Oliveira Suilane Coelho Ribeiro, Moniz Camila Motta Venchiarutti, Riechelmann Rachel, Alex Alexandra Kichfy, Braghirolli Maria Ignez, Bariani Giovanni, Nahas Caio, Hoff Paulo Marcelo Gehm
Universidade de Sao Paulo, Sao Paulo, Sao Paulo, Brazil.
J Gastrointest Cancer. 2016 Mar;47(1):75-81. doi: 10.1007/s12029-015-9790-4.
This was a phase II study of capecitabine in substitution of 5-fluorouracil (5-FU) in the chemoradiotherapy regimen for patients with localized squamous cell carcinoma of the anal canal.
Combined chemoradiation with infusional 5-FU and mitomycin is the standard treatment for localized squamous cell carcinoma (SCC) of the anal canal. Capecitabine is an oral fluoropirimidine that has been shown to be equally effective to 5-FU in many solid tumors. However, the efficacy of the substitution of 5-FU for capecitabine in anal SCC needs confirmation.
Patients with SCC of anal cancer T2-4N0M0 or T (any) N1-3M0, with good performance status and normal blood and renal function, were treated with capecitabine 825 mg/m(2) bid during radiotherapy associated with a single dose of mitomycin 15 mg/m(2) on day 1. The primary objective was local control rate at 6 months determined by clinical examination and radiological assessment. Sample size was calculated using the Fleming single-stage design.
From November 2010 to February 2014, N = 51 patients were initially included; however, 43 patients were assessed. Seventeen patients (39.5%) were stage II, 11 patients (25.6%) stage IIIA, and 15 patients (34.9%) stage IIIB. Four patients (9.3%) were HIV positive. With a median follow-up of 23.1 months (range 4 to 44.4 months), 3 patients (7%) presented partial response, 37 (86%) had complete response, and 3 patients developed progression of the disease (7%) at 6 months. The colostomy rate was 18.6%. It was observed a locoregional control of 86% in 6 months (CI 95% 0.72-0.94). The main grade 3-4 toxicities were grade 3 radiodermitis in 10 patients (23.2%), grade 3 lymphopenia in 5 patients (11.6%), and grade 3 neutropenia in 2 patients (6.9%). One HIV-positive patient had septic shock, pneumonia, herpetic encephalitis, atrial fibrillation, and macrophage activation syndrome.
Capecitabine can safely substitute infusional 5-FU in the standard chemoradiation regimen for SCC of the anal cancer, with a locoregional control of 86% in 6 months (CI 95% 0.72-0.94).
这是一项关于卡培他滨替代5-氟尿嘧啶(5-FU)用于肛管局部鳞状细胞癌患者放化疗方案的II期研究。
联合输注5-FU和丝裂霉素进行放化疗是肛管局部鳞状细胞癌(SCC)的标准治疗方法。卡培他滨是一种口服氟嘧啶,已证实在许多实体瘤中其疗效与5-FU相当。然而,在肛管SCC中用卡培他滨替代5-FU的疗效尚需证实。
肛管癌T2-4N0M0或T(任何)N1-3M0、身体状况良好且血液和肾功能正常的患者,在放疗期间接受卡培他滨825mg/m²,每日两次,第1天联合单次剂量丝裂霉素15mg/m²治疗。主要目标是通过临床检查和影像学评估确定6个月时的局部控制率。样本量采用弗莱明单阶段设计计算。
2010年11月至2014年2月,最初纳入N = 51例患者;然而,有43例患者接受了评估。17例患者(39.5%)为II期,11例患者(25.6%)为IIIA期,15例患者(34.9%)为IIIB期。4例患者(9.3%)为HIV阳性。中位随访23.1个月(范围4至44.4个月),6个月时3例患者(7%)出现部分缓解,37例(86%)完全缓解,3例患者疾病进展(7%)。结肠造口率为18.6%。观察到6个月时局部区域控制率为86%(95%CI 0.72 - 0.94)。主要的3 - 4级毒性反应为10例患者(23.2%)出现3级放射性皮炎,5例患者(11.6%)出现3级淋巴细胞减少,2例患者(6.9%)出现3级中性粒细胞减少。1例HIV阳性患者发生感染性休克、肺炎、疱疹性脑炎、心房颤动和巨噬细胞活化综合征。
在肛管癌SCC的标准放化疗方案中,卡培他滨可安全替代输注用5-FU,6个月时局部区域控制率为86%(95%CI 0.72 - 0.94)。