Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia; The Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia.
The Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Department of Molecular Imaging, Peter MacCallum Cancer Centre, Melbourne, Australia.
Int J Radiat Oncol Biol Phys. 2020 Sep 1;108(1):204-211. doi: 10.1016/j.ijrobp.2020.02.636. Epub 2020 Mar 7.
Patients with abscopal regressions of lymphoma after palliative involved-site radiation therapy (ISRT), detected on sequential F-fluorodeoxyglucose positron emission tomography (FDG-PET), were identified by audit. A retrospective analysis was subsequently conducted to estimate the frequency of abscopal regression in follicular lymphoma (FL).
Potential cases were identified at multidisciplinary lymphoma meetings and fulfilled these criteria: (1) palliative ISRT given for histologically confirmed lymphoma, (2) >2 lesions visualized on FDG-PET, (3) >1 unirradiated lesion(s) outside ISRT volume, (4) no systemic therapy delivered <2 months before radiation therapy or between radiation therapy and response assessment, (5) complete metabolic response (CMR) in ≥1 unirradiated lesions detected on serial FDG-PET/CT. All ISRT patients with FL treated in 2016 to 2018 were systematically reviewed.
Seven cases of abscopal regression were identified, including 4 patients with FL. In all cases, a CMR was apparent both within the ISRT volume and in ≥1 unirradiated lesions. One patient each was identified with mantle cell lymphoma (4 Gy in 2 fractions), Hodgkin lymphoma (20 Gy in 3 fractions, then 30 Gy in 15 fractions to the same volume), and Richter transformation of chronic lymphatic leukemia (30 Gy in 10 fractions). The 4 patients with FL received either 4 Gy in 2 fractions (n = 3) or 4 Gy followed 8 months later by 30 Gy in 15 fractions (n = 1). From 2016 to 2018, 29 courses of ISRT were prescribed for multifocal FL, after which 4 of 29 (13.8%) abscopal responses were detected, including in 4 of 9 (44.4%) patients with serial PET scans. Two patients, with relapsed disease after initial abscopal responses, experienced durable CMRs with immunotherapies.
In 4 of 7 cases, PET-detected abscopal regression of lymphoma occurred after 4 Gy, in 2 of 7 cases after repeated ISRT to the same volume, and in 2 of 7 was associated with subsequent complete response to immunotherapy, consistent with an immune basis for the abscopal effect. Abscopal regressions in FL appear to be more common than previously suspected.
通过审核,确定了姑息性累及部位放射治疗(ISRT)后淋巴瘤患者的远处退缩反应,这些患者在连续氟-18 氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)上得到了检测。随后进行了回顾性分析,以估计滤泡性淋巴瘤(FL)中远处退缩反应的频率。
在多学科淋巴瘤会议上确定了潜在病例,并符合以下标准:(1)因组织学证实的淋巴瘤给予姑息性 ISRT;(2)FDG-PET 上可见>2 处病变;(3)ISRT 体积外有>1 处未照射的病变;(4)在放射治疗前<2 个月或在放射治疗和反应评估之间没有给予全身治疗;(5)在连续 FDG-PET/CT 上检测到的≥1 处未照射病变中完全代谢缓解(CMR)。对 2016 年至 2018 年治疗的所有 FL 累及部位放射治疗患者进行了系统性回顾。
共发现 7 例远处退缩反应,其中 4 例为 FL。在所有病例中,ISRT 体积内和≥1 处未照射的病变均出现了 CMR。分别有 1 例为套细胞淋巴瘤(2 次分割,每次 4 Gy)、霍奇金淋巴瘤(3 次分割,每次 20 Gy,然后在同一部位给予 15 次分割,每次 30 Gy)和慢性淋巴细胞白血病的 Richter 转化(10 次分割,每次 30 Gy)。4 例 FL 患者分别接受 2 次分割 4 Gy(n=3)或 4 Gy 后 8 个月接受 15 次分割 30 Gy(n=1)。2016 年至 2018 年,共进行了 29 次 ISRT 治疗多灶性 FL,随后在 29 例患者中检测到 4 例(13.8%)远处退缩反应,其中 9 例患者(44.4%)进行了连续 PET 扫描。2 例初始远处退缩反应后复发的患者接受免疫治疗后,获得了持久的 CMR。
在 7 例患者中,4 例(7 例中的 4 例)在接受 4 Gy 后,2 例(7 例中的 2 例)在对同一部位进行重复 ISRT 后,2 例(7 例中的 2 例)在随后对免疫治疗产生完全反应时,PET 检测到淋巴瘤的远处退缩反应,这与远处效应的免疫基础一致。FL 中的远处退缩反应似乎比以前怀疑的更常见。