Ramucirumab plus docetaxel versus placebo plus docetaxel in patients

Abstract

Background Few treatments with a distinct mechanism of action are available for patients with platinum-refractory advanced or metastatic urothelial carcinoma. We assessed the efficacy and safety of treatment with docetaxel plus either ramucirumab-a human IgG1 VEGFR-2 antagonist-or placebo in this patient population.

Methods We did a randomised, double-blind, phase 3 trial in patients with advanced or metastatic urothelial carcinoma who progressed during or after platinum-based chemotherapy. Patients were enrolled from 124 sites in 23 countries. Previous treatment with one immune-checkpoint inhibitor was permitted. Patients were randomised (1:1) using an interactive web response system to receive intravenous docetaxel 75 mg/m(2) plus either intravenous ramucirumab 10 mg/kg or matching placebo on day 1 of repeating 21-day cycles, until disease progression or other discontinuation criteria were met. The primary endpoint was investigator-assessed progression-free survival, analysed by intention-to-treat in the first 437 randomised patients. This study is registered with ClinicalTrials.gov, number NCT02426125.

Findings Between July, 2015, and April, 2017, 530 patients were randomly allocated either ramucirumab plus docetaxel (n=263) or placebo plus docetaxel (n=267). Progression-free survival was prolonged significantly in patients allocated ramucirumab plus docetaxel versus placebo plus docetaxel (median 4.07 months [95% CI 2.96-4.47] vs 2.76 months [2.60-2.96]; hazard ratio [HR] 0.757, 95% CI 0.607-0.943; p=0.0118). A blinded independent central analysis was consistent with these results. An objective response was achieved by 53 (24.5%, 95% CI 18.8-30.3) of 216 patients allocated ramucirumab and 31 (14.0%, 9.4-18.6) of 221 assigned placebo. The most frequently reported treatment-emergent adverse events, regardless of causality, in either treatment group (any grade) were fatigue, alopecia, diarrhoea, decreased appetite, and nausea. These events occurred predominantly at grade 1-2 severity. The frequency of grade 3 or worse adverse events was similar for patients allocated ramucirumab and placebo (156 [60%] of 258 vs 163 [62%] of 265 had an adverse event), with no unexpected toxic effects. 63 (24%) of 258 patients allocated ramucirumab and 54 (20%) of 265 assigned placebo had a serious adverse event that was judged by the investigator to be related to treatment. 38 (15%) of 258 patients allocated ramucirumab and 43 (16%) of 265 assigned placebo died on treatment or within 30 days of discontinuation, of which eight (3%) and five (2%) deaths were deemed related to treatment by the investigator. Sepsis was the most common adverse event leading to death on treatment (four [2%] vs none [0%]). One fatal event of neutropenic sepsis was reported in a patient allocated ramucirumab.

Interpretation To the best of our knowledge, ramucirumab plus docetaxel is the first regimen in a phase 3 study to show superior progression-free survival over chemotherapy in patients with platinum-refractory advanced urothelial carcinoma. These data validate inhibition of VEGFR-2 signalling as a potential new therapeutic treatment option for patients with urothelial carcinoma.

C1 [Petrylak, Daniel P.] Yale Univ, Sch Med, 333 Cedar St, New Haven, CT 06520 USA.

[de Wit, Ronald] Erasmus MC Canc Inst, Rotterdam, Netherlands.

[Chi, Kim N.] British Columbia Canc Agcy, Vancouver, BC, Canada.

[Drakaki, Alexandra] UCLA, David Geffen Sch Med, Los Angeles, CA 90095 USA.

[Sternberg, Cora N.] San Camillo & Forlanini Hosp, Rome, Italy.

[Nishiyama, Hiroyuki] Univ Tsukuba, Tsukuba, Ibaraki, Japan.

[Castellano, Daniel] Hosp Univ 12 Octubre CiberOnc, Madrid, Spain.

[Hussain, Syed] Plymouth Univ, Peninsula Sch Med & Dent, Plymouth, Devon, England.

[Flechon, Aude] Ctr Leon Berard, Lyon, France.

[Bamias, Aristotelis] Univ Athens, Athens, Greece.

[Yu, Evan Y.] Univ Washington, Seattle, WA 98195 USA.

[van der Heijden, Michiel S.] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Amsterdam, Netherlands.

[Matsubara, Nobuaki] Hosp East, Natl Canc Ctr, Chiba, Japan.

[Alekseev, Boris] PA Herzen Moscow Oncol Res Inst, Moscow, Russia.

[Necchi, Andrea] Fdn IRCCS Ist Nazl Tumori, Milan, Italy.

[Geczi, Lajos] Natl Inst Oncol, Budapest, Hungary.

[Ou, Yen-Chuan] Taichung Vet Gen Hosp, Taichung, Taiwan.

[Coskun, Hasan Senol] Akdeniz Univ, Sch Med, Antalya, Turkey.

[Su, Wen-Pin] Natl Cheng Kung Univ, Coll Med, Inst Clin Med, Tainan, Taiwan.

[Su, Wen-Pin] Natl Cheng Kung Univ Hosp, Coll Med, Dept Internal Med, Tainan, Taiwan.

[Hegemann, Miriam] Univ Hosp, Tubingen, Germany.

[Percent, Ivor J.] Florida Canc Specialists, Port Charlotte, FL USA.

[Lee, Jae-Lyun] Univ Ulsan, Coll Med, Asan Med Ctr, Seoul, South Korea.

[Tucci, Marcello] Univ Turin, San Luigi Gonzaga Hosp, Dept Oncol, Div Med Oncol, Turin, Italy.

[Semenov, Andrey] RBHI Ivanovo Reg Oncol Dispensary, Ivanovo, Russia.

[Laestadius, Fredrik] Ctr Oscar Lambret, Lille, France.

[Peer, Avivit] Rambam Hlth Care Campus, Haifa, Israel.

[Tortora, Giampaolo] Univ Verona, Verona, Italy.

[Tortora, Giampaolo] Azienda Osped Univ Integrata, Verona, Italy.

[Safina, Sufia] Tatarstan Reg Canc Ctr, Kazan, Russia.

[Garcia del Muro, Xavier] Univ Barcelona, IDIBELL, Inst Catala Oncol Hosp, Barcelona, Spain.

[Rodriguez-Vida, Alejo] Hosp Mar, Barcelona, Spain.

[Cicin, Irfan] Trakya Univ, Edirne, Turkey.

[Harputluoglu, Hakan] Inonu Univ, Malatya, Turkey.

[Widau, Ryan C.; Liepa, Astra M.; Walgren, Richard A.; Hamid, Oday; Zimmermann, Annamaria H.; Bell-McGuinn, Katherine M.] Eli Lilly & Co, Indianapolis, IN 46285 USA.

[Powles, Thomas] Queen Mary Univ London, Barts Canc Inst, London, England.