-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

1511 Phase Ib/II Study of CPX-351 in Combination with Venetoclax in Patients with Newly Diagnosed, High Risk Acute Myeloid Leukemia

Program: Oral and Poster Abstracts
Session: 617. Acute Myeloid Leukemias: Commercially Available Therapies: Poster I
Hematology Disease Topics & Pathways:
Clinical trials, Research, Combination therapy, Clinical Research, Treatment Considerations
Saturday, December 7, 2024, 5:30 PM-7:30 PM

Emmanuel Almanza, MD1*, Wei-Ying Jen, MD, FRCPath, MA1*, Courtney D. DiNardo, MD, MSc2, Kelly S. Chien, MD3, Danielle Hammond, MD1, Yesid Alvarado Valero, MD1, Naveen Pemmaraju, MD4, Lucia Masarova, MD1, Sherry Pierce, BSN, BA1*, Naval Daver, MD5, Alex Bataller, MD, PhD1*, Guillermo Garcia-Manero, MD1, Amin M. Alousi, MD6*, Nicholas J. Short, MD1, Farhad Ravandi, MBBS7, Hagop M. Kantarjian, MD1 and Tapan M. Kadia, MD1

1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
2Department of Leukemia, UT MD Anderson Cancer Center, Houston, TX
3Department of Leukemia, MD Anderson, Houston, TX
4Department of Leukemia, The University of Texas MD Anderson Cancer Center, Bellaire, TX
5MD Anderson Cancer Center, Houston, TX
6Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX
7Department of Leukemia, University of Texas- MD Anderson Cancer Center, Houston, TX

Background

CPX-351 is a nanoscale liposome of a fixed 5:1 molar ratio of cytarabine and daunorubicin which has improved survival in pts with secondary acute myeloid leukemia (AML). Venetoclax (ven) is a BCL2 inhibitor which, in combination with azacitidine or cytarabine, has become the standard of care for older pts with AML. Ven has demonstrated synergy with intensive chemotherapy, with high complete remission rates in newly diagnosed (ND) and relapsed/refractory (RR) AML. In this study, we aim to assess the efficacy and safety of CPX-351 plus ven (CPX-ven) in ND AML.

Methods

This is a phase Ib/II study to assess the combination of CPX-351 and Venetoclax in newly diagnosed AML patients. Pts aged 18 – 69 with ND AML with adequate liver, renal, and cardiac function, and ECOG performance status ≤2 were enrolled. Patients who had received hypomethylating agents (HMAs) for a prior MDS or CMML (treated secondary AML , tsAML) were eligible. A phase Ib safety lead-in and dose finding cohort determined the recommended phase 2 dose: CPX-351 (daunorubicin 44 mg/m2 and cytarabine 100 mg/m2 IV on D1, 3 and 5 of induction, and daunorubicin 22 mg/m2 IV on D1 and 3 during consolidation). Ven was given on D2-8 of each cycle at a dose of 300mg daily and modified appropriately for concomitant CYP3A inhibitors. The primary outcome measure was complete remission (CR) or CR with incomplete count recovery (CRi). Overall survival (OS), Relapse-free survival (RFS) and Event-free survival (EFS) were analyzed by using Kaplan-Meier method.

Results

Eighteen patients have been treated. 11 (61%) are male. Median age was 59 yrs (range, 43-69). 12 pts (67%) had prior myeloid malignancies (3 (17%) CMML and 9 (50%) MDS). 5 (28%) pts had a previous non-myeloid malignancy. Adverse risk karyotype was present in 13 (72%) pts. Specifically, karyotype was Diploid in 4 (22%) pts, -7/7q- in 4 (22%) pts, and complex in 8 (46%) pts. Mutations in TP53 were present in 5 (28%) pts, ASXL1 in 4 (22%), NRAS in 4 (22%), and IDH2 in 2 (11%) pts. Among the patients with prior myeloid malignancies, 9 (75%) had received treatment with HMAs prior to their diagnosis of AML (ts-AML). Median number of cycles received were 2 (1-5). Overall response rate (ORR) was 78% (14/18) including 5 CR (28%), 8 CRi (44%), and 1 MLFS (6%). Of the responding patients, 5 (38%) achieved undetectable measurable residual disease (MRD) by flow cytometry. Among the responding pts, 12 (67%) underwent stem cell transplantation (SCT). With a median follow up of 11.5 months, the OS, RFS, and EFS were 12.9, 26.5, and 8.7 months, respectively. The most common serious adverse events reported were: neutropenic fever in 3 (17%) pts, and hemorrhage in 1 (6%) pt. The 4- and 8-week mortality rates were 0% and 11%, respectively. Of the 9 pts who had ts-AML, 5 (55%) proceeded to SCT, 2 pts died during treatment, and 1 pt did not respond.

Conclusions:

The combination of CPX-351 and 7 days of Venetoclax is a tolerable and effective regimen for patients with newly diagnosed high-risk AML, including those with tsAML. The regimen produced a high ORR and allowed most patients to proceed to SCT. Further prospective controlled trials to evaluate this combination are warranted.

