A phase II trial of docetaxel plus capecitabine in patients with previously treated non-small cell lung cancer.

Lee, Jae Jin; Han, Ji-Youn; Lee, Dae Ho; Kim, Hyae Young; Chun, Jong Ho; Lee, Hong Gi; Yoon, Seong Min; Lee, Sung Young; Lee, Jin Soo
Japanese journal of clinical oncology
2006Dec ; 36 ( 12 ) :761-7.
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Lee, Jae Jin -
Han, Ji-Youn -
Lee, Dae Ho -
Kim, Hyae Young -
Chun, Jong Ho -
Lee, Hong Gi -
Yoon, Seong Min -
Lee, Sung Young -
Lee, Jin Soo -
ABSTRACT
BACKGROUND: A combination of docetaxel (T) and capecitabine (X) showed synergistic effects in preclinical studies and phase III randomized trials of metastatic breast cancer. We conducted this phase II study to examine its efficacy in previously treated non-small cell lung cancer (NSCLC) patients.

METHODS: Patient eligibility required advanced NSCLC with measurable lesion(s), at least one prior regimen failure and Eastern Cooperative Oncology Group (ECOG) performance status 0-2. Treatment consisted of T 36 mg/m(2) i.v. on days 1 and 8 plus X 1000 mg/m(2) p.o. b.i.d. on days 1-14 of a 21-day cycle (level I) or T 30 mg/m(2) i.v. on days 1 and 8 plus X 625 mg/m(2) p.o. b.i.d. on days 1-14 of a 21-day cycle (level II).

RESULTS: A total of 35 patients (M/F=24/11) were enrolled; 29 had received one prior regimen and 19 had received platinum-based regimens. Significant non-hematologic toxicities were observed after the treatment given at level I, including one treatment-related death. Subsequently 29 patients were treated at level II. The treatment at level II was well tolerated with grade 3 or 4 neutropenia only in 10%, grade 3 asthenia in 21% and stomatitis in 14% of patients. Four (15%) of 27 evaluable patients had partial response (PR) at level II and eight (30%) had stable disease (SD).

CONCLUSIONS: The TX regimen showed modest antitumor effects in patients with previously treated NSCLC. For further studies, we recommend T 30 mg/m(2) i.v. on days 1 and 8 plus X 625 mg/m(2) p.o. b.i.d. on days 1-14 of a 21-day cycle.
docetaxel, capecitabine, non-small cell lung cancer, second-line treatment
MESH
Adenocarcinoma/drug therapy/metabolism/pathology, Adult, Aged, Antineoplastic Combined Chemotherapy Protocols/*therapeutic use, Capecitabine, Carcinoma, Large Cell/drug therapy/metabolism/pathology, Carcinoma, Non-Small-Cell Lung/*drug therapy/metabolism/pathology, Carcinoma, Squamous Cell/drug therapy/metabolism/pathology, Deoxycytidine/administration & dosage/analogs & derivatives, Disease-Free Survival, Dose-Response Relationship, Drug, Female, Fluorouracil/administration & dosage/analogs & derivatives, Humans, Lung Neoplasms/*drug therapy/metabolism/pathology, Male, Middle Aged, Survival Rate, Taxoids/administration & dosage, Treatment Outcome
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The TX regimen showed modest antitumor effects in patients with previously treated NSCLC. This study recommend T 30 mg/m2 i.v. on days 1 and 8 plus X 625 mg/m2 p.o. b.i.d. on days 1?4 of a 21-day cycle.
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DOI
10.1093/jjco/hyl106
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ICD 03
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