Vulvar Recurrences After Intensity-modulated Radiation Therapy for Squamous Cell Carcinoma of the Anus

被引:4
|
作者
Bagshaw, Hilary P. [1 ]
Sause, William T. [2 ]
Gawlick, Ute [3 ]
Kim, H. Tae [3 ]
Whisenant, Jonathan [4 ]
Cannon, George M. [2 ]
机构
[1] Stanford Univ Hosp & Clin, Stanford, CA USA
[2] Intermt Healthcare Radiat Oncol, Salt Lake City, UT USA
[3] Intermt Colon & Rectal Surg, Salt Lake City, UT USA
[4] Huntsman Canc Inst, Salt Lake City, UT USA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2018年 / 41卷 / 05期
关键词
anal cancer; radiotherapy; IMRT; CONCURRENT CHEMOTHERAPY; NECK-CANCER; RADIOTHERAPY; MITOMYCIN; CHEMORADIATION; TRIAL; FLUOROURACIL; COMBINATION; CISPLATIN; TOXICITY;
D O I
10.1097/COC.0000000000000322
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: The objective is to determine localregional control (LRC), distant metastasis free survival, disease-free survival, overall survival (OS), and toxicity for patients with squamous cell carcinoma of the anus treated with definitive chemotherapy and intensity-modulated radiation therapy (IMRT). Materials and Methods: We conducted a retrospective review of patients treated using IMRT for squamous cell carcinoma of the anus at our institution since 2005. Patients with local recurrences were identified and reviewed. The Kaplan-Meier curves were used for LRC and OS. Results: From 2005 to 2014, 52 patients were treated with IMRT-based chemoradiation for squamous cell carcinoma of the anus. Median dose to the primary tumor was 54 Gy. LRC, distant metastasis free survival, OS, and disease-free survival were 92.3%, 88.5%, 86.5%, and 84.6%, respectively, with a median follow-up of 20 months. Two local failures occurred at the anal primary site and 2 in the vulva. Despite subsequent palliative radiotherapy and chemotherapy, neither patient with a vulvar recurrence achieved disease control. Conclusions: In a cohort of patients treated with IMRT-based chemoradiation, 2 vulvar recurrences were identified within the avoided external genitalia despite limited recurrence rates within the cohort overall. This experience suggests that for patients with a locally advanced primary tumor and bulky bilateral inguinal or pelvic disease, the in-transit vulvar dermal lymphatics may be at risk for subclinical involvement and subsequent recurrence. If substantiated by a similar pattern of recurrence at other institutions, the external genitalia may need to be reclassified from an avoidance structure to a clinical treatment volume in patients with locally advanced anal cancer.
引用
收藏
页码:492 / 496
页数:5
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