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The Efficacy and Safety of Padexol(R) (Paclitaxel) and Cisplatin for Treating Advanced Non-small Cell Lung Cancer / Journal of the Korean Cancer Association, 대한암학회지
Cancer Research and Treatment ; : 66-70, 2006.
Article in English | WPRIM | ID: wpr-58681
ABSTRACT

PURPOSE:

The authors conducted a multicenter study to evaluate the efficacy and safety of combination chemotherapy with Padexol(R) and cisplatin for treating patients with advanced non-small cell lung cancer (NSCLC). MATERIALS AND

METHODS:

From November 2003 to April 2005, 42 chemo-naive patients with advanced NSCLC were enrolled into this study from 4 hospitals. The treatment consisted of Padexol(R) 175 mg/m2 as a 3-hr infusion, and this was followed by cisplatin 75 mg/m2 administered as an intravenous infusion with standard premedication. The treatment was repeated every 3 weeks.

RESULTS:

Among the 42 patients (pts), 33 pts were evaluable for response. On the per protocol analysis, 1 patient (pt) (3.0%) achieved complete response (CR), 17 pts (51.5%) achieved partial response (PR), 6 pts (18.2%) achieved stable disease (SD), and 9 pts (27.3%) progressed; therefore, the overall response rate was 54.6% (95% CI 37.6~71.5%). On the intention-to-treat analysis, 1 pt (2.4%) achieved CR, 18 pts (42.9%) achieved PR, 11 pts (26.2%) achieved SD, and 9 pts (21.4%) progressed; therefore, the overall response rate was 45.2% (95% CI 30.2~60.3%). The response, as evaluated by the investigators, was independently reviewed by 2 external radiologists and it was as follows; 13 PR (43.3%), 14 SD (46.7%) and 3 progressive disease (10%). The median duration of response was 5.9 months. The median follow-up duration was 10.3 months (range 1.3 to 22.1 months). The median time to progression was 5.8 months (95% CI 4.7 to 7.4 months). The median survival time on the intention-to-treat analysis was 10.5 months (95% CI 8.1 to 18.8 months). The most common grade 3 or 4 hematologic toxicities were neutropenia (26/180 cycles, 14.4%), anemia (7/180 cycles, 3.9%) and febrile neutropenia (2/180 cycles, 1.1%). The most frequent grade 3 or 4 non-hematologic toxicities were nausea (14/42 patients, 14.3%), anorexia (3/42 patients, 7.1%) and myalgia (3/42 patients, 7.1%).

CONCLUSION:

The authors observed that Padexol(R) was as good as the other paclitaxel (Taxol(R) or Genexol(R)) formulations when combined with cisplatin for treating patients with advanced NSCLC.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Premedication / Research Personnel / Infusions, Intravenous / Anorexia / Follow-Up Studies / Cisplatin / Paclitaxel / Carcinoma, Non-Small-Cell Lung / Drug Therapy / Drug Therapy, Combination Type of study: Controlled clinical trial / Practice guideline / Observational study / Prognostic study Limits: Humans Language: English Journal: Cancer Research and Treatment Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Premedication / Research Personnel / Infusions, Intravenous / Anorexia / Follow-Up Studies / Cisplatin / Paclitaxel / Carcinoma, Non-Small-Cell Lung / Drug Therapy / Drug Therapy, Combination Type of study: Controlled clinical trial / Practice guideline / Observational study / Prognostic study Limits: Humans Language: English Journal: Cancer Research and Treatment Year: 2006 Type: Article