Henkenberens Christoph, Meinecke Daniela, Michael Stoll, Bremer Michael, Christiansen Hans
Department of Radiation Oncology, Klinik für Strahlentherapie und Spezielle Onkologie, Medizinische Hochschule Hannover, Hannover Medical School, Carl-Neuberg-Str.1, 30625, Hannover, Germany.
End- und Dickdarmzentrum Hannover, Hannover, Germany.
Strahlenther Onkol. 2015 Nov;191(11):845-54. doi: 10.1007/s00066-015-0885-4. Epub 2015 Aug 26.
Chemoradiation (CRT) is the standard of care in patients with node-positive (cN+) and node-negative (cN0) anal cancer. Depending on the tumor size (T-stage), total doses of 50-60 Gray (Gy) in daily fractions of 1.8-2.0 Gy are usually applied to the tumor site. Inguinal and iliac lymph nodes usually receive a dose of ≥ 45 Gy. Since 2010, our policy has been to apply a reduced total dose of 39.6 Gy to uninvolved nodal regions. This paper provides preliminary results of the efficacy and safety of this protocol.
Overall, 30 patients with histologically confirmed and node-negative anal cancer were treated in our department from 2009-2014 with definitive CRT. Histology all cases showed squamous cell carcinoma. A total dose of 39.6 Gy [single dose (SD) 1.8 Gy] was delivered to the iliac/inguinal lymph nodes. The area of the primary tumor received 50-59.4 Gy, depending on the T-stage. In parallel with the irradiation, 5-fluorouracil (5-FU) at a dose of 1000 mg/m(2) was administered by continuous intravenous infusion over 24 h on days 1-4 and 29-32, and mitomycin C (MMC) at a dose of 10 mg/m(2) (maximum absolute dose 14 mg) was administered on days 1 and 29. The distribution of the tumor stages was as follows: T1, n = 8; T2, n = 17; T3 n = 3. Overall survival (OS), local control (LC) of the lymph nodes, colostomy-free survival (CFS), and acute and chronic toxicities were assessed.
The median follow-up was 27.3 months (range 2.7-57.4 months). Three patients (10.0 %) died, 2 of cardiopulmonary diseases and one of liver failure, yielding a 3-year OS of 90.0 %. Two patients (6.7 %) relapsed early and received salvage colostomies, yielding a 3-year CFS of 93.3 %. No lymph node relapses were observed, giving a lymph node LC of 100 %. According to the Common Terminology Criteria for Adverse Events Version 4.0 (CTCAE V. 4.0), there were no grade IV gastrointestinal or genitourinary acute toxicities. Seven patients showed acute grade III perineal skin toxicity. Acute grade III groin skin toxicity was not observed.
Reducing the total irradiation dose to uninvolved nodal regions to 39.6 Gy in chemoradiation protocols for anal carcinoma was safe and effective, and a prospective evaluation in future clinical trials is warranted.
放化疗(CRT)是淋巴结阳性(cN+)和淋巴结阴性(cN0)肛管癌患者的标准治疗方案。根据肿瘤大小(T分期),通常对肿瘤部位给予1.8 - 2.0Gy的每日分次剂量,总剂量为50 - 60Gy。腹股沟和髂淋巴结通常接受≥45Gy的剂量。自2010年以来,我们的策略是对未受累的淋巴结区域给予39.6Gy的降低总剂量。本文提供了该方案疗效和安全性的初步结果。
2009年至2014年期间,我们科室共对30例经组织学确诊且淋巴结阴性的肛管癌患者进行了根治性放化疗。所有病例组织学均显示为鳞状细胞癌。对髂/腹股沟淋巴结给予39.6Gy的总剂量[单次剂量(SD)1.8Gy]。根据T分期,原发肿瘤区域接受50 - 59.4Gy的剂量。在放疗的同时,于第1 - 4天和第29 - 32天,通过持续静脉输注给予剂量为1000mg/m² 的5 - 氟尿嘧啶(5 - FU),持续24小时,并且在第1天和第29天给予剂量为10mg/m²(最大绝对剂量14mg)的丝裂霉素C(MMC)。肿瘤分期分布如下:T1,n = 8;T2,n = 17;T3,n = 3。评估总生存期(OS)、淋巴结局部控制率(LC)、无结肠造口生存期(CFS)以及急性和慢性毒性。
中位随访时间为27.3个月(范围2.7 - 57.4个月)。3例患者(10.0%)死亡,2例死于心肺疾病,1例死于肝功能衰竭,3年总生存率为90.0%。2例患者(6.7%)早期复发并接受了挽救性结肠造口术,3年无结肠造口生存期为93.3%。未观察到淋巴结复发,淋巴结局部控制率为100%。根据不良事件通用术语标准第4.0版(CTCAE V. 4.0),未出现IV级胃肠道或泌尿生殖系统急性毒性。7例患者出现急性III级会阴皮肤毒性。未观察到急性III级腹股沟皮肤毒性。
在肛管癌放化疗方案中,将未受累淋巴结区域的总照射剂量降低至39.6Gy是安全有效的,未来临床试验有必要进行前瞻性评估。