (n = 4, 2.9%), Egypt (n = 2, 1.5%), Nigeria (n = 2, 1.5%), and the Russian Federation (n = 2, 1.5%). Single centres participated from Ethiopia, Kazakhstan, Saudi Arabia, and Thailand [Fig 1].

Private hospitals or clinics accounted for most participating centres (51.1%), followed by academic or university hospitals (26.3%) and government or public hospitals (19.0%). Dedicated theragnostic services were established in 71.3% of centres, while 25.0% were still developing and 3.7% had no such service [Table 2].
| Characteristic | Category | Number | Percentage (%) |
|---|---|---|---|
| Centre type | Private hospital/clinic | 70 | 51.1 |
| Academic/University hospital | 36 | 26.3 | |
| Government/Public hospital | 26 | 19.0 | |
| Research institute | 4 | 2.9 | |
| Other | 1 | 0.7 | |
| Dedicated theragnostic service | Established | 97 | 70.8 |
| Developing | 34 | 24.8 | |
| Not available | 5 | 3.6 | |
| Not reported | 1 | 0.7 |
BRICS: BRICS member and associate member states
Annual theragnostic procedure volumes varied widely [Fig 2]. Most centres performed fewer than 200 procedures annually, with 34.3% reporting <50 procedures and 31.4% reporting 50–200 procedures per year. A smaller proportion of centres reported higher volumes, while 4.4% did not report activity levels.

PSMA-based theragnostics, which primarily target prostate-specific membrane antigen (PSMA) in prostate cancer and other PSMA-expressing tumours, were offered by 82.3% of the participating centres. DOTATATE-based therapies, aimed at somatostatin receptor-positive neuroendocrine tumours and related malignancies, were reported by 70.8% of centres. Notably, many institutions offered both platforms simultaneously [Table 3]. With regard to therapeutic radionuclides, iodine-131 (131I) was the most widely administered agent overall (86.1%), followed by lutetium-177 (177Lu) at 73.7%. The leading clinical indications treated with radionuclide therapy were thyroid cancer (90.8%), prostate cancer (82.4%), neuroendocrine tumours (70.2%), and bone metastases (60.3%) [Fig 3].
| Parameter | Category/Indicator | Number of centres | Percentage (%) |
|---|---|---|---|
| Theragnostic platforms (n = 130) | DOTATATE-based theragnostic (for neuroendocrine and other somatostatin receptor– expressing tumours) | 92 | 70.8 |
| PSMA-based theragnostic (primarily for prostate and other PSMA-expressing tumours) | 107 | 82.3 |
BRICS: BRICS member and associate member states; DOTATATE: DOTA-(Tyr3)-octreotate; PSMA: Prostate-specific membrane antigen

Therapeutic radionuclide utilisation was dominated by 131I, which was used by 118 centres (86.1%), followed by 177Lu in 101 centres (73.7%). In contrast, alpha-emitting 225Ac was employed by 20 centres (14.6%), while emerging radionuclides such as 161Tb and 188Re were used less frequently (10 centres, 7.3% and 6 centres, 4.4%, respectively), with other radionuclides reported by 36 centres (26.3%) [Fig 4].

Participants were asked to report the approximate number of therapeutic doses administered per year for each of five radionuclides: 177Lu, 131I, 225Ac, 161Tb, and 188Re. 177Lu was the most widely used radionuclide, with 29.9% of centres (n = 41) administering 11–50 doses annually and 18.2% (n = 25) administering 1–10 doses per year. Only 7 centres (5.1%) reported not using 177Lu at all. 131I was also extensively used, with 34 centres (24.8%) reporting 51–100 doses and a further 43 centres (31.4%) administering more than 100 doses annually. In contrast, 225Ac and 161Tb demonstrated considerably lower values, with nearly half the centres leaving dose volumes unreported, suggesting limited or nascent implementation. 188Re showed a similar pattern. The distribution of annual dose volumes by radionuclide is presented in Table 4.
