| Literature DB >> 29185155 |
Shin-Ichiro Fujiwara1, Yuya Shirato1, Takashi Ikeda1, Shin-Ichiro Kawaguchi1, Yumiko Toda1, Shoko Ito1, Shin-Ichi Ochi1, Takashi Nagayama1, Kiyomi Mashima1, Kento Umino1, Daisuke Minakata1, Hirofumi Nakano1, Kaoru Morita1, Ryoko Yamasaki1, Yasufumi Kawasaki1, Miyuki Sugimoto1, Masahiro Ashizawa1, Chihiro Yamamoto1, Kaoru Hatano1, Kazuya Sato1, Iekuni Oh1, Ken Ohmine1, Kazuo Muroi1, Yoshinobu Kanda2.
Abstract
Tyrosine kinase inhibitors (TKIs) are standard therapy for chronic myeloid leukemia (CML). However, the effects of these agents on mature B cell lymphoma are not well known. We describe a 50-year-old man who was diagnosed with CML in the chronic phase and treated with imatinib. After 3 years of imatinib therapy that achieved a complete cytogenetic response of CML, he developed Philadelphia-negative follicular lymphoma (FL). Rituximab monotherapy induced a partial response of FL, and he subsequently achieved a major molecular response (MMR) of CML. Three years later, however, the MMR was lost, followed by the progression of FL. Imatinib was switched to nilotinib for the treatment of CML, while we chose watchful waiting for FL. He achieved MMR again under treatment with nilotinib for 8 months including one month of substitutional use of dasatinib due to adverse events, but thereafter nilotinib was switched to bosutinib due to hyperbilirubinemia. With the administration of second-generation TKIs (2G-TKIs) for a total of 18 months, he achieved a complete response to FL without antilymphoma treatment. This is the first report to suggest that 2G-TKIs may have direct or indirect effects on FL.Entities:
Keywords: CML; FL; Second-generation TKI
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Year: 2017 PMID: 29185155 DOI: 10.1007/s12185-017-2378-y
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490