Long-term results of neoadjuvant chemotherapy and combined chemoradiotherapy before surgery in the management of locally advanced oesophageal cancer: a single-centre experience

被引:6
|
作者
Diaz, Robert [1 ]
Reynes, Gaspar [1 ]
Tormo, Alejandro [3 ]
de Juan, Manuel [2 ]
Girones, Regina [1 ]
Segura, Angel [1 ]
Aparicio, Jorge [1 ]
Richart, Paula [1 ]
de la Cueva, Helena [1 ]
Garcia, Jose [1 ]
机构
[1] Univ Hosp La Fe, Med Oncol Unit, ES-46009 Valencia, Spain
[2] Univ Hosp La Fe, Dept Surg, ES-46009 Valencia, Spain
[3] Univ Hosp La Fe, Radiotherapy Unit, ES-46009 Valencia, Spain
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2009年 / 11卷 / 12期
关键词
Oesophageal cancer; Adenocarcinoma; Chemotherapy; Radiotherapy; SQUAMOUS-CELL CARCINOMA; ENDOSCOPIC ULTRASOUND; CHEMORADIATION; THERAPY; RADIOTHERAPY; TRIAL; US;
D O I
10.1007/s12094-009-0452-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Neoadjuvant chemoradiotherapy before surgery is an option in the treatment of locally advanced resectable oesophageal cancer (EC). However toxicity is substantial and the improvement in overall survival (OS) with this approach is controversial. Methods This was a prospective, single-centre study of neoadjuvant chemotherapy and concomitant chemoradiotherapy with CDDP and 5-FU and 50.4 Gy of external radiotherapy before possible radical surgery in patients with locally advanced resectable EC. If surgery was not possible, a second-phase radiotherapy boost of 10 Gy and one cycle of modified dose chemotherapy were used. Results Seventy-three patients included between 1998 and 2007: 96% males, median age 61, 83% squamous cell carcinomas, 23% lower third tumours, 36% stage II and 54% stage III and 47% local lymph node involvement. Eighty-six percent completed the combined protocol. Main grade 3-4 toxicities: mucositis (19%) and infections (8%); 4 toxic deaths. Clinical response rates: complete response 54%, partial response 27%, stable disease 8%. Twenty-five patients proceeded to surgery, with radical resection in 24. Pathological response rate: complete response 32%, partial response 52%, progression 16%. There were 7 postoperative deaths and 16 of 34 patients that did not have surgery received the second-phase RT boost. Survival analysis: Median follow-up of 64 months (range 6-134 months). Median OS of 10.33 months. 2-year and 5-year OS of 22 and 16%. The only significant prognostic factor in OS is the clinical complete response rate: 13.9 vs. 7.7 months (p=0.0049). Conclusions Our protocol offers a high rate of clinical activity although it is relatively toxic and seems to increase the postoperative mortality, which would blunt any small improvement in survival. The achievement of a complete response is a powerful prognostic factor.
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收藏
页码:835 / 841
页数:7
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