Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.
Northwestern University, Feinberg School of Medicine, Chicago, IL.
Blood Adv. 2024 May 28;8(10):2592-2599. doi: 10.1182/bloodadvances.2023011996.
Chimeric antigen receptor (CAR) T-cell (CAR-T) immunotherapy is an effective therapy for relapsed/refractory B-cell non-Hodgkin lymphoma (r/r B-NHL). However, data are limited on the impact of the convergence of race and social determinants of health on outcomes for patients treated with CAR-T therapy. We examined the impact of interactions between race and insurance type on health care use and outcomes in patients treated with CAR-T therapy for aggressive B-NHL. Adult patients with r/r B-NHL treated with CD19 CAR-Ts were identified between 2015 and 2021 across 13 US academic centers. Insurance type, demographic, and clinical data were collected and analyzed. In total, 466 adult patients were included in our analysis. Median follow-up after CAR-T therapy was 12.7 months. Median progression-free survival (mPFS) was longer for Caucasians (11.5 months) than for African Americans (3.5 months; hazard ratio [HR], 1.56 [1.03-2.4]; P = .04) or Asians (2.7 months; HR, 1.7 [1.02-2.67]; P = .04). Differences in median overall survival (mOS) were not significant. For Medicare (n = 206) vs Medicaid (n = 33) vs private insurance (n = 219) vs self-pay (n = 7): mPFS was 15.9 vs 4.2 vs 6.0 vs 0.9 months (P < .001), respectively; and mOS was 31.2 vs 12.8 vs 21.5 vs 3.2 months (P < .001), respectively. Our multicenter retrospective analysis showed that race and insurance status can affect outcomes for patients treated with CAR-T therapy.
嵌合抗原受体 (CAR) T 细胞 (CAR-T) 免疫疗法是治疗复发/难治性 B 细胞非霍奇金淋巴瘤 (r/r B-NHL) 的有效方法。然而,关于种族和健康社会决定因素的融合对接受 CAR-T 治疗的患者结局的影响的数据有限。我们研究了种族和保险类型之间的相互作用对接受 CAR-T 治疗的侵袭性 B-NHL 患者的医疗保健使用和结局的影响。在 13 个美国学术中心,我们在 2015 年至 2021 年期间确定了接受 CD19 CAR-T 治疗的 r/r B-NHL 成年患者。收集和分析了保险类型、人口统计学和临床数据。共有 466 名成年患者纳入我们的分析。CAR-T 治疗后中位随访时间为 12.7 个月。与非裔美国人 (3.5 个月;风险比 [HR],1.56 [1.03-2.4];P =.04) 或亚洲人 (2.7 个月;HR,1.7 [1.02-2.67];P =.04) 相比,白种人 (11.5 个月) 的中位无进展生存期 (mPFS) 更长。中位总生存期 (mOS) 的差异无统计学意义。对于医疗保险 (n = 206)、医疗补助 (n = 33)、私人保险 (n = 219) 和自付 (n = 7):mPFS 分别为 15.9、4.2、6.0 和 0.9 个月 (P <.001);mOS 分别为 31.2、12.8、21.5 和 3.2 个月 (P <.001)。我们的多中心回顾性分析表明,种族和保险状况可能会影响接受 CAR-T 治疗的患者的结局。