Abstract 1975P
Background
In the JAVELIN Bladder 100 phase 3 trial (NCT02603432), avelumab 1L maintenance + best supportive care (BSC) significantly prolonged overall survival (OS) and progression-free survival (PFS) vs BSC alone in pts with aUC that had not progressed with 1L platinum-based chemotherapy (PBC). Here, we report conditional survival estimates and safety in pts treated with avelumab for ≥1 or ≥2 years.
Methods
Eligible pts with unresectable locally advanced or metastatic UC without progression after 1L PBC were randomized 1:1 to receive avelumab + BSC (n=350) or BSC alone (n=350). The primary endpoint was OS (from randomization); secondary endpoints included PFS and safety.
Results
Among 350 pts randomized to avelumab + BSC, treatment duration was ≥1 year in 118 pts (33.7%) and ≥2 years in 68 (19.4%). Compared with the overall avelumab + BSC arm, a higher proportion of pts with ≥2 years of treatment had received 1L gemcitabine + cisplatin (64.7% vs 52.3%), had nonvisceral metastases (58.8% vs 45.4%), and had PD-L1+ tumors (64.7% vs 54.0%). In pts who received ≥1 year of treatment, the probability of surviving for an additional 1 or 1.5 years was 93.2% and 86.8%, respectively; the probability of surviving for an additional 6 months or 1 year without progression was 77.9% and 66.7%, respectively. In pts who received ≥2 years of treatment, the probability of surviving for an additional 1 or 1.5 years was 95.8% and 90.3%, respectively; the probability of surviving an additional 6 months or 1 year without progression was 82.9% and 66.7%, respectively. Among pts treated for ≥1 or ≥2 years, any-grade treatment-related adverse events (TRAEs) occurred after ≥1 year in 50.0% and after ≥2 years in 35.3%; grade ≥3 TRAEs occurred in 11.9% and 5.9%, respectively.
Conclusions
Pts with aUC who received ≥1 or ≥2 years of avelumab 1L maintenance treatment in JAVELIN Bladder 100 had a high probability of surviving for an additional 1 year or more. No new safety concerns were identified with longer treatment duration. These results can inform prognosis and further support avelumab 1L maintenance as a standard of care in pts with aUC without progression after 1L PBC.
Clinical trial identification
NCT02603432; first posted November 11, 2015.
Editorial acknowledgement
Medical writing support was provided by Sophie Saunders of Nucleus Global and was funded by Merck.
Legal entity responsible for the study
Merck.
Funding
This trial was sponsored by Pfizer and was previously conducted under an alliance between Merck (CrossRef Funder ID: 10.13039/100009945) and Pfizer. This analysis was sponsored by Merck.
Disclosure
P. Grivas: Financial Interests, Personal, Advisory Role: AADI, AbbVie, Asieris Pharmaceuticals, Astellas Pharma, AstraZeneca, BostonGene, Bristol Myers Squibb, CG Oncology, Fresenius Kabi, G1 Therapeutics, Gilead Sciences, lmmunityBio, Janssen, Lucence Health, Merck, MSD, Pfizer, PureTech, Roche, Seagen, Silverback Therapeutics, Strata Oncology; Financial Interests, Institutional, Research Funding: Acrivon Therapeutics, ALX Oncology, Bristol Myers Squibb, G1 Therapeutics, Genentech, Gilead Sciences, GSK, Merck, Mirati Therapeutics, MSD, Pfizer, QED Therapeutics. S.H. Park: Financial Interests, Personal, Other, Honoraria: Merck, Ono Pharmaceutical, Pfizer; Financial Interests, Personal, Advisory Role: Janssen Oncology; Financial Interests, Institutional, Research Funding: MSD. W. Demey: Financial Interests, Personal, Advisory Role: Pfizer, Merck. P.C. Fong: Financial Interests, Personal, Advisory Role: MSD; Financial Interests, Personal, Other, Travel and accommodation expenses: Pfizer; Financial Interests, Institutional, Research Funding: MSD. J.A. Garcia: Financial Interests, Personal, Other, Personal fees: Aptitude Health, Pfizer, US Food and Drug Administration, MJH, Astellas. N. Jacob: