| Literature DB >> 29846829 |
Tomonori Nakazato1, Noriyoshi Iriyama2, Michihide Tokuhira3, Maho Ishikawa4, Eriko Sato5, Tomoiku Takaku6, Kei-Ji Sugimoto7, Hiroyuki Fujita8, Isao Fujioka6, Yuta Kimura3, Yoshinobu Aisa9, Eisaku Iwanaga10, Norio Asou4, Masahiro Kizaki3, Yoshihiro Hatta2, Norio Komatsu6, Tatsuya Kawaguchi10.
Abstract
We performed a retrospective study to evaluate the incidence of second malignancies (SMs) in chronic myeloid leukemia (CML) patients treated with tyrosine kinase inhibitors (TKIs). We analyzed data from 339 patients with CML who were extracted from the CML Cooperative Study Group database. The standardized incidence ratio (SIR) was calculated to assess the risk of SMs using data from the Cancer Registries in Japan. The median follow-up was 65 months. SMs developed in 14 patients (4.1%, 10 men, 4 women) after the start of TKIs. The median age was 69 years at the time of the CML diagnosis and 72.5 years at the time of the SM diagnosis. Ten patients were treated with imatinib, three with dasatinib, and one with nilotinib as the initial treatment. The SIR for all malignancies was 1.05 (95% CI 0.50-1.93) for men and 1.08 (95% CI 0.29-2.76) for women. The difference in the overall survival (OS) of patients with or without SMs was not statistically significant (5-year OS: 82.5% vs. 92.9%; p = 0.343). A subgroup analysis of 166 patients treated with second-generation TKIs (92 dasatinib, 74 nilotinib) showed that the SIRs for all malignancies were 1.33 (95% CI 0.36-3.41) for men and 0 for women. In conclusion, the incidence of SMs in CML patients during TKI treatment was the same as that in the general Japanese population. There was no evidence of an increase in the incidence of SMs during second-generation TKI treatment. Furthermore, the occurrence of SMs during TKI treatment did not affect the survival or mortality in our cohort.Entities:
Keywords: Chronic myeloid leukemia; Second malignancies; Standardized incidence ratio; Tyrosine kinase inhibitor
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Year: 2018 PMID: 29846829 DOI: 10.1007/s12032-018-1159-7
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064