| Literature DB >> 29845460 |
Kazuyuki Sato1, Hirotaka Sakai2, Yusuke Saiki1, Akiko Uchida1, Yu Uemura1, Satoshi Yokoi1, Yuka Tsuruoka1, Yuji Nishio1, Manabu Matsunawa1, Yoshinori Suzuki1, Yasushi Isobe1, Masayuki Kato1, Naoto Tomita1, Yasuyuki Inoue1, Ikuo Miura1.
Abstract
The introduction of all-trans retinoic acid (ATRA) has made acute promyelocytic leukemia (APL) a curable disease; however, early death prior to the completion of treatment remains a problem. In quantitative evaluation of response to ATRA treatment, lymphocytes must be excluded as they do not originally have t(15;17). We categorized peripheral blood leukocytes by nuclear morphology into polymorphonuclear cells (PMNs) comprising segmented granulocytes, and non-polymorphonuclear cells (NPMs) which includes lymphocytes, monocytes, band cells, and immature myeloid cells. We consecutively evaluated the ratio of t(15;17)-positive cells using fluorescence in situ hybridization in eight newly diagnosed patients with APL. We confirmed the differentiation of APL cells until cytogenetic complete remission; the association of a decrease of t(15;17)-positive NPMs and an increase of t(15;17)-positive PMNs was followed by a decrease of t(15;17)-positive PMNs. The kinetic pattern of t(15;17)-positive NPMs and PMNs was consistent in most patients, irrespective of leukocyte counts at diagnosis, additional chromosomal changes, and ATRA with or without chemotherapies. Kinetic analysis enables us to evaluate treatment response and the recovery of normal hematopoiesis in individuals.Entities:
Keywords: Early death; Fluorescence in situ hybridization; PML–RARA; t(15;17)
Mesh:
Substances:
Year: 2018 PMID: 29845460 DOI: 10.1007/s12185-018-2472-9
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490