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非霍奇金淋巴瘤 CAR-T 细胞治疗后第 +30 天残留氟脱氧葡萄糖活性的巩固性放疗

英文原题:Consolidative radiotherapy for residual fluorodeoxyglucose activity on day +30 post CAR T-cell therapy in non-Hodgkin lymphoma.

查看英文原题

Consolidative radiotherapy for residual fluorodeoxyglucose activity on day +30 post CAR T-cell therapy in non-Hodgkin lymphoma.

PubMed 2023/11/01(内容时间) Haematologica Q1 · IF 8.2(JCR 2025)

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中文摘要

多数非霍奇金淋巴瘤(NHL)患者在CAR-T 细胞治疗后第30天仅达到部分缓解(PR)或疾病稳定(SD),随后会进展,只有约30%可自发达到完全缓解(CR)。

本研究首次评估CAR-T 后第30天仍有氟脱氧葡萄糖(FDG)残留活性时,巩固放疗(cRT)的作用。研究回顾性纳入61例接受CAR-T 且第30天达到PR或SD的NHL患者,并自CAR-T 输注起评估无进展生存期(PFS)、总生存期(OS)和局部无复发生存期(LRFS)。cRT分为全面放疗(覆盖所有FDG高摄取病灶)和局灶放疗。第30天正电子发射断层扫描后,45例患者接受观察,16例接受cRT。观察组中15例(33%)自发达到CR,27例(60%)进展,所有复发均涉及初始FDG残留病灶。cRT组中10例(63%)达到CR,4例(25%)进展,照射部位均未复发。cRT照射部位2年LRFS为100%,观察部位为31%(P<0.001);cRT组与观察组的2年PFS分别为73%和37%(P=0.025),2年OS分别为78%和43%(P=0.12)。与观察或局灶放疗患者相比,接受全面cRT的NHL患者(n=13)2年PFS(83%比37%;P=0.008)和2年OS(86%比43%;P=0.047)更优。CAR-T 后仍有FDG残留活性的NHL患者局部进展风险较高。CAR-T 后第30天针对残留FDG活性进行cRT,似乎可改变复发模式并改善LRFS和PFS。

展开英文摘要原文

Majority of non-Hodgkin lymphoma (NHL) patients who achieve partial response (PR) or stable disease (SD) to CAR T-cell therapy (CAR T) on day +30 progress and only 30% achieve spontaneous complete response (CR).

This study is the first to evaluate the role of consolidative radiotherapy (cRT) for residual fluorodeoxyglucose (FDG) activity on day +30 post- CAR T in NHL.

We retrospectively reviewed 61 patients with NHL who received CAR T and achieved PR or SD on day +30. Progression-free survival (PFS), overall survival (OS), and local relapse-free survival (LRFS) were assessed from CAR T infusion. cRT was defined as comprehensive - treated all FDG-avid sites - or focal. Following day +30 positron emission tomography scan, 45 patients were observed and 16 received cRT. Fifteen (33%) observed patients achieved spontaneous CR, and 27 (60%) progressed with all relapses involving initial sites of residual FDG activity. Ten (63%) cRT patients achieved CR, and four (25%) progressed with no relapses in the irradiated sites.

The 2-year LRFS was 100% in the cRT sites and 31% in the observed sites (P<0. 001). The 2-year PFS was 73% and 37% (P=0. 025) and the 2-year OS was 78% and 43% (P=0. 12) in the cRT and observation groups, respectively. Patients receiving comprehensive cRT (n=13) had superior 2- year PFS (83% vs. 37%; P=0.

008) and 2-year OS (86% vs. 43%; P=0. 047) compared to observed or focal cRT patients (n=48). NHL patients with residual FDG activity following CAR T are at high risk of local progression. cRT for residual FDG activity on day +30 post-CAR T appears to alter the pattern of relapse and improve LRFS and PFS.

论文信息

作者
Saifi O、Breen WG、Lester SC、Rule WG、Stish BJ、Rosenthal A、Munoz J、Lin Y
第一作者单位
Department of Radiation Oncology, Mayo Clinic Jacksonville, FL.United States
通讯作者单位
Department of Radiation Oncology, Mayo Clinic Jacksonville, FL. hoppe.bradford@mayo.edu.United States
期刊
Haematologica2023 Nov 1
原文标识
PubMed 37317888 · DOI 10.3324/haematol.2023.283311