Outcomes of Third-Line Docetaxel-Based Chemotherapy in Advanced Gastric Cancer Who Failed Previous Oxaliplatin-Based and Irinotecan-Based Chemotherapies
- Authors
- Lee, Min Jeong; Hwang, In Gyu; Jang, Joung-Soon; Choi, Jin Hwa; Park, Byeong-Bae; Chang, Myung Hee; Kim, Seung Tae; Park, Se Hoon; Kang, Myoung Hee; Kang, Jung Hun
- Issue Date
- Dec-2012
- Publisher
- KOREAN CANCER ASSOCIATION
- Keywords
- Stomach neoplasms; Docetaxel; Oxaliplatin; Irinotecan
- Citation
- CANCER RESEARCH AND TREATMENT, v.44, no.4, pp 235 - 241
- Pages
- 7
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- CANCER RESEARCH AND TREATMENT
- Volume
- 44
- Number
- 4
- Start Page
- 235
- End Page
- 241
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/106775
- DOI
- 10.4143/crt.2012.44.4.235
- ISSN
- 1598-2998
2005-9256
- Abstract
- Purpose Little is known about outcomes in the use of third-line chemotherapy in cases of advanced gastric cancer (AGC). The primary aim of this retrospective study was to evaluate outcomes of docetaxel-based chemotherapy in patients with AGC that progressed after both oxaliplatin-based and irinotecan-based regimens. Materials and Methods Eligible patients were those with AGC who had previous chemotherapy including fluoropyrimidine and oxaliplatin as well as fluoropyrimidine and irinotecan and who received subsequent docetaxel-based chemotherapy. Thirty-five patients were retrospectively recruited from 5 medical centers in Korea. Patients received either weekly or 3 weekly with docetaxel +/- cisplatin. Results Thirty-one out of 35 patients were evaluated for treatment response. A total of 94 cycles of chemotherapy (median, 2; range, 1 to 7) were administered. The overall response rate was 14.3%, and the disease control rate was 45.7%. The median progression-free survival (PFS) was 1.9 months (95% confidence interval [Cl], 1.1 to 2.7 months). The median overall survival (OS) was 3.6 months (95% Cl, 2.8 to 4.4 months). PFS and OS were significantly prolonged in patients of the Eastern Cooperative Oncology Group, with performance status of 0 or 1 in multivariate analysis (PFS: hazard ratio[HR], 0.411; 95% Cl, 0.195 to 0.868; p=0.020 and OS: HR, 0.390; 95% Cl, 0.184 to 0.826; p=0.014, respectively). Four of the 35 patients enrolled in the study died due to infection associated with neutropenia. Conclusion Our findings suggest that salvage docetaxel-based chemotherapy is a feasible treatment option for AGC patients with good performance status (PS), whereas chemotherapy for patients with poor PS (PS <= 2) should be undertaken with caution for those who previously failed oxaliplatin- and irinotecan-based regimens.
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