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Phase 3 randomized trial of chemotherapy with or without oblimersen in older AML patients: CALGB 10201 (Alliance)
- Source :
- Blood Adv
- Publication Year :
- 2021
- Publisher :
- American Society of Hematology, 2021.
-
Abstract
- Overexpression of B-cell leukemia/lymphoma 2 (BCL2) renders acute myeloid leukemia (AML) cells resistant to chemotherapy and has been associated with unfavorable outcomes. Oblimersen (G3139) is a phosphorothioate 18-mer antisense oligonucleotide directed against the first 6 BCL2 codons. In a phase 1 study of AML patients treated with G3139, cytarabine, and daunorubicin induction with cytarabine consolidation, no antisense-related toxicity was reported, and BCL2 downregulation occurred in patients achieving complete remission. In this phase 3 trial, untreated older AML patients were randomized to cytarabine (100 mg/m2 per day on days 4-10) and daunorubicin (60 mg/m2 per day on days 4-6) followed by cytarabine consolidation (2000 mg/m2 per day on days 4-8) with (arm A) or without (arm B) G3139 (7 mg/m2 per day on days 1-10 [induction] or days 1-8 [consolidation]). A total of 506 patients were enrolled. No differences in toxicity were observed between arms. Estimated overall survival (OS) at 1 year was 43% for arm A and 40% for arm B (1-sided log rank P = .13), with no differences in disease-free (DFS; P = .26) or event-free survival (P = .80). Subgroup analyses showed patients age
- Subjects :
- 0301 basic medicine
Oncology
medicine.medical_specialty
Myeloid
Clinical Trials and Observations
Daunorubicin
Chronic lymphocytic leukemia
medicine.medical_treatment
03 medical and health sciences
0302 clinical medicine
hemic and lymphatic diseases
Internal medicine
Antineoplastic Combined Chemotherapy Protocols
medicine
Humans
neoplasms
Aged
Chemotherapy
business.industry
Oblimersen
Cytarabine
Hematology
Thionucleotides
medicine.disease
Chemotherapy regimen
Leukemia, Myeloid, Acute
Leukemia
030104 developmental biology
medicine.anatomical_structure
030220 oncology & carcinogenesis
business
medicine.drug
Subjects
Details
- ISSN :
- 24739537 and 24739529
- Volume :
- 5
- Database :
- OpenAIRE
- Journal :
- Blood Advances
- Accession number :
- edsair.doi.dedup.....3f7671c710703addff6c62614702ad9d
- Full Text :
- https://doi.org/10.1182/bloodadvances.2021004233