Abstract
1709P Outcomes with novel combinations in non-clear cell renal cell carcinoma (nccRCC): ORACLE study
Annals of oncology, Vol.35(Supplement 2), pp.S1024-S1025
09/2024
DOI: 10.1016/j.annonc.2024.08.1802
Abstract
Background
There is a paucity of data to guide management of nccRCC due to the heterogeneity and rarity of these tumors. Limited data exists regarding the clinical activity of combination therapies in subtypes of advanced nccRCC.
Methods
In this multicenter retrospective analysis, we evaluated the efficacy of combination systemic therapy from 2012-2024. in patients(pts) with nccRCC. Eligible pts included those with nccRCC and receipt of any combination regimens including IO-IO, IO-VEGF, mTOR-VEGF during any line of treatment. The primary endpoint was objective response rate (ORR) assessed by investigator review. Secondary endpoints were progression- free survival (PFS), disease control rate (DCR), and overall survival (OS).
Results
253 pts received combination regimens. The median age was 59 years; 72% were male and 64% white. Histologies included papillary (38%), unclassified (34%), chromophobe (16%), translocation (8%), and other (4%). 23% had sarcomatoid and/or rhabdoid differentiation. 73% had prior nephrectomy, 82% were IMDC intermediate/poor risk. 23% and 28% had liver and bone metastasis respectively. The majority (69%) received combination treatment as first line. Comparison of outcomes based on treatment regimen and subtype is shown in the table. ORR/DCR/PFS was significantly lower when combination regimens were utilized in second or later line compared to front line setting.
Conclusions
Limited antitumor activity was observed with novel combinations in nccRCC in both frontline and later line setting. nccRCC subsets appear to respond differentially based on the type of combination regimen. Optimal management of nccRCC remains an unmet need.
Details
- Title: Subtitle
- 1709P Outcomes with novel combinations in non-clear cell renal cell carcinoma (nccRCC): ORACLE study
- Creators
- D. Kilari - Medical College of WisconsinA. Szabo - Medical College of WisconsinM.A. Bilen - Winship Cancer InstituteY. Ged - Johns Hopkins HospitalB.L. Maughan - University of UtahC. Hwang - Henry Ford Health SystemH. McManus - Duke UniversityP.M. Coelho Barata - University Hospitals Seidman Cancer CenterA. Desai - University of California, San FranciscoY. Zakharia - University of IowaH. Emamekhoo - University of Wisconsin Carbone Cancer CenterA. Tripathi - City Of Hope National Medical CenterT. Rose - UNC Lineberger Comprehensive Cancer CenterP. Ghatalia - Fox Chase Cancer CenterM.A. Reimers - Washington University in St. Louis School of MedicineE. Heath - The Barbara Ann Karmanos Cancer InstituteJ.M. King - Indiana UniversityB.I. Rini - Vanderbilt-Ingram Cancer CenterJ. Brugarolas - The University of Texas Southwestern Medical CenterR.R. McKay - University of California, San Diego
- Resource Type
- Abstract
- Publication Details
- Annals of oncology, Vol.35(Supplement 2), pp.S1024-S1025
- Publisher
- Elsevier Ltd
- DOI
- 10.1016/j.annonc.2024.08.1802
- ISSN
- 0923-7534
- Language
- English
- Date published
- 09/2024
- Academic Unit
- Hematology, Oncology, and Blood & Marrow Transplantation; Internal Medicine
- Record Identifier
- 9984708762602771
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