| Dose range | 177Lu | 131I | 225Ac | 161Tb | 188Re |
|---|---|---|---|---|---|
| Not used | 7 (5.1) | 2 (1.5) | 20 (14.6) | 21 (15.3) | 22 (16.1) |
| 0 doses | 13 (9.5) | 3 (2.2) | 30 (21.9) | 36 (26.3) | 35 (25.5) |
| 1–10 | 25 (18.2) | 6 (4.4) | 10 (7.3) | 4 (2.9) | 4 (2.9) |
| 11–50 | 41 (29.9) | 29 (21.2) | 4 (2.9) | 5 (3.6) | < 5 (< 3.6) |
| 51–100 | 18 (13.1) | 34 (24.8) | 1 (0.7) | 0 (0) | 0 (0) |
| > 100 | 11 (8.0) | 43 (31.4) | 1 (0.7) | 0 (0) | 0 (0) |
| Not | 22 (16.1) | 20 (14.6) | 71 (51.8) | 71 (51.8) | 76 (55.5) |
Note: Values represent the number of centres (n) and column percentages (%) within each dose range category. ‘Not reported’ includes blank responses and entries coded as data entry errors (e.g., date-format artefacts). Centres reporting 0 doses were distinguished from those explicitly indicating the radionuclide was not used. Lu: Lutetium; I: Iodine; Ac: Actinium; Tb: Terbium; Re: Rhenium.
Patient-specific dosimetry remained limited. Slightly more than half of the participating centres (n = 70, 51.1%) reported that patient-specific dosimetry was not performed. Among the remaining centres, it was conducted selectively in 35.8% (n = 49) and routinely in 8.0% (n = 11). SPECT/CT was the most commonly used imaging modality for dosimetry. When applied, the most frequently cited indications were 131I therapy, 177Lu therapies, and research protocols. A substantial proportion of centres (n = 43, 31.4%) did not specify an applicable indication. Dosimetry-related findings, including barriers, are detailed in Table 5.
| Characteristic | n | % |
|---|---|---|
| Patient-specific dosimetry performed | ||
| No | 70 | 51.1 |
| Yes, selectively | 49 | 35.8 |
| Yes, routinely | 11 | 8.0 |
| Not reported | 7 | 5.1 |
| Dosimetry imaging modality used | ||
| Not performed | 54 | 39.4 |
| SPECT/CT only | 27 | 19.7 |
| SPECT/CT + PET/CT | 13 | 9.5 |
| SPECT/CT + Planar imaging | 15 | 10.9 |
| SPECT/CT + PET/CT + Planar imaging | 10 | 7.3 |
| PET/CT only | 4 | 2.9 |
| Planar imaging only | 4 | 2.9 |
| Not reported | 10 | 7.3 |
| Indications for which dosimetry is applied | ||
| 131I therapies only | 22 | 16.1 |
| 177Lu therapies only | 19 | 13.9 |
| 177Lu + 131I therapies | 13 | 9.5 |
| Research protocols only | 26 | 19.0 |
| Multiple combined indications | 14 | 10.2 |
| Not applicable / not reported | 43 | 31.4 |
Note: All 137 centres responded. “Not reported” includes blank entries. Imaging modalities were consolidated from free-text and multi-select responses. “Multiple combined indications” refers to responses citing three or more indications. SPECT/CT: Single photon emission tomography/computed tomography; PET/CT: Positron emission tomography/computed tomography
Among the 124 centres that indicated at least one barrier to dosimetry implementation, the most commonly cited obstacle was limited software or hardware (estimated n = 93, 75.0% of respondents), followed by time constraints (n = 66, 53.2%), and lack of expertise or training (n = 56, 45.2%). Lack of reimbursement was noted by approximately one third of responding centres (n = 45, 36.3%), whereas regulatory limitations were reported less frequently (n = 12, 9.7%). Thirteen centres (9.5%) indicated that barriers were not applicable, consistent with the subsection of centres already performing dosimetry routinely. Barrier frequencies are presented in Table 6.
| Barrier | n* | %* |
|---|---|---|
| Limited software or hardware | 93 | 75.0 |
| Time constraints | 66 | 53.2 |
| Lack of expertise/training | 56 | 45.2 |
| Not reimbursed | 45 | 36.3 |
| Regulatory limitations | 12 | 9.7 |
| No barrier reported (not applicable) | 13 | 9.5 |
Note: As this was a “select all that apply” item, responses consisted of unique combination strings. Barrier frequencies were estimated by counting the occurrence of each barrier across all combinations and are marked with an asterisk (*). Percentages are based on the 124 centres that reported at least one barrier and may therefore exceed 100%.
