Department of Radiation Oncology, University of Texas M.D. Anderson Cancer Center, Unit 97, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Department of Radiation Oncology, Shandong Cancer Hospital Affiliated to Shandong University, 440 Jiyan Road, SD, CN, Jinan, China.
J Immunother Cancer. 2019 Sep 4;7(1):237. doi: 10.1186/s40425-019-0718-6.
Preclinical evidence suggests that low-dose radiation may overcome the inhibitory effects of the tumor stroma and improve a tumor's response to immunotherapy, when combined with high-dose radiation to another tumor. The aim of this study was to evaluate tumor responses to this combination in a clinical setting.
A post-hoc analysis of 3 ongoing immunoradiation trials was performed. Twenty-six (of 155) patients received low-dose radiation (1-20 Gy total), either as scatter from high-dose radiation or from intentional treatment of a second isocenter with low-dose radiation, were evaluated for response. The low-dose lesions were compared to lesions that received no radiation (< 1 Gy total). Response rates, both defined as complete and partial responses as defined by RECIST criteria were used to compare lesion types.
The 26 patients had a total of 83 lesions for comparison (38 receiving low-dose, 45 receiving no-dose). The average dose given to low-dose lesions was 7.3 Gy (1.1-19.4 Gy), and the average time to response was 56 days. Twenty-two out of 38 (58%) low-dose lesions met the PR/CR criteria for RECIST compared with 8 out of 45 (18%) no-dose lesions (P = 0.0001). The median change for longest diameter size for low-dose lesions was - 38.5% compared to 8% in no-dose lesions (P < 0.0001). Among the low-dose lesions that had at least one no-dose lesion within the same patient as a control (33 and 45 lesions respectively), 12 low-dose lesions (36%) responded without a corresponding response in their no-dose lesions; Conversely, two (4%) of the no-dose lesions responded without a corresponding response in their low-dose lesion (P = 0.0004).
Low-dose radiation may increase systemic response rates of metastatic disease treated with high-dose radiation and immunotherapy.
临床前证据表明,低剂量辐射与高剂量辐射联合应用于另一个肿瘤时,可能会克服肿瘤基质的抑制作用,并改善肿瘤对免疫治疗的反应。本研究旨在评估该联合治疗在临床环境中的肿瘤反应。
对 3 项正在进行的免疫放疗试验进行了事后分析。26 名(155 名患者中的 26 名)患者接受了低剂量辐射(总剂量为 1-20Gy),这些患者要么是从高剂量辐射中散射而来,要么是从低剂量辐射的第二个等中心故意治疗而来,评估了他们的反应。将低剂量病变与未接受任何辐射的病变(总剂量<1Gy)进行比较。根据 RECIST 标准,使用完全缓解和部分缓解的反应率来比较病变类型。
26 名患者共有 83 个病变进行比较(38 个接受低剂量,45 个接受无剂量)。低剂量病变的平均剂量为 7.3Gy(1.1-19.4Gy),平均反应时间为 56 天。38 个低剂量病变中有 22 个(58%)符合 RECIST 的 PR/CR 标准,而 45 个无剂量病变中只有 8 个(18%)(P=0.0001)。低剂量病变的最长直径变化中位数为-38.5%,而无剂量病变为 8%(P<0.0001)。在至少有一个无剂量病变作为对照的同一患者的低剂量病变中(分别为 33 个和 45 个病变),12 个低剂量病变(36%)没有相应的无剂量病变反应而出现了缓解;相反,有两个(4%)无剂量病变没有相应的低剂量病变反应而出现了缓解(P=0.0004)。
低剂量辐射可能会提高高剂量辐射和免疫治疗治疗转移性疾病的全身反应率。