European urology oncology
September 11, 2026 · via Europe PMC
Feasibility and Characterization of Immune-related Pathologic Response Criteria in Renal Cell Carcinoma.
Croll BJ, Yahya HA, Fredette J, +15 more, Geynisman DM.
AI summary — for doctors, generated from the abstract only
Immune-related pathologic response criteria were feasible in all 37 RCC tumors after systemic combination therapy, identifying major pathologic response in 35% and revealing poor correlation with radiographic response.
What was studied
Retrospective cohort of 35 patients (37 tumors) with RCC resected after systemic combination therapy, applying irPRC endorsed by the International Neoadjuvant Kidney Cancer Consortium.
Key findings
- irPRC applicable in all cases
- Major pathologic response in 35% of tumors
- Substantial heterogeneity in tumor bed components beyond tumor fraction
- All 11 patients recurring within 6 months had necrosis-predominant tumor beds with no tissue repair features
- Nearly one-third of major pathologic responders lacked significant radiographic improvement
Clinical relevance
This supports standardized immune-related pathologic reporting in RCC research and cautions against relying on imaging alone to judge response, though the cohort is small and retrospective.
Who should care
Limitations
Small retrospective cohort; heterogeneous systemic therapies; exploratory associations with recurrence.
Pathology after immunotherapy in kidney cancer can reveal responses imaging misses, and standardized criteria make that assessment feasible.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Pathologic assessment of treatment response in renal cell carcinoma (RCC) after systemic combination therapy is increasingly relevant, yet traditional reporting methods fail to capture unique immune-mediated changes, and a lack of standardized reporting recommendations has led to discordant clinical trial definitions. We evaluated the feasibility and implementation of immune-related pathologic response criteria (irPRC), recently endorsed by the International Neoadjuvant Kidney Cancer Consortium, in a retrospective cohort of 35 patients (37 tumors). Application of irPRC was feasible in all cases and identified major pathologic response in 35% of the tumors. Tumor bed evaluation based on irPRC components revealed substantial heterogeneity, highlighting the limitations of relying on tumor fraction alone. All patients (N = 11) experiencing recurrence within 6 mo of surgery exhibited necrosis-predominant tumor beds and a complete absence of tissue repair features, suggesting an area for additional research. In addition, radiographic response correlated poorly with pathologic findings; nearly one-third of major pathologic responders lacked significant radiographic improvement. These findings support the feasibility of irPRC in RCC and underscore the limitations of current radiographic and traditional pathologic response assessments. Broader adoption of standardized immune-related pathologic response frameworks may improve consistency in reporting and better reflect underlying tumor biology in clinical research.
DOI
10.1016/j.euo.2026.08.007
PMID
42728152
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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