Literature DB >> 27803064

Randomized, Placebo-Controlled, Phase II Study of Veliparib in Combination with Carboplatin and Paclitaxel for Advanced/Metastatic Non-Small Cell Lung Cancer.

Suresh S Ramalingam1, Normand Blais2, Julien Mazieres3, Martin Reck4, C Michael Jones5, Erzsebet Juhasz6, Laszlo Urban7, Sergey Orlov8, Fabrice Barlesi9, Ebenezer Kio10, Ulrich Keiholz11, Qin Qin12, Jiang Qian12, Caroline Nickner13, Juliann Dziubinski12, Hao Xiong12, Peter Ansell12, Mark McKee12, Vincent Giranda12, Vera Gorbunova14.   

Abstract

Purpose: PARP plays an important role in DNA repair. Veliparib, a PARP inhibitor, enhances the efficacy of platinum compounds and has been safely combined with carboplatin and paclitaxel. The primary endpoint of this phase II trial determined whether addition of veliparib to carboplatin and paclitaxel improved progression-free survival (PFS) in previously untreated patients with advanced/metastatic non-small cell lung cancer.Experimental Design: Patients were randomized 2:1 to carboplatin and paclitaxel with either veliparib or placebo. Veliparib (120 mg) or placebo was given on days 1 to 7 of each 3-week cycle, with carboplatin (AUC = 6 mg/mL/min) and paclitaxel (200 mg/m2) administered on day 3, for a maximum of 6 cycles.
Results: Overall, 158 were included (median age, 63 years; male 68%, squamous histology 48%). Median PFS was 5.8 months in the veliparib group versus 4.2 months in the placebo group [HR, 0.72; 95% confidence interval (CI), 0.45-1.15; P = 0.17)]. Median overall survival (OS) was 11.7 and 9.1 months in the veliparib and placebo groups, respectively (HR, 0.80; 95% CI, 0.54-1.18; P = 0.27). In patients with squamous histology, median PFS (HR, 0.54; 95% CI, 0.26-1.12; P = 0.098) and OS (HR, 0.73; 95% CI, 0.43-1.24; P = 0.24) favored veliparib treatment. Objective response rate was similar between groups (veliparib: 32.4%; placebo: 32.1%), but duration of response favored veliparib treatment (HR, 0.47; 95% CI, 0.16-1.42; P = 0.18). Grade III/IV neutropenia, thrombocytopenia, and anemia were comparable between groups.Conclusions: Veliparib combination with carboplatin and paclitaxel was well-tolerated and demonstrated a favorable trend in PFS and OS versus chemotherapy alone. Patients with squamous histology had the best outcomes with veliparib combination. Clin Cancer Res; 23(8); 1937-44. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27803064     DOI: 10.1158/1078-0432.CCR-15-3069

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  27 in total

1.  Impact of Advantage in Tumor Response on the Correlation Between Progression-Free Survival and Overall Survival: Meta-Analysis of Clinical Trials in Patients with Advanced Non-Small Cell Lung Cancer.

Authors:  Yosuke Yoshida; Masayuki Kaneko; Mamoru Narukawa
Journal:  Pharmaceut Med       Date:  2021-01-23

2.  EGFR and c-MET Cooperate to Enhance Resistance to PARP Inhibitors in Hepatocellular Carcinoma.

Authors:  Qiongzhu Dong; Yi Du; Hui Li; Chunxiao Liu; Yongkun Wei; Mei-Kuang Chen; Xixi Zhao; Yu-Yi Chu; Yufan Qiu; Lunxiu Qin; Hirohito Yamaguchi; Mien-Chie Hung
Journal:  Cancer Res       Date:  2018-12-20       Impact factor: 12.701

3.  A phase I study of intravenous or intraperitoneal platinum based chemotherapy in combination with veliparib and bevacizumab in newly diagnosed ovarian, primary peritoneal and fallopian tube cancer.