Centres were asked to identify major challenges across three domains: logistics and supply chain, regulatory and policy, and clinical and operational. As shown in Table 6, the dominant logistics challenge was limited availability of radionuclides, cited by an estimated 82.4% of responding centres (n = 98 of 119). Import and export delays constituted the second most common supply-chain barrier (n = 67, 56.3%). In the regulatory domain, lack of harmonised regulations was the most frequently identified challenge (n = 74, 72.5% of 102 respondents), followed by licensing and authorisation delays (n = 57, 55.9%). Restrictions specifically pertaining to alpha-emitting radionuclides were noted by 42.2% of regulatory-domain respondents (n = 43). Clinically, reimbursement and funding difficulties were cited by the largest proportion of responding centres (n = 96, 77.4% of 124), with insufficient trained personnel (n = 83, 67.0%) and patient referral pathway deficiencies (n = 79, 63.7%) also emerging as prominent concerns [Table 7].
| Domain | Category | n | % |
|---|---|---|---|
| Logistics and supply chain (n= 119 respondents) | Limited availability of radionuclides | 98 | 82.4 |
| Import/export delays | 67 | 56.3 | |
| Transportation and cold-chain issues | 29 | 24.4 | |
| Short half-life constraints | 27 | 22.7 | |
| Reimbursement and funding issues | 1 | 0.8 | |
| Regulatory and policy (n= 102 respondents) | Lack of harmonised regulations | 74 | 72.5 |
| Licensing and authorisation delays | 57 | 55.9 | |
| Radiation safety compliance burden | 45 | 44.1 | |
| Restrictions on alpha-emitting radionuclides | 43 | 42.2 | |
| Clinical and operational (n= 124 respondents) | Patient referral pathways | 79 | 63.7 |
| Reimbursement and funding issues | 96 | 77.4 | |
| Insufficient trained personnel | 83 | 67.0 | |
| Infrastructure limitations (hot labs, isolation wards) | 39 | 31.5 |
Note: Challenges were assessed using three separates ‘select all that apply’ items. Individual frequencies were estimated by tallying each challenge across all response combination strings. Percentages within each domain may exceed 100% as multiple challenges could be selected.
Among the 130 centres that responded regarding preferred solutions, the most frequently requested support included the development of multicentre clinical protocols (66.9%), fellowships or exchange programmes (62.3%), structured training programmes in radionuclide therapy (59.2%), hands-on dosimetry workshops (58.5%), and regional radionuclide supply coordination (57.7%). These priorities reflect a strong collective desire for practical capacity-building, harmonised guidelines, and improved logistical support.
Centres demonstrated a high willingness to engage in future collaborative initiatives. The majority (n = 100, 73.0%) indicated readiness to participate in all three proposed initiative types: multicentre research studies, training and capacity-building initiatives, and guideline development projects. A further 6.6% (n = 9) indicated willingness to participate in multicentre research studies alone, and 4.4% (n = 6) in training initiatives alone. Only a small minority restricted their willingness to guideline development exclusively (n = 1, 0.7%), and 5.1% (n = 7) did not provide a response. Collectively, 95.6% of responding centres expressed willingness to participate in at least one type of collaborative initiative. The distribution of participation preferences is summarised in Table 8.
