Thind Govin, Johal Bal, Follwell Matthew, Kennecke Hagen Fritz
Division of Medical Oncology, British Columbia Cancer Agency - Vancouver Center, Vancouver, BC V5Z 4E6, Canada.
Radiat Oncol. 2014 May 29;9:124. doi: 10.1186/1748-717X-9-124.
Standard therapy for patients with stage I-III squamous cell carcinoma (SCC) of the anal canal is chemo-radiotherapy with 5-fluorouracil (5-FU) and mitomycin C (MMC). While there is limited published evidence to substitute capecitabine (CAP) for 5-FU, the objectives of the study were to describe the toxicity, dose intensity and outcomes of a sequential cohort of patients treated with chemo-radiotherapy with CAP and MCC in a population-based setting.
Patients with stage I-III malignancies of the anal canal referred between February 2010 and March 2012 were included. Dose intensity was calculated by comparing delivered versus planned radiation and chemotherapy treatments and toxicity was retrospectively graded according to standard protocol-specified criteria.
Among 66 eligible patients, median planned dose of radiation was 51.9 Gy over 5.5 weeks, range 25.0 to 63 Gy, and dose intensity was 98%. Median delivered dose of MCC delivered was 12 mg/m2 on day one, week one while median CAP dose was 825 mg/m2 twice daily on radiation days. CAP dose reductions due to toxicity were recorded for 13 patients (20%). Median follow-up was 20 months and 94% of patients with squamous cell histology had no evidence of relapse.
Chemo-radiation with CAP plus MMC is well tolerated and may be a reasonable consideration for patients with stage I-III SCC of the anal canal. A range of planned radiation dose was observed and longer follow-up is necessary to ensure that patients who received lower doses of radiation have similar outcomes to those who received larger doses.
肛管I - III期鳞状细胞癌(SCC)患者的标准治疗方案是采用5 - 氟尿嘧啶(5 - FU)和丝裂霉素C(MMC)进行放化疗。虽然将卡培他滨(CAP)替代5 - FU的已发表证据有限,但本研究的目的是描述在基于人群的环境中接受CAP和MMC放化疗的连续队列患者的毒性、剂量强度和治疗结果。
纳入2010年2月至2012年3月转诊的肛管I - III期恶性肿瘤患者。通过比较实际给予的放疗和化疗与计划的治疗来计算剂量强度,并根据标准方案指定的标准对毒性进行回顾性分级。
在66例符合条件的患者中,计划放疗的中位剂量为5.5周内51.9 Gy,范围为25.0至63 Gy,剂量强度为98%。MMC在第1周第1天给予的中位剂量为12 mg/m²,而CAP在放疗日的中位剂量为825 mg/m²,每日两次。13例患者(20%)因毒性记录了CAP剂量减少。中位随访时间为20个月,94%的鳞状细胞组织学患者无复发证据。
CAP加MMC的放化疗耐受性良好,对于肛管I - III期SCC患者可能是一个合理的选择。观察到一系列计划放疗剂量,需要更长时间的随访以确保接受较低放疗剂量的患者与接受较高剂量的患者有相似的治疗结果。