Ladbury Colton, Dandapani Savita, Hao Claire, Fabros Mildred, Amini Arya, Sampath Sagus, Glaser Scott, Sokolov Karen, Yeh Jekwon, Baird John H, Thiruvengadam Swetha Kambhampati, Herrera Alex, Mei Matthew, Nikolaenko Liana, Shouse Geoffrey, Budde Lihua E
Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA 91010, USA.
Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA 91010, USA.
Cancers (Basel). 2023 Mar 14;15(6):1747. doi: 10.3390/cancers15061747.
Bridging therapy (BT) with systemic therapy (ST), radiation therapy (RT), or combined-modality therapy (CMT) is increasingly being utilized prior to chimeric antigen receptor (CAR) T-cell therapy for large B-cell lymphoma (LBCL). We report the long-term outcomes of the patients who received commercial CAR T-cell therapy with or without BT.
The patients with LBCL who underwent infusion of a commercial CD19 CAR T product were eligible. The radiation was stratified as comprehensive or focal. The efficacy outcomes and toxicity were analyzed.
In total, 156 patients were included and, of them, 52.5% of the patients received BT. The median progression-free survival (PFS) was 0.65 years in the BT cohort compared to 1.45 years in the non-BT cohort. The median overall survival (OS) was 3.16 years in the BT cohort and was not reached in the non-BT cohort. The patients who received comprehensive radiation (versus focal) had significantly improved PFS and OS, achieving a 1-year PFS of 100% vs. 9.1% and 1-year OS of 100% vs. 45.5%. There was no difference in the severe toxicity between any of the nonbridging or BT cohorts.
BT did not appear to compromise outcomes with respect to response rates, disease control, survival, and toxicity. The patients with limited disease treated with RT had favorable outcomes.
在嵌合抗原受体(CAR)T细胞治疗大B细胞淋巴瘤(LBCL)之前,越来越多地采用全身治疗(ST)、放射治疗(RT)或联合治疗(CMT)进行桥接治疗(BT)。我们报告了接受或未接受BT的商业CAR T细胞治疗患者的长期疗效。
符合条件的患者为接受商业CD19 CAR T产品输注的LBCL患者。放疗分为全面放疗或局部放疗。分析疗效和毒性。
共纳入156例患者,其中52.5%的患者接受了BT。BT组的中位无进展生存期(PFS)为0.65年,而非BT组为1.45年。BT组的中位总生存期(OS)为3.16年,非BT组未达到。接受全面放疗(与局部放疗相比)的患者PFS和OS显著改善,1年PFS分别为100%和9.1%,1年OS分别为100%和45.5%。非桥接组或BT组之间的严重毒性没有差异。
BT似乎在缓解率、疾病控制率、生存率和毒性方面未影响疗效。接受RT治疗的疾病局限患者预后良好。