Financial Interests, Personal, Full or part-time Employment: Merck. A. Gerhold-Ay: Financial Interests, Personal, Full or part-time Employment: Merck. K. Tyroller: Financial Interests, Personal, Full or part-time Employment: EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA; Financial Interests, Personal, Stocks/Shares: Merck. J. Hoffman: Financial Interests, Personal, Full or part-time Employment: EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA; Financial Interests, Personal, Stocks or ownership: Merck, MSD, Pfizer. J. Bellmunt: Financial Interests, Personal, Advisory Role: Astellas Pharma, AstraZeneca/MedImmune, Bristol Myers Squibb, Genentech, Merck, Novartis, Pfizer, Pierre Fabre; Financial Interests, Personal, Other, Travel and accommodation expenses: Ipsen, MSD, Pfizer; Financial Interests, Personal, Royalties: UpToDate; Financial Interests, Personal, Stocks or ownership: Rainier Therapeutics; Financial Interests, Personal, Other, Honoraria: UpToDate; Financial Interests, Institutional, Research Funding: Merck, Millennium, Pfizer, Sanofi. T.B. Powles: Financial Interests, Personal, Advisory Role: Astellas Pharma, AstraZeneca, Bristol Myers Squibb, Eisai, Exelixis, Incyte, Ipsen, Johnson & Johnson, Merck, MSD, Pfizer, Roche, Seagen, MashupMD; Financial Interests, Personal, Other, Travel and accommodations expenses: Pfizer, AstraZeneca, Ipsen, MSD, Pfizer, Roche; Financial Interests, Personal, Other, Honoraria: Astellas Pharma, AstraZeneca, Bristol Myers Squibb, Eisai, Exelixis, Incyte, Ipsen, Johnson & Johnson/Janssen, MashupMD, Merck, MSD, Novartis, Pfizer, Roche, Seagen; Financial Interests, Personal, Research Funding: Astellas Pharma, AstraZeneca, Bristol Myers Squibb, Eisai, Exelixis, Ipsen, Johnson & Johnson, Merck, MSD, Novartis, Pfizer, Roche, Seagen. All other authors have declared no conflicts of interest.
Resources from the same session
1998P - Preliminary results from a phase I study of T3011, an oncolytic HSV expressing IL-12 and anti-PD-1 antibody, for BCG-failure non-muscle-invasive bladder cancer (NMIBC)
Presenter: Dingwei Ye
Session: Poster session 13
1999P - Expression heterogeneity of ADC-related targets between primary tumors and metastatic lymph nodes in advanced urothelial cancers
Presenter: Xingliang Tan
Session: Poster session 13
2001P - Epidemiology and treatment patterns of patients with locally advanced or metastatic urothelial cancer in France: A non-interventional database study
Presenter: Florence Joly Lobbedez
Session: Poster session 13
2002P - Efficacy and biomarker analysis of neoadjuvant disitamab vedotin combined immunotherapy in patients with muscle-invasive bladder cancer: A multi-center real-world study
Presenter: Luzhe Yan
Session: Poster session 13
2003P - Clinical outcomes of patients with metastatic urothelial carcinoma (mUC) discontinuing enfortumab vedotin (EV) monotherapy (mono) without disease progression
Presenter: Michal Sternschuss
Session: Poster session 13
2004P - The combination of high levels of serum cytokeratin fragment 21-1 and VI-RADS≧4 has diagnostic and prognostic value in high-stage bladder cancer
Presenter: Shunsuke Ikuma
Session: Poster session 13
2005P - Prediction of response and identification of mechanisms of resistance to neoadjuvant chemotherapy according to molecular subtypes in muscle-invasive bladder carcinoma
Presenter: Alvaro Pinto Marin
Session: Poster session 13
2006P - Prognostic factors in metastatic urothelial cancer (mUC): Developing an accessible model for predicting patient survival
Presenter: Sevinc Balli
Session: Poster session 13
2007P - Similar genetic profile in early and late-stage urothelial tract cancer suggests that early genomic testing bears the potential of timely personalized treatment in clinical trials
Presenter: Dag Rune Stormoen
Session: Poster session 13