Disclosures: DiNardo: Amgen: Consultancy; AstraZeneca: Honoraria; Riegel: Honoraria; Gilead: Consultancy; ImmuneOnc: Research Funding; Notable Labs: Honoraria; Astex: Research Funding; Cleave: Research Funding; Immunogen: Honoraria; Foghorn: Research Funding; GSK: Consultancy, Honoraria; Rigel: Research Funding; Loxo: Research Funding; BMS: Consultancy, Honoraria, Research Funding; Abbvie: Consultancy, Honoraria, Research Funding; GenMab: Consultancy, Honoraria, Other: data safety board; Genetech: Honoraria; Servier: Consultancy, Honoraria, Other: meetingsupport, Research Funding; Schrodinger: Consultancy, Honoraria; Astellas: Consultancy, Honoraria; Jazz: Consultancy, Honoraria; Stemline: Consultancy. Chien: AbbVie: Consultancy; Rigel Pharmaceuticals: Consultancy. Pemmaraju: Triptych Health Partners: Consultancy; Affymetrix/Thermo Fisher Scientific: Research Funding; Roche Molecular Diagnostics: Honoraria; Stemline Therapeutics: Honoraria, Other: Travel Expenses, Research Funding; Mustang Bio: Honoraria, Other: Travel Expenses, Research Funding; LFB Biotechnologies: Honoraria; Incyte: Honoraria; Celgene: Honoraria, Other: Travel Expenses; Bristol-Myers Squibb: Consultancy; Novartis: Honoraria, Research Funding; Aptitude Health: Honoraria; Neopharm: Honoraria; Protagonist Therapeutics: Consultancy; CareDx: Honoraria; Pacylex: Consultancy; DAVA Oncology: Honoraria, Other: Travel Expenses; Plexxikon: Research Funding; Daiichi Sankyo: Research Funding; Cellectis: Research Funding; ClearView Healthcare Partners: Consultancy; Springer Science + Business Media: Honoraria; Blueprint Medicines: Consultancy, Honoraria; Immunogen: Consultancy; ASH Committee on Communications ASCO Cancer.NET Editorial Board: Other: Leadership; Samus Therapeutics: Research Funding; Blueprint Medicines OncLive PeerView Institute for Medical Education: Consultancy, Other: advisory board; CTI BioPharma: Consultancy; Astellas: Consultancy; AbbVie: Honoraria, Other: Travel Expenses, Research Funding; Karger Publishers: Other: Licenses; National Institute of Health/National Cancer Institute (NIH/NCI): Research Funding; HemOnc Times/Oncology Times: Other: uncompensated. Masarova: MorphoSys: Other: Advisory Board Participant; PharmaEssentia: Other: Advisory Board Participant; GSK: Consultancy, Other: Travel support; Cogent: Other: Advisory Board Participant. Daver: KITE: Research Funding; Novartis: Consultancy; Agios: Consultancy; Trillium: Consultancy, Research Funding; Syndax: Consultancy; Pfizer: Consultancy, Research Funding; Gilead: Consultancy, Research Funding; Bristol Myers Squibb: Consultancy, Research Funding; Arog: Consultancy; Genentech: Consultancy, Research Funding; Trovagene: Research Funding; Hanmi: Research Funding; Shattuck Labs: Consultancy; Astellas: Consultancy, Research Funding; Celgene: Consultancy; Jazz: Consultancy; Servier: Consultancy, Research Funding; FATE Therapeutics: Other: Consulting Fees, Research Funding; Daiichi-Sankyo: Consultancy, Research Funding; Novimmune: Research Funding; Menarini Group: Consultancy; Glycomimetics: Research Funding. Garcia-Manero: Janssen: Research Funding; Genentech: Research Funding; Forty Seven: Research Funding; H3 Biomedicine: Research Funding; Curis: Research Funding; Onconova: Research Funding; Merck: Research Funding; Astex: Research Funding; Novartis: Research Funding; AbbVie: Research Funding; Helsinn: Research Funding; Bristol Myers Squibb: Other: Personal fees, Research Funding; Aprea: Research Funding; Genentech: Other: Personal fees; Astex: Other: Personal fees; Helsinn: Other: Personal fees; Amphivena: Research Funding. Short: NextCure: Research Funding; Sanofi: Honoraria; Takeda Oncology: Honoraria, Research Funding; Stemline Therapeutics: Research Funding; Amgen: Honoraria; Astellas Pharma, Inc.: Honoraria, Research Funding; Xencor: Research Funding; Novartis: Honoraria; GSK: Consultancy, Research Funding; Adaptive Biotechnologies: Honoraria; Pfizer Inc.: Honoraria; Autolus: Honoraria; BeiGene: Honoraria. Ravandi: Syros: Consultancy, Honoraria, Research Funding; Xencor: Research Funding; Astellas: Consultancy, Honoraria; Amgen: Research Funding; Abbvie: Consultancy, Honoraria; BMS: Consultancy, Honoraria; Prelude: Consultancy, Honoraria, Research Funding; Astyex/Taiho: Research Funding; Syndax: Honoraria. Kantarjian: AbbVie, Amgen, Ascentage, Ipsen Biopharmaceuticals, KAHR Medical, Novartis, Pfizer, Shenzhen Target Rx, Stemline,Takeda: Consultancy, Honoraria. Kadia: Cellenkos: Research Funding; Novartis: Honoraria; Abbvie: Consultancy, Research Funding; Regeneron: Research Funding; BMS: Consultancy, Research Funding; Amgen: Research Funding; Genentech: Consultancy, Research Funding; Pfizer: Research Funding; Incyte: Research Funding; Ascentage: Research Funding; JAZZ: Research Funding; Rigel: Honoraria; Servier: Consultancy; AstraZeneca: Research Funding; ASTEX: Research Funding; DrenBio: Consultancy, Research Funding; Sellas: Consultancy, Research Funding.

OffLabel Disclosure: CPX-351 will be used in combination with venetoclax, which is an off-label use of both drugs.

*signifies non-member of ASH