| Domain | Category | n | % |
|---|---|---|---|
| Solutions most beneficial to centres (n= 130) | Structured training programs in radionuclide therapy | 77 | 59.2 |
| Hands-on dosimetry workshops (SPECT/PET) | 76 | 58.5 | |
| Multicentre clinical protocols | 87 | 66.9 | |
| Regulatory guidance and harmonisation efforts | 62 | 47.7 | |
| Regional radionuclide supply coordination | 75 | 57.7 | |
| Fellowships/exchange programs | 81 | 62.3 | |
| Willingness to participate in BRICS collaboration (n= 137) | All three (multicentre research + training + guideline development) | 100 | 73.0 |
| Multicentre research studies only | 9 | 6.6 | |
| Training and capacity-building only | 6 | 4.4 | |
| Multicentre research + training | 6 | 4.4 | |
| Guideline development only | 1 | 0.7 | |
| Multicentre research + guideline development | 3 | 2.2 | |
| Multicentre research + training + guideline (alt. format) | 4 | 2.9 | |
| Training + guideline development | 1 | 0.7 | |
| Not reported | 7 | 5.1 |
Note: Categories reflect the original multi-select response combinations as captured in the dataset. The entry “Multicentre research + training + guideline (alt. format)” includes four responses recorded with forward slashes instead of commas; these are semantically equivalent to the main “all three” category. BRICS: BRICS member and associate member states; SPECT/PET: Single photon emission computed tomography/computed tomography
Seventy-one respondents provided additional narrative comments. These comments most commonly reinforced themes of radionuclide supply constraints, treatment affordability and reimbursement issues, workforce shortages, and the urgent need for affordable dosimetry software and structured training. Several centres also highlighted the development of referral networks and cross-border collaboration as important enablers of programme growth.
DISCUSSION
The BRICS Multicentre Theragnostic Survey 2026 represents a landmark collaborative effort among nuclear medicine centres across BRICS member and partner countries. This first-of-its-kind multicentre study systematically characterises current theragnostic practices, identifies key operational and systemic challenges, and highlights strategic opportunities to advance precision radionuclide therapy across the region. Building on decades of progress since the early clinical application of radioactive iodine in the 1940s, nuclear medicine has evolved into a multidisciplinary field that integrates functional and molecular imaging with targeted radionuclide therapy. This transformation has enabled increasingly precise, non-invasive characterisation of disease at the cellular level and expanded the role of nuclear medicine across a wide range of clinical specialties. Within this evolving landscape, theragnostic has emerged as a pivotal advancement, enabling integrated diagnosis, treatment, and response assessment within a single molecular pathway, thereby enhancing clinical decision-making and therapeutic precision. However, a marked global disparity in nuclear medicine infrastructure persists. High-income countries typically have substantially greater densities of facilities and trained workforce—often 5–20 times higher per million population—compared with BRICS member and partner countries, many of which have only 0.3–1 centre or scanner per million inhabitants.[18] This imbalance underscores the critical need for scalable, decentralised, and collaborative models to expand equitable access to theragnostic services across the BRICS network.
Current landscape of theragnostic practices in BRICS and oncology burden
The foundation for enhanced BRICS collaboration in nuclear medicine and theragnostics was laid at the first BRICS International Forum on Nuclear Medicine, held in Saint Petersburg, Russia, from 19–21 June 2024. Jointly organised by the Russian Ministry of Health and the State Corporation Rosatom, the forum brought together approximately 200 participants from BRICS member countries (Brazil, Russia, India, China, and South Africa) as well as associate members from Iran, the United Arab Emirates, Saudi Arabia, Egypt, and Ethiopia. Over four technical sessions, delegates addressed critical topics including education and training in nuclear medicine and radiopharmacy, radiopharmacy industry growth, equipment availability, production of key radionuclides (99Mo, 131I, 177Lu, and 225Ac), clinical trials and regulatory harmonisation, and the development of innovative radiopharmaceuticals.[19] This landmark meeting underscored the growing momentum for regional cooperation and directly contributed to the establishment of the BRICS Nuclear Medicine Working Group, reflecting growing momentum for coordinated regional action.
