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734 A Phase II Trial of Venetoclax in Combination with Cladribine, Idarubicin, and Cytarabine in Newly Diagnosed Acute Myeloid Leukemia and High-Risk Myelodysplastic Syndrome

Program: Oral and Poster Abstracts
Type: Oral
Session: 616. Acute Myeloid Leukemias: Investigational Drug and Cellular Therapies: New Treatment Approaches for AML
Hematology Disease Topics & Pathways:
Research, Clinical trials, Acute Myeloid Malignancies, AML, Adult, Clinical Research, Diseases, Myeloid Malignancies, Study Population, Human, Measurable Residual Disease
Monday, December 9, 2024: 10:45 AM

Ian M. Bouligny, MD1, Hagop M. Kantarjian, MD1, Musa Yilmaz, MD1*, Naval Daver, MD2, Gautam Borthakur, MD3, Courtney D. DiNardo, MD, MSc1, Guillermo Montalban-Bravo, MD1, Nicholas J. Short, MD1, Yesid Alvarado Valero, MD1, Elias Jabbour, MD1, Nitin Jain, MD1, Naveen Pemmaraju, MD4, Danielle Hammond, MD1, Kelly S. Chien, MD5, Koichi Takahashi, MD, PhD6, Ghayas C. Issa, MD1, Hussein A. Abbas, MD, PhD1, Guillermo Garcia-Manero, MD1, Farhad Ravandi, MBBS7 and Tapan M. Kadia, MD1

1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
2MD Anderson Cancer Center, Houston, TX
3Section of Molecular Hematology and Therapy, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
4Department of Leukemia, The University of Texas MD Anderson Cancer Center, Bellaire, TX
5Department of Leukemia, MD Anderson, Houston, TX
6Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX
7Department of Leukemia, University of Texas- MD Anderson Cancer Center, Houston, TX

Introduction

The combination of the BCL2 inhibitor venetoclax with intensive chemotherapy with cladribine, idarubicin, and cytarabine (CLIA) has been shown to be safe and effective in younger, fit patients with newly diagnosed acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS). Here, we report on an expanded cohort with mature longer-term follow-up and subgroup analyses of the phase II study of venetoclax combined with CLIA as first-line induction therapy.


Methods

This phase II trial (NCT02115295) enrolled patients aged ≤65 years with newly diagnosed AML, mixed phenotype acute leukemia (MPAL), high-risk MDS (defined as ≥10% blasts or IPSS risk ≥2), or myeloid blast phase CML (BP-CML). Patients received cladribine 5 mg/m2 D1–5, cytarabine 1–1.5 mg/m2 D1–5, idarubicin 8–10 mg/m2 D1–3, and venetoclax 400 mg on days 2–8, with dose adjustments for CYP3A inhibitors. Patients in remission underwent up to 5 additional cycles of dose-attenuated consolidation. Antimicrobial prophylaxis and, after an amendment, G-CSF support were administered to all patients. Eligible patients proceeded to allogeneic stem cell transplant (SCT).


Results

Ninety-five patients have been treated, including 85 (90%) with AML, 3 (3%) with MPAL, and 7 (7%) with MDS. Over one-third of patients were from racial and ethnic minority groups (15% Hispanic, 14% Black, 6% of Middle-Eastern descent, and 2% Asian). The median age at diagnosis was 49 (range, 18–64) years among patients with AML and 46 (36–58) years among those with MDS. Among patients with AML, the ELN 2022 risk was 25% favorable, 34% intermediate, and 41% adverse. AML was classified as therapy-related in 8% and secondary in 4%; 14% had AML-MRC. NPM1 was the most common mutation in the overall cohort at 31%; additional mutations included: 18% FLT3-ITD, 16% NRAS, 13% IDH2, 9% IDH1, 9% KRAS, 8% FLT3-TKD, and 4% TP53.

Patients were given a median of 2 (1–6) cycles of therapy, with a median of 1 (1–4) cycles to remission. The composite complete response (CRc) rate was 93%, including 84% CR and 8% CRi. One (1%) patient with MDS achieved HI and one (1%) with AML achieved PR; the overall response rate was 95% (ORR: CR + CRi + HI + PR). Among AML patients achieving CRc, 82% achieved MRD-negative CR measured by multiparameter flow cytometry. The ORR was 100%, 97%, and 89% for AML patients classified as favorable, intermediate, and adverse risk by ELN 2022, respectively.

With a median follow-up time of 2.5 years, the median overall survival was not reached. In patients with AML, the probability of OS was 85% at 1 year, 73% at 2 years, and 71% at 4 years. The relapse-free survival (RFS) was 78% at 1 year and 75% at 2 years. In patients with MDS, the 1- and 2-year probability of OS was 100%. The RFS for patients with MDS was 86% at 1 year and 86% at 2 years. Sixty-five patients (74%) with AML underwent allogeneic SCT in the first remission. In a landmark analysis, the 1- and 2-year OS was 88% and 82% for those receiving SCT after CLIA-venetoclax vs. 82% and 59% for those who did not (log-rank for overall survival, p = 0.229).

