Feasibility and Safety of 3-Weekly Carboplatin/Paclitaxel Regimen in Advanced Squamous cell Carcinoma of the Anal Canal

A. Dornellas, R. Bonadio, P. M. Moraes, M. Braghiroli, R. Polizio, P. Hoff, C. Moniz
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Abstract

Introduction: Anal cancer is a rare disease, and there is a lack of phase 3 studies in the advanced setting. Currently, the standard treatment is based on interAACT phase 2 study using Carboplatin (C) (AUC 5, D1q28) plus Paclitaxel (P) (80 mg/m2, D1,8,15q28). This study demonstrated a median OS of 20m, a response rate of 59% and serious adverse events in 36% of patients (pts). However, this regimen requires more infusions and hospital visits than a 3-weekly CP regimen, resulting in high social and financial cost. Objective: To retrospectively access safety and efficacy of treatment with 3-weekly CP in advanced SCCA. Methods: We performed a single-center retrospective analysis of patients (pts) who received first-line treatment with 3-weekly CP for inoperable locally recurrent or metastatic SCCA between Jun/2011 and Jun/2018. Study data were collected using REDCap®. Survival analyses were estimated with the Kaplan-Meier method and compared by log-rank test. Prognostic factors were evaluated by Cox regression. Results: 47 patients were included. Median age was 57 years, 60% (n=28) were female and 21% (n=10) HIV positive.16% (n=7) had metastatic disease at diagnosis. The majority of pts (n=42) were treated with paclitaxel (P) 175 mg/m2 plus carboplatin (C) AUC 5 every 3 weeks. The median number of cycles was 4 and dose reduction by toxicity was necessary for 30% (n=14). Grade 3/4 adverse events were neutropenia 19% (n=9), anemia 4% (n=2), fatigue 4% (n=2), neuropathy 2% (n=1). Two pts had interruption due to toxicity and no treatment-related death. 64% of patients benefited from treatment, 4% with complete response. The median overall survival (OS) was 10 months(m). In a multivariable analysis, HIV-positive (HIV+) status (HR 3.1; 95%CI 1.8-8.4; p 0.001) and ECOG 2/3 (HR 3.9; 95%CI 1.2-8.1; p 0.01) showed a negative impact on OS. Median OS was 16m for HIV- vs 4m for HIV+ group; and 20m for ECOG 0/1 vs 4m for ECOG 2/3. Conclusion: The present study suggests that 3-weekly CP has similar outcomes to the InterAACT regimen. Nevertheless, pts who are HIV+ or have ECOG 2/3 had poor outcomes and other treatment strategies should be studied for these pts.
3周卡铂/紫杉醇方案治疗晚期肛管鳞状细胞癌的可行性和安全性
简介:肛门癌是一种罕见的疾病,在晚期环境中缺乏3期研究。目前,标准治疗是基于interAACT 2期研究,使用卡铂(C) (AUC 5, D1q28)加紫杉醇(P) (80 mg/m2, D1,8,15q28)。该研究显示,中位总生存期为20m,缓解率为59%,36%的患者(pts)发生严重不良事件。然而,与3周CP方案相比,该方案需要更多的输液和医院就诊,导致较高的社会和经济成本。目的:回顾性评价3周CP治疗晚期SCCA的安全性和有效性。方法:我们对2011年6月至2018年6月期间接受3周CP一线治疗的局部复发或转移性SCCA患者(pts)进行了单中心回顾性分析。使用REDCap®收集研究数据。生存分析采用Kaplan-Meier法估计,log-rank检验比较。采用Cox回归评价预后因素。结果:纳入47例患者。中位年龄为57岁,60% (n=28)为女性,21% (n=10)为HIV阳性。16% (n=7)在诊断时有转移性疾病。大多数患者(n=42)每3周接受紫杉醇(P) 175 mg/m2加卡铂(C) AUC 5治疗。中位周期数为4个,30%需要毒性减量(n=14)。3/4级不良事件为中性粒细胞减少19% (n=9),贫血4% (n=2),疲劳4% (n=2),神经病变2% (n=1)。2名患者因毒性而中断治疗,无治疗相关死亡。64%的患者从治疗中受益,4%的患者完全缓解。中位总生存期(OS)为10个月。在多变量分析中,HIV阳性(HIV+)状态(HR 3.1;95%可信区间1.8 - -8.4;p 0.001)和ECOG 2/3 (HR 3.9;95%可信区间1.2 - -8.1;p < 0.01)对OS有负面影响。HIV组的中位OS为1600万,HIV+组为400万;ECOG 0/1为20m, ECOG 2/3为4m。结论:目前的研究表明,3周CP与InterAACT方案具有相似的结果。然而,HIV阳性或ECOG 2/3的患者预后较差,应针对这些患者研究其他治疗策略。
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