Theragnostics has evolved as a key modality in precision oncology, integrating molecular imaging and targeted radionuclide therapy via shared tumour-specific biomarkers. This “see-and-treat” strategy employs PET or SPECT for patient stratification and disease characterisation, followed by administration of the same ligand labelled with β- or α-emitting radionuclides. Table 9 describes the currently approved therapeutic radionuclide therapies in oncology as of March 2026. Most approved therapies are beta-emitting agents, with increasing adoption of alpha-emitter therapies and ongoing development of novel radionuclides and molecular targets expanding the theragnostic landscape. Randomised trials, including the NETTER-1, NETTER-2 trials and VISION trial, have demonstrated significant improvements in overall survival and quality of life, reinforcing its clinical utility across diverse tumour types, including breast, pancreatic, sarcoma, hepatocellular and colorectal cancers.[7-14]
| Agent (trade names) | Radionuclide | Emission | Molecular target | Primary indication | Regulatory approval |
|---|---|---|---|---|---|
| Lutetium-177 dotatate (Lutathera®; generic formulations) | 177Lu | B;γ | Somatostatin receptor (SSTR2) | Gastroenteropancreatic neuroendocrine tumours (GEP-NETs); SSTR2-positive tumours | FDA (2018; paediatrics extension 2024), EMA (2017) |
| Lutetium-177 vipivotide tetraxetan (Pluvicto®) | 177Lu | B;γ | PSMA | PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) | FDA (2022; expanded 2025), EMA (2022) |
| Radium-223 dichloride (Xofigo®) | 223Ra | α | Bone metastases (calcium analogue) | Symptomatic bone metastases in mCRPC | FDA (2013), EMA (2013) |
| Ibritumomab tiuxetan (Zevalin®) | 90Y | β | CD20 (B-cells) | Relapsed/refractory low-grade or follicular non-Hodgkin lymphoma | FDA (2002); limited EMA use |
| Sodium iodide I-131 | 131I | B;γ | Sodium iodide symporter | Thyroid cancer and hyperthyroidism | Longstanding FDA/EMA approval |
| Iobenguane I-131 (Azedra®) | 131I | B;γ | Norepinephrine transporter | Pheochromocytoma/paraganglioma | FDA (2018); limited availability |
| Strontium-89 chloride (Metastron®; generics) | 89Sr | β | Bone metastases (calcium analogue) | Pain palliation in metastatic bone disease | FDA (1993); limited current use |
Keynote: Most approved therapies are beta-emitting agents, with increasing adoption of alpha-emitter therapies and ongoing development of novel radionuclides and molecular targets expanding the theragnostic landscape. β=Beta-emitter, γ=Gamma emitter; α=Alpha-emitter. GEP-NETs: Gastroenteropancreatic neuroendocrine tumours; PSMA: Positive metastatic castration-resistant prostate cancer; FDA: Food and Drug Administration (United States of America); EMA: European Medicines Agency; mCRPC: Metastatic castration-resistant prostate cancer; CD20: Cluster of differentiation 20; SSTR2: Somatostatin receptor subtype 2; α: Alpha emitter; β: Beta emitter; γ: Gamma emitter
Despite these advances, BRICS nations—representing approximately 4.0 billion people, nearly half of the global population—face a disproportionately high and rapidly increasing cancer burden.[20] However, theragnostic infrastructure remains limited relative to demand, with advanced services concentrated in major urban centres. This imbalance underscores the urgent need for decentralised and scalable theragnostic models, including the development of satellite centres, to improve access and meet the growing demand for precision oncology across the BRICS network.
Institutional profile and annual theragnostic workload
The survey of 137 centres from 14 countries provides the first comprehensive snapshot of theragnostic practices within the BRICS ecosystem. The participating centres showed notable diversity in institutional type, with private hospitals or clinics comprising the majority (51.1%), followed by academic or university hospitals (26.3%) and government or public hospitals (19.0%). Dedicated theragnostic services were already established in 71.3% of the 136 centres reporting this information, while 25.0% were still developing, and 3.7% had no such service among centres reporting annual theragnostic activity; most operated at low to moderate procedural volumes. A total of 47 centres (34.3%) performed fewer than 50 procedures per year, while 43 centres (31.4%) reported performing between 50 and 200 procedures annually. Higher-volume activity was less common, with 23 centres (16.8%) performing 201–500 procedures and 18 centres (13.1%) reporting more than 500 procedures per year. A small proportion of centres (6, 4.4%) did not report their annual procedural volume. The predominance of low- to moderate-volume centres suggests that, while theragnostic services are increasingly established across the BRICS network, they have not yet reached full operational scale. Most centres continue to deliver services at relatively modest procedural volumes, with only a small proportion functioning as high-volume hubs. This distribution reflects an early-to-intermediate stage of programme maturity, where infrastructure and clinical capability are in place but not yet optimally utilised. It also underscores the need for targeted capacity-building initiatives, improved referral pathways, and strategic decentralisation to expand access and enhance service efficiency across the region.
