Haematology, SA Pathology, Adelaide, Australia.
Blood. 2013 Jul 25;122(4):515-22. doi: 10.1182/blood-2013-02-483750. Epub 2013 May 23.
Most patients with chronic myeloid leukemia (CML) treated with imatinib will relapse if treatment is withdrawn. We conducted a prospective clinical trial of imatinib withdrawal in 40 chronic-phase CML patients who had sustained undetectable minimal residual disease (UMRD) by conventional quantitative polymerase chain reaction (PCR) on imatinib for at least 2 years. Patients stopped imatinib and were monitored frequently for molecular relapse. At 24 months, the actuarial estimate of stable treatment-free remission was 47.1%. Most relapses occurred within 4 months of stopping imatinib, and no relapses beyond 27 months were seen. In the 21 patients treated with interferon before imatinib, a shorter duration of interferon treatment before imatinib was significantly associated with relapse risk, as was slower achievement of UMRD after switching to imatinib. Highly sensitive patient-specific BCR-ABL DNA PCR showed persistence of the original CML clone in all patients with stable UMRD, even several years after imatinib withdrawal. No patients with molecular relapse after discontinuation have progressed or developed BCR-ABL mutations (median follow-up, 42 months). All patients who relapsed remained sensitive to imatinib re-treatment. These results confirm the safety and efficacy of a trial of imatinib withdrawal in stable UMRD with frequent, sensitive molecular monitoring and early rescue of molecular relapse.
大多数接受伊马替尼治疗的慢性髓性白血病(CML)患者如果停止治疗将会复发。我们对 40 例慢性期 CML 患者进行了前瞻性临床试验,这些患者在接受伊马替尼治疗至少 2 年后,通过常规定量聚合酶链反应(PCR)检测到微小残留疾病(UMRD)持续不可检测。患者停止伊马替尼治疗,并频繁监测分子复发情况。在 24 个月时,无治疗缓解的稳定估计存活率为 47.1%。大多数复发发生在停止伊马替尼治疗后的 4 个月内,27 个月后未见复发。在伊马替尼之前接受干扰素治疗的 21 例患者中,伊马替尼之前干扰素治疗的持续时间较短与复发风险显著相关,而在转为伊马替尼后达到 UMRD 的速度较慢也与复发风险相关。高度敏感的患者特异性 BCR-ABL DNA PCR 显示,所有 UMRD 稳定的患者中,即使在停止伊马替尼治疗数年后,原始 CML 克隆仍持续存在。停止治疗后分子复发的患者均未进展或出现 BCR-ABL 突变(中位随访时间为 42 个月)。所有复发患者对伊马替尼重新治疗仍敏感。这些结果证实了在频繁、敏感的分子监测下,对稳定 UMRD 进行伊马替尼停药试验的安全性和有效性,并且可以早期挽救分子复发。