Prediction of Response to FDA-Approved Targeted Therapy and Immunotherapy in Acute Lymphoblastic Leukemia (ALL).

IF 3.8 2区 医学 Q2 ONCOLOGY
Current Treatment Options in Oncology Pub Date : 2024-09-01 Epub Date: 2024-08-05 DOI:10.1007/s11864-024-01237-w
Zakaria Yahya Khawaji, Nussaiba Yahya Khawaji, Mohammed Abdullah Alahmadi, Abeer Abd Elmoneim
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引用次数: 0

Abstract

Opinion statement: Acute lymphoblastic leukemia (ALL) represents the predominant cancer in pediatric populations, though its occurrence in adults is relatively rare. Pre-treatment risk stratification is crucial for predicting prognosis. Important factors for assessment include patient age, white blood cell (WBC) count at diagnosis, extramedullary involvement, immunophenotype, and cytogenetic aberrations. Minimal residual disease (MRD), primarily assessed by flow cytometry following remission, plays a substantial role in guiding management plans. Over the past decade, significant advancements in ALL outcomes have been witnessed. Conventional chemotherapy has remarkably reduced mortality rates; however, its intensive nature raises safety concerns and has led to the emergence of treatment-resistant cases with recurrence of relapses. Consequently, The U.S. Food and Drug Administration (FDA) has approved several novel treatments for relapsed/refractory ALL due to their demonstrated efficacy, as indicated by improved complete remission and survival rates. These treatments include tyrosine kinase inhibitors (TKIs), the anti-CD19 monoclonal antibody blinatumomab, anti-CD22 inotuzumab ozogamicin, anti-CD20 rituximab, and chimeric antigen receptor (CAR) T-cell therapy. Identifying the variables that influence treatment decisions is a pressing necessity for tailoring therapy based on heterogeneous patient characteristics. Key predictive factors identified in various observational studies and clinical trials include prelymphodepletion disease burden, complex genetic abnormalities, and MRD. Furthermore, the development of serious adverse events following treatment could be anticipated through predictive models, allowing for appropriate prophylactic measures to be considered. The ultimate aim is to incorporate the concept of precision medicine in the field of ALL through valid prediction platform to facilitate the selection of the most suitable treatment approach.

预测急性淋巴细胞白血病 (ALL) 对 FDA 批准的靶向疗法和免疫疗法的反应。
意见陈述:急性淋巴细胞白血病(ALL)是儿科最常见的癌症,但在成人中的发病率相对较低。治疗前的风险分层对于预测预后至关重要。重要的评估因素包括患者年龄、诊断时的白细胞(WBC)计数、髓外受累情况、免疫表型和细胞遗传学畸变。最小残留病(MRD)主要通过缓解后的流式细胞术进行评估,在指导管理计划方面发挥着重要作用。过去十年间,ALL 的治疗效果取得了重大进展。传统化疗显著降低了死亡率;然而,其强化治疗的性质引发了安全问题,并导致耐药病例的出现和复发。因此,美国食品和药物管理局(FDA)批准了几种治疗复发/难治性 ALL 的新型疗法,因为这些疗法的疗效已得到证实,完全缓解率和生存率均有所提高。这些疗法包括酪氨酸激酶抑制剂(TKIs)、抗CD19单克隆抗体blinatumomab、抗CD22伊妥珠单抗奥佐米星、抗CD20利妥昔单抗和嵌合抗原受体(CAR)T细胞疗法。确定影响治疗决策的变量是根据不同患者特征定制治疗方案的迫切需要。在各种观察性研究和临床试验中发现的主要预测因素包括淋巴细胞耗竭前的疾病负担、复杂的基因异常和 MRD。此外,还可以通过预测模型预测治疗后严重不良事件的发生,从而考虑采取适当的预防措施。最终目的是通过有效的预测平台,将精准医疗的概念纳入 ALL 领域,以促进选择最合适的治疗方法。
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
CiteScore
7.10
自引率
0.00%
发文量
113
审稿时长
>12 weeks
期刊介绍: This journal aims to review the most important, recently published treatment option advances in the field of oncology. By providing clear, insightful, balanced contributions by international experts, the journal intends to facilitate worldwide approaches to cancer treatment. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas, such as endocrine tumors, lymphomas, neuro-oncology, and cancers of the breast, head and neck, lung, skin, gastrointestinal tract, and genitourinary region. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. We also provide commentaries from well-known oncologists, and an international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research.
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