Amin Neha P, Zainib Maliha, Parker Sean M, Agarwal Manuj, Mattes Malcolm D
Department of Radiation Oncology, University of Maryland, School of Medicine, Baltimore, Maryland.
University of Maryland School of Medicine, Baltimore, Maryland.
Adv Radiat Oncol. 2018 May 24;3(3):399-404. doi: 10.1016/j.adro.2018.04.015. eCollection 2018 Jul-Sep.
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.
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.
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.
Concurrent RT-nivolumab did not appear to increase the toxicity profile from the previously reported toxicity rates from nivolumab or radiation alone.
放射治疗(RT)和纳武单抗是多种晚期和转移性癌症的标准疗法,但对于它们联合治疗的毒性特征了解甚少。据报道,纳武单抗单药治疗和单纯放射姑息治疗的≥3级毒性发生率分别为10%至18%和0%至26%。我们回顾了我们的经验,以评估同步放化疗联合纳武单抗的急性毒性特征。
对2015年1月至2017年5月期间在4个不同中心接受同步放化疗联合纳武单抗的所有连续患者进行回顾性研究。同步放化疗联合纳武单抗的定义为在首次纳武单抗输注前3天至最后一次纳武单抗输注后28天内完成放疗。
在接受纳武单抗治疗的261例患者中,46例(17.6%)接受了同步放疗,共照射67个部位。中位随访时间为3.3个月(四分位间距,1.7 - 6.1个月),1年总生存率为22%。在最后一次分析时存活的46例患者中的11例(24%),中位随访时间为12.8个月(四分位间距,8.3 - 14.9个月)。最常见的组织学类型、放疗处方和治疗部位分别是非小细胞肺癌(46例患者中的23例;50%)、10次分割照射30 Gy(67例患者中的24例;35.8%)以及腹部/盆腔(67例患者中的16例;24%)。4例黑色素瘤患者同时接受了伊匹单抗治疗,并被排除在放化疗联合纳武单抗的最终毒性分析之外。在放化疗联合纳武单抗治疗的3个月内,42例患者中有4例(9.5%)出现3级毒性,其中2例患者的毒性明确归因于放疗的添加:全脑放疗后出现3级听力丧失,立体定向体部放疗至左肾上腺后出现3级胰腺炎。1例因转氨酶升高死亡仅归因于纳武单抗,因为放疗野未覆盖肝脏。
同步放化疗联合纳武单抗似乎并未使毒性特征高于先前报道的纳武单抗或单纯放疗的毒性发生率。