Boer Judith M, Ilan Uri, Boeree Aurélie, Langenberg Karin P S, Koster Jan, Koudijs Marco J, Hehir-Kwa Jayne Y, Nierkens Stefan, Rossi Corinne, Molenaar Jan J, Goemans Bianca F, den Boer Monique L, Zwaan C Michel
Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Amsterdam UMC University of Amsterdam, Center for Experimental and Molecular Medicine, Laboratory of Experimental Oncology and Radiobiology Amsterdam The Netherlands.
Hemasphere. 2024 Jul 15;8(7):e122. doi: 10.1002/hem3.122. eCollection 2024 Jul.
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.
在过去10年中,针对复发或难治性儿童癌症设立了机构和国家分子肿瘤委员会,以便根据可操作的致癌病变为个体化治疗确定靶向药物的优先顺序,其中包括荷兰的iTHER平台。血液系统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,我们将细胞表面标志物和致癌畸变视为可操作事件,并对6例患者补充了体外药敏试验。在iTHER登记之前,34%的患者接受了异基因造血细胞移植(HCT),18%的患者接受了CAR-T治疗。对于51例患者(91%),获得了综合诊断检测所需的足够肿瘤比例(≥20%)的样本。49/51例患者中确定了多达10个致癌可操作事件,并且在所有分析的患者中都鉴定出了免疫治疗靶点。51例患者中有24例(47%)接受了基于iTHER建议的靶向治疗,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匹配的靶向药物治疗,1例患者接受了基于体外药敏试验的药物治疗,大多数患者产生了客观反应并为HCT架起了桥梁。总之,对复发/难治性血液系统恶性肿瘤进行全面分析显示,精准医学方法有多个致癌和免疫治疗靶点,这需要多学科专业知识来为这个罕见的、经过大量预处理的儿科人群确定最佳治疗方案的优先顺序。