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利妥昔单抗与苯达莫司汀联合作为一线治疗方案在清除滤泡性淋巴瘤微小残留病方面疗效显著:一项意大利回顾性研究

The Combination of Rituximab and Bendamustine as First-Line Treatment Is Highly Effective in the Eradicating Minimal Residual Disease in Follicular Lymphoma: An Italian Retrospective Study.

作者信息

Galimberti Sara, Ciabatti Elena, Ercolano Giacomo, Grassi Susanna, Guerrini Francesca, Cecconi Nadia, Rousseau Martina, Cervetti Giulia, Mazziotta Francesco, Iovino Lorenzo, Falzetti Franca, Falcinelli Flavio, Bosi Alberto, Rigacci Luigi, Kovalchuk Sofia, Vallisa Daniele, Macchia Lucia, Ciancia Eugenio, Petrini Mario

机构信息

Section of Hematology, Department of Clinical and Experimental Medicine, University of PisaPisa, Italy.

Doctoral School of Genetics, Oncology and Clinical Medicine (GeNOMEC), University of SienaSiena, Italy.

出版信息

Front Pharmacol. 2017 Jun 29;8:413. doi: 10.3389/fphar.2017.00413. eCollection 2017.

Abstract

R-Bendamustine is an effective treatment for follicular lymphoma (FL). Previous large trials demonstrated the prognostic role of the molecular minimal residual disease (MRD) during the most frequently adopted chemotherapeutic regimens, but there are not yet conclusive data about the effect of combination of rituximab (R) and bendamustine in terms of MRD clearance. Thus, the aim of this retrospective study was to assess if and in what extent the combination of rituximab and bendamustine would exert a significant reduction of the molecular disease in 48 previously untreated FL patients. The molecular marker at baseline was found in the 62.5% of cases; no significant differences were observed between patients with or without the molecular marker in respect of the main clinical features. Moreover, the quantization of the baseline molecular tumor burden showed a great variability: the median value was 1.4 × 10 copies, ranging from 3 × 10 to 4 × 10. The initial molecular tumor burden did not correlate with clinical features and did not impact on the subsequent quality of response. After treatment, 93% of cases became MRD-negative; the median reduction of the load was 4 logs. The 2-years PFS was 85%; it was significantly longer for patients in complete than for those in partial response (91 vs. 57%; = 0.002), and for cases with lower FLIPI-2 score (88 vs. 60%; = 0.004). On the contrary, PFS did not differ between patients with or without the molecular marker at baseline; a molecular tumor burden 15 times higher was observed in the relapsed subgroup in comparison to the relapse-free one, but this difference did not change the PFS length. The 2-years OS was 93.6%; the only variable that significantly impacted on it was the FLIPI-2 score; the presence of the molecular marker at baseline or its behavior after treatment did not impact on survival. This study, even if retrospective and conducted on a small series of patients, would represent a proof of concept that R-bendamustine is able to so efficaciously eradicate MRD that it could be able to by-pass the prognostic significance of MRD already demonstrated for other chemotherapeutic regimens in FL.

摘要

利妥昔单抗联合苯达莫司汀(R - Bendamustine)是滤泡性淋巴瘤(FL)的一种有效治疗方法。以往的大型试验证明了分子微小残留病(MRD)在最常用化疗方案中的预后作用,但关于利妥昔单抗(R)和苯达莫司汀联合用药在清除MRD方面的效果尚无确凿数据。因此,这项回顾性研究的目的是评估利妥昔单抗和苯达莫司汀联合用药是否以及在多大程度上能使48例初治FL患者的分子疾病显著减少。在62.5%的病例中发现了基线分子标志物;在主要临床特征方面,有或无分子标志物的患者之间未观察到显著差异。此外,基线分子肿瘤负荷的量化显示出很大的变异性:中位数为1.4×10拷贝,范围从3×10到4×10。初始分子肿瘤负荷与临床特征无关,也不影响后续的缓解质量。治疗后,93%的病例变为MRD阴性;肿瘤负荷的中位数降低了4个对数。2年无进展生存期(PFS)为85%;完全缓解的患者明显长于部分缓解的患者(91%对57%;P = 0.002),FLIPI - 2评分较低的患者也是如此(88%对60%;P = 0.004)。相反,基线时有或无分子标志物的患者之间PFS无差异;复发亚组的分子肿瘤负荷比无复发亚组高15倍,但这种差异并未改变PFS的长度。2年总生存期(OS)为93.6%;唯一对其有显著影响的变量是FLIPI - 2评分;基线时分子标志物的存在或治疗后其变化情况对生存无影响。这项研究,即使是回顾性的且针对一小部分患者进行,也将代表一个概念验证,即R - Bendamustine能够如此有效地根除MRD,以至于它可能能够绕过已在FL的其他化疗方案中证明的MRD的预后意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7e9/5489595/84c54a560603/fphar-08-00413-g0001.jpg

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