CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Molecularly Targeted Small Molecule Inhibitor Therapy for Pediatric Acute Lymphoblastic Leukemia: A Comprehensive Review of Clinical Trials.
Molecularly Targeted Small Molecule Inhibitor Therapy for Pediatric Acute Lymphoblastic Leukemia: A Comprehensive Review of Clinical Trials.
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在过去的几十年中,急性白血病的生物学和遗传学特征研究取得了显著进展,风险适应性多药联合治疗方案的优化也大幅提高了儿童急性淋巴细胞白血病(ALL)的治愈率和生活质量。尽管取得了这些理想的结果,但复发或化疗难治性(R/R)疾病患者或具有高风险遗传特征的患者仍面临不令人满意的结局。
进一步强化传统化疗已在达到理想疗效而不产生过度副作用方面达到了极限,需要创新方法来提高治愈率,同时继续最大限度地减少与化疗和造血干细胞移植相关的毒性。在精准医学时代,血液肿瘤学领域出现了两种关键的治疗策略:分子靶向治疗和免疫治疗。基于抗体的免疫治疗和细胞免疫治疗无疑重塑了儿童ALL治疗的格局,并具有在当前和未来一线方案中发挥主导作用的巨大潜力;这些重要疗法在近期综述中已有详细阐述。分子靶向小分子抑制剂治疗仍然是精准医学的基石,下一代测序的最新进展为其提供了支持,使得转录组学和基因组学分析数据能够应用于风险分层和治疗优化。儿童ALL的临床试验在完善治疗和改善结局方面发挥了重要作用,随着治疗策略日益复杂,这一范式仍然至关重要。这篇综述聚焦于儿童ALL的分子靶向治疗方法,旨在总结已完成临床试验的结果,突出当前正在进行和即将开展的试验格局,并为儿童B-ALL和T-ALL精准驱动治疗优化的未来方向提供见解。
In the past decades, significant advancements in the biological and genetic characterization of acute leukemias and optimization of risk-adapted multi-agent treatment protocols have dramatically improved cure rates and quality of life for children with acute lymphoblastic leukemia (ALL). Despite these optimal results, patients with relapsed or chemotherapy-refractory (R/R) disease or with high-risk genetic features still face unsatisfactory outcomes.
Further intensification of conventional chemotherapy has reached its limits in achieving the desired efficacy without undue side effects, necessitating innovative approaches to improve cure rates while continuing to minimize the toxicities associated with chemotherapy and hematopoietic stem cell transplantation. In the era of precision medicine, two key therapeutic strategies have emerged in hemato-oncology: molecularly targeted therapies and immunotherapies. Antibody-based and cellular immunotherapies have undoubtedly reshaped the landscape of childhood ALL treatment and have significant potential to play leading roles in current and future frontline regimens; these important therapies are well delineated in recent reviews.
Molecularly targeted small molecule inhibitor therapies remain a cornerstone of precision medicine, supported by recent advancements in next-generation sequencing, which have enabled the application of transcriptomic and genomic profiling data to risk stratification and therapy optimization. Clinical trials for children with ALL have been instrumental in refining therapies and improving outcomes, a paradigm that remains critical as treatment strategies become increasingly complex.
This comprehensive review focuses upon molecularly targeted therapy approaches for childhood ALL and aims to summarize findings from completed clinical trials to highlight the current landscape of ongoing and upcoming trials and to provide insights into future directions for the precision-driven optimization of pediatric B-ALL and T-ALL treatment.
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