Ponatinib Improved the Prognosis of Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: A Japanese Single-Center Cohort Study.

acute lymphocytic leukemia allogeneic hematopoietic stem cell transplantation cd20 maintenance therapy molecular complete remission philadelphia chromosome ponatinib treatment-free remission tyrosine kinase inhibitor

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Dec 2023
Historique:
accepted: 12 12 2023
medline: 15 1 2024
pubmed: 15 1 2024
entrez: 15 1 2024
Statut: epublish

Résumé

Introduction The overall survival (OS) of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) has improved with the combination of tyrosine kinase inhibitor (TKI) with intensive chemotherapy. In recent years, there has been increased interest in the possibility of long-term survival without allogeneic hematopoietic stem cell transplantation (HSCT) or maintenance therapy. The aim of this study was to determine the effectiveness of treatment and the resultant outcomes in Ph+ALL patients using real-world data. Methods We performed a single-center retrospective analysis utilizing Akita University Hospital data (Akita, Japan) from November 2000 to June 2023 to evaluate the outcomes of TKI with intensive chemotherapy for Ph+ALL. Results Twenty-three patients with Ph+ALL were treated with intensive chemotherapy combined with TKI, including six imatinib, four dasatinib, and 13 ponatinib. The median patient age was 53 years (range; 28-67). Eighteen patients (78%) achieved complete molecular remission (CMR) within three months. HSCT was performed in 16 patients (70%), all of whom did not receive post-transplant TKI maintenance therapy. Six of the seven patients who did not undergo HSCT received maintenance therapy with ponatinib after intensive chemotherapy. The three-year OS was 81%. Ponatinib treatment resulted in a much higher OS rate than imatinib/dasatinib (100% vs. 60%; 

Identifiants

pubmed: 38222242
doi: 10.7759/cureus.50416
pmc: PMC10784717
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e50416

Informations de copyright

Copyright © 2023, Tozawa et al.

Déclaration de conflit d'intérêts

The authors have declared financial relationships, which are detailed in the next section.

Auteurs

Nagi Tozawa (N)

Department of Hematology, Akita University Hospital, Akita, JPN.

Takaya Yamashita (T)

Department of Hematology, Akita University Hospital, Akita, JPN.

Miho Nara (M)

Department of Hematology, Akita University Hospital, Akita, JPN.

Yuki Fujioka (Y)

Department of Hematology, Akita University Hospital, Akita, JPN.

Sho Ikeda (S)

Department of Hematology, Akita University Hospital, Akita, JPN.

Takahiro Kobayashi (T)

Department of Hematology, Akita University Hospital, Akita, JPN.

Isuzu Kobayashi (I)

Department of Hematology, Akita University Hospital, Akita, JPN.

Akihiro Kitadate (A)

Department of Hematology, Akita University Hospital, Akita, JPN.

Yoshihiro Kameoka (Y)

Department of Hematology, Akita University Hospital, Akita, JPN.

Naoto Takahashi (N)

Department of Hematology, Akita University Hospital, Akita, JPN.

Classifications MeSH