Avelumab (Ave) first-line (1L) maintenance plus best supportive care (BSC) versus BSC alone for advanced urothelial carcinoma (UC): JAVELIN Bladder 100 Japanese subgroup analysis.

Authors

null

Norihiko Tsuchiya

Department of Urology, Yamagata University Faculty of Medicine, Yamagata, Japan

Norihiko Tsuchiya , Yoshiaki Yamamoto , Hirotsugu Uemura , Hiro-Omi Kanayama , Masatoshi Eto , Hideaki Miyake , Thomas Powles , Mizuki Yoshida , Yuichiro Koide , Yoshiko Umeyama , Alessandra Di Pietro , Yoshihiko Tomita

Organizations

Department of Urology, Yamagata University Faculty of Medicine, Yamagata, Japan, Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Japan, Department of Urology, Kindai University Faculty of Medicine, Osaka, Japan, Department of Urology, Graduate School, The University of Tokushima, Tokushima, Japan, Department of Urology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan, Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan, Barts Cancer Institute, Experimental Cancer Medicine Centre, Queen Mary University of London, St Bartholomew’s Hospital, London, United Kingdom, Pfizer R&D Japan, Tokyo, Japan, Pfizer SRL, Milan, Italy, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan

Research Funding

Pharmaceutical/Biotech Company
Pfizer, as part of an alliance between Pfizer and Merck KGaA, Darmstadt, Germany

Background: A randomized phase III trial (JAVELIN Bladder 100; NCT02603432) to investigate avelumab (anti–PD-L1) as 1L maintenance therapy in patients with advanced UC met its primary objective, demonstrating significantly prolonged overall survival (OS) with Ave + BSC vs BSC alone in all randomized patients and in patients with PD-L1+ tumors. We report efficacy and safety in Japanese patients enrolled in this study. Methods: Eligible patients with unresectable locally advanced or metastatic UC that had not progressed with 4-6 cycles of gemcitabine with either cisplatin or carboplatin were randomized 1:1 to receive maintenance Ave (10 mg/kg IV every 2 weeks) + BSC or BSC alone, stratified by best response to 1L chemotherapy (complete/partial response vs stable disease) and by visceral vs nonvisceral disease when initiating 1L chemotherapy. The primary endpoint was OS, assessed from randomization in all randomized patients and in patients with PD-L1+ tumors (Ventana SP263 assay). Secondary endpoints included progression-free survival (PFS) per blinded independent central review and safety. Results: Japanese patients (n=73) were randomized to receive Ave + BSC (n=36) or BSC alone (n=37); 52.8% vs 62.2% had PD-L1+ tumors, respectively. Median OS (95% CI) was 24.7 months (18.2-not estimable [NE]) with Ave + BSC vs 18.7 months (12.8-33.0) with BSC alone (HR, 0.81 [95% CI; 0.409-1.585]) in all randomized patients and 18.6 months (9.4-NE) with Ave + BSC vs 19.4 months (11.7-33.0) with BSC alone (HR, 1.00 [95% CI, 0.413-2.412]) in patients with PD-L1+ tumors. Median PFS (95% CI) was 5.6 months (1.9-9.4) with Ave + BSC vs 1.9 months (1.9-3.8) with BSC alone (HR, 0.63 [95% CI, 0.358-1.113]) in all randomized patients and 5.6 months (1.8-11.2) with Ave + BSC vs 1.9 months (1.9-3.8) with BSC alone (HR, 0.62 [95% CI, 0.298-1.301]) in patients with PD-L1+ tumors. The most common treatment-emergent adverse events (all grade; grade ≥3) in the Ave + BSC arm were pyrexia (10 [27.8%]; 0), nasopharyngitis (7 [19.4%]; 0), and anemia (7 [19.4%]; 4 [11.1%]). Conclusions: Ave 1L maintenance + BSC was efficacious and tolerable in Japanese patients with advanced UC, and results were generally consistent with those in the overall population. Clinical trial information: NCT02603432

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Abstract Details

Meeting

2021 Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session: Urothelial Carcinoma

Track

Urothelial Carcinoma

Sub Track

Therapeutics

Clinical Trial Registration Number

NCT02603432

Citation

J Clin Oncol 39, 2021 (suppl 6; abstr 425)

DOI

10.1200/JCO.2021.39.6_suppl.425

Abstract #

425

Poster Bd #

Online Only

Abstract Disclosures