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滤泡性淋巴瘤患者一线治疗后PET-CT的预后价值:三项多中心研究中中心扫描回顾的汇总分析

Prognostic value of PET-CT after first-line therapy in patients with follicular lymphoma: a pooled analysis of central scan review in three multicentre studies.

作者信息

Trotman Judith, Luminari Stefano, Boussetta Sami, Versari Annibale, Dupuis Jehan, Tychyj Christelle, Marcheselli Luigi, Berriolo-Riedinger Alina, Franceschetto Antonella, Julian Anne, Ricard Fabien, Guerra Luca, Haioun Corinne, Biasoli Irene, Tilly Hervé, Federico Massimo, Salles Gilles, Meignan Michel

机构信息

Haematology Department, Concord Hospital, University of Sydney, Sydney, NSW, Australia.

Department of Diagnostic, Clinical and Public Health Medicine, University of Modena and Reggio Emilia, Modena, Italy.

出版信息

Lancet Haematol. 2014 Oct;1(1):e17-27. doi: 10.1016/S2352-3026(14)70008-0. Epub 2014 Sep 17.

Abstract

BACKGROUND

The value of (18)F-fluorodeoxyglucose (FDG) PET-CT (PET) imaging in response assessment after first-line rituximab chemotherapy for follicular lymphoma has been documented. We analysed the application of the five-point Deauville scale (5PS; used to score FDG uptake on PET images) in a large cohort derived from three studies, to assess the correlation between post-induction PET status and survival in patients with follicular lymphoma.

METHODS

In this pooled analysis, we used data from three multicentre prospective studies of first-line rituximab chemotherapy for patients with high-tumour-burden follicular lymphoma (the PRIMA study, the PET-Folliculaire study, and the Fondazione Italiana Linfomi FOLL05 study). Patients included in this analysis received at least six cycles of rituximab and chemotherapy before response assessment with conventional contrast-enhanced CT and PET low-dose CT (PET). We included only patients who had a PET scan within 3 months of the last dose of induction rituximab. Patient data, including conventional CT-based response assessment, were recorded for all patients undergoing PET review. Scans undergoing central PET review were scored independently by three reviewers according to the 5PS. The primary endpoints were progression-free survival and overall survival according to the 5PS score of post-induction PET scan (ie, positive [≥4 points] or negative [<4 points]), analysed in the central review population.

FINDINGS

Between Dec 24, 2004, and Sept 22, 2010, 439 of the patients enrolled in the three studies underwent local PET assessment, 246 of whom had centrally reviewed post-induction scans. 41 (17%) of 246 patients had a positive post-induction PET scan according to a cutoff of 4 or higher on the 5PS, with substantial reporter concordance. With a median follow-up of 54·8 months (IQR 39·7-68·5; range 7·7-90·1), the hazard ratio (HR) for progression-free survival for patients with a positive PET scan versus those with a negative PET scan was 3·9 (95% CI 2·5-5·9; p<0·0001), and for overall survival was 6·7 (2·4-18·5; p=0·0002). For patients with a positive PET scan, 23·2% (95% CI 11·1-37·9) of patients were progression free at 4 years compared with 63·4% (55·9-70·0) of those who had a negative PET scan (p<0·0001); 4-year overall survival was 87·2% (95% CI 71·9-94·5) versus 97·1% (93·2-98·8), respectively (p<0·0001). Conventional CT-based response (ie, complete response or unconfirmed complete response vs partial response) was weakly predictive of progression-free survival (HR 1·7 [95% CI 1·1-2·5]; p=0·017).

INTERPRETATION

PET-CT rather than contrast-enhanced CT scanning should be considered as a new standard for response assessment of follicular lymphoma in clinical practice, and could help guide response-adapted therapy.

FUNDING

Groupe d'Etude des Lymphomes de l'Adulte (Paris, France), now LYSA (Lymphoma Study Association), Direction de la Recherche Clinique de l'Assistance Publique-Hôpitaux de Paris, Fondazione Italiana Linfomi, and the Italian Ministry of Health.

摘要

背景

(18)F - 氟脱氧葡萄糖(FDG)PET - CT成像在滤泡性淋巴瘤一线利妥昔单抗化疗后的疗效评估中的价值已有文献记载。我们分析了五点Deauville量表(5PS;用于对PET图像上的FDG摄取进行评分)在来自三项研究的大型队列中的应用,以评估诱导化疗后PET状态与滤泡性淋巴瘤患者生存率之间的相关性。

方法

在这项汇总分析中,我们使用了三项多中心前瞻性研究的数据,这些研究针对高肿瘤负荷滤泡性淋巴瘤患者进行一线利妥昔单抗化疗(PRIMA研究、PET - Folliculaire研究和意大利淋巴瘤基金会FOLL05研究)。纳入本分析的患者在使用传统增强CT和PET低剂量CT(PET)进行疗效评估之前接受了至少六个周期的利妥昔单抗和化疗。我们仅纳入在最后一剂诱导性利妥昔单抗后3个月内进行PET扫描的患者。记录了所有接受PET检查的患者的患者数据,包括基于传统CT的疗效评估。由三位审阅者根据5PS对接受中心PET检查的扫描进行独立评分。主要终点是根据诱导化疗后PET扫描的5PS评分(即阳性[≥4分]或阴性[<4分])的无进展生存期和总生存期,在中心审查人群中进行分析。

结果

在2004年12月24日至2010年9月22日期间,三项研究中纳入的439例患者接受了局部PET评估,其中246例患者接受了诱导化疗后的中心审查扫描。根据5PS评分4分或更高的临界值,246例患者中有41例(17%)诱导化疗后PET扫描为阳性,报告者之间有高度一致性。中位随访时间为54.8个月(IQR 39.7 - 68.5;范围7.7 - 90.1),PET扫描阳性患者与阴性患者的无进展生存期风险比(HR)为3.9(95%CI 2.5 - 5.9;p<0.0001),总生存期风险比为6.7(2.4 - 18.5;p = 0.0002)。对于PET扫描阳性的患者,4年时23.2%(95%CI 11.1 - 37.9)的患者无进展,而PET扫描阴性的患者为63.4%(55.9 - 70.0)(p<0.0001);4年总生存率分别为87.2%(95%CI 71.9 - 94.5)和97.1%(93.2 - 98.8)(p<0.0001)。基于传统CT的疗效(即完全缓解或未确认的完全缓解与部分缓解)对无进展生存期的预测较弱(HR 1.7 [95%CI 1.1 - 2.5];p = 0.017)。

解读

在临床实践中,PET - CT而非增强CT扫描应被视为滤泡性淋巴瘤疗效评估的新标准,并有助于指导适应性治疗。

资助

成人淋巴瘤研究组(法国巴黎),现LYSA(淋巴瘤研究协会),巴黎公共援助 - 医院临床研究部,意大利淋巴瘤基金会,以及意大利卫生部。

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