학술논문

Results of a randomized phase 3 study of oral sapacitabine in elderly patients with newly diagnosed acute myeloid leukemia (SEAMLESS)
Document Type
article
Source
Cancer. 127(23)
Subject
Biomedical and Clinical Sciences
Oncology and Carcinogenesis
Hematology
Clinical Trials and Supportive Activities
Clinical Research
Rare Diseases
Cancer
Evaluation of treatments and therapeutic interventions
6.1 Pharmaceuticals
Aged
Arabinonucleosides
Azacitidine
Cytosine
Decitabine
Humans
Leukemia
Myeloid
Acute
Treatment Outcome
acute myeloid leukemia
decitabine
hypomethylation
sapacitabine
therapy
Public Health and Health Services
Oncology & Carcinogenesis
Oncology and carcinogenesis
Public health
Language
Abstract
BackgroundAcute myeloid leukemia (AML) is fatal in elderly patients who are unfit for standard induction chemotherapy. The objective of this study was to evaluate the survival benefit of administering sapacitabine, an oral nucleoside analogue, in alternating cycles with decitabine, a low-intensity therapy, to elderly patients with newly diagnosed AML.MethodsThis randomized, open-label, phase 3 study (SEAMLESS) was conducted at 87 sites in 11 countries. Patients aged ≥70 years who were not candidates for or chose not to receive standard induction chemotherapy were randomized 1:1 to arm A (decitabine in alternating cycles with sapacitabine) received 1-hour intravenous infusions of decitabine 20 mg/m2 once daily for 5 consecutive days every 8 weeks (first cycle and subsequent odd cycles) and sapacitabine 300 mg twice daily on 3 consecutive days per week for 2 weeks every 8 weeks (second cycle and subsequent even cycles) or to control arm C who received 1-hour infusions of decitabine 20 mg/m2 once daily for 5 consecutive days every 4 weeks. Prior hypomethylating agent therapy for preexisting myelodysplastic syndromes or myeloproliferative neoplasms was an exclusion criterion. Randomization was stratified by antecedent myelodysplastic syndromes or myeloproliferative neoplasms, white blood cell count (