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停用伊马替尼治疗达到缓解的可行性:在慢性髓性白血病慢性期研究中使用非专利伊马替尼的试验结果。

Feasibility of treatment-free remission with generic imatinib: Results of generic imatinib-free trial-in-chronic myeloid leukaemia-chronic phase study.

机构信息

Department of Clinical Hematology and Medical Oncology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

Department of Hematology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.

出版信息

Indian J Med Res. 2023 Jan;157(1):87-91. doi: 10.4103/ijmr.ijmr_1090_21.

Abstract

BACKGROUND & OBJECTIVES: Both innovator and generic imatinib are approved for the treatment of Chronic Myeloid Leukaemia-Chronic phase (CML-CP). Currently, there are no studies on the feasibility of treatment-free remission (TFR) with generic imatinib. This study attempted to determine the feasibility and efficacy of TFR in patients on generic Imatinib.

METHODS

In this single-centre prospective Generic Imatinib-Free Trial-in-CML-CP study, twenty six patients on generic imatinib for ≥3 yr and in sustained deep molecular response (BCR ABL ≤0.01% for more than two years) were included. After treatment discontinuation, patients were monitored with complete blood count and BCR ABL by real-time quantitative PCR monthly for one year and three monthly thereafter. Generic imatinib was restarted at single documented loss of major molecular response (BCR ABL>0.1%).

RESULTS

At a median follow up of 33 months (interquartile range 18.7-35), 42.3 per cent patients (n=11) continued to be in TFR. Estimated TFR at one year was 44 per cent. All patients restarted on generic imatinib regained major molecular response. On multivariate analysis, attainment of molecularly undetectable leukaemia (>MR) prior to TFR was predictive of TFR [P=0.022, HR 0.284 (0.096-0.837)].

INTERPRETATION & CONCLUSIONS: The study adds to the growing literature that generic imatinib is effective and can be safely discontinued in CML-CP patients who are in deep molecular remission.

摘要

背景与目的

原研伊马替尼和仿制药伊马替尼均被批准用于治疗慢性髓性白血病慢性期(CML-CP)。目前,尚无关于仿制药伊马替尼实现无治疗缓解(TFR)的可行性的研究。本研究试图确定 CML-CP 患者使用仿制药伊马替尼实现 TFR 的可行性和疗效。

方法

在这项单中心前瞻性 CML-CP 仿制药无治疗试验中,纳入了 26 名接受仿制药伊马替尼治疗≥3 年且持续深度分子反应(BCR ABL<0.01%持续两年以上)的患者。停药后,每月通过实时定量 PCR 监测全血细胞计数和 BCR ABL,持续 1 年,此后每 3 个月监测一次。在单一记录的主要分子反应丧失(BCR ABL>0.1%)时重新开始使用仿制药伊马替尼。

结果

中位随访 33 个月(四分位间距 18.7-35)时,42.3%的患者(n=11)持续处于 TFR 状态。预计 1 年的 TFR 为 44%。所有重新开始使用仿制药伊马替尼的患者均恢复了主要分子反应。多变量分析显示,TFR 前达到分子学不可检测白血病(>MR)与 TFR 相关[P=0.022,HR 0.284(0.096-0.837)]。

解释与结论

本研究增加了越来越多的文献证据,证明在 CML-CP 患者中,深度分子缓解时,仿制药伊马替尼是有效且安全的,可以停药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e0/10284370/463174207203/IJMR-157-87-g001.jpg

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