Lung Cancer
Volume 70, Issue 1 , Pages 71-76, October 2010

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

  • Hyeong Su Kim

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
    • These authors contributed equally to this study.
  • ,
  • Gyeong-Won Lee

      Affiliations

    • Department of Internal Medicine, Gyeongsang National University College of Medicine, Jinju, Republic of Korea
    • Gyeongsang Institute of Health Science, Jinju, Republic of Korea
    • Gyeongnam Regional Cancer Center, Jinju, Republic of Korea
    • These authors contributed equally to this study.
  • ,
  • Jung Han Kim

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
    • Corresponding Author InformationCorresponding author at: Department of Internal Medicine, Kangnam Sacred-Heart Hospital, Hallym University Medical Center, 948-1, Daerim-1 dong, Yeongdeungpo-gu, Seoul 150-950, Republic of Korea. Tel.: +82 2 829 5414; fax: +82 2 846 4669.
  • ,
  • Ho Young Kim

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Jung Hye Kwon

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Hun Ho Song

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Hyo Jung Kim

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Joo Young Jung

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Geundoo Jang

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Dae Ro Choi

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Sang Myeon Park

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Tae Rim Shin

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Hee-sung Lee

      Affiliations

    • Department of Chest Surgery, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea
  • ,
  • Dae Young Zang

      Affiliations

    • Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea

Received 20 October 2009; received in revised form 18 December 2009; accepted 26 December 2009. published online 22 January 2010.

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 500mg/m2 over a 10-min intravenous infusion and carboplatin at an AUC 5mg/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.

Keywords: Pemetrexed, Carboplatin, Non-small cell lung cancer, Salvage

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0169-5002(10)00002-4

doi:10.1016/j.lungcan.2009.12.015

Lung Cancer
Volume 70, Issue 1 , Pages 71-76, October 2010