Stereotactic Ablative Radiotherapy (SABR) for Large Renal Tumors

医学 SABR波动模型 不良事件通用术语标准 肾细胞癌 肾切除术 实体瘤疗效评价标准 离格 进行性疾病 置信区间 放射治疗 恶心 肺炎 外科 不利影响 放射科 内科学 化疗 金融经济学 经济 随机波动 波动性(金融)
作者
Rohann Correa,George Rodrigues,Hanbo Chen,Andrew Warner,Belal Ahmad,Alexander V. Louie
出处
期刊:American Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:41 (6): 568-575 被引量:35
标识
DOI:10.1097/coc.0000000000000329
摘要

Objectives: Metastatic renal cell carcinoma represents a clinical scenario where aggressive treatment to the primary tumor (ie, cytoreductive nephrectomy) is associated with a survival benefit. We hypothesized that stereotactic ablative radiotherapy (SABR) could be a safe alternative local modality for inoperable metastatic renal cell carcinoma patients. Our study objectives were to report on technical considerations, toxicity, and clinical outcomes of our institutional experience with renal SABR. Materials and Methods: Patients who underwent renal SABR at our institution between January 2008 and June 2015 were reviewed. Toxicity was quantified using the Common Terminology Criteria for Adverse Events version 4.0. Radiographic response was evaluated using the Response Evaluation Criteria in Solid Tumors classification. Median overall survival and follow-up were calculated using the Kaplan-Meier and reverse Kaplan-Meier methods, respectively. Results: We identified 11 patients that met study criteria. SABR was directed to the tumor or whole kidney in 5 fractions to a dose of 25 to 40 Gy. Median tumor diameter and planning target volume were 9.5 cm (range, 7.5 to 24.4) and 819.3 cm 3 (range, 313.4 to 5704.3), respectively. Median follow-up was 3.9 years (95% confidence interval, 0.6-4.9). Five cases of grade 1 toxicity were reported. In the patient with the largest target, grade 2 diarrhea and probable grade 3 nausea were observed. In patients with available follow-up imaging (7/11), stable disease (n=5), partial response (n=1), and progressive disease (n=1) were observed. Median overall survival was 20.4 months (95% confidence interval, 2.30-N/A). Conclusions: In this small cohort, renal SABR was delivered with minimal toxicity. A prospective study is underway at our institution to determine maximum tolerable and optimal dosing (NCT02264548).
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