Authors:  Kathleen N Moore; Austin Miller; Katherine M Bell-McGuinn; Russell J Schilder; Joan L Walker; Roisin E O'Cearbhaill; Saketh R Guntupalli; Deborah K Armstrong; Andrea R Hagemann; Heidi J Gray; Linda R Duska; Cara A Mathews; Alice Chen; David O'Malley; Sarah Gordon; Paula M Fracasso; Carol Aghajanian
Journal:  Gynecol Oncol       Date:  2019-11-07       Impact factor: 5.482

4.  Synthetic Lethality of PARP Inhibition and Ionizing Radiation is p53-dependent.

Authors:  Steven T Sizemore; Rahman Mohammad; Gina M Sizemore; Somaira Nowsheen; Hao Yu; Michael C Ostrowski; Arnab Chakravarti; Fen Xia
Journal:  Mol Cancer Res       Date:  2018-03-28       Impact factor: 5.852

5.  Veliparib in Combination With Platinum-Based Chemotherapy for First-Line Treatment of Advanced Squamous Cell Lung Cancer: A Randomized, Multicenter Phase III Study.

Authors:  Suresh S Ramalingam; Silvia Novello; Salih Zeki Guclu; Dmitry Bentsion; Zanete Zvirbule; Maria Szilasi; Reyes Bernabe; Konstantinos Syrigos; Lauren Averett Byers; Philip Clingan; Jair Bar; Everett E Vokes; Ramaswamy Govindan; Martin Dunbar; Peter Ansell; Lei He; Xin Huang; Vasudha Sehgal; Jaimee Glasgow; Bruce A Bach; Julien Mazieres
Journal:  J Clin Oncol       Date:  2021-08-26       Impact factor: 44.544

6.  Phase 1 study of veliparib (ABT-888), a poly (ADP-ribose) polymerase inhibitor, with carboplatin and paclitaxel in advanced solid malignancies.

Authors:  Leonard J Appleman; Jan H Beumer; Yixing Jiang; Yan Lin; Fei Ding; Shannon Puhalla; Leigh Swartz; Taofeek K Owonikoko; R Donald Harvey; Ronald Stoller; Daniel P Petro; Hussein A Tawbi; Athanassios Argiris; Sandra Strychor; Marie Pouquet; Brian Kiesel; Alice P Chen; David Gandara; Chandra P Belani; Edward Chu; Suresh S Ramalingam
Journal:  Cancer Chemother Pharmacol       Date:  2019-09-23       Impact factor: 3.333

Review 7.  Breakthroughs in the treatment of advanced squamous-cell NSCLC: not the neglected sibling anymore?

Authors:  Georgios Tsironis; Dimitrios C Ziogas; Anastasios Kyriazoglou; Marita Lykka; Konstantinos Koutsoukos; Aristotelis Bamias; Meletios-Athanasios Dimopoulos
Journal:  Ann Transl Med       Date:  2018-04

Review 8.  PARP Inhibition in Cancer: An Update on Clinical Development.

Authors:  Esha Sachdev; Roya Tabatabai; Varun Roy; B J Rimel; Monica M Mita
Journal:  Target Oncol       Date:  2019-12       Impact factor: 4.493

9.  A phase I trial adding poly(ADP-ribose) polymerase inhibitor veliparib to induction carboplatin-paclitaxel in patients with head and neck squamous cell carcinoma: Alliance A091101.

Authors:  Michael J Jelinek; Nathan R Foster; Alex J Zoroufy; Gary K Schwartz; Pamela N Munster; Tanguy Y Seiwert; Jonas A de Souza; Everett E Vokes
Journal:  Oral Oncol       Date:  2021-01-26       Impact factor: 5.337

10.  Olaparib Suppresses MDSC Recruitment via SDF1α/CXCR4 Axis to Improve the Anti-tumor Efficacy of CAR-T Cells on Breast Cancer in Mice.

Authors:  Ruixin Sun; Hong Luo; Jingwen Su; Shengmeng Di; Min Zhou; Bizhi Shi; Yansha Sun; Guoxiu Du; Honghong Zhang; Hua Jiang; Zonghai Li
Journal:  Mol Ther       Date:  2020-09-26       Impact factor: 11.454

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