International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) classification and regression tree analysis to characterize objective response rates (ORR) in metastatic renal cell carcinoma (mRCC).

4532 Background: Therapies for mRCC have evolved significantly, making treatment decisions more complex. We used machine learning (ML) to identify whether this could help identify subgroups of patients who have a high probability of response. Methods: Patients from IMDC were identified and a ML classification and regression tree analysis was conducted, in which we grew a complex tree up to a depth of 30 with a minimum node split size of 2 with no constraints on the cost-complexity parameter. The resulting tree was pruned according to the cost-complexity parameter that minimized the leave one out cross-validated error rate and had a minimum bucket size of 25 patients. Results: 2,549 patients were included, 73.2% male, 13.5% non-clear cell histology, 70.3% nephrectomy, and 19.4%, 54.2%, and 26.4% had favorable, intermediate and poor IMDC risk respectively. 1L treatment regimens consisted of VEGF inhibitors (51.5%), IO-IO combinations (32.3%), and IO-TKI combinations (16.2%). The ORR was 36.0% overall, with 29.6% for VEGF inhibitors, 39.1% for IO-IO, and 50.2% for IO-TKI combinations. ML identified 5 hierarchal variables —therapy type, prior nephrectomy (PN), lung metastasis (LM), other metastases, and age— that divided patients into 7 different categories with different response probabilities (see Table). VEGF therapy showed the poorest response, with no additional variables able to predict response. The best ORR was observed in patients treated with IO-TKI and PN; and in those treated with IO-IO, PN, and only lung metastasis. Factors associated with poorer responses included non-clear cell histology, older age, bone and liver metastases, poor performance status, elevated neutrophils, and poor IMDC risk score. Conclusions: This large-scale ML analysis identified five key clinical variables that predict treatment response in mRCC, with treatment type emerging as the primary determinant. These results suggest that treatment selection for mRCC could potentially be optimized by considering these hierarchical variables, though further validation is needed. ML analysis results: Groups of patients and associated outcomes. Risk Groups N (%) ORR (%) Odd Ratio TTNT 18-month survival 1) VEGF 1313 (51.5) 29.6 Ref. 9.4 (8.6-10.3) 0.62 (0.59-0.65) 2) IO-IO or IO-TKI and no PN 443 (17.4) 35.0 1.28 (1.02-1.60) 10.2 (8.8-11.3) 0.59 (0.55-0.65) 3) IO-IO and PN a) No LM 137 (5.4) 29.2 0.98 (0.66-1.43) 17.2 (10.6-30.1) 0.85 (0.78-0.92) b) LM and other met 267 (10.5) 43.8 1.87 (1.42-2.44) 13.0 (10.1-20.5) 0.78 (0.72-0.83) c) Only LM 85 (3.3) 60.0 3.56 (2.28-5.63) 39.2 (14.4-NA) 0.93 (0.87-0.99) 4)IO-TKI and PN a) Age 70+ 78 (3.2) 43.6 1.84 (1.15-2.91) 35.7 (19.8-NA) 0.80 (0.71-0.91) b) Age < 70 226 (8.9) 58.4 3.34 (2.50-4.47) 24.7 (22.4-36.4) 0.88 (0.84-0.93) Overall 2549 36.0 11.5 (10.7-12.2) 0.68 (0.67-0.70)

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Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.4532
Primary Topic
Renal cell carcinoma treatment
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article

International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) classification and regression tree analysis to characterize objective response rates (ORR) in metastatic renal cell carcinoma (mRCC).

Martín Zarbá, David Maj, Razane El Hajj Chehade, J. Connor Wells et al.
Journal of Clinical Oncology
Renal cell carcinoma treatment
article

International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) classification and regression tree analysis to characterize objective response rates (ORR) in metastatic renal cell carcinoma (mRCC).

