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Combination antiangiogenic tyrosine kinase inhibition and anti-PD1 immunotherapy in metastatic renal cell carcinoma: A retrospective analysis of safety, tolerance, and clinical outcomes.
- Source :
-
Cancer medicine [Cancer Med] 2021 Apr; Vol. 10 (7), pp. 2341-2349. Date of Electronic Publication: 2021 Mar 01. - Publication Year :
- 2021
-
Abstract
- Introduction: Two separate antiangiogenic tyrosine kinase inhibitors (TKIs) and immunotherapy (IO) combinations are FDA-approved as front-line treatment for metastatic renal cell carcinoma (mRCC). Little is known about off-protocol and post-front-line experience with combination TKI-IO approaches.<br />Methods: We conducted a retrospective analysis of mRCC patients who received combination TKI-IO post-first-line therapy between November 2015 and January 2019 at MD Anderson Cancer Center and Duke Cancer Institute. Chart review detailed patient characteristics, treatments, toxicity, and survival. Independent radiologists, blinded to clinical data, assessed best radiographic response using RECIST v1.1.<br />Results: We identified 48 mRCC patients for inclusion: median age 65 years, 75.0% clear cell histology, 68.8% IMDC intermediate risk, and median two prior systemic therapies. TKI-IO combinations included nivolumab-cabozantinib (N +C; 24 patients), nivolumab-pazopanib (N+P; 13), nivolumab-axitinib (6), nivolumab-lenvatinib (2), and nivolumab-ipilimumab-cabozantinib (3). The median progression-free survival was 11.6 months and the median overall survival was not reached. Response data were available in 45 patients: complete response (CR; n = 3, 6.7%), partial response (PR; 20, 44.4%), stable disease (SD; 19, 42.2%), and progressive disease (3, 6.7%). Overall response rate was 51% and disease control rate (CR+PR+SD) was 93%. Only one patient had a grade ≥3 adverse event.<br />Conclusion: To our knowledge, this is the first case series reporting off-label use of combination TKI-IO for mRCC. TKI-IO combinations, particularly N+P and N+C, are well tolerated and efficacious. Although further prospective research is essential, slow disease progression on IO or TKI monotherapy may be safely controlled with addition of either TKI or IO.<br /> (© 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.)
- Subjects :
- Adult
Aged
Aged, 80 and over
Angiogenesis Inhibitors administration & dosage
Anilides administration & dosage
Axitinib administration & dosage
Carcinoma, Renal Cell immunology
Carcinoma, Renal Cell metabolism
Carcinoma, Renal Cell pathology
Female
Humans
Immune Checkpoint Inhibitors administration & dosage
Indazoles administration & dosage
Ipilimumab administration & dosage
Kidney Neoplasms immunology
Kidney Neoplasms metabolism
Kidney Neoplasms pathology
Male
Middle Aged
Nivolumab administration & dosage
Phenylurea Compounds administration & dosage
Programmed Cell Death 1 Receptor immunology
Pyridines administration & dosage
Pyrimidines administration & dosage
Quinolines administration & dosage
Retrospective Studies
Sulfonamides administration & dosage
Survival Rate
Treatment Outcome
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Carcinoma, Renal Cell drug therapy
Kidney Neoplasms drug therapy
Programmed Cell Death 1 Receptor antagonists & inhibitors
Protein-Tyrosine Kinases antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 2045-7634
- Volume :
- 10
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Cancer medicine
- Publication Type :
- Academic Journal
- Accession number :
- 33650321
- Full Text :
- https://doi.org/10.1002/cam4.3812