Faculty, Staff and Student Publications

Publication Date

12-20-2024

Journal

Journal of Clinical Oncology

DOI

10.1200/JCO.24.00272

PMID

39028925

PMCID

PMC12360455

PubMedCentral® Posted Date

8-19-2025

PubMedCentral® Full Text Version

Author MSS

Abstract

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.In this analysis, we update our experience with the chemotherapy-free regimen of blinatumomab and ponatinib in 60 patients with newly diagnosed Philadelphia chromosome (Ph)-positive ALL. At a median follow-up of 24 months, the complete molecular response rate by reverse transcriptase-polymerase chain reaction was 83% (67% at the end of course one), and the rate of measurable residual disease negativity by next-generation clono-sequencing was 98% (45% at the end of course one). Only two patients underwent hematopoietic stem cell transplantation (HSCT). Seven patients relapsed: two with systemic disease, four with isolated CNS relapse, and one with extramedullary Ph-negative, CRLF2-positive pre-B ALL. The estimated 3-year overall survival rate was 91% and event-free survival rate was 77%. Three patients discontinued blinatumomab because of adverse events (related, n = 1; unrelated, n = 2) and nine discontinued ponatinib because of cerebrovascular ischemia, coronary artery stenosis, persistent rash, elevated liver function tests with drug-induced fatty liver, atrial thrombus, severe arterial occlusive disease of lower extremities, pleuro-pericardial effusion, and debilitation. In conclusion, the simultaneous combination of ponatinib and blinatumomab is a highly effective and relatively safe nonchemotherapy regimen. This regimen also reduces the need for intensive chemotherapy and HSCT in first remission in the majority of patients.

Keywords

Humans, Pyridazines, Imidazoles, Middle Aged, Male, Antibodies, Bispecific, Female, Adult, Antineoplastic Combined Chemotherapy Protocols, Aged, Philadelphia Chromosome, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Young Adult, Hematopoietic Stem Cell Transplantation, Adolescent

Comments

Trial registration: ClinicalTrials.gov NCT03263572.

Published Open-Access

yes

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