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).
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Martin Zarba
Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada
Dylan O'Sullivan
University of Calgary, Calgary, AB, Canada
David Maj
Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada
Winson Y. Cheung
Department of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada
Lisa Ludwig
Eli Lilly, Indianapolis
Connor Wells
Evan Ferrier
Tom Baker Cancer Centre, Calgary, AB, Canada
Razane El Hajj Chehade
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
Frede Donskov
University Hospital of Southern Denmark, Esbjerg, Denmark
Marc Eid
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
Sumanta Kumar Pal
Department of Medical Oncology City of Hope Comprehensive Cancer Center Duarte California USA
Benoit Beuselinck
University Hospital Leuven, KU Leuven, Leuven, Belgium
Rana R. McKay
Department of Medicine, Urology, and Radiation Medicine and Applied Sciences University of California‐San Diego La Jolla California USA
Lori Wood
Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, NS, Canada
Jae Lyun Lee
Cristina Suarez
Department of Medical Oncology Vall d'Hebron Institute of Oncology Hospital Universitari Vall d'Hebron Barcelona Spain
Kosuke Takemura
Faculty of Economics, Shiga University
Ignacio Duran
Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain
Toni K. Choueiri
Department of Medical Oncology Dana‐Farber Cancer Institute Boston Massachusetts USA
Daniel Yick Chin Heng
Department of Medical Oncology, Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada