儿科血癌患者匹配治疗的致癌和免疫学靶点:荷兰 iTHER 研究经验。

IF 7.6 2区 医学 Q1 HEMATOLOGY HemaSphere Pub Date : 2024-07-15 DOI:10.1002/hem3.122
Judith M. Boer, Uri Ilan, Aurélie Boeree, Karin P. S. Langenberg, Jan Koster, Marco J. Koudijs, Jayne Y. Hehir-Kwa, Stefan Nierkens, Corinne Rossi, Jan J. Molenaar, Bianca F. Goemans, Monique L. den Boer, C. Michel Zwaan
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引用次数: 0

摘要

在过去 10 年中,针对复发或难治性儿童癌症实施了机构和国家分子肿瘤委员会,以便根据可作用的致癌病变(包括荷兰 iTHER 平台)优先选择靶向药物进行个体化治疗。血液恶性肿瘤在精准医学研究中占少数。在此,我们报告了 56 例 iTHER 白血病/淋巴瘤患者的情况,我们将细胞表面标志物和致癌畸变视为可操作事件,并补充了 6 例患者的体内外药物敏感性。在 iTHER 登记之前,34% 的患者接受过异体造血细胞移植 (HCT),18% 的患者接受过 CAR-T 疗法。51名患者(91%)获得了全面诊断检测所需的足够肿瘤比例(≥20%)的样本。在 49/51 例患者中,有多达 10 个致癌可操作事件被优先考虑,所有被分析的患者都确定了免疫疗法靶点。根据 iTHER 的建议,对 51 例患者中的 24 例(47%)进行了靶向治疗,其中 17 例患者接受了免疫治疗,12 例患者接受了与致癌畸变相匹配的靶向药物治疗,1 例患者接受了基于体内外药物敏感性的药物治疗。总之,对复发/难治性血液恶性肿瘤的全面分析表明,精准医疗方法有多个致癌和免疫治疗靶点,这需要多学科专业知识,才能为这一罕见、接受过大量预处理的儿科人群优先选择最佳治疗方案。
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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Oncogenic and immunological targets for matched therapy of pediatric blood cancer patients: Dutch iTHER study experience

Over the past 10 years, institutional and national molecular tumor boards have been implemented for relapsed or refractory pediatric cancer to prioritize targeted drugs for individualized treatment based on actionable oncogenic lesions, including the Dutch iTHER platform. Hematological malignancies form a minority in precision medicine studies. Here, we report on 56 iTHER leukemia/lymphoma patients for which we considered cell surface markers and oncogenic aberrations as actionable events, supplemented with ex vivo drug sensitivity for six patients. Prior to iTHER registration, 34% of the patients had received allogeneic hematopoietic cell transplantation (HCT) and 18% CAR-T therapy. For 51 patients (91%), a sample with sufficient tumor percentage (≥20%) required for comprehensive diagnostic testing was obtained. Up to 10 oncogenic actionable events were prioritized in 49/51 patients, and immunotherapy targets were identified in all profiled patients. Targeted treatment(s) based on the iTHER advice was given to 24 of 51 patients (47%), including immunotherapy in 17 patients, a targeted drug matching an oncogenic aberration in 12 patients, and a drug based on ex vivo drug sensitivity in one patient, resulting in objective responses and a bridge to HCT in the majority of the patients. In conclusion, comprehensive profiling of relapsed/refractory hematological malignancies showed multiple oncogenic and immunotherapy targets for a precision medicine approach, which requires multidisciplinary expertise to prioritize the best treatment options for this rare, heavily pretreated pediatric population.

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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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