Department of Radiation Oncology, University of Washington, Seattle, Washington.
University of Washington School of Medicine, Seattle, Washington.
Int J Radiat Oncol Biol Phys. 2018 Oct 1;102(2):330-339. doi: 10.1016/j.ijrobp.2018.05.075. Epub 2018 Jun 5.
Patients with Merkel cell carcinoma (MCC) with chronic immunosuppression (IS) have worse outcomes, but the mechanisms are not well understood. We hypothesized that these differences may be mediated in part by differential response to treatment, and we evaluated whether radiation therapy (RT) efficacy is altered among IS compared with immune-competent (IC) patients with MCC.
Among 805 patients with MCC, recurrence-free survival (RFS) and patterns of first recurrence were compared between 89 IS and 716 IC patients with stage I to III MCC treated with curative intent. We used a Fine and Gray's competing risk multivariable analysis to estimate associations with RFS.
IS and IC patients with MCC had similar demographic and disease characteristics. Most (77% IC, 86% IS) were irradiated (median, 50.4 Gy IC, 50.3 Gy IS), although more IS patients were irradiated to the primary site (97% vs 81%). With a median follow-up of 54.4 months, IS patients had inferior RFS (2-year: 30% vs 57%; P < .0001) and higher rates of local recurrence as the first site of relapse (25% vs 12%; P = .0002). The association between RT and RFS differed by immune status (interaction P = .01). Although RT was associated with significantly improved RFS among IC patients (hazard ratio 0.56, 95% confidence interval 0.44-0.72), no difference in RFS was observed with RT among IS patients (hazard ratio 1.49, 95% confidence interval 0.70-3.17).
Radiation therapy efficacy at current standard RT doses for MCC is impaired among immunosuppressed patients with MCC. Although a strong link between durability of RT response and immune function does not appear to be evident in most cancers, our results may reflect an especially dynamic interaction between immune status and RT efficacy in MCC.
患有慢性免疫抑制(IS)的 Merkel 细胞癌(MCC)患者预后较差,但发病机制尚不清楚。我们假设这些差异可能部分是由于对治疗的反应不同,因此评估了与免疫功能正常(IC)的 MCC 患者相比,IS 患者的放射治疗(RT)疗效是否会发生变化。
在 805 例 MCC 患者中,比较了 89 例 IS 患者和 716 例 IC 患者的无复发生存期(RFS)和首次复发模式,这些患者均接受根治性治疗,分期为 I 至 III 期 MCC。我们使用 Fine 和 Gray 的竞争风险多变量分析来估计与 RFS 相关的因素。
MCC 的 IS 和 IC 患者具有相似的人口统计学和疾病特征。大多数患者(IC 为 77%,IS 为 86%)接受了放疗(中位剂量 50.4Gy,IC 为 50.3Gy,IS 为 50.3Gy),尽管更多的 IS 患者接受了原发部位的放疗(97%对 81%)。中位随访 54.4 个月后,IS 患者的 RFS 较差(2 年:30%对 57%;P<0.0001),且首次复发部位为局部复发的比例较高(25%对 12%;P=0.0002)。RT 与 RFS 的相关性因免疫状态而异(交互 P=0.01)。尽管 RT 与 IC 患者的 RFS 显著相关(危险比 0.56,95%置信区间 0.44-0.72),但在 IS 患者中,RT 对 RFS 无影响(危险比 1.49,95%置信区间 0.70-3.17)。
目前标准 RT 剂量治疗 MCC 时,免疫抑制的 MCC 患者的 RT 疗效受损。尽管在大多数癌症中,RT 反应的持久性与免疫功能之间没有明显的联系,但我们的结果可能反映了免疫状态与 RT 疗效在 MCC 中的一种特别动态的相互作用。