Qi Wen-Jing, Xu Xue-Ju, Li Bai, Wang Tao, Sheng Guang-Yao, Zhu Ping, Wang Chun-Mei
Department of Children's Hematology and Oncology, First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2024 Oct 15;26(10):1093-1100. doi: 10.7499/j.issn.1008-8830.2406014.
To explore the current application of high-throughput drug sensitivity (HDS) testing in children with relapsed and refractory acute leukemia (RR-AL) and analyze the feasibility of salvage treatment plans.
A retrospective collection of clinical data from children with RR-AL who underwent HDS testing at the Department of Children's Hematology and Oncology of the First Affiliated Hospital of Zhengzhou University from November 2021 to October 2023 was conducted, followed by an analysis of drug sensitivity results and treatment outcomes.
A total of 17 children with RR-AL underwent HDS testing, including 7 cases of relapsed refractory acute myeloid leukemia and 10 cases of relapsed refractory acute lymphoblastic leukemia. The detection rate of highly sensitive chemotherapy drugs/regimens was 53% (9/17), while the detection rate of moderately sensitive chemotherapy drugs/regimens was 100% (17/17). Among the 17 RR-AL patients with highly and moderately sensitive chemotherapy drugs and regimens, the MOACD regimen (mitoxantrone + vincristine + cytarabine + cyclophosphamide + dexamethasone) accounted for 100%, with the highest inhibition rate for single-agent mitoxantrone (94%, 16/17), and the highest inhibition rate for targeted therapy being bortezomib (94%, 16/17). Nine patients adjusted their chemotherapy based on HDS testing results, with 4 undergoing hematopoietic stem cell transplantation. Four patients achieved disease-free survival, while 5 died. Eight patients received empirical chemotherapy, with 2 undergoing hematopoietic stem cell transplantation; 4 achieved disease-free survival, while 4 died.
HDS testing can identify highly sensitive drugs/regimens for children with RR-AL, improving the rate of re-remission and creating conditions for subsequent hematopoietic stem cell transplantation.
探讨高通量药物敏感性(HDS)检测在复发难治性急性白血病(RR-AL)患儿中的应用现状,并分析挽救治疗方案的可行性。
回顾性收集2021年11月至2023年10月在郑州大学第一附属医院儿童血液肿瘤科接受HDS检测的RR-AL患儿的临床资料,随后分析药物敏感性结果及治疗结局。
共有17例RR-AL患儿接受了HDS检测,其中复发难治性急性髓系白血病患者7例,复发难治性急性淋巴细胞白血病患者10例。高敏化疗药物/方案的检出率为53%(9/17),中敏化疗药物/方案的检出率为100%(17/17)。在17例具有高敏和中敏化疗药物及方案的RR-AL患者中,MOACD方案(米托蒽醌+长春新碱+阿糖胞苷+环磷酰胺+地塞米松)占100%,单药米托蒽醌的抑制率最高(94%,16/17),靶向治疗中硼替佐米的抑制率最高(94%,16/17)。9例患者根据HDS检测结果调整了化疗方案,4例接受了造血干细胞移植。4例患者实现无病生存,5例死亡。8例患者接受经验性化疗,2例接受造血干细胞移植;4例实现无病生存,4例死亡。
HDS检测可识别RR-AL患儿的高敏药物/方案,提高再缓解率,并为后续造血干细胞移植创造条件。