Your browser doesn't support javascript.
loading
Clinical outcomes of second-generation tyrosine kinase inhibitors versus imatinib in older patients with CML.
Ono, Takaaki; Takahashi, Naoto; Kizaki, Masahiro; Kawaguchi, Tatsuya; Suzuki, Ritsuro; Yamamoto, Kazuhito; Ohnishi, Kazunori; Naoe, Tomoki; Matsumura, Itaru.
Afiliación
  • Ono T; Department of Transfusion and Cell Therapy, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
  • Takahashi N; Department of Hematology, Nephrology, and Rheumatology, Akita University School of Medicine, Akita, Japan.
  • Kizaki M; Department of Hematology, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.
  • Kawaguchi T; Department of Medical Technology, Kumamoto Health Science University, Kumamoto, Japan.
  • Suzuki R; Department of Hematology and Oncology, Faculty of Medicine, Shimane University, Izumo, Japan.
  • Yamamoto K; Department of Hematology and Cell Therapy, Aichi Cancer Center, Nagoya, Japan.
  • Ohnishi K; Shubun University Faculty of Medical Sciences, Ichinomiya, Japan.
  • Naoe T; National Hospital Organization, Nagoya Medical Center, Nagoya, Japan.
  • Matsumura I; Department of Hematology and Rheumatology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Cancer Sci ; 114(3): 995-1006, 2023 Mar.
Article en En | MEDLINE | ID: mdl-36336963
ABSTRACT
Age and comorbidities are important factors to be considered in the selection of tyrosine kinase inhibitors (TKIs) for first-line treatment in patients with chronic myeloid leukemia in chronic phase (CML-CP). However, it is yet unclear whether TKI selection, particularly, imatinib versus second-generation TKIs (2GTKIs), impacts treatment outcomes in the clinical practice. To address this, we compared the clinical outcomes of prospectively registered 452 patients with CML-CP treated with imatinib and 2GTKIs, taking into consideration their age and/or comorbidities. A total of 136 patients (30.1%) were classified into an older cohort (≥65 years) and 316 (69.9%) into a younger cohort (18-64 years). The TKI selection did not vary based on age (70.6% received 2GTKIs in the younger cohort and 66.2% in the older cohort). The median follow-up period was 5.4 years. Treatment responses including the cumulative incidence of deep molecular response (BCR-ABL1 international scale ≤0.0032%) at any time were similar between the two age cohorts regardless of the type of TKI. The 5-year overall survival (OS) in the older cohort was lower than that in the younger cohort (95.9% vs 83.8%; p < 0.0001), whereas the 5-year OS in patients treated with 2GTKIs was not influenced by age factors and comorbidities. Therefore, our results suggest that the selection of 2GTKIs as first-line treatment is an effective option for both younger and older CML-CP patients with or without comorbidities. This trial was registered at UMIN-CTR as 00003581.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva Límite: Aged / Humans Idioma: En Revista: Cancer Sci Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva Límite: Aged / Humans Idioma: En Revista: Cancer Sci Año: 2023 Tipo del documento: Article País de afiliación: Japón