Phase III Study of Pemetrexed Plus Carboplatin Compared With Etoposide Plus Carboplatin in Chemotherapy-Naive Patients With Extensive-Stage Small-Cell Lung Cancer

Author:

Socinski Mark A.1,Smit Egbert F.1,Lorigan Paul1,Konduri Kartik1,Reck Martin1,Szczesna Aleksandra1,Blakely Johnetta1,Serwatowski Piotr1,Karaseva Nina A.1,Ciuleanu Tudor1,Jassem Jacek1,Dediu Mircea1,Hong Shengyan1,Visseren-Grul Carla1,Hanauske Axel-Rainer1,Obasaju Coleman K.1,Guba Susan C.1,Thatcher Nick1

Affiliation:

1. From the Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC; Vrije University Medical Center, Amsterdam; Eli Lilly Netherlands, Utrecht, the Netherlands; Christie Hospital, Manchester, United Kingdom; US Oncology, Houston, TX; Hospital Grosshansdorf, Grosshansdorf; Department of Medicine and Medical Oncology, St Georg Hospital, Hamburg, Germany; Mazovian Center of Lung Diseases and Tuberculosis, Otwock; Sokolowski Specialist Hospital in Szczecin-Zdunowo; Medical...

Abstract

Purpose Following a phase II trial in which pemetrexed-platinum demonstrated similar activity to that of historical etoposide-platinum controls, a phase III study was conducted to compare pemetrexed-carboplatin with etoposide-carboplatin for the treatment of extensive-stage small-cell lung cancer (ES-SCLC). Patients and Methods Chemotherapy-naive patients with ES-SCLC and an Eastern Cooperative Oncology Group performance status of zero to 2 were randomly assigned to receive pemetrexed-carboplatin (pemetrexed 500 mg/m2 on day 1; carboplatin at area under the serum concentration-time curve [AUC] 5 on day 1) or etoposide-carboplatin (etoposide 100 mg/m2 on days 1 through 3; carboplatin AUC 5 on day 1) every 3 weeks for up to six cycles. The primary objective of the study was noninferiority of pemetrexed-carboplatin overall survival with a 15% margin. Results Accrual was terminated with 908 of 1,820 patients enrolled after results of a planned interim analysis. In the final analysis, pemetrexed-carboplatin was inferior to etoposide-carboplatin for overall survival (median, 8.1 v 10.6 months; hazard ratio [HR],1.56; 95% CI, 1.27 to 1.92; log-rank P < .01) and progression-free survival (median, 3.8 v 5.4 months; HR, 1.85; 95% CI, 1.58 to 2.17; log-rank P < .01). Objective response rates were also significantly lower for pemetrexed-carboplatin (31% v 52%; P < .001). Pemetrexed-carboplatin had lower grade 3 to 4 neutropenia, febrile neutropenia, and leukopenia than etoposide-carboplatin; grade 3 to 4 thrombocytopenia was comparable between arms and anemia was higher in the pemetrexed-carboplatin arm. Conclusion Pemetrexed-carboplatin is inferior for the treatment of ES-SCLC. Planned translational research and pharmacogenomic analyses of tumor and blood samples may help explain the study results and provide insight into new treatment strategies.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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