Literature DB >> 20096475

A phase II study of pemetrexed and carboplatin as a salvage therapy for platinum-pretreated patients with non-small cell lung cancer.

Hyeong Su Kim1, Gyeong-Won Lee, Jung Han Kim, Ho Young Kim, Jung Hye Kwon, Hun Ho Song, Hyo Jung Kim, Joo Young Jung, Geundoo Jang, Dae Ro Choi, Sang Myeon Park, Tae Rim Shin, Hee-sung Lee, Dae Young Zang.   

Abstract

BACKGROUND: Although platinum-based doublet chemotherapy is considered as standard of care for patients with advanced non-small cell lung cancer (NSCLC), most of them are eventually supposed to experience disease progression. Pemetrexed, docetaxel, erlotinib, and gefitinib have been shown to be active as monotherapy for pretreated patients. In this study, the efficacy of pemetrexed and carboplatin as a salvage therapy for patients with advanced NSCLC is evaluated. PATIENTS AND METHODS: From March 2007 to February 2009, 32 patients who were diagnosed with inoperable NSCLC and treated with one or more prior cisplatin-based chemotherapies were enrolled. Treatment consisted of pemetrexed 500 mg/m(2) over a 10-min intravenous infusion and carboplatin at an AUC 5 mg/mL/min over a 30-min intravenous infusion on Day 1 of a 21-day cycle. All patients were supplemented with folic acid and vitamin B12 to reduce the hematological toxicity of pemetrexed.
RESULTS: There were one (3.1%) complete response and five partial (15.6%) responses. The overall response rate was 18.8% and the median response duration was 4.4 months. Among the responders, four patients had adenocarcinoma and two had squamous cell carcinoma. Nine patients had stable disease, and the disease control rate was 46.9%. With a median follow up duration of 9.4 months, the median time to progression was 2.3 months and the median OS was 9.4 months. Seven patients (21.9%) experienced grade 3 and 4 hematologic toxicities; one anemia (3.1%), six neutropenia (18.8%), and six thrombocytopenia (18.8%). Two patients experienced grade 4 febrile neutropenia with infection. Four patients (12.5%) experienced grade 3 non-hematologic toxicities; four asthenia (12.5%), two anorexia (6.3%), and one stomatitis (3.1%). Grade 1-2 peripheral neuropathy developed in 13 patients (40.6%).
CONCLUSION: The combination of pemetrexed and carboplatin showed favorable toxicity profiles and activity in the pretreated patients with advanced NSCLC. It is suggested that this regimen can be a good chemotherapeutic option as a salvage therapy for patients with NSCLC. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20096475     DOI: 10.1016/j.lungcan.2009.12.015

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  4 in total

1.  Third-line therapy for advanced non-small-cell lung cancer patients: feasible drugs for feasible patients.

Authors:  Zhengbo Song; Yongfeng Yu; Zhiwei Chen; Shun Lu
Journal:  Med Oncol       Date:  2010-11-30       Impact factor: 3.064

2.  [Analysis of the efficacy and survival of third-line treatment in advanced non-small cell lung cancer].

Authors:  Lan Shao; Zhengbo Song; Lin Hu; Fajun Xie; Guangyuan Lou; Wei Hong; Cuiping Gu; Dan Hong; Baochai Lin; Yiping Zhang
Journal:  Zhongguo Fei Ai Za Zhi       Date:  2012-06

3.  Efficacy of platinum agents for stage III non-small-cell lung cancer following platinum-based chemoradiotherapy: a retrospective study.

Authors:  Eriko Miyawaki; Hirotsugu Kenmotsu; Yasushi Shintani; Ikuo Sekine; Takehito Shukuya; Koichi Takayama; Akira Inoue; Isamu Okamoto; Katsuyuki Kiura; Kazuhisa Takahashi; Nobuyuki Yamamoto; Tomoya Kawaguchi; Etsuo Miyaoka; Ichiro Yoshino; Hiroshi Date
Journal:  BMC Cancer       Date:  2022-03-29       Impact factor: 4.430

4.  Sunitinib combined with pemetrexed and carboplatin in patients with advanced solid malignancies--results of a phase I dose-escalation study.

Authors:  Normand Blais; D Ross Camidge; Derek J Jonker; Denis Soulières; Scott A Laurie; Sami G Diab; Ana Ruiz-Garcia; Aron Thall; Ke Zhang; Richard C Chao; Laura Q Chow
Journal:  Invest New Drugs       Date:  2013-08-22       Impact factor: 3.850

  4 in total

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