Key clinical activity and practice patterns
Clinical activity and practice patterns revealed a strong focus on prostate and neuroendocrine tumours, alongside the long-standing dominance of thyroid cancer management. The widespread adoption of PSMA-based theragnostics highlights the rapid uptake of prostate cancer–focused radioligand therapy across BRICS centres. In this survey, PSMA-targeted therapies were available in 82.3% of centres, while DOTATATE-based therapies were reported by 70.8%, reflecting the broad integration of targeted radioligand therapy into clinical practice. This high level of adoption underscores the central role of prostate cancer and neuroendocrine tumours as primary drivers of theragnostic implementation in the region. Notably, the substantial overlap between PSMA and DOTATATE platforms suggests that advanced theragnostic capabilities are concentrated within centres that have already established the necessary infrastructure, expertise, and multidisciplinary workflows. Collectively, these findings indicate not only strong momentum in the uptake of established theragnostic applications but also a solid foundation for expanding into emerging molecular targets and novel radionuclide therapies across the BRICS network. In addition to these established targets, several centres reported using Fibroblast Activation Protein Inhibitor (FAPI)-based theragnostics and other emerging agents.
Regarding therapeutic radionuclides, 131I was the most frequently used (86.1%), followed by 177Lu (73.7%). Other radionuclides were reported by 24.1% of centres, while 225Ac was employed by 14.6%, 161Tb by 6.6%, and 188Re by 2.9%. Notably, 188Re benefits from on-site generator production, offering greater logistical efficiency and more reliable therapy access in resource-limited settings. Meanwhile, 161Tb, with its combined beta and Auger electron emission, is showing promising theragnostic results in early clinical studies.[21-23]
The leading clinical indications were thyroid cancer (90.8%), prostate cancer (82.4%), neuroendocrine tumours (70.2%), and bone metastases (60.3%). Hepatocellular carcinoma was treated in 29.8% of centres, with a smaller proportion reporting lymphoma and other malignancies. These patterns indicate that while core theragnostic applications are well established, there is growing interest in expanding to additional molecular targets and tumour types across the BRICS region.
Patient-specific dosimetry practice, imaging modalities, dosimetry indications, and implementation barriers
Patient-specific dosimetry was performed in less than half of the participating centres. Slightly more than half (51.1%, n = 70) reported that they did not perform patient-specific dosimetry at all, while it was applied selectively in 35.8% (n = 49) and routinely in only 8.0% (n = 11). Among centres that did perform dosimetry, SPECT/CT was the predominant imaging modality, used either alone or in combination with other techniques. When dosimetry was implemented, it was most commonly applied to 131I therapies, 177Lu therapies, or research protocols. A notable proportion of centres (31.4%, n = 43) did not specify any particular indication for dosimetry, which aligns with the large number of centres that reported not performing it. The limited adoption of patient-specific dosimetry represents a significant gap between guideline recommendations and real-world clinical practice. As detailed in Tables 5 and 6, quantitative dosimetry remains underutilised across BRICS centres, with most institutions either not implementing it or applying it selectively. This disparity highlights key barriers, including limited access to appropriate software and hardware, insufficient training, and the lack of standardised, practical protocols. Addressing these challenges will be essential to support wider implementation of dosimetry, optimise treatment personalisation, and align clinical practice with evolving international standards in theragnostic care.[24,25]
Major challenges identified
The survey revealed several interconnected challenges that currently limit the expansion of theragnostic services across BRICS nations. In the logistics and supply chain domain, limited availability of therapeutic radionuclides was the most prominent barrier, reported by 82.4% of responding centres, followed by import/export delays (56.3%). Regulatory and policy challenges were also substantial, with a lack of harmonised regulations cited by 72.5% and licensing or authorisation delays by 55.9% of respondents in this domain. Restrictions on alpha-emitting radionuclides further complicated practice for 42.2% of centres. On the clinical and operational side, reimbursement and funding issues emerged as the leading concern (77.4%), followed closely by insufficiently trained personnel (67.0%) and suboptimal patient referral pathways (63.7%). Infrastructure limitations, including inadequate hot laboratories and isolation wards, were noted by 31.5% of centres. These findings highlight systemic barriers spanning supply security, regulatory fragmentation, workforce capacity, and financial constraints that collectively hinder equitable access to theragnostic therapies.
