{"title":"阿扎胞苷加Venetoclax与强化化疗治疗急性髓系白血病的安全性和有效性比较:倾向评分匹配分析。","authors":"Yu-Cheng Chang, Hao-Kuen Lin, Yu-Che Lee, Cho-Han Chiang, Wenli Gao","doi":"10.1159/000547415","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Azacitidine plus venetoclax (HMA&Ven) is a well-established treatment for acute myeloid leukemia (AML) in older or medically unfit patients, given its favorable efficacy and safety profile. Recently, there has been growing interest in extending its use to younger, fitter patients who are traditionally treated with intensive chemotherapy (IC). However, prior studies comparing HMA&Ven to IC have been limited by small sample sizes and inconclusive results.</p><p><strong>Methods: </strong>We conducted a propensity score-matched cohort study using the TriNetX database to compare mortality and safety outcomes between HMA&Ven and IC in this population. We included patients aged 60-75 years with a diagnosis of AML who received either HMA&Ven or IC as induction therapy. Patients who underwent bone marrow transplantation or chimeric antigen receptor T-cell therapy following induction were excluded. We matched patients on predetermined variables, such as age, sex, race, comorbidities, medication, socioeconomic status, and healthcare utilization.</p><p><strong>Results: </strong>The final analysis included 370 patients in each treatment group. At the 1-year follow-up, HMA&Ven demonstrated comparable all-cause mortality to IC (HR: 1.16 [95% CI: 0.93-1.44], p value = 0.186). However, HMA&Ven was associated with significantly lower rates of neutropenia (HR: 0.72 [95% CI: 0.60-0.87], p value <0.001) and sepsis (HR: 0.72 [95% CI: 0.56-0.92], p value = 0.009).</p><p><strong>Conclusion: </strong>Among AML patients aged 60-75, HMA&Ven showed similar 1-year all-cause mortality compared to IC, while offering a significantly better safety profile with reduced risks of neutropenia and sepsis.</p>","PeriodicalId":19497,"journal":{"name":"Oncology","volume":" ","pages":"1-6"},"PeriodicalIF":1.8000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative Safety and Effectiveness of Azacitidine plus Venetoclax versus Intensive Chemotherapy in Acute Myeloid Leukemia: A Propensity Score-Matched Analysis.\",\"authors\":\"Yu-Cheng Chang, Hao-Kuen Lin, Yu-Che Lee, Cho-Han Chiang, Wenli Gao\",\"doi\":\"10.1159/000547415\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Azacitidine plus venetoclax (HMA&Ven) is a well-established treatment for acute myeloid leukemia (AML) in older or medically unfit patients, given its favorable efficacy and safety profile. Recently, there has been growing interest in extending its use to younger, fitter patients who are traditionally treated with intensive chemotherapy (IC). However, prior studies comparing HMA&Ven to IC have been limited by small sample sizes and inconclusive results.</p><p><strong>Methods: </strong>We conducted a propensity score-matched cohort study using the TriNetX database to compare mortality and safety outcomes between HMA&Ven and IC in this population. We included patients aged 60-75 years with a diagnosis of AML who received either HMA&Ven or IC as induction therapy. Patients who underwent bone marrow transplantation or chimeric antigen receptor T-cell therapy following induction were excluded. We matched patients on predetermined variables, such as age, sex, race, comorbidities, medication, socioeconomic status, and healthcare utilization.</p><p><strong>Results: </strong>The final analysis included 370 patients in each treatment group. At the 1-year follow-up, HMA&Ven demonstrated comparable all-cause mortality to IC (HR: 1.16 [95% CI: 0.93-1.44], p value = 0.186). However, HMA&Ven was associated with significantly lower rates of neutropenia (HR: 0.72 [95% CI: 0.60-0.87], p value <0.001) and sepsis (HR: 0.72 [95% CI: 0.56-0.92], p value = 0.009).</p><p><strong>Conclusion: </strong>Among AML patients aged 60-75, HMA&Ven showed similar 1-year all-cause mortality compared to IC, while offering a significantly better safety profile with reduced risks of neutropenia and sepsis.</p>\",\"PeriodicalId\":19497,\"journal\":{\"name\":\"Oncology\",\"volume\":\" \",\"pages\":\"1-6\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1159/000547415\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1159/000547415","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
Comparative Safety and Effectiveness of Azacitidine plus Venetoclax versus Intensive Chemotherapy in Acute Myeloid Leukemia: A Propensity Score-Matched Analysis.
Introduction: Azacitidine plus venetoclax (HMA&Ven) is a well-established treatment for acute myeloid leukemia (AML) in older or medically unfit patients, given its favorable efficacy and safety profile. Recently, there has been growing interest in extending its use to younger, fitter patients who are traditionally treated with intensive chemotherapy (IC). However, prior studies comparing HMA&Ven to IC have been limited by small sample sizes and inconclusive results.
Methods: We conducted a propensity score-matched cohort study using the TriNetX database to compare mortality and safety outcomes between HMA&Ven and IC in this population. We included patients aged 60-75 years with a diagnosis of AML who received either HMA&Ven or IC as induction therapy. Patients who underwent bone marrow transplantation or chimeric antigen receptor T-cell therapy following induction were excluded. We matched patients on predetermined variables, such as age, sex, race, comorbidities, medication, socioeconomic status, and healthcare utilization.
Results: The final analysis included 370 patients in each treatment group. At the 1-year follow-up, HMA&Ven demonstrated comparable all-cause mortality to IC (HR: 1.16 [95% CI: 0.93-1.44], p value = 0.186). However, HMA&Ven was associated with significantly lower rates of neutropenia (HR: 0.72 [95% CI: 0.60-0.87], p value <0.001) and sepsis (HR: 0.72 [95% CI: 0.56-0.92], p value = 0.009).
Conclusion: Among AML patients aged 60-75, HMA&Ven showed similar 1-year all-cause mortality compared to IC, while offering a significantly better safety profile with reduced risks of neutropenia and sepsis.
期刊介绍:
Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.