A multi-center phase II study of oxaliplatin, irinotecan, and capecitabine in advanced gastric/gastroesophageal junction carcinoma

被引:21
作者
Brell, Joanna M. [1 ,2 ]
Krishnamurthi, Smitha S. [1 ,2 ]
Javle, Milind [3 ]
Saltzman, Joel [4 ]
Wollner, Ira [5 ]
Pelley, Robert [6 ]
Dowlati, Afshin [1 ,2 ]
Kantharaj, Belagodu N. [7 ]
Schluchter, Mark D. [8 ]
Rath, Linda [1 ,2 ]
Ivy, S. Percy [9 ]
Remick, Scot C. [10 ]
机构
[1] Univ Hosp Case Med Ctr, Dept Med, Cleveland, OH 44106 USA
[2] Case Comprehens Canc Ctr, Dev Therapeut Program, Cleveland, OH USA
[3] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[4] Lake Univ, Ireland Canc Ctr, Mentor, OH USA
[5] Henry Ford Hlth Syst, Detroit, MI USA
[6] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[7] Community Hlth Partners, Elyria, OH USA
[8] Case Comprehens Canc Ctr, Div Biostat, Cleveland, OH USA
[9] NCI, Invest Drug Branch, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
[10] W Virginia Univ, Mary Babb Randolph Canc Ctr, Morgantown, WV 26506 USA
关键词
Gastric cancer; Phase II; Chemotherapy; Metastatic; ADVANCED GASTRIC-CANCER; FOLINIC ACID; TRIAL; FLUOROURACIL; CISPLATIN; 5-FLUOROURACIL; DOXORUBICIN; TOXICITY; CHEMOTHERAPY; METHOTREXATE;
D O I
10.1007/s00280-008-0807-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
There is no standard first-line therapy for advanced gastric and gastroesophageal junction (GEJ) adenocarcinoma and the prognosis remains poor. Our institution conducted a phase I study of oxaliplatin, irinotecan, and capecitabine given in a novel, weekly schedule. The regimen was tolerated; pharmacodynamic studies revealed no drug interactions, and there was one confirmed response in a gastric cancer patient. We performed a phase II trial in advanced gastric and GEJ adenocarcinoma to determine response rate and response duration. This was a multi-center single treatment arm study involving six sites. Only prior adjuvant therapy was allowed. Patients had ECOG performance status of 0-2, adequate organ function, and were able to tolerate oral medications. All patients received oxaliplatin 60 mg/m(2) intravenously (IV) and irinotecan 50 mg/m(2) IV weekly times 4 weeks with a 2-week rest period. Capecitabine 450 mg bid orally was received on days 1 through 5 every week for 4 weeks, followed by a 2-week rest. Patients were assessed for response after the first two cycles; response duration, overall survival, and adverse events were also recorded. We estimated an improvement in historical response rate by 30% would have clinical meaning. A total of 39 patients were accrued and all were assessed for toxicity; 30 patients were evaluable for response. The median age was 57.8 years (31-79 years) and 74% were male. Two patients had a complete response, with nine patients achieving a partial response. The total response rate was 28%, with nine patients not evaluable for response. The median response duration was noted at 5.97 months and median overall survival was 8.98 months. There were no grade 5 treatment related events, with all deaths secondary to disease progression. Only five grade 4 events occurred (neutropenia, hyperkalemia, hypokalemia (2), thrombosis/embolism) without grade 4 diarrhea or sensory neuropathy. Oxaliplatin, irinotecan, and capecitabine given in a novel, weekly schedule does induce responses in advanced gastric and GEJ adenocarcinoma. However, the total response rate is modest and not an improvement over other regimens.
引用
收藏
页码:851 / 857
页数:7
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