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局部晚期直肠癌新辅助放化疗的初步研究:一项II期研究的回顾性分析

Pilot study of intense neoadjuvant chemoradiotherapy for locally advanced rectal cancer: retrospective review of a phase II study.

作者信息

Xu Ben-Hua, Chi Pan, Guo Jin-Hua, Guan Guo-Xian, Tang Tian-Lan, Yang Ying-Hong, Chen Ming-Qiu, Song Jian-Yuan, Feng Chang-Yin

出版信息

Tumori. 2014 Mar-Apr;100(2):149-57. doi: 10.1177/030089161410000206.


DOI:10.1177/030089161410000206
PMID:24852858
Abstract

AIMS AND BACKGROUND: Locally advanced rectal adenocarcinoma is typically treated with neoadjuvant chemoradiotherapy and surgery. We assessed the effect of an additional cycle of capecitabine/oxaliplatin chemotherapy before surgery in 57 patients with T3/4, N+/- or T1/2, N+ rectal cancer. MATERIALS AND STUDY DESIGN: Radiotherapy (total dose, 50.4 Gy) was combined with three cycles of chemotherapy (two cycles concomitant with radiotherapy), and each cycle consisted of oxaliplatin (130 mg/m2 on day 1) and capecitabine (825 mg/m2, twice per day from day 1 to day 14) for 21 days. In addition to assessing the safety of this treatment, the primary endpoint was pathological complete response (pCR). The secondary endpoint was the change in primary tumor and node stage from pre-treatment to post-surgery. RESULTS: Eleven patients (19%) experienced complete tumor regression and 23 patients (40%) experienced tumor regression grade 3. Tumor down-staging occurred in 31 patients (54.4%) and down-staging of nodes occurred in 25 patients (43.9%). There was a significant difference in tumor stage between pre-treatment and post-surgery (P <0.001). Patients with less advanced N stages had significantly better recurrence-free survival but similar metastasis-free survival and overall survival. Tumor regression grade was not associated with overall survival, recurrence-free survival or metastasis-free survival. The most common adverse events were pulmonary infection (n = 6, 10.5%) and intestinal obstruction (n = 6, 10.5%): CONCLUSIONS. An additional cycle of chemotherapy given after chemoradiotherapy and before surgery provided good efficacy and had a satisfactory safety profile in patients with locally advanced rectal cancer.

摘要

目的与背景:局部晚期直肠腺癌通常采用新辅助放化疗及手术治疗。我们评估了57例T3/4、N±或T1/2、N+直肠癌患者在手术前额外增加一个周期的卡培他滨/奥沙利铂化疗的效果。 材料与研究设计:放疗(总剂量50.4 Gy)与三个周期的化疗联合(两个周期与放疗同步),每个周期由奥沙利铂(第1天130 mg/m²)和卡培他滨(825 mg/m²,第1天至第14天每日两次)组成,为期21天。除评估该治疗的安全性外,主要终点为病理完全缓解(pCR)。次要终点为从治疗前到手术后原发肿瘤和淋巴结分期的变化。 结果:11例患者(19%)出现肿瘤完全消退,23例患者(40%)出现3级肿瘤消退。31例患者(54.4%)出现肿瘤降期,25例患者(43.9%)出现淋巴结降期。治疗前和手术后肿瘤分期有显著差异(P<0.001)。N分期较晚的患者无复发生存期明显更好,但无转移生存期和总生存期相似。肿瘤消退分级与总生存期、无复发生存期或无转移生存期无关。最常见的不良事件是肺部感染(n = 6,10.5%)和肠梗阻(n = 6,10.5%)。 结论:在放化疗后手术前额外增加一个周期的化疗对局部晚期直肠癌患者疗效良好且安全性令人满意。

相似文献

[1]
Pilot study of intense neoadjuvant chemoradiotherapy for locally advanced rectal cancer: retrospective review of a phase II study.

Tumori. 2014

[2]
A phase II trial of neoadjuvant IMRT-based chemoradiotherapy followed by one cycle of capecitabine for stage II/III rectal adenocarcinoma.

Radiat Oncol. 2013-5-29

[3]
Oxaliplatin added to fluorouracil-based preoperative chemoradiotherapy and postoperative chemotherapy of locally advanced rectal cancer (the German CAO/ARO/AIO-04 study): final results of the multicentre, open-label, randomised, phase 3 trial.

Lancet Oncol. 2015-7-15

[4]
A phase II study of neoadjuvant chemoradiotherapy with oxaliplatin and capecitabine for rectal cancer.

Cancer Lett. 2011-7-5

[5]
Concomitant boost IMRT-based neoadjuvant chemoradiotherapy for clinical stage II/III rectal adenocarcinoma: results of a phase II study.

Radiat Oncol. 2014-3-7

[6]
Radiation Therapy Oncology Group 0247: a randomized Phase II study of neoadjuvant capecitabine and irinotecan or capecitabine and oxaliplatin with concurrent radiotherapy for patients with locally advanced rectal cancer.

Int J Radiat Oncol Biol Phys. 2011-7-19

[7]
Phase II trial of preoperative radiochemotherapy with concurrent bevacizumab, capecitabine and oxaliplatin in patients with locally advanced rectal cancer.

Radiat Oncol. 2013-4-15

[8]
Four-week neoadjuvant intensity-modulated radiation therapy with concurrent capecitabine and oxaliplatin in locally advanced rectal cancer patients: a validation phase II trial.

Int J Radiat Oncol Biol Phys. 2011-11-11

[9]
[Preoperative chemoradiotherapy for rectal cancer: experience from one centre].

Cancer Radiother. 2015-4

[10]
Pre-operative bevacizumab, capecitabine, oxaliplatin and radiation among patients with locally advanced or low rectal cancer: a phase II trial.

Eur J Cancer. 2011-6-12

引用本文的文献

[1]
Signet ring cell component predicts the response to neoadjuvant chemoradiotherapy in rectal cancer. Long interim results of a single institution experience.

Am J Cancer Res. 2022-3-15

[2]
The survival benefit of intensified full-dose XELOX chemotherapy concomitant to radiotherapy and then resting-period consolidation chemotherapy in locally advanced rectal cancer.

J Cancer. 2019-1-1

[3]
Apparent Diffusion Coefficient Predicts Pathology Complete Response of Rectal Cancer Treated with Neoadjuvant Chemoradiotherapy.

PLoS One. 2016-4-21

[4]
Is the irradiated small bowel volume still a predictor for acute lower gastrointestinal toxicity during preoperative concurrent chemo-radiotherapy for rectal cancer when using intensity-modulated radiation therapy?

Radiat Oncol. 2015-12-18

[5]
Circadian gene expression predicts patient response to neoadjuvant chemoradiation therapy for rectal cancer.

Int J Clin Exp Pathol. 2015-9-1

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