Outcomes after intensity-modulated compared with 3-dimensional conformal radiotherapy with chemotherapy for squamous cell carcinoma of the anal canal

被引:0
|
作者
Agarwal, M. S. [1 ]
Hitchcock, K. E. [1 ]
Morris, C. G. [1 ]
George, T. J., Jr. [2 ]
Mendenhall, W. M. [1 ]
Zlotecki, R. A. [1 ]
机构
[1] Univ Florida, Coll Med, Dept Radiat Oncol, Gainesville, FL USA
[2] Univ Florida, Coll Med, Dept Med, Gainesville, FL USA
关键词
Radiation oncology; anal carcinoma; intensity-modulated radiotherapy; 3-dimensional conformal radiotherapy; SIMULTANEOUS INTEGRATED BOOST; RADIATION-THERAPY; CONCURRENT CHEMOTHERAPY; RANDOMIZED-TRIAL; CANCER-PATIENTS; MITOMYCIN; CHEMORADIATION; 5-FLUOROURACIL; FLUOROURACIL; COMBINATION;
D O I
10.3747/co.26.4311
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We report our institution's treatment techniques, disease outcomes, and complication rates after radiotherapy for the management of anal canal carcinoma with intensity-modulated radiotherapy (mni) and concurrent chemotherapy relative to prior cases managed with 3-dimensional conformal radiotherapy (3D-CRT). Methods In a retrospective review of the medical records of 21 patients diagnosed with biopsy-proven stage I (23%), stage II (27%), or stage III (50%) squamous-cell carcinoma of the anal canal treated with curative chemotherapy and IMRT between July 2009 and December 2014, patient outcomes were determined. Results for patients treated with 3D-car by the same group were previously reported. The median initial radiation dose to the pelvic and inguinal nodes at risk was 45 Gy (range: 36-50.4 Gy), and the median total dose, including local anal canal primary tumour boost, was 59.4 Gy (range: 41.4-61.2 Gy). Patients received those doses over a median of 32 fractions (range: 23-34 fractions). Chemotherapy consisted of 2 cycles of concurrent fluorouracil-cisplatin (45%) or fluorouracil-mitomycin C (55%). Results Median follow-up was 3.1 years (range: 0.38-6.4 years). The mean includes a patient who died of septic shock at 38 days. The 3-year rates of overall survival, metastasis-free survival, locoregional control, and colostomy-free survival were 95%, 100%, 100%, and 100% respectively. No patients underwent abdominoperitoneal resection after chemoradiotherapy or required diverting colostomy during or after treatment. Those outcomes compare favourably with the previously published series that used 3D-CRT with or without brachytherapy in treating anal canal cancers. Of the 21 patients in the present series, 10 (48%) experienced acute grade 3, 4, or 5 toxicities related to treatment. Conclusions The recommended use of IMRT with concurrent chemotherapy as an improvement over 3D-CRT for management of anal canal carcinoma achieves a high probability of local control and colostomy-free survival without excessive risk for acute or late treatment-related toxicities.
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收藏
页码:E515 / E521
页数:7
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