Final results of a phase 3 study of trebananib plus weekly paclitaxel in recurrent ovarian cancer (TRINOVA-1): Long-term survival, impact of ascites, and progression-free survival-2

被引:74
作者
Monk, Bradley J. [1 ]
Poveda, Andres [2 ]
Vergote, Ignace [3 ]
Raspagliesi, Francesco [4 ]
Fujiwara, Keiichi [5 ]
Bae, Duk-Soo [6 ]
Oaknin, Ana [7 ]
Ray-Coquard, Isabelle [8 ]
Provencher, Diane M. [9 ]
Karlan, Beth Y. [10 ]
Lhomme, Catherine [11 ]
Richardson, Gary [12 ]
Rincon, Dolores Gallardo [13 ]
Coleman, Robert L. [14 ]
Marth, Christian [15 ]
Brize, Arija [16 ]
Fabbro, Michel [17 ]
Redondo, Andres [18 ]
Bamias, Aristotelis [19 ]
Ma, Haijun [20 ]
Vogl, Florian D. [21 ]
Bach, Bruce A. [21 ]
Oza, Amit M. [22 ]
机构
[1] Univ Arizona, Canc Ctr Dign Hlth, St Josephs Hosp & Med Ctr, Dept Obstet & Gynecol, Phoenix, AZ USA
[2] Fdn Inst Valenciano Oncol, Area Clin Oncol Ginecol, Valencia, Spain
[3] Katholieke Univ Leuven, European Union, Dept Obstet & Gynecol, Univ Hosp Leuven,Leuven Canc Inst, Leuven, Belgium
[4] Fdn IRCCS, Gynecol Oncol Unit, Ist Nazl Cura & Studio Tumori, Milan, Italy
[5] Saitama Med Univ, Dept Gynecol Oncol, Int Med Ctr, Hidaka, Saitama, Japan
[6] Samsung Med Ctr, Dept Obstet & Gynecol, Seoul, South Korea
[7] Vail dHebron Univ Hosp, Vall dHebron Inst Oncol, Barcelona, Spain
[8] Univ Lyon 1, Ctr Leon Berard, Lyon, France
[9] Ctr Hosp Univ Montreal, Div Gynecol Oncol, Montreal, PQ, Canada
[10] Cedars Sinai Med Ctr, Womens Canc Program, Samuel Oschin Comprehens Canc Ctr, Los Angeles, CA 90048 USA
[11] Inst Gustave Roussy, Dept Med, Villejuif, France
[12] Cabrini Hosp, Acad Haematol & Oncol, Malvern, Vic, Australia
[13] Inst Nacl Cancerol, Subdirecc Med Interna, Mexico City, DF, Mexico
[14] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol & Reprod Med, Houston, TX 77030 USA
[15] Med Univ Innsbruck, Univ Klin Gynakol & Geburtshilfe, Innsbruck, Austria
[16] Riga Eastern Clin Univ Hosp, Latvian Oncol Ctr, Riga, Latvia
[17] Reg Canc Inst Montpellier, Montpellier, France
[18] Hosp Univ La Paz Idi Paz, Madrid, Spain
[19] Natl & Kapodistrian Univ Athens, Alexandra Hosp, Dept Clin Therapeut, Athens, Greece
[20] Amgen Inc, Global Biostat Sci, Thousand Oaks, CA 91320 USA
[21] Amgen Inc, Global Dev Oncol, Thousand Oaks, CA 91320 USA
[22] Univ Toronto, Princess Margaret Hosp, Dept Med, Toronto, ON M5S 1A1, Canada
关键词
Trebananib; TRINOVA-1; Recurrent epithelial ovarian cancer; Overall survival; Ascites; Time to second disease progression; ADVANCED EPITHELIAL OVARIAN; MALIGNANT ASCITES; FALLOPIAN-TUBE; DOUBLE-BLIND; CLINICAL-TRIAL; END-POINTS; BEVACIZUMAB; ANGIOGENESIS; CHEMOTHERAPY; THERAPY;
D O I
10.1016/j.ygyno.2016.07.112
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpbse. Trebananib, a peptibody that blocks binding of angiopoietin-1 and -2 to Tie2, significantly prolonged progression-free survival (PFS) in patients with recurrent epithelial ovarian cancer in the phase 3 TRINOVA-1 study. We report overall survival (OS) in the interit-to-treat population and clinically relevant subgroups and time to second disease progression (PFS-2)., Patients and methods. Women with recurrent disease (platinum-free interval < 12 months) were randomized to receive intravenous paclitaxel 80 mg/m(2) (3 weeks on/1 week off) plus intravenous trebananib 15 mg/kg or placebo, weekly. OS in the intent-to-treat population was a key secondary endpoint. Exploratory analysis of PFS-2 was conducted according to guidance by the European Medicines Agency. Results. Median OS was not significantly improved with trebananib compared with placebo (19.3 versus 18.3 months, HR, 0.95; 95% CI, 0.81-1.11; P = 0.52) in the intent-to-treat population (n = 919). In subgroup analysis, trebananib improved median OS compared with placebo (14.5 versus 12.3 months; HR, 0.72; 95% CI, 0.55-0.93; P = 0.011) in patients with ascites at baseline (n = 295). In the intent-to-treat population, trebananib significantly improved median PFS-2 compared with placebo (12.5 versus 10.9 months; HR, 0.85; 95% CI, 0.74-0.98; P = 0.024). The incidence and type of adverse events in this updated analysis was consistent with that described in the primary analysis; no new safety signals were detected. Conclusions. OS was not significantly longer in the intent-to-treat population, although there was an improvement in OS in patients with ascites receiving trebananib. PFS-2 confirmed that the PFS benefit associated with trebananib was maintained through the second disease progression independent of the choice of subsequent therapy. (C) 2016 Elsevier Inc. All rights reserved.
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页码:27 / 34
页数:8
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