The most common grade ≥3 toxicities in patients with AML were hematologic: all patients had grade ≥3 anemia, leukopenia, neutropenia, and thrombocytopenia. Sixty-five (74%) patients had neutropenic fever in the first cycle, and 72 (82%) had neutropenic fever in any cycle. Additional grade ≥3 toxicities included: 28% bacteremia, 22% pneumonia, 19% ALT elevation, 14% colitis, 7% AST elevation, and 7% bilirubin elevation. The median time to count recovery during induction was 27 (18–52) days. In the overall cohort, the 30- and 60-day mortality was 1% and 2%, respectively.


Conclusion

CLIA-venetoclax is associated with a CRc exceeding 90%, with most patients achieving an MRD-negative response. High complete response rates and low early mortality rates facilitate the majority of patients to allogeneic SCT. Low relapse rates following SCT translate to an estimated overall survival of 71% at 4 years in patients with newly diagnosed AML. CLIA-venetoclax is a highly effective regimen, producing deep and durable remissions in patients with newly diagnosed AML.

Disclosures: Kantarjian: AbbVie, Amgen, Ascentage, Ipsen Biopharmaceuticals, KAHR Medical, Novartis, Pfizer, Shenzhen Target Rx, Stemline,Takeda: Consultancy, Honoraria. Yilmaz: daiichi sankyo: Honoraria, Research Funding. Daver: Hanmi: Research Funding; Menarini Group: Consultancy; Pfizer: Consultancy, Research Funding; Agios: Consultancy; Genentech: Consultancy, Research Funding; Gilead: Consultancy, Research Funding; Syndax: Consultancy; Novartis: Consultancy; KITE: Research Funding; Shattuck Labs: Consultancy; Servier: Consultancy, Research Funding; Jazz: Consultancy; Celgene: Consultancy; Trillium: Consultancy, Research Funding; Astellas: Consultancy, Research Funding; Daiichi-Sankyo: Consultancy, Research Funding; Arog: Consultancy; Bristol Myers Squibb: Consultancy, Research Funding; Glycomimetics: Research Funding; Novimmune: Research Funding; FATE Therapeutics: Other: Consulting Fees, Research Funding; Trovagene: Research Funding. Borthakur: Astex Pharmaceuticals, Ryvu, PTC Therapeutics: Research Funding; Pacylex, Novartis, Cytomx, Bio Ascend: Membership on an entity's Board of Directors or advisory committees; Catamaran Bio, AbbVie, PPD Development, Protagonist Therapeutics, Janssen: Consultancy. DiNardo: Riegel: Honoraria; Genetech: Honoraria; Notable Labs: Honoraria; Servier: Consultancy, Honoraria, Other: meetingsupport, Research Funding; Stemline: Consultancy; Amgen: Consultancy; ImmuneOnc: Research Funding; Foghorn: Research Funding; GSK: Consultancy, Honoraria; Astex: Research Funding; GenMab: Consultancy, Honoraria, Other: data safety board; Astellas: Consultancy, Honoraria; Loxo: Research Funding; Cleave: Research Funding; Gilead: Consultancy; Jazz: Consultancy, Honoraria; Rigel: Research Funding; Schrodinger: Consultancy, Honoraria; Immunogen: Honoraria; BMS: Consultancy, Honoraria, Research Funding; AstraZeneca: Honoraria; Abbvie: Consultancy, Honoraria, Research Funding. Montalban-Bravo: Rigel: Research Funding; Takeda: Research Funding. Short: Xencor: Research Funding; Stemline Therapeutics: Research Funding; Pfizer Inc.: Honoraria; Novartis: Honoraria; Sanofi: Honoraria; Takeda Oncology: Honoraria, Research Funding; GSK: Consultancy, Research Funding; Amgen: Honoraria; Astellas Pharma, Inc.: Honoraria, Research Funding; Autolus: Honoraria; Adaptive Biotechnologies: Honoraria; NextCure: Research Funding; BeiGene: Honoraria. Jabbour: AbbVie, Adaptive Biotechnologies, Amgen, Astellas Pharma, BMS, Genentech, Incyte, Pfizer, Takeda: Consultancy; AbbVie, Adaptive Biotechnologies, Amgen, Ascentage Pharma Group, Pfizer, Takeda: Research Funding. Jain: TransThera Sciences: Research Funding; NovalGen: Research Funding; TG Therapeutics: Consultancy, Honoraria, Other: Travel Support; Loxo Oncology: Research Funding; BeiGene: Consultancy, Honoraria, Other: Travel Support; Precision Biosciences: Consultancy, Honoraria, Other: Travel Support, Research Funding; Pfizer: Research Funding; Takeda: Research Funding; Janssen: Consultancy, Honoraria, Other: Travel Support; Genentech: Consultancy, Honoraria, Other: Travel Support, Research Funding; ADC Therapeutics: Research Funding; Newave: Research Funding; Medisix: Research Funding; Fate Therapeutics: Research Funding; Pharmacyclics: Consultancy, Honoraria, Other: Travel Support, Research Funding; MingSight: Honoraria, Research Funding; CareDx: Consultancy, Honoraria, Other: Travel Support; Cellectis: Consultancy, Honoraria, Other: