[Clinical Characteristics of Acute Leukemia Patients with PICALM∷MLLT10 Fusion Gene Positivity and Prognostic Analysis of Combined Venetoclax Targeted Therapy].

Q4 Medicine
Cheng-Sen Cai, Zhen Yao, Ming-Zhu Xu, Zheng Li, Yan-Jun Wu, Sheng-Li Xue
{"title":"[Clinical Characteristics of Acute Leukemia Patients with <i>PICALM∷MLLT10</i> Fusion Gene Positivity and Prognostic Analysis of Combined Venetoclax Targeted Therapy].","authors":"Cheng-Sen Cai, Zhen Yao, Ming-Zhu Xu, Zheng Li, Yan-Jun Wu, Sheng-Li Xue","doi":"10.19746/j.cnki.issn.1009-2137.2025.03.013","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the clinical characteristics and prognostic of venetoclax (VEN) combined targeted therapy in acute leukemia (AL) patients with <i>PICALM∷MLLT10</i> fusion gene positivity.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 16 <i>PICALM∷MLLT10</i>-positive AL patients treated at the First Affiliated Hospital of Soochow University from January 2021 to August 2024. These patients were diagnosed by targeted RNA sequencing (RNA-seq) or reverse transcription multiplex PCR, including newly diagnosed and relapsed/refractory (R/R) cases. The immunophenotypes, genetic features, gene mutations, and the efficacy of VEN combination targeted therapy of patients were evaluated.</p><p><strong>Results: </strong>Among the 16 cases, 3 were confirmed by reverse transcription multiplex PCR, and 13 were detected through targeted RNA-seq among 528 AL patients, with a detection rate of 2.46%. The averge age of patients was (28.0±8.58) years. Patients exhibited diverse immunophenotypes, including 7 cases of acute myeloid leukemia, 5 of acute T-lymphoblastic leukemia, 1 of acute B-lymphoblastic leukemia, 1 of acute undifferentiated leukemia, and 2 of mixed-phenotype acute leukemia. Among them, 11 had extramedullary disease (EMD), 14 expressed CD7, and 12 expressed CD33. Major co-occurring mutations included <i>PHF6</i> (6 cases), <i>NOTCH1</i> (5 cases), and 7 cases with complex karyotypes. Of the 12 patients who received standard induction therapy, 7 did not achieve remission (PR+NR). All 4 patients treated with VEN combination therapy achieved complete remission (CR). Among the 7 induction failure cases, 4 achieved CR upon re-induction with VEN, while the remaining 3 re-induced with standard therapy, did not achieve CR. Thirteen patients received allogeneic hematopoietic stem cell transplantation, including 6 who received maintenance therapy with hypomethylating agents (HMA) alone or in combination with VEN, and seven were followed up. Survival analysis showed that the overall survival was better in the maintenance therapy group (<i>P</i> =0.044).</p><p><strong>Conclusion: </strong><i>PICALM∷MLLT10</i>-positive AL involves multiple lineages and demonstrates poor response to conventional chemotherapy. VEN combination therapy shows promising efficacy in both newly diagnosed and R/R patients. Post-transplant maintenance therapy with HMA alone or combined with VEN may extend survival; however, further clinical validation is required.</p>","PeriodicalId":35777,"journal":{"name":"中国实验血液学杂志","volume":"33 3","pages":"711-719"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国实验血液学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.19746/j.cnki.issn.1009-2137.2025.03.013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To investigate the clinical characteristics and prognostic of venetoclax (VEN) combined targeted therapy in acute leukemia (AL) patients with PICALM∷MLLT10 fusion gene positivity.

Methods: A retrospective analysis was conducted on 16 PICALM∷MLLT10-positive AL patients treated at the First Affiliated Hospital of Soochow University from January 2021 to August 2024. These patients were diagnosed by targeted RNA sequencing (RNA-seq) or reverse transcription multiplex PCR, including newly diagnosed and relapsed/refractory (R/R) cases. The immunophenotypes, genetic features, gene mutations, and the efficacy of VEN combination targeted therapy of patients were evaluated.

Results: Among the 16 cases, 3 were confirmed by reverse transcription multiplex PCR, and 13 were detected through targeted RNA-seq among 528 AL patients, with a detection rate of 2.46%. The averge age of patients was (28.0±8.58) years. Patients exhibited diverse immunophenotypes, including 7 cases of acute myeloid leukemia, 5 of acute T-lymphoblastic leukemia, 1 of acute B-lymphoblastic leukemia, 1 of acute undifferentiated leukemia, and 2 of mixed-phenotype acute leukemia. Among them, 11 had extramedullary disease (EMD), 14 expressed CD7, and 12 expressed CD33. Major co-occurring mutations included PHF6 (6 cases), NOTCH1 (5 cases), and 7 cases with complex karyotypes. Of the 12 patients who received standard induction therapy, 7 did not achieve remission (PR+NR). All 4 patients treated with VEN combination therapy achieved complete remission (CR). Among the 7 induction failure cases, 4 achieved CR upon re-induction with VEN, while the remaining 3 re-induced with standard therapy, did not achieve CR. Thirteen patients received allogeneic hematopoietic stem cell transplantation, including 6 who received maintenance therapy with hypomethylating agents (HMA) alone or in combination with VEN, and seven were followed up. Survival analysis showed that the overall survival was better in the maintenance therapy group (P =0.044).

Conclusion: PICALM∷MLLT10-positive AL involves multiple lineages and demonstrates poor response to conventional chemotherapy. VEN combination therapy shows promising efficacy in both newly diagnosed and R/R patients. Post-transplant maintenance therapy with HMA alone or combined with VEN may extend survival; however, further clinical validation is required.

【PICALM∷MLLT10融合基因阳性急性白血病患者临床特点及联合维妥乐靶向治疗预后分析】。
目的:探讨venetoclax (VEN)联合靶向治疗PICALM∷MLLT10融合基因阳性急性白血病(AL)患者的临床特点及预后。方法:对2021年1月至2024年8月在苏州大学第一附属医院就诊的16例PICALM∷mllt10阳性AL患者进行回顾性分析。这些患者通过靶向RNA测序(RNA-seq)或逆转录多重PCR诊断,包括新诊断和复发/难治性(R/R)病例。评估患者的免疫表型、遗传特征、基因突变及VEN联合靶向治疗的疗效。结果:16例AL患者中,逆转录多重PCR确诊3例,528例AL患者中靶向RNA-seq检出13例,检出率为2.46%。患者平均年龄(28.0±8.58)岁。患者免疫表型多样,急性髓性白血病7例,急性t淋巴细胞白血病5例,急性b淋巴细胞白血病1例,急性未分化白血病1例,混合表型急性白血病2例。其中EMD 11例,CD7表达14例,CD33表达12例。主要共发生突变包括PHF6(6例)、NOTCH1(5例)和7例复杂核型。在接受标准诱导治疗的12例患者中,7例未达到缓解(PR+NR)。经VEN联合治疗的4例患者均达到完全缓解(CR)。7例诱导失败病例中,4例经VEN再诱导后达到CR,其余3例经标准治疗再诱导后未达到CR。13例患者接受同种异体造血干细胞移植,其中6例接受低甲基化药物(HMA)单用或联合VEN维持治疗,7例随访。生存分析显示,维持治疗组总生存期较维持治疗组好(P =0.044)。结论:PICALM∷mllt10阳性AL涉及多个谱系,对常规化疗反应较差。VEN联合治疗在新诊断和R/R患者中均显示出良好的疗效。移植后维持治疗单独使用HMA或联合VEN可延长生存期;然而,需要进一步的临床验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
期刊介绍:
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信