Cancer Res Treat.  2006 Apr;38(2):66-70.

The Efficacy and Safety of Padexol(R) (Paclitaxel) and Cisplatin for Treating Advanced Non-small Cell Lung Cancer

Affiliations
  • 1Department of Internal Medicine, St. Vincent's Hospital, The Catholic Unviersity of Korea, Korea. kimhoonkyo@yahoo.co.kr
  • 2Department of Internal Medicine, Korea University Medical Center, Korea.
  • 3Division of Hemato-Oncology, Department of Internal Medicine, Daegu Catholic University Medical Center, Korea.
  • 4Department of Internal Medicine, Daegu Fatima Hospital, Korea.

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.

Keyword

Non-small cell lung cancer; Chemotherapy; Padexol(R); Cisplatin

MeSH Terms

Anemia
Anorexia
Carcinoma, Non-Small-Cell Lung*
Cisplatin*
Drug Therapy
Drug Therapy, Combination
Febrile Neutropenia
Follow-Up Studies
Humans
Infusions, Intravenous
Myalgia
Nausea
Neutropenia
Paclitaxel
Premedication
Research Personnel
Cisplatin
Paclitaxel

Figure

  • Fig. 1 Overall survival. The Kaplan-Meier estimate of median overall survival was 10.5 months (95% CI, 8.1 to 18.8 months).

  • Fig. 2 Time to disease progression. The Kaplan-Meier estimate of median time to disease progression was 5.8 months (95% CI, 4.7 to 7.4 months).


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