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Phase II Study of Venetoclax Added to Cladribine Plus Low-Dose Cytarabine Alternating With 5-Azacitidine in Older Patients With Newly Diagnosed Acute Myeloid Leukemia

医学 威尼斯人 阿扎胞苷 克拉屈滨 内科学 阿糖胞苷 中性粒细胞减少症 养生 不利影响 髓系白血病 胃肠病学 白血病 肿瘤科 化疗 慢性淋巴细胞白血病 生物化学 基因表达 化学 DNA甲基化 基因
作者
Tapan M. Kadia,Patrick K. Reville,Xuemei Wang,Caitlin R. Rausch,Gautam Borthakur,Naveen Pemmaraju,Naval Daver,Courtney D. DiNardo,Koji Sasaki,Ghayas C. Issa,Maro Ohanian,Guillermo Montalban‐Bravo,Nitin Jain,Alessandra Ferrajoli,Kapil N. Bhalla,Koichi Takahashi,Rashmi Malla,Kelly Quagliato,Rashmi Kanagal‐Shamanna,Uday Popat,Michael Andreeff,Guillermo Garcia‐Manero,Marina Konopleva,Farhad Ravandi,Hagop M. Kantarjian
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:40 (33): 3848-3857 被引量:43
标识
DOI:10.1200/jco.21.02823
摘要

PURPOSE The combination of venetoclax and 5-azacitidine (5-AZA) for older or unfit patients with acute myeloid leukemia (AML) improves remission rates and survival compared with 5-AZA alone. We hypothesized that the addition of venetoclax to cladribine (CLAD)/low-dose araC (low-dose cytarabine [LDAC]) alternating with 5-AZA backbone may further improve outcomes for older patients with newly diagnosed AML. METHODS This is a phase II study investigating the combination of venetoclax and CLAD/LDAC alternating with venetoclax and 5-AZA in older (≥ 60 years) or unfit patients with newly diagnosed AML. The primary objective was composite complete response (CR) rate (CR plus CR with incomplete blood count recovery); secondary end points were overall survival, disease-free survival (DFS), overall response rate, and toxicity. RESULTS A total of 60 patients were treated; median age was 68 years (range, 57-84 years). By European LeukemiaNet, 23%, 33%, and 43% were favorable, intermediate, and adverse risk, respectively. Fifty-six of 60 evaluable patients responded (composite CR: 93%) and 84% were negative for measurable residual disease. There was one death (2%) within 4 weeks. With a median follow-up of 22.1 months, the median overall survival and DFS have not yet been reached. The most frequent grade 3/4 nonhematologic adverse events were febrile neutropenia (n = 33) and pneumonia (n = 14). One patient developed grade 4 tumor lysis syndrome. CONCLUSION Venetoclax and CLAD/LDAC alternating with venetoclax and 5-AZA is an effective regimen among older or unfit patients with newly diagnosed AML. The rates of overall survival and DFS are encouraging. Further study of this non–anthracycline-containing backbone in younger patients, unfit for intensive chemotherapy, as well as comparisons to standard frontline therapies is warranted.
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