Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy

被引:20
作者
Amin, Neha P. [1 ]
Zainib, Maliha [2 ]
Parker, Sean M. [3 ]
Agarwal, Manuj [1 ]
Mattes, Malcolm D. [4 ]
机构
[1] Univ Maryland, Sch Med, Dept Radiat Oncol, 22 S Green St, Baltimore, MD 21201 USA
[2] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[3] West Virginia Univ, Sch Med, Morgantown, WV 26506 USA
[4] West Virginia Univ, Dept Radiat Oncol, Morgantown, WV 26506 USA
关键词
D O I
10.1016/j.adro.2018.04.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Radiation therapy (RT) and nivolumab are standard therapies for a wide range of advanced and metastatic cancers, yet little is known about the toxicity profile of their combined treatment. The rate of grade >= 3 toxicities from nivolumab monotherapy and radiation-only palliative treatments has been reported at 10% to 18% and 0% to 26%, respectively. We reviewed our experience to assess the acute toxicity profile of concurrent RT-nivolumab. Methods and materials: A retrospective review of all consecutive patients from January 2015 to May 2017 who received concurrent RT-nivolumab was conducted at 4 separate centers. Concurrent RT-nivolumab was defined as RT completed between 3 days prior to initial nivolumab infusion and 28 days after the last nivolumab infusion. Results: Of the 261 patients who received nivolumab, 46 (17.6%) had concurrent RT to 67 treatment sites. The median follow-up was 3.3 months (interquartile range, 1.7-6.1 months) and the 1-year overall survival rate was 22%. For the 11 of 46 patients (24%) who were alive at last analysis, the median follow-up was 12.8 months (interquartile range, 8.3-14.9 months). The most common histology, RT prescription, and treatment site were non-small cell lung cancer (23 of 46 patients; 50%), 30 Gy in 10 fractions (24 of 67 patients; 35.8%), and abdomen/pelvis (16 of 67 patients; 24%), respectively. Four patients with melanoma had concurrent ipilimumab and were removed from the final toxicity analysis of RT-nivolumab. Within 3 months of treatment with RT-nivolumab, 4 of 42 patients (9.5%) experienced grade 3 toxicity and 2 of these patients' toxicities were attributed specifically to the addition of RT: grade 3 hearing loss after whole brain RT and grade 3 pancreatitis after stereotactic body RT to the left adrenal gland. One death from transaminitis was attributed to nivolumab alone because the RT field did not encompass the liver. Conclusions: Concurrent RT-nivolumab did not appear to increase the toxicity profile from the previously reported toxicity rates from nivolumab or radiation alone. (C) 2018 The Author(s). Published by Elsevier Inc. on behalf of the American Society for Radiation Oncology.
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收藏
页码:399 / 404
页数:6
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