Updated results of the chemotherapy-free regimen of blinatumomab and ponatinib in patients with newly diagnosed Philadelphia-positive B-cell acute lymphoblastic leukemia.

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Authors: Lewis Fady Nasr, Hannah E. Goulart, Nicholas James Short, Nitin Jain, Maria Hachem, Tapan M. Kadia, Courtney Denton Dinardo, Naval Guastad Daver, Naveen Pemmaraju, Kelly Sharon Chien, Fadi Haddad, Jayastu Senapati
+8 more Rita Khouri, Farhad Ravandi-Kashani, Guillermo Garcia-Manero, Wuliamatu Deen, Ejiroghene Mayor, Rebecca S. Garris, HM Kantarjian, Elias Jabbour
Cited by: 1

Abstract

6514 Background: Chemotherapy-free regimens incorporating blinatumomab (blina) and ponatinib have demonstrated promising activity in frontline Philadelphia-positive (Ph+) B-cell acute lymphoblastic leukemia (B-ALL). We report the long-term outcomes from an ongoing, phase II study of blina with ponatinib in adults with newly diagnosed (ND) Ph+ B-ALL. Methods: Patients (pts) ≥18 yrs with Ph+ B-ALL received up to 5 simultaneous cycles of blina with ponatinib 30 mg daily, reduced to 15 mg daily upon complete molecular response (CMR). Pts continued ponatinib for at least 5 yrs. IT chemo was increased from 12 to 15 with pt #64 to reduce the risk of central nervous system (CNS) relapse. Protocol was amended to add 2 cycles of high-dose methotrexate (MTX) and cytarabine for pts with WBC >70x10 9 /L. Results: As of January 2025, 88 pts were enrolled (median age of 50 yrs [range, 18-83]; 19%>70 yrs). Median baseline WBC was 15.2 x10 9 /L (0.6-322). 78% of pts had BCR::ABL1 p190 transcripts, 20% had p210. 25 out of 48 pts (52%) with SNP array testing had IKZF1+ genotype. The objective response rate was 96%, with a complete remission (CR) rate of 95%. Measurable residual disease (MRD)-negativity by next-generation sequencing (NGS) was achieved in 95% of evaluable pts; 43% after 1 cycle. CMR rates by RT-PCR was 83%, 67% after 1 cycle. Median follow-up was 3 yrs. 70 pts (79%) remain in molecular remission without allogeneic stem cell transplant (SCT). Of these, 1 received inotuzumab for MRD-positivity and 1 received CAR T-cell therapy. 2 pts (2%) went to SCT in CR1 due to persistent positive p190 transcripts; neither pt had NGS-MRD available. 11 pts (12%) relapsed (10 with p190 transcripts) after a median of 20 months (8-33) from CR: 5 were bone marrow only, 5 CNS only, and 1 extramedullary only; 7/11 relapsed pts (64%) had baseline WBC>70x10 9 /L. Three of the 11 relapsed pts died. There were 2 early deaths, and 3 pts died in CR. Since increasing IT chemo to 15, there has been 1 CNS relapse. 3 pts received 2 cycles of high-dose MTX and cytarabine for WBC>70x10 9 /L; none have relapsed. Median event-free survival (EFS) and overall (OS) have not yet been reached; 3-yr EFS and OS rates are 79% and 89%, respectively. Outcomes did not differ significantly by transcript type nor by NGS MRD clearance after C1. For pts with WBC≥70x10 9 /L vs. WBC

Fields of Study & Subjects

Acute Lymphoblastic Leukemia research Chronic Myeloid Leukemia Treatments CAR-T cell therapy research

Publication details

Journal / source
Journal of Clinical Oncology
Publisher
American Society of Clinical Oncology (ASCO)
Volume
44
Issue
16_suppl
Pages
6514–6514
Publication date
27 May 2026
Language
EN