Zhai Z W, Zhang K N, Wang C, Han J G, Ma H C, Wei G H, Yang Y, Wang Z J
Department of General Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.
Department of Pathology, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2020 Mar 25;23(3):274-280. doi: 10.3760/cma.j.cn.441530-20190819-00312.
To compare the short-term efficacy and perioperative safety of neoadjuvant chemoradiotherapy (nCRT) with total neoadjuvant treatment (TNT) in patients with locally advanced rectal cancer (LARC). A retrospective cohort analysis was carried out. Inclusion criteria: (1) rectal adenocarcinoma confirmed by pathology with a distance from tumor inferior border to anal verge within 12 cm; (2) clinical stage cT3-4N0 or cT1-4N1-2 diagnosed by magnetic resonance imaging (MRI) or endorectal ultrasonography; (3) a single rectal tumor confirmed by colonoscopy; (4) patients suitable for chemoradiotherapy; (5) no previous history of other tumors. Exclusion criteria: (1)patients with previous rectal cancer surgery and local recurrence; (2) those who did not complete nCRT course; (3) those with distant metastases; (4) those with defective clinicopathological data. According to the above criteria, a total of 134 LARC patients at the Department of General Surgery of Beijing Chaoyang Hospital from January 2016 to January 2019 were enrolled, including 82 males and 52 females, with a male-female ratio of 1.58∶1.00 and mean age of (59.6±11.2) (26-81) years. Based on neoadjuvant regimen, patients were divided into nCRT group (=55) and TNT group (=79). There were no statistically significant differences in baseline data, such as age, sex, distance from tumor to anal verge, Eastern Cooperative Oncology Group (ECOG) performance status and clinical TNM stage, between the two groups (all >0.05). All the patients received pelvic intensity-modulated radiotherapy (IMRT) with a total dose of 50.4 Gy in 28 fractions. Patients in nCRT group received oral capecitabine chemotherapy during radiotherapy and underwent surgery 6-8 weeks after chemoradiation. Patients in TNT group received one cycle of induction CapeOX (oxaliplatin and capecitabine) and concurrent chemoradiotherapy, then underwent a radical surgery two weeks after completion of consolidation chemotherapy. The efficacy of neoadjuvant therapy, adverse events of chemoradiotherapy and perioperative safety were compared between the two groups. Patients of two groups completed the course of neoadjuvant therapy. There were no statistically significant differences between nCRT group and TNT group in the incidence of adverse events in neutropenia [7.3% (4/55) vs. 10.1% (8/79)], anemia [3.6% (2/55) vs. 3.8% (3/79)], thrombocytopenia [5.5% (3/55) vs. 7.6% (6/79)], gastrointestinal dysfunction [3.6% (2/55) vs. 6.3% (5/79)] and radiation enteritis [9.1% (5/55) vs. 8.9% (7/79)] (all >0.05). One hundred and thirty patients completed TME surgery, including 54 patients in nCRT group and 76 patients in the TNT group. Compared with the nCRT group, the proportion of abdominoperineal resection (APR) was higher in the TNT group [31.6% (25/76) vs. 13.0% (7/54), χ(2)=9.382, =0.009]. No statistically significant differences in morbidity of postoperative complication, operation time, intraoperative blood loss and postoperative hospital stay between the two groups were found (all >0.05). The distal and circumferential margins were negative in all the patients. Seventeen patients in the TNT group 22.4% (17/76) got pathologic complete response (pCR), which was significantly higher than 7.4% (4/54) in nCRT group (χ(2)=5.217, =0.022). There were no statistically significant differences in ypTNM classification, perineural invasion and venous invasion between the two groups (all >0.05). The pCR of TNT is higher than that of nCRT without increasing the incidence of toxicity and complications of radiotherapy and chemotherapy for patients with locally advanced rectal cancer.
比较新辅助放化疗(nCRT)与全新辅助治疗(TNT)在局部晚期直肠癌(LARC)患者中的短期疗效及围手术期安全性。进行了一项回顾性队列分析。纳入标准:(1)经病理确诊为直肠腺癌,肿瘤下缘距肛缘距离在12 cm以内;(2)经磁共振成像(MRI)或直肠内超声诊断为临床分期cT3 - 4N0或cT1 - 4N1 - 2;(3)经结肠镜检查确诊为单一直肠肿瘤;(4)适合放化疗的患者;(5)既往无其他肿瘤病史。排除标准:(1)既往有直肠癌手术及局部复发史的患者;(2)未完成nCRT疗程的患者;(3)有远处转移的患者;(4)临床病理资料不全的患者。根据上述标准,选取2016年1月至2019年1月在北京朝阳医院普通外科就诊的134例LARC患者,其中男性82例,女性52例,男女比例为1.58∶1.00,平均年龄为(59.6±11.2)(26 - 81)岁。根据新辅助治疗方案,将患者分为nCRT组(n = 55)和TNT组(n = 79)。两组患者的年龄、性别、肿瘤距肛缘距离、东部肿瘤协作组(ECOG)体能状态及临床TNM分期等基线数据比较,差异均无统计学意义(均P>0.05)。所有患者均接受盆腔调强放疗(IMRT),总剂量50.4 Gy,分28次照射。nCRT组患者在放疗期间口服卡培他滨化疗,并在放化疗后6 - 8周接受手术。TNT组患者接受1周期诱导化疗CapeOX(奥沙利铂和卡培他滨)及同步放化疗,巩固化疗结束后2周接受根治性手术。比较两组新辅助治疗的疗效、放化疗不良反应及围手术期安全性。两组患者均完成新辅助治疗疗程。nCRT组与TNT组在中性粒细胞减少[7.3%(4/55) vs. 10.1%(8/79)]、贫血[3.6%(2/55) vs. 3.8%(3/79)]、血小板减少[5.5%(3/55) vs. 7.6%(6/79)]、胃肠功能障碍[3.6%(2/55) vs. 6.3%(5/79)]及放射性肠炎[9.1%(5/55) vs. 8.9%(7/79)]的不良反应发生率方面比较,差异均无统计学意义(均P>0.05)。130例患者完成了全直肠系膜切除术(TME),其中nCRT组54例,TNT组76例。与nCRT组比较,TNT组腹会阴联合切除术(APR)比例更高[31.6%(25/76) vs. 13.0%(7/54),χ² = 9.382,P = 0.009]。两组患者术后并发症发生率、手术时间、术中出血量及术后住院时间比较,差异均无统计学意义(均P>0.05)。所有患者切缘远端及环周均为阴性。TNT组17例患者(22.4%,17/76)达到病理完全缓解(pCR),显著高于nCRT组的7.4%(4/54)(χ² = 5.217,P = 0.022)。两组患者ypTNM分期、神经侵犯及脉管侵犯比较,差异均无统计学意义(均P>0.05)。对于局部晚期直肠癌患者,TNT的pCR高于nCRT,且未增加放化疗的毒性及并发症发生率。