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博舒替尼作为T315I阳性淋巴母细胞期慢性髓性白血病患者的四线治疗:一例报告

Bosutinib as a fourth-line therapy for a patient with T315I-positive lymphoid blastic phase chronic myeloid leukemia: A case report.

作者信息

Komeno Yukiko, Uchida Naoyuki, Satoh Yumiko, Uryu Hideki, Iwata Yuko, Masuda Akiko, Iihara Kuniko, Yatomi Yutaka, Taniguchi Shuichi, Ryu Tomiko

机构信息

Department of Hematology, Japan Community Healthcare Organization (JCHO) Tokyo Yamate Medical Center, Hyakunin-cho, Shinjuku, