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早期滤泡性淋巴瘤的微小残留病灶监测可预测预后,并可在放疗后用利妥昔单抗进行治疗。

Minimal residual disease monitoring in early stage follicular lymphoma can predict prognosis and drive treatment with rituximab after radiotherapy.

机构信息

Haematology, Department of Translational and Precision Medicine, Sapienza University, Rome, Italy.

National Centre for Global Health, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Br J Haematol. 2020 Jan;188(2):249-258. doi: 10.1111/bjh.16125. Epub 2019 Aug 5.

DOI:10.1111/bjh.16125
PMID:31385309
Abstract

Since 2000, we have investigated 67 consecutive patients with stage I/II follicular lymphoma (FL) for the presence of BCL2/IGH rearrangements by polymerase chain reaction (PCR), real time quantitative PCR (RQ-PCR) and digital droplet PCR (ddPCR). All patients were treated with involved-field radiotherapy (IF-RT) (24-30 Gy). From 2005, patients with minimal residual disease (MRD) after IF-RT received rituximab (R) (375 mg/m , 4 weekly administrations). The median follow-up is 82 months (17-196). At diagnosis, 72% of patients were BCL2/IGH+. Progression-free survival (PFS) was significantly better in patients with undetectable/low levels (<10 ) of circulating BCL2/IGH+ cells at diagnosis and in those who were persistently MRD- during follow-up (P = 0·0038). IF-RT induced an MRD- status in 50% of cases; 16/19 (84%) MRD+ patients after IF-RT became MRD- after R treatment. A significantly longer PFS was observed in MRD+ patients treated with R compared to untreated MRD+ patients (P = 0·049). In early stage FL, both circulating levels of BCL2/IGH+ cells at diagnosis and MRD status during follow-up bear prognostic implications. Standard IF-RT fails to induce an MRD-negative status in half of patients. Most patients become MRD- following treatment with R and this is associated with a significantly better PFS.

摘要

自 2000 年以来,我们通过聚合酶链反应(PCR)、实时定量 PCR(RQ-PCR)和数字液滴 PCR(ddPCR)连续研究了 67 例 I/II 期滤泡淋巴瘤(FL)患者,以检测 BCL2/IGH 重排。所有患者均接受累及野放疗(IF-RT)(24-30 Gy)。从 2005 年开始,接受 IF-RT 后有微小残留病灶(MRD)的患者接受利妥昔单抗(R)(375mg/m ,每周 4 次)治疗。中位随访时间为 82 个月(17-196)。在诊断时,72%的患者 BCL2/IGH+。在诊断时循环 BCL2/IGH+细胞水平不可检测/低水平(<10 )和随访期间持续 MRD-的患者无进展生存(PFS)显著更好(P=0.0038)。IF-RT 可使 50%的病例达到 MRD-状态;19 例 IF-RT 后 MRD+患者中的 16 例(84%)在接受 R 治疗后成为 MRD-。与未经治疗的 MRD+患者相比,接受 R 治疗的 MRD+患者的 PFS 显著更长(P=0.049)。在早期 FL 中,诊断时循环 BCL2/IGH+细胞水平和随访期间的 MRD 状态均具有预后意义。标准 IF-RT 无法使一半的患者达到 MRD-状态。大多数患者在接受 R 治疗后成为 MRD-,这与显著更好的 PFS 相关。

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