Identifying Regional Kidney Cancer Needs Via International Collaboration

Commentary
Video

Large international meetings may facilitate conversations regarding disparities of care outside of high-income countries.

According to Regina Barragan-Carrillo, MD, establishing trust between high-income countries and their international counterparts could be beneficial in building programs for clinical collaboration in kidney cancer, bringing contemporary research to countries with income disparities.

CancerNetwork® spoke with Barragan-Carrillo, postdoctoral fellow of medical oncology and medical therapeutics at City of Hope Comprehensive Cancer Center in Duarte, CA, about what other institutions can do or keep in mind to help mitigate disparities in clinical trial availability for renal cell carcinoma (RCC).

Barragan-Carrillo expressed that the scope of the issue was beyond anything a single institution could solve, emphasizing that the issue required international collaboration to mitigate. To this end, she expressed that the establishment of trust between institutions in high-income countries and their international counterparts may help in building connections that prevent research gatekeeping.

Furthermore, she explained that meetings like the 2025 ASCO Genitourinary Cancers Symposium may help facilitate the conversations necessary to identify the needs of international practices and to discuss the establishment of programs to address these issues. She further iterated that a lack of open discussion regarding these disparities will result in greater difficulty in overcoming these barriers.

Results from a real-world analysis study Barragan-Carrillo presented at the ASCO Genitourinary Cancers Symposium revealed that RCC clinical trials were disproportionately concentrated in high-income countries (HICs), with only a fraction of trials accessible to upper-middle-income countries (UMICs), lower-middle-income-countries (LMICs), and lower-income countries (LICs). Furthermore, a direct association between expenditure for health, mortality, age standardized incidence rate, and trial availability was found.

Data from the trial revealed that of 357 clinical trials included in the analysis, 84 were available in UMICs, LMICs, and LICs in addition to HICs, as opposed to 273 that were only available in HICs. Additionally, 92.3% (odds ratio [OR], 0.056; 95% CI, 0.018-0.176; P <.001) of LMICs and 100% (OR, 0.013; 95% CI, 0.001-0.228; P = .003) of LICs had no RCC trials available.

Transcript:

To be honest, I do not think [RCC trial availability] is something that a single institution would be able to solve, being such an international problem. But something important on the institutional level is to trust the partners we have in other countries, to start building these bridges and not gatekeeping your research efforts in a certain region. This meeting, for example, the ASCO [Genitourinary Cancers Symposium], is a great way to establish conversations and to reach out to people from other nations and to understand their needs. How can we start building these programs? Because if we do not talk about it, and if we do not make a statement and understand that the problem is existing in many countries, it is going to be hard to start taking actions to solve it.

Reference

Barragan-Carrillo R, Zugman M, Castro D, et al. Assessing global disparities in clinical trial availability for renal cell carcinoma (RCC). J Clin Oncol. 2025;43(suppl 5):449. doi:10.1200/JCO.2025.43.5_suppl.449


Newsletter

Stay up to date on recent advances in the multidisciplinary approach to cancer.

Recent Videos
“It’s a drug that I’m very comfortable with, and it is a drug I’ll likely use primarily in the first-line setting,” stated Jorge Nieva, MD, on taletrectinib in non–small cell lung cancer.
Those being treated for peritoneal carcinomatosis may not have to experience the complication rates or prolonged recovery associated with surgical options.
For patients with peritoneal carcinomatosis, integrating PIPAC into a treatment regimen does not interrupt their systemic therapy.
According to Benjamin J. Golas, MD, PIPAC could be used as a bridging therapy before surgical debulking or between subsequent large surgical operations.
“If you have a [patient in the] fourth or fifth line, [JNJ-5322] could be a valid drug of choice,” said Rakesh Popat, BSc, MBBS, MRCP, FRCPath, PhD.
Earlier treatment with daratumumab may be better tolerated for patients with pretreated MRD-negative multiple myeloma.
The trispecific antibody JNJ-5322 demonstrated superior efficacy vs approved agents in multiple myeloma in results shared at the 2025 EHA Congress.
Despite CD19 CAR T-cell therapy exhibiting efficacy in patients with relapsed/refractory large B-cell lymphoma, less than half achieve long-term remission.
Related Content