Capacity building, infrastructure solutions, and strategic advantages
We recognise that BRICS nations are diverse in culture, population size, and healthcare infrastructure. Nevertheless, the burden of cancer and its associated morbidity and mortality is shared uniformly across the region.[20] Theragnostic offers life-saving treatment options for a wide range of malignancies, including prostate cancer, neuroendocrine tumours, and thyroid cancer, with potential expansion to many other tumour types, while providing a favourable therapeutic index and better quality of life compared with many conventional therapies.[7-14] Given the rapidly increasing demand and the current concentration of advanced services in a limited number of urban centres, the expansion and decentralisation of theragnostic services must be prioritised. To address the growing demand and enhance access across diverse settings, the establishment of satellite and decentralised theragnostic therapy centres presents a feasible and strategically important solution. A basic functional theragnostic centre requires SPECT or SPECT/CT for imaging, diagnostic receptor imaging using 99mTc with peptide kits, baseline renogram, and post-therapy scanning with SPECT or SPECT/CT. Safe preparation of 177Lu-labelled therapies necessitates a dedicated hot laboratory with appropriate shielding, validated quality control, and regulatory compliance.[26] Manual labelling with reagent kits remains the most flexible, cost-effective, and easily teachable approach for new or smaller centres, making it particularly suitable for decentralised expansion across BRICS nations.
A distinct strength of the BRICS network lies in the advanced and efficient domestic radionuclide production capabilities of Russia, China, South Africa, and Iran. These countries have demonstrated reliable capacity to supply key therapeutic isotopes, including 131I, 177Lu, and 225Ac (as well as 99mMo for generator-based imaging). Complementing this production advantage is the availability of highly experienced experts within the BRICS Nuclear Medicine community, who are well-positioned to provide training, mentorship, and technical support for infrastructure development in emerging centres. This unique combination of manufacturing capacity and human expertise represents a major regional asset that can significantly accelerate the safe expansion and decentralisation of theragnostic services across BRICS nations.[19]
Opportunities for BRICS collaboration
Despite these limitations, this study represents the largest multicentre assessment of theragnostic practices across BRICS nations to date, providing valuable real-world insights into current capabilities and challenges. The findings highlight clear priorities for strengthening theragnostic capacity, with a strong emphasis on workforce development, standardisation, and collaborative infrastructure.
Key areas identified include the development of multicentre clinical protocols (66.9%), fellowships or exchange programmes (62.3%), and structured training programmes in radionuclide therapy (59.2%), closely followed by hands-on dosimetry workshops (58.5%) and improved regional coordination of radionuclide supply (57.7%). Together, these priorities underscore the critical role of training and harmonised clinical practice in addressing disparities arising from variable expertise, infrastructure, and resource availability across participating countries.
Additionally, nearly half of centres emphasised the need for regulatory guidance and harmonisation (47.7%), reflecting persistent challenges related to fragmented regulatory frameworks and inconsistent approval pathways. Encouragingly, willingness to engage in collaborative BRICS initiatives was high, with 73.0% of centres expressing readiness to participate across all major domains, including multicentre research, training, and guideline development. Overall, more than 95% of centres indicated willingness to engage in at least one form of collaboration, demonstrating strong momentum for coordinated, network-driven approaches to advancing theragnostic services across the region.
