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).

M Martin Zarba (Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada) D Dylan O'Sullivan (University of Calgary, Calgary, AB, Canada) D David Maj (Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada) W Winson Y. Cheung (Department of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada) L Lisa Ludwig (Eli Lilly, Indianapolis) C Connor Wells E Evan Ferrier (Tom Baker Cancer Centre, Calgary, AB, Canada) R Razane El Hajj Chehade (Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA) F Frede Donskov (University Hospital of Southern Denmark, Esbjerg, Denmark) M Marc Eid (Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA) S Sumanta Kumar Pal (Department of Medical Oncology City of Hope Comprehensive Cancer Center Duarte California USA) B Benoit Beuselinck (University Hospital Leuven, KU Leuven, Leuven, Belgium) R Rana R. McKay (Department of Medicine, Urology, and Radiation Medicine and Applied Sciences University of California‐San Diego La Jolla California USA) L Lori Wood (Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, NS, Canada) J Jae Lyun Lee C Cristina Suarez (Department of Medical Oncology Vall d'Hebron Institute of Oncology Hospital Universitari Vall d'Hebron Barcelona Spain) K Kosuke Takemura (Faculty of Economics, Shiga University) I Ignacio Duran (Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain) T Toni K. Choueiri (Department of Medical Oncology Dana‐Farber Cancer Institute Boston Massachusetts USA) D Daniel Yick Chin Heng (Department of Medical Oncology, Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada)

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)

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 4532-4532
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

M

Martin Zarba

Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada

D

Dylan O'Sullivan

University of Calgary, Calgary, AB, Canada

D

David Maj

Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada

W

Winson Y. Cheung

Department of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada

L

Lisa Ludwig

Eli Lilly, Indianapolis

C

Connor Wells

E

Evan Ferrier

Tom Baker Cancer Centre, Calgary, AB, Canada

R

Razane El Hajj Chehade

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

F

Frede Donskov

University Hospital of Southern Denmark, Esbjerg, Denmark

M

Marc Eid

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

S

Sumanta Kumar Pal

Department of Medical Oncology City of Hope Comprehensive Cancer Center Duarte California USA

B

Benoit Beuselinck

University Hospital Leuven, KU Leuven, Leuven, Belgium

R

Rana R. McKay

Department of Medicine, Urology, and Radiation Medicine and Applied Sciences University of California‐San Diego La Jolla California USA

L

Lori Wood

Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, NS, Canada

J

Jae Lyun Lee

C

Cristina Suarez

Department of Medical Oncology Vall d'Hebron Institute of Oncology Hospital Universitari Vall d'Hebron Barcelona Spain

K

Kosuke Takemura

Faculty of Economics, Shiga University

I

Ignacio Duran

Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain

T

Toni K. Choueiri

Department of Medical Oncology Dana‐Farber Cancer Institute Boston Massachusetts USA

D

Daniel Yick Chin Heng

Department of Medical Oncology, Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada