Phase II trial of preoperative chemoradiotherapy with oxaliplatin, cisplatin, and 5-FU in locally advanced esophageal and gastric cancer

被引:30
|
作者
Pera, M. [1 ,2 ]
Gallego, R. [3 ]
Montagut, C. [2 ,4 ]
Martin-Richard, M. [5 ]
Iglesias, M. [6 ]
Conill, C. [3 ]
Reig, A. [7 ]
Balague, C. [8 ]
Petriz, L. [9 ]
Momblan, D. [10 ]
Bellmunt, J. [2 ,4 ]
Maurel, J. [3 ]
机构
[1] Univ Autonoma Barcelona, Sect Gastrointestinal Surg, Hosp Univ del Mar, Barcelona 08003, Spain
[2] Univ Autonoma Barcelona, Inst Recerca Hosp del Mar IMIM, Barcelona 08003, Spain
[3] Univ Barcelona Med Sch, Dept Med Oncol & Radiat Therapy, Hosp Clin Barcelona, Inst Invest Biomed August Pi & Sunyer IDIBAPS, Barcelona, Spain
[4] Hosp Univ del Mar, Med Oncol Serv, Barcelona, Spain
[5] Hosp Santa Creu & Sant Pau, Med Oncol Serv, Barcelona, Spain
[6] Hosp Univ del Mar, Serv Pathol, Barcelona, Spain
[7] Hosp Univ del Mar, Serv Radiotherapy, Barcelona, Spain
[8] Hosp Santa Creu & Sant Pau, Serv Digest Surg, Barcelona, Spain
[9] Hosp Santa Creu & Sant Pau, Serv Radiat Therapy, Barcelona, Spain
[10] Hosp Clin Barcelona, Serv Gastrointestinal Surg, Barcelona, Spain
关键词
chemoradiotherapy; esophageal cancer; gastric cancer; oxaliplatin; pathologic response; preoperative therapy; SQUAMOUS-CELL CARCINOMA; DNA MISMATCH REPAIR; NEOADJUVANT CHEMOTHERAPY; ONCOLOGY-GROUP; SURGERY; METAANALYSIS; THERAPY; CHEMORADIATION; CLASSIFICATION; 5-FLUOROURACIL;
D O I
10.1093/annonc/mdr291
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Based on a phase I study showing the feasibility of combining of oxaliplatin, cisplatin, and 5-fluorouracil (5-FU) (OCF) with radiation therapy (RT) in esophageal cancer, the efficacy of this regimen in esophageal, gastroesophageal (GE), and gastric (G) cancer was assessed in this phase II multicenter study. Patients and methods: Patients with resectable tumors were eligible. Treatment included two cycles of oxaliplatin 85 mg/m(2), cisplatin 55 mg/m(2), and continuously infused 5-FU 3 g/m(2) in 96 h and concurrent RT (45 Gy), followed by surgery after 6-8 weeks. Primary end point was complete pathologic response (pCR). Results: Forty-one patients were enrolled. Tumor location was esophagus 39% (squamous 10/adenocarcinoma 6), GE junction 32%, and stomach 29%. G3-G4 adverse events included asthenia (27%) and neutropenia (14%). One toxic death occurred. Thirty-one patients (75.6%) underwent surgery (R0 in 94%). Pathologic response was achieved in 58% of patients, with pCR in 50% and 16% of esophageal and GE/G cancer, respectively. pCR was achieved in 67% of squamous cell carcinoma. Survival: median follow-up, 50.4 months; median progression-free survival and overall survival were 23.2 and 28.4 months, respectively. Conclusion: Preoperative OCF plus RT showed an acceptable toxicity and promising activity especially in squamous cell esophageal cancer.
引用
收藏
页码:664 / +
页数:7
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