Travel Support, Research Funding; Aprea Therapeutics: Research Funding; Dialectic Therapeutics: Research Funding; Incyte: Research Funding; Bristol Myers Squibb: Consultancy, Honoraria, Other: Travel Support, Research Funding; Servier: Research Funding; Ipsen: Consultancy, Honoraria, Other: Travel Support; MEI Pharma: Consultancy, Honoraria, Other: Travel Support; Kite, a Gilead Company: Consultancy, Honoraria, Other: Travel Support, Research Funding; AstraZeneca: Consultancy, Honoraria, Other: Travel Support, Research Funding; Adaptive Biotechnologies: Consultancy, Honoraria, Other: Travel Support, Research Funding; AbbVie: Consultancy, Honoraria, Other: Travel Support, Research Funding. Pemmaraju: LFB Biotechnologies: Honoraria; Roche Molecular Diagnostics: Honoraria; Neopharm: Honoraria; Bristol-Myers Squibb: Consultancy; Incyte: Honoraria; Mustang Bio: Honoraria, Other: Travel Expenses, Research Funding; Stemline Therapeutics: Honoraria, Other: Travel Expenses, Research Funding; Celgene: Honoraria, Other: Travel Expenses; Springer Science + Business Media: Honoraria; Protagonist Therapeutics: Consultancy; ClearView Healthcare Partners: Consultancy; Aptitude Health: Honoraria; DAVA Oncology: Honoraria, Other: Travel Expenses; Novartis: Honoraria, Research Funding; Pacylex: Consultancy; CareDx: Honoraria; Blueprint Medicines: Consultancy, Honoraria; Immunogen: Consultancy; CTI BioPharma: Consultancy; Triptych Health Partners: Consultancy; Affymetrix/Thermo Fisher Scientific: Research Funding; Cellectis: Research Funding; Daiichi Sankyo: Research Funding; Plexxikon: Research Funding; Samus Therapeutics: Research Funding; Blueprint Medicines OncLive PeerView Institute for Medical Education: Consultancy, Other: advisory board; Astellas: Consultancy; AbbVie: Honoraria, Other: Travel Expenses, Research Funding; ASH Committee on Communications ASCO Cancer.NET Editorial Board: Other: Leadership; Karger Publishers: Other: Licenses; National Institute of Health/National Cancer Institute (NIH/NCI): Research Funding; HemOnc Times/Oncology Times: Other: uncompensated. Chien: AbbVie: Consultancy; Rigel Pharmaceuticals: Consultancy. Issa: AstraZeneca: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees; AbbVie: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees; Celgene: Research Funding; Syndax Pharmaceuticals, Inc.: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees, Research Funding; Novartis: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees, Research Funding; NuProbe: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees, Research Funding; Astex: Research Funding; Kura Oncology: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees, Research Funding; Sanofi: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: consultancy/ad board fees; Merck: Research Funding. Abbas: Enzyme By Design: Research Funding; Blueprint Medicines Corporation: Research Funding; GlaxoSmithKline: Research Funding; Genentech: Research Funding; Illumina: Honoraria, Other: Inkind Support, Research Funding; Alamar Biosciences: Honoraria; Molecular Partners: Consultancy; Ascentage: Research Funding. Garcia-Manero: Genentech: Research Funding; Astex: Research Funding; Forty Seven: Research Funding; Bristol Myers Squibb: Other: Personal fees, Research Funding; Amphivena: Research Funding; Onconova: Research Funding; AbbVie: Research Funding; Astex: Other: Personal fees; H3 Biomedicine: Research Funding; Merck: Research Funding; Aprea: Research Funding; Helsinn: Other: Personal fees; Helsinn: Research Funding; Novartis: Research Funding; Curis: Research Funding; Janssen: Research Funding; Genentech: Other: Personal fees. Ravandi: BMS: Consultancy, Honoraria; Astellas: Consultancy, Honoraria; Syndax: Honoraria; Amgen: Research Funding; Abbvie: Consultancy, Honoraria; Syros: Consultancy, Honoraria, Research Funding; Xencor: Research Funding; Prelude: Consultancy, Honoraria, Research Funding; Astyex/Taiho: Research Funding. Kadia: ASTEX: Research Funding; Incyte: Research Funding; Servier: Consultancy; Sellas: Consultancy, Research Funding; Rigel: Honoraria; Cellenkos: Research Funding; Novartis: Honoraria; Regeneron: Research Funding; JAZZ: Research Funding; Abbvie: Consultancy, Research Funding; DrenBio: Consultancy, Research Funding; AstraZeneca: Research Funding; Ascentage: Research Funding; Genentech: Consultancy, Research Funding; BMS: Consultancy, Research Funding; Pfizer: Research Funding; Amgen: Research Funding.

*signifies non-member of ASH