CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Consolidative radiotherapy for residual fluorodeoxyglucose activity on day +30 post CAR T-cell therapy in non-Hodgkin lymphoma.
Consolidative radiotherapy for residual fluorodeoxyglucose activity on day +30 post CAR T-cell therapy in non-Hodgkin lymphoma.
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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。
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.
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