Treatment-free remission as a new goal in the management of chronic myeloid leukemia: Clinical and biological aspects

IF 3.3 4区 医学 Q2 HEMATOLOGY
Daniele Cattaneo, Cristina Bucelli, Valentina Bellani, Barbara Mora, Alessandra Iurlo
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引用次数: 0

Abstract

The therapeutic armamentarium of chronic myeloid leukemia (CML) has dramatically improved after small molecule tyrosine kinase inhibitors (TKIs) targeting BCR::ABL1 became available, with a life expectancy now close to that of the general population. Although highly effective, these drugs also have a toxicity profile that is often mild to moderate, but sometimes severe. Indeed, long-term treatment with TKIs can lead to chronic adverse events that can negatively affect patients' quality of life and can promote significant morbidity and mortality, particularly in the case of second- or third-generation TKIs. Treatment discontinuation has therefore become an emerging goal for CML patients and numerous studies have evaluated in off-TKI subjects what requirements are appropriate for an attempt at treatment-free remission (TFR). TFR eligibility is currently limited to a small population of subjects with both deep and sustained molecular responses to TKIs. For those attempting TFR, average success rates are promising, with 25%–30% of patients experiencing prolonged TFR. In case of failure to maintain sustained TFR, safety results to date are reassuring, with almost all patients responding successfully to resumption of TKIs, and advanced-phase disease progression representing a very rare event. The purpose of this review is to discuss guidelines for TKI discontinuation, clinical advances from clinical trials and real-life experiences, and describe areas of research, particularly regarding the biological factors capable of predicting the success of TFR.

无治疗缓解作为慢性髓性白血病治疗的新目标:临床和生物学方面
以 BCR::ABL1 为靶点的小分子酪氨酸激酶抑制剂(TKIs)问世后,慢性髓性白血病(CML)的治疗手段大为改观,患者的预期寿命已接近普通人群。这些药物虽然疗效显著,但也有毒性,通常为轻度至中度毒性,但有时也会出现严重毒性。事实上,TKIs 的长期治疗可导致慢性不良反应,对患者的生活质量产生负面影响,并可导致严重的发病率和死亡率,尤其是第二代或第三代 TKIs。因此,停止治疗已成为 CML 患者的一个新目标,许多研究评估了非 TKI 受试者尝试无治疗缓解(TFR)的适当要求。目前,符合 TFR 条件的患者仅限于少数对 TKIs 有深度和持续分子反应的受试者。对于尝试 TFR 的患者来说,平均成功率很高,25%-30% 的患者可获得长期的 TFR。如果未能维持持续的 TFR,迄今为止的安全性结果令人欣慰,几乎所有患者都能对 TKIs 的恢复成功做出反应,而晚期疾病进展则是非常罕见的情况。本综述旨在讨论 TKI 停药指南、临床试验的临床进展和实际经验,并介绍研究领域,尤其是能够预测 TFR 成功与否的生物学因素。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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