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Volume 69, Issue 1, Pages 94-98 (July 2010)


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Phase II study of a biweekly schedule of docetaxel and cisplatin in patients with metastatic non-small cell lung cancer

Su-Hee Choabc1, Se-Il Goabc1, Gyeong-Won LeeabcCorresponding Author Informationemail address, Jung Hun Kangabc, Hoon-Gu Kimabc, Seok Hyun Kima, Yu Ji Choab, Yi Yeong Jeongabc, Ho-Cheol Kimabc, Jong Duk Leeabc, Young Sil Hwangabc

Received 30 June 2009; received in revised form 3 September 2009; accepted 8 September 2009. published online 05 October 2009.

Abstract 

Purpose

We investigated the efficacy and toxicity of a biweekly schedule of docetaxel and cisplatin in patients with metastatic non-small cell lung cancer (NSCLC).

Methods

In this study, 48 patients with previously untreated metastatic NSCLC were given combination chemotherapy consisting of docetaxel 40mg/m2 and cisplatin 40mg/m2; both drugs were given biweekly, on days 1 and 15, every 4 weeks.

Results

A partial response and stable disease were observed in 25 patients (52.1%, 95% CI: 38.7–66.9%) and ten patients (20.8%), respectively. The overall median survival was 14.0 months (95% CI: 7.10–20.9 months). There was no treatment-related mortality. The major toxicity was grade 2 asthenia (35.4%). Grade 4 neutropenia was observed in two patients (4.2%), as was grade 3 infection (4.2%).

Conclusions

As a front-line chemotherapy in an outpatient setting for patients with metastatic NSCLC, the biweekly schedule of docetaxel and cisplatin showed effective antitumor activity with a marked reduction in hematologic toxicity, comparable to the results of previous studies using 3-week or weekly schedules. Further randomized studies are needed before this can be accepted as a standard schedule.

a Department of Internal Medicine, School of medicine Gyeongsang National University, Jinju, Republic of Korea

b Gyeongsang Institute of Health Science, Jinju, Republic of Korea

c Gyeongnam Regional Cancer Center, Jinju, Republic of Korea

Corresponding Author InformationCorresponding author at: Division of Hematology-Oncology, Department of Internal Medicine, School of Medicine Gyeongsang National University, 660-702 Jinju, Republic of Korea. Tel.: +82 55 750 8066; fax: +82 55 758 9122.

1 These authors contributed equally to this work.

PII: S0169-5002(09)00489-9

doi:10.1016/j.lungcan.2009.09.005


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