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Pemetrexed and cisplatin in patients with advanced gastric cancer: a Korean cancer study group multicenter phase II study.

Authors
 Yeul Hong Kim  ;  Hyun Cheol Chung  ;  Won Ki Kang  ;  Sook Ryun Park  ;  Chul Soo Kim  ;  Tae-Yue Kim  ;  Sang Won Shin  ;  Byung-Joo Park  ;  Soo Jin Cha  ;  Yung-Jue Bang 
Citation
 CANCER CHEMOTHERAPY AND PHARMACOLOGY, Vol.62(2) : 263-270, 2008 
Journal Title
CANCER CHEMOTHERAPY AND PHARMACOLOGY
ISSN
 0344-5704 
Issue Date
2008
MeSH
Adenocarcinoma/drug therapy* ; Adenocarcinoma/mortality ; Adenocarcinoma/pathology ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols/administration & dosage ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use* ; Cisplatin/administration & dosage ; Cisplatin/adverse effects ; Cisplatin/therapeutic use ; Disease-Free Survival ; Female ; Glutamates/administration & dosage ; Glutamates/adverse effects ; Glutamates/therapeutic use ; Guanine/administration & dosage ; Guanine/adverse effects ; Guanine/analogs & derivatives ; Guanine/therapeutic use ; Humans ; Infusions, Intravenous ; Korea ; Male ; Middle Aged ; Neoplasm Invasiveness ; Pemetrexed ; Stomach Neoplasms/drug therapy* ; Stomach Neoplasms/mortality ; Stomach Neoplasms/pathology
Keywords
Advanced gastric cancer ; Chemotherapy ; Cisplatin ; Pemetrexed ; Phase II trial
Abstract
BACKGROUND: Pemetrexed is a multitargeted antifolate enzyme inhibitor, which has activity against a variety of tumors, including advanced gastric cancer (AGC). The aim of this study was to assess efficacy and safety of pemetrexed plus cisplatin (PemCis) combination in the treatment of AGC in Korean patients.

PATIENTS AND METHODS: This was a multicenter, single arm, open label study. Patients with no prior palliative chemotherapy received pemetrexed 500 mg/m(2) and cisplatin 75 mg/m(2) day 1, every 3 weeks plus folic acid and vitamin B(12) supplementation. Response rate was assessed according to response evaluation criteria in solid tumors (RECIST) criteria.

RESULTS: Of the 50 patients evaluable for efficacy, 13 had partial response for an overall response rate of 26% (95% CI, 14.6-40.3%) and 15 (30%) had stable disease. Median time to progression was 2.8 months (95%CI, 2.2-4.4 months), and median overall survival was 6.6 months (95% CI, 4.8-10.4 months). Of the 51 patients evaluable for safety, the most frequent NCI-CTC grade 3/4 toxicities were neutropenia in 49% of patients (25% of cycles) and anorexia in 10% of patients (4% of cycles).

CONCLUSION: PemCis has a modest activity and acceptable toxicity profile in patients with AGC. Clinical trials with different combinations and dose regimens are, therefore, warranted.
Full Text
http://link.springer.com/article/10.1007%2Fs00280-007-0600-y
DOI
10.1007/s00280-007-0600-y
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Chung, Hyun Cheol(정현철) ORCID logo https://orcid.org/0000-0002-0920-9471
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/106388
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