Augustin Alix, Le Gouill Steven, Gressin Rémy, Bertaut Aurélie, Monnereau Alain, Woronoff Anne-Sophie, Trétarre Brigitte, Delafosse Patricia, Troussard Xavier, Moreau Anne, Hermine Olivier, Maynadié Marc
Registre des hémopathies malignes de Côte d'Or, Faculté des Sciences de Santé, Inserm UMR 1231, Université de Bourgogne F-Comté, 7 Bd Jeanne d'Arc, 21079, Dijon Cedex, France.
Service Hématologie clinique, Centre Hospitalier Universitaire de de Nantes Hôtel-Dieu, Place Alexis Ricordeau, 44000, Nantes, France.
J Cancer Res Clin Oncol. 2018 Apr;144(4):629-635. doi: 10.1007/s00432-017-2529-9. Epub 2017 Oct 11.
Mantle cell lymphoma (MCL) is a rare non-Hodgkin's lymphoma entity with a poor prognosis. Therapeutic advances have improved the survival of patients enrolled in clinical trials; however, their impact on patients outside clinical trials remains unclear. In this work, we compared patient outcome inside and outside clinical trials.
We identified MCL patients recorded in six French population-based registries between 2008 and 2012 to perform a comparison with patients enrolled in two prospective multicenter MCL clinical trials conducted by the LYSA group during the same period. Variables associated with inclusion in a clinical trial were identified using a logistic regression. Pohar-Perme estimator and Nelson et al. flexible parametric model was used to estimate net survival probabilities and prognosis factors on excess mortality.
A total of 312 registry patients were compared to the 372 patients enrolled in LYSA clinical trials. Patients included in clinical trials were younger (median age 60 vs 74, p < 0.001). Age and Ann Arbor stage IV were independently associated with enrollment [OR = 0.09 (0.06-0.12) and OR = 1.61 (1.11-2.34), respectively]. The 4 year net survival was better in clinical trials [79.9% (75.9-84.7) vs 60.3% (53.6-67.0)]. This result was confirmed in multivariate analysis in patients older than 65 years with a lower excess mortality rate [0.33 (0.17-0.66)].
MCL included in trials are highly selected patients who are not representative of MCL patients who are encountered in everyday practice. With widened inclusion criteria, clinical trial patients could be more representative of the general population.
套细胞淋巴瘤(MCL)是一种罕见的非霍奇金淋巴瘤,预后较差。治疗进展改善了参加临床试验患者的生存率;然而,它们对未参加临床试验患者的影响仍不明确。在本研究中,我们比较了临床试验内外患者的预后。
我们确定了2008年至2012年间在六个法国基于人群的登记处记录的MCL患者,以便与同期由LYSA组进行的两项前瞻性多中心MCL临床试验中入组的患者进行比较。使用逻辑回归确定与纳入临床试验相关的变量。使用Pohar-Perme估计器和Nelson等人的灵活参数模型来估计净生存概率和超额死亡率的预后因素。
总共312名登记处患者与372名参加LYSA临床试验的患者进行了比较。纳入临床试验的患者更年轻(中位年龄60岁对74岁,p<0.001)。年龄和Ann Arbor IV期与入组独立相关[OR分别为0.09(0.06 - 0.12)和OR为1.61(1.11 - 2.34)]。临床试验中的4年净生存率更高[79.9%(75.9 - 84.7)对60.3%(53.6 - 67.0)]。在对65岁以上患者进行的多变量分析中,这一结果得到证实,超额死亡率较低[0.33(0.17 - 0.66)]。
试验中纳入的MCL患者是经过高度筛选的,不能代表日常临床中遇到的MCL患者。随着纳入标准的放宽,临床试验患者可能更能代表一般人群。