Martín Zarbá, David Maj, Razane El Hajj Chehade, J. Connor Wells, Benoit Beuselinck, Ignacio Durán, Daniel Yick Chin Heng, Winson Y. Cheung, Sumanta Kumar Pal, Lisa Ludwig, Dylan Edmund O'Sullivan, Toni K. Choueiri, Rana R. McKay, Frede Donskov, Jae‐Lyun Lee, Kosuke null Takemura, Lori Wood, Cristina Suárez, Marc Eid, Evan Ferrier
article en

Abstract

4532 Background: Therapies for mRCC have evolved significantly, making treatment decisions more complex. We used machine learning (ML) to identify whether this could help identify subgroups of patients who have a high probability of response. Methods: Patients from IMDC were identified and a ML classification and regression tree analysis was conducted, in which we grew a complex tree up to a depth of 30 with a minimum node split size of 2 with no constraints on the cost-complexity parameter. The resulting tree was pruned according to the cost-complexity parameter that minimized the leave one out cross-validated error rate and had a minimum bucket size of 25 patients. Results: 2,549 patients were included, 73.2% male, 13.5% non-clear cell histology, 70.3% nephrectomy, and 19.4%, 54.2%, and 26.4% had favorable, intermediate and poor IMDC risk respectively. 1L treatment regimens consisted of VEGF inhibitors (51.5%), IO-IO combinations (32.3%), and IO-TKI combinations (16.2%). The ORR was 36.0% overall, with 29.6% for VEGF inhibitors, 39.1% for IO-IO, and 50.2% for IO-TKI combinations. ML identified 5 hierarchal variables —therapy type, prior nephrectomy (PN), lung metastasis (LM), other metastases, and age— that divided patients into 7 different categories with different response probabilities (see Table). VEGF therapy showed the poorest response, with no additional variables able to predict response. The best ORR was observed in patients treated with IO-TKI and PN; and in those treated with IO-IO, PN, and only lung metastasis. Factors associated with poorer responses included non-clear cell histology, older age, bone and liver metastases, poor performance status, elevated neutrophils, and poor IMDC risk score. Conclusions: This large-scale ML analysis identified five key clinical variables that predict treatment response in mRCC, with treatment type emerging as the primary determinant. These results suggest that treatment selection for mRCC could potentially be optimized by considering these hierarchical variables, though further validation is needed. ML analysis results: Groups of patients and associated outcomes. Risk Groups N (%) ORR (%) Odd Ratio TTNT 18-month survival 1) VEGF 1313 (51.5) 29.6 Ref. 9.4 (8.6-10.3) 0.62 (0.59-0.65) 2) IO-IO or IO-TKI and no PN 443 (17.4) 35.0 1.28 (1.02-1.60) 10.2 (8.8-11.3) 0.59 (0.55-0.65) 3) IO-IO and PN a) No LM 137 (5.4) 29.2 0.98 (0.66-1.43) 17.2 (10.6-30.1) 0.85 (0.78-0.92) b) LM and other met 267 (10.5) 43.8 1.87 (1.42-2.44) 13.0 (10.1-20.5) 0.78 (0.72-0.83) c) Only LM 85 (3.3) 60.0 3.56 (2.28-5.63) 39.2 (14.4-NA) 0.93 (0.87-0.99) 4)IO-TKI and PN a) Age 70+ 78 (3.2) 43.6 1.84 (1.15-2.91) 35.7 (19.8-NA) 0.80 (0.71-0.91) b) Age < 70 226 (8.9) 58.4 3.34 (2.50-4.47) 24.7 (22.4-36.4) 0.88 (0.84-0.93) Overall 2549 36.0 11.5 (10.7-12.2) 0.68 (0.67-0.70)

Journal of Clinical OncologyVol. 43(16_suppl)
Ulsan College (KR), Dalhousie University (CA), Harvard University (US), Queen Mary University of London (GB), University of Calgary (CA), Universitair Ziekenhuis Leuven (BE), Queen Elizabeth II Health Sciences Centre (CA), Asan Medical Center (KR), University of California San Diego (US), University of Ulsan (KR), City of Hope (US), Occupational Cancer Research Centre (CA), Instituto de Investigación Marqués de Valdecilla (ES), Dana-Farber Cancer Institute (US), Vall d'Hebron Hospital Universitari (ES), Hospital South West Jutland (DK), Japanese Foundation For Cancer Research (JP), Vall d'Hebron Institute of Oncology (ES)
Openalex Percentile: Top 80%
Renal cell carcinoma treatment
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