Rationale and Design of a Prospective, Multicentre, Stop Tyrosine Kinase Inhibitor Trial of Paediatric Patients with Chronic Myeloid Leukaemia with Sustained Complete Molecular Response (STKI-14)

Q4 Medicine
H. Shimada, A. Kada, H. Shima, C. Tono, Y. Yuza, H. Kurosawa, A. Watanabe, Masaki Ito, Hideko Uryu, K. Kamibeppu, N. Kiyokawa, S. Adachi, A. Saito, A. Tanizawa
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引用次数: 1

Abstract

Chronic myeloid leukaemia (CML) is a relatively rare disease in children, accounting for 2–3% of all paediatric leukaemia cases. Generally, children with CML can avoid hematopoietic stem cell transplantation and achieve molecular responses with tyrosine kinase inhibitors (TKI). However, CML stem cells are thought to survive in many patients, even after TKI treatment. Many aspects of the toxic effects of prolonged exposure to TKIs during childhood remain unclear, particularly those regarding growth impairment. This lack of clarity underscores the importance of the present clinical trial, which aims to clarify the feasibility of treatment-free remission (TFR) in children following TKI treatment. We aim to examine the long-term outcomes and complications of TKIs before and after cessation to better understand the unknown complications that could arise in adulthood. This trial targets patients who were diagnosed with CML at an age younger than 20 years, were in the chronic or accelerated phase at initial diagnosis and remained in complete molecular remission for at least 2 years after TKI administration. We will examine the utility of TKI cessation and assess the treatment results of patients who resumed TKI therapy after losing a major molecular response. We will also investigate factors related to the feasibility of a TFR after TKI cessation.
一项前瞻性、多中心、终止酪氨酸激酶抑制剂试验的原理和设计,该试验针对具有持续完全分子反应的慢性髓性白血病患儿(STKI-14)
慢性粒细胞白血病(CML)是一种相对罕见的儿童疾病,占所有儿童白血病病例的2-3%。一般来说,患有慢性粒细胞白血病的儿童可以避免造血干细胞移植,并使用酪氨酸激酶抑制剂(TKI)实现分子反应。然而,CML干细胞被认为在许多患者中存活,即使在TKI治疗后也是如此。儿童时期长期接触TKIs的毒性影响的许多方面仍不清楚,尤其是与生长障碍有关的方面。这种缺乏明确性的情况突显了目前临床试验的重要性,该试验旨在阐明TKI治疗后儿童无治疗缓解(TFR)的可行性。我们的目的是检查TKIs在停止前后的长期结果和并发症,以更好地了解成年后可能出现的未知并发症。该试验针对的是20岁以下被诊断为慢性粒细胞白血病的患者,在最初诊断时处于慢性或加速期,并且在TKI给药后至少2年内保持完全分子缓解。我们将研究停止TKI的效用,并评估在失去主要分子反应后恢复TKI治疗的患者的治疗结果。我们还将研究TKI停止后TFR可行性的相关因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hiroshima journal of medical sciences
Hiroshima journal of medical sciences Medicine-Medicine (all)
CiteScore
0.30
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