Dellas Kathrin, Höhler Thomas, Reese Thomas, Würschmidt Florian, Engel Erik, Rödel Claus, Wagner Wolfgang, Richter Michael, Arnold Dirk, Dunst Jürgen
Radiat Oncol. 2013 Apr 15;8:90. doi: 10.1186/1748-717X-8-90.
Preoperative radiochemotherapy (RCT) with 5-FU or capecitabine is the standard of care for patients with locally advanced rectal cancer (LARC). Preoperative RCT achieves pathological complete response rates (pCR) of 10-15%. We conducted a single arm phase II study to investigate the feasibility and efficacy of addition of bevacizumab and oxaliplatin to preoperative standard RCT with capecitabine.
Eligible patients had LARC (cT3-4; N0/1/2, M0/1) and were treated with preoperative RCT prior to planned surgery. Patients received conventionally fractionated radiotherapy (50.4 Gy in 1.8 Gy fractions) and simultaneous chemotherapy with capecitabine 825 mg/m2 bid (d1-14, d22-35) and oxaliplatin 50 mg/m2 (d1, d8, d22, d29). Bevacizumab 5 mg/kg was added on days 1, 15, and 29. The primary study objective was the pCR rate.
70 patients with LARC (cT3-4; N0/1, M0/1), ECOG < 2, were enrolled at 6 sites from 07/2008 through 02/2010 (median age 61 years [range 39-89], 68% male). At initial diagnosis, 84% of patients had clinical stage T3, 62% of patients had nodal involvement and 83% of patients were M0. Mean tumor distance from anal verge was 5.92 cm (± 3.68). 58 patients received the complete RCT (full dose RT and full dose of all chemotherapy). During preoperative treatment, grade 3 or 4 toxicities were experienced by 6 and 2 patients, respectively: grade 4 diarrhea and nausea in one patient (1.4%), respectively, grade 3 diarrhea in 2 patients (3%), grade 3 obstipation, anal abscess, anaphylactic reaction, leucopenia and neutropenia in one patient (1.4%), respectively. In total, 30 patients (46%) developed postoperative complications of any grade including one gastrointestinal perforation in one patient (2%), wound-healing problems in 7 patients (11%) and bleedings in 2 patients (3%). pCR was observed in 12/69 (17.4%) patients. Pathological downstaging (ypT < cT and ypN ≤ cN) was achieved in 31 of 69 patients (44.9%). All of the 66 operated patients had a R0 resection. 47 patients (68.1%) underwent sphincter preserving surgery.
The addition of bevacizumab and oxaliplatin to RCT with capecitabine was well tolerated and did not increase perioperative morbidity or mortality. However, the pCR rate was not improved in comparison to other trials that used capecitabine or capecitabine/oxaliplatin in preoperative radiochemotherapy.
术前使用5-氟尿嘧啶(5-FU)或卡培他滨进行放化疗(RCT)是局部晚期直肠癌(LARC)患者的标准治疗方案。术前RCT的病理完全缓解率(pCR)为10%-15%。我们开展了一项单臂II期研究,以探讨在术前使用卡培他滨的标准RCT基础上加用贝伐单抗和奥沙利铂的可行性和疗效。
符合条件的患者患有LARC(cT3-4;N0/1/2,M0/1),并在计划手术前接受术前RCT治疗。患者接受常规分割放疗(50.4 Gy,每次1.8 Gy),同时接受卡培他滨825 mg/m²,每日两次(第1-14天,第22-35天)和奥沙利铂50 mg/m²(第1天、第8天、第22天、第29天)化疗。在第1天、第15天和第29天添加贝伐单抗5 mg/kg。主要研究目标是pCR率。
2008年7月至2010年2月期间,在6个地点招募了70例LARC患者(cT3-4;N0/1,M0/1),ECOG<2(中位年龄61岁[范围39-89岁],68%为男性)。初始诊断时,84%的患者为临床T3期,62%的患者有淋巴结受累,83%的患者为M0。距肛缘的平均肿瘤距离为5.92 cm(±3.68)。58例患者接受了完整的RCT(全量放疗和全量化疗)。在术前治疗期间,分别有6例和2例患者出现3级或4级毒性反应:1例患者(1.4%)分别出现4级腹泻和恶心,2例患者(3%)出现3级腹泻,1例患者(1.4%)分别出现了3级便秘、肛周脓肿、过敏反应、白细胞减少和中性粒细胞减少。总共有30例患者(46%)出现了任何级别的术后并发症,包括1例患者(2%)出现胃肠道穿孔,7例患者(11%)出现伤口愈合问题,2例患者(3%)出现出血。69例患者中有12例(17.4%)观察到pCR。69例患者中有31例(44.9%)实现了病理降期(ypT<cT且ypN≤cN)。所有66例接受手术的患者均实现了R0切除。47例患者(68.1%)接受了保肛手术。
在使用卡培他滨的RCT基础上加用贝伐单抗和奥沙利铂耐受性良好,且未增加围手术期发病率或死亡率。然而,与术前放化疗中使用卡培他滨或卡培他滨/奥沙利铂的其他试验相比,pCR率并未提高。