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Avelumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma.

Robert J Motzer ,
Konstantin Penkov ,
John Haanen ,
Brian Rini ,
Laurence Albiges ,
Matthew T Campbell ,
Balaji Venugopal ,
Christian Kollmannsberger ,
Sylvie Negrier ,
Motohide Uemura ,
Jae L Lee ,
Aleksandr Vasiliev ,
Wilson H Miller ,
Howard Gurney ,
Manuela Schmidinger ,
James Larkin ,
Michael B Atkins ,
Jens Bedke ,
Boris Alekseev ,
Jing Wang ,
Mariangela Mariani ,
Paul B Robbins ,
Aleksander Chudnovsky ,
Camilla Fowst ,
Subramanian Hariharan ,
Bo Huang ,
Alessandra di Pietro ,
Toni K Choueiri

Abstract

METHODS

We randomly assigned patients in a 1:1 ratio to receive avelumab (10 mg per kilogram of body weight) intravenously every 2 weeks plus axitinib (5 mg) orally twice daily or sunitinib (50 mg) orally once daily for 4 weeks (6-week cycle). The two independent primary end points were progression-free survival and overall survival among patients with programmed death ligand 1 (PD-L1)-positive tumors. A key secondary end point was progression-free survival in the overall population; other end points included objective response and safety.

CONCLUSIONS

Progression-free survival was significantly longer with avelumab plus axitinib than with sunitinib among patients who received these agents as first-line treatment for advanced renal-cell carcinoma. (Funded by Pfizer and Merck [Darmstadt, Germany]; JAVELIN Renal 101 ClinicalTrials.gov number, NCT02684006.).

RESULTS

A total of 886 patients were assigned to receive avelumab plus axitinib (442 patients) or sunitinib (444 patients). Among the 560 patients with PD-L1-positive tumors (63.2%), the median progression-free survival was 13.8 months with avelumab plus axitinib, as compared with 7.2 months with sunitinib (hazard ratio for disease progression or death, 0.61; 95% confidence interval [CI], 0.47 to 0.79; P<0.001); in the overall population, the median progression-free survival was 13.8 months, as compared with 8.4 months (hazard ratio, 0.69; 95% CI, 0.56 to 0.84; P<0.001). Among the patients with PD-L1-positive tumors, the objective response rate was 55.2% with avelumab plus axitinib and 25.5% with sunitinib; at a median follow-up for overall survival of 11.6 months and 10.7 months in the two groups, 37 patients and 44 patients had died, respectively. Adverse events during treatment occurred in 99.5% of patients in the avelumab-plus-axitinib group and in 99.3% of patients in the sunitinib group; these events were grade 3 or higher in 71.2% and 71.5% of the patients in the respective groups.

BACKGROUND

In a single-group, phase 1b trial, avelumab plus axitinib resulted in objective responses in patients with advanced renal-cell carcinoma. This phase 3 trial involving previously untreated patients with advanced renal-cell carcinoma compared avelumab plus axitinib with the standard-of-care sunitinib.

More about this publication

The New England journal of medicine

Volume 380
Issue nr. 12
Pages 1103-1115
Publication date 21-03-2019

Full text links

Publisher website (DOI) 10.1056/NEJMoa1816047
Europe PubMed Central 30779531
Pubmed 30779531

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