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病理完全缓解可能并非食管癌术前治疗后生存情况的最佳替代指标。

Pathologic complete response may not represent the optimal surrogate for survival after preoperative therapy for esophageal cancer.

作者信息

Blackstock A William, Aklilu Mabea, Lovato James, Farmer Michael R, Mishra Girish, Melin Susan A, Oaks Timothy, Geisinger Kim, Levine Edward A

机构信息

Department of Radiation Oncology, Wake Forest University School of Medicine, Winston Salem, NC 27157, USA.

出版信息

Int J Gastrointest Cancer. 2006;37(1):7-14. doi: 10.1385/IJGC:37:1:7.

Abstract

BACKGROUND

We designed a phase II trial to examine the benefit of preoperative hyperfractionated radiation therapy (XRT) and concurrent chemotherapy for patients with locally advanced esophageal cancer (LAEC).

AIM OF STUDY

The pathologic complete response (pCR) was the primary endpoint to estimate efficacy.

METHODS

Twenty-three patients with LAEC received twice-daily XRT during wk 1 and 5 and once-daily XRT during wk 2-4 (59 Gy). Cisplatin (100 mg/m(2)) was given on d 1, while 5-fluorouracil (1000 mg/m(2)) was given by continuous infusion the first and fifth weeks of the XRT.

RESULTS

The pCR for the 19 patients undergoing esophagectomy was 16%. The study was closed at the interim analysis having not met the required minimum pCR rate of 20%. Hematologic toxicities consisted of grades III and IV neutropenia observed in 33% and 14% of patients, respectively. Grade III nausea and vomiting was seen in 38% of patients. One grade V pulmonary toxicity occurred. The median survival was 44.6 mo with 65% of patients alive at 2 yr.

CONCLUSIONS

The pCR rate in this trial did not meet the predetermined statistical minimum. With the encouraging 2-yr survival, it is not clear that pCR is a reliable surrogate endpoint to discern treatment efficacy.

摘要

背景

我们设计了一项II期试验,以研究术前超分割放疗(XRT)联合同步化疗对局部晚期食管癌(LAEC)患者的益处。

研究目的

病理完全缓解(pCR)是评估疗效的主要终点。

方法

23例LAEC患者在第1周和第5周接受每日两次的XRT,在第2 - 4周接受每日一次的XRT(59 Gy)。顺铂(100 mg/m²)在第1天给药,而5-氟尿嘧啶(1000 mg/m²)在XRT的第1周和第5周持续输注。

结果

19例行食管切除术的患者的pCR率为16%。该研究在中期分析时因未达到所需的最低pCR率20%而提前结束。血液学毒性包括分别在33%和14%的患者中观察到的III级和IV级中性粒细胞减少。38%的患者出现III级恶心和呕吐。发生了1例V级肺部毒性。中位生存期为44.6个月,2年时65%的患者存活。

结论

该试验中的pCR率未达到预定的统计学最小值。鉴于令人鼓舞的2年生存率,尚不清楚pCR是否是辨别治疗疗效的可靠替代终点。

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