Ansarian Mohammad Amin, Fatahichegeni Mahsa, Ren Juan, Wang Xiaoning
Medical College, Xi'an Jiaotong University, Xi'an 710061, China.
Department of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.
Curr Oncol. 2025 Mar 31;32(4):204. doi: 10.3390/curroncol32040204.
Biological sex and gender factors significantly influence the pathogenesis, progression, and treatment response in hematologic malignancies. This comprehensive review examines sex-specific differences in acute myeloid leukemia, acute lymphoblastic leukemia, chronic myeloid leukemia, and multiple myeloma through systematic analysis of the peer-reviewed literature published between 2014-2024 and identified through structured searches of PubMed, Web of Science, and MEDLINE databases. Epidemiological data demonstrate higher disease incidence (57% male vs. 43% female in MM, 63% male vs. 37% female in AML hospitalizations for ages 18-39) and inferior outcomes in male patients across malignancy types (5-year relative survival rates of 48.8% vs. 60.4% in females with AML), while female patients exhibit superior survival despite experiencing greater treatment-related toxicities. Our analysis reveals consistent sex-specific patterns in molecular mechanisms, including distinct mutational profiles, differences in immune system function, and sex-based pharmacokinetic variations that collectively suggest the necessity for sex-differentiated treatment approaches. The review identifies reproducible patterns across diseases, particularly in cytogenetic and molecular characteristics, with females demonstrating favorable prognostic mutations in leukemias and higher rates of chromosomal abnormalities in multiple myeloma. Despite these identifiable patterns, significant knowledge gaps persist regarding the underlying mechanisms of sex-based outcome differences. Incorporating sex and gender considerations into precision medicine frameworks represents a critical advancement toward optimizing treatment strategies and improving clinical outcomes for patients with hematologic malignancies.
生物性别和社会性别因素显著影响血液系统恶性肿瘤的发病机制、进展及治疗反应。本综述通过系统分析2014年至2024年间发表的、经同行评审的文献(通过对PubMed、科学网和医学期刊数据库进行结构化检索确定),研究了急性髓系白血病、急性淋巴细胞白血病、慢性髓系白血病和多发性骨髓瘤中的性别差异。流行病学数据显示,在各类恶性肿瘤中,男性患者的疾病发病率更高(多发性骨髓瘤中男性占57%,女性占43%;18至39岁急性髓系白血病住院患者中男性占63%,女性占37%),且预后较差(急性髓系白血病女性患者的5年相对生存率为60.4%,男性为48.8%),而女性患者尽管经历了更大的治疗相关毒性,但生存率更高。我们的分析揭示了分子机制中一致的性别特异性模式,包括不同的突变谱、免疫系统功能差异以及基于性别的药代动力学变化,这些共同表明了采用性别差异化治疗方法的必要性。该综述确定了不同疾病间可重复的模式,特别是在细胞遗传学和分子特征方面,女性在白血病中表现出有利的预后突变,在多发性骨髓瘤中染色体异常率更高。尽管存在这些可识别的模式,但关于基于性别的预后差异的潜在机制仍存在重大知识空白。将性别因素纳入精准医学框架是优化血液系统恶性肿瘤患者治疗策略和改善临床结局的关键进展。