To address the identified gaps, the BRICS Nuclear Medicine Working Group has outlined several priority solutions as part of a sustained post-survey initiative. These include structured capacity building to establish new theragnostic centres, radiopharmaceutical support, clinical expertise sharing, and improved access to essential resources. In particular, the development of regional regulatory harmonisation frameworks, centralised radionuclide procurement models, and designated training hubs will be critical to reducing fragmentation, improving supply reliability, and strengthening workforce capacity across the network. Collaboration can be further enhanced through improved logistics coordination, streamlined customs clearance processes, reliable regional isotope supply chains, multicentre clinical trials, regular networking events, joint task forces, and the development of standardised clinical protocols. Additional key actions include promoting the decentralisation of theragnostic services through the establishment of basic SPECT and hot-lab facilities as accessible therapy entry points, alongside regulatory alignment to facilitate more efficient and timely patient care [Fig 5].

Successful implementation of these strategies will require sustained commitment and coordination among key stakeholders — including governments, regulatory authorities, academic institutions, and industry partners — to ensure scalable and equitable expansion of theragnostic services. The BRICS Nuclear Medicine Working Group provides a strong platform to support this effort through structured training programmes, expert mentorship, infrastructure guidance, and regional collaboration, enabling established centres to support emerging programmes and collectively advance theragnostic care across the region.
CONCLUSION
The BRICS Multicentre Theragnostic Survey 2026 highlights both substantial progress and persistent disparities in the implementation of theragnostic services across BRICS member and partner countries. While dedicated services are established in the majority of centres and key platforms such as PSMA- and DOTATATE-based therapies are widely adopted, important challenges remain, particularly in radionuclide availability, reimbursement and funding, regulatory fragmentation, infrastructure limitations, and workforce capacity. BRICS nations are uniquely positioned to develop resilient and collaborative theragnostic ecosystems by leveraging their combined expertise, production capabilities, and expanding clinical networks. Coordinated action through the BRICS Nuclear Medicine Working Group will be critical to translating this potential into scalable, cost-effective, and sustainable solutions. Strategic priorities include strengthening regional radionuclide supply chains, advancing regulatory harmonisation, expanding structured training programmes, and supporting the decentralisation of services through accessible SPECT and hot-lab infrastructure, alongside the promotion of multicentre research initiatives.
Collectively, these efforts have the potential to accelerate equitable access to high-quality theragnostic care and improve clinical outcomes for patients across a broad spectrum of malignancies. If successfully implemented, these coordinated strategies could position the BRICS network as a global leader in delivering equitable, scalable, cost-effective, and innovation-driven theragnostic care.
Acknowledgement:
The authors would like to express their sincere gratitude to all the Heads of Departments and responsible persons from the participating nuclear medicine and theragnostic centres for their valuable time, cooperation, and willingness to contribute to this multicentre survey. Their active participation and insightful responses have been instrumental in providing a comprehensive overview of theragnostic practices across the BRICS nations and partner countries, and in advancing collaborative efforts within the BRICS healthcare framework.
Author contributions:
MM, OM, VR, and PE: Conceived and designed the study, developed the survey methodology, coordinated data collection, performed data analysis and interpretation, and contributed substantially to the drafting, critical revision, and final approval of the manuscript; YT, OM, PSD, PSC, OUK, JA, MA, TSD, SL, TG, ECE, TT, and HM: Contributed to data acquisition and validation from their respective countries and institutions, provided critical review and scientific input, assisted with manuscript revisions, and approved the final version for publication. All authors reviewed and approved the final manuscript and agree to be accountable for all aspects of the work.
Ethical approval:
Institutional Review Board approval is not required as it involved the collection of anonymous, aggregated institutional-level data without any patient identifiers or individual participant information. The survey was conducted in accordance with the ethical principles of the Declaration of Helsinki.
Declaration of patient consent:
Patient's consent is not required as patients’ identity is not disclosed or compromised.
Conflicts of interest:
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
Financial support and sponsorship: Nil.
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