Department of a Internal Medicine, Houston Methodist Research Institute, Houston, Texas 77030.
b Department of Pathology and Genomic Medicine, Houston Methodist Research Institute, Houston, Texas 77030.
Radiat Res. 2018 Sep;190(3):322-329. doi: 10.1667/RR15048.1. Epub 2018 Jun 27.
Until recently, patients with relapsed Hodgkin's lymphoma after brentuximab vedotin (Bv) treatments had poor treatment outcomes. Checkpoint inhibitors such as nivolumab and pembrolizumab that bind to and inhibit programmed cell death protein-1 (PD-1), have demonstrated an overall response rate of 70% in Hodgkin's lymphoma patients; however, complete response is still low at 20% with median progression-free survival of 14 months. There are ongoing clinical studies to seek out synergistic combinations, with the goal of improving the complete response rates for the cure of Hodgkin's lymphoma. Although radiotherapy has a limited survival benefit in such refractory patients, several preclinical models and anecdotal clinical evidence have suggested that combining local tumor irradiation with checkpoint inhibitors can produce systemic regression of distant tumors, an abscopal effect. Most of these reported studies on the response with local conformal radiotherapy and checkpoint inhibitors in combination with the anti-cytotoxic T-lymphocyte associated antigen-4 (CTLA-4) antibody-ipilimumab are in melanoma. Here we report in our case series that the checkpoint inhibitors that block CTLA4 and B7-homolog 1 (B7-H1) or PD-1 in preclinical radiotherapy models have shown an increased the rate of tumor regression. Our case series demonstrates that combining local irradiation with anti-PD-1 checkpoint blockade treatment is feasible and synergistic in refractory Hodgkin's lymphoma. Correlative studies also suggest that the expression of programmed death-ligand 1 (PD-L1), DNA damage response and mutational tumor burden can be used as potential biomarkers for treatment response.
直到最近,接受 Brentuximab vedotin(Bv)治疗后复发的霍奇金淋巴瘤患者的治疗效果仍然较差。针对程序性死亡蛋白-1(PD-1)的检查点抑制剂,如 nivolumab 和 pembrolizumab,在霍奇金淋巴瘤患者中的总缓解率为 70%;然而,完全缓解率仍较低,为 20%,中位无进展生存期为 14 个月。目前正在进行临床研究以寻求协同组合,目标是提高霍奇金淋巴瘤的完全缓解率以实现治愈。尽管在这些难治性患者中放射治疗的生存获益有限,但几项临床前模型和临床经验证据表明,将局部肿瘤照射与检查点抑制剂联合使用可以产生远处肿瘤的全身消退,即远隔效应。这些关于局部适形放疗与检查点抑制剂联合使用抗细胞毒性 T 淋巴细胞相关抗原-4(CTLA-4)抗体 ipilimumab 治疗反应的大多数报告研究均在黑色素瘤中进行。在这里,我们报告了一系列病例,在临床前放射治疗模型中,阻断 CTLA4 和 B7-同源物 1(B7-H1)或 PD-1 的检查点抑制剂可增加肿瘤消退率。我们的病例系列表明,局部照射与抗 PD-1 检查点阻断治疗联合使用在难治性霍奇金淋巴瘤中是可行且协同的。相关研究还表明,程序性死亡配体 1(PD-L1)、DNA 损伤反应和突变肿瘤负担的表达可用作治疗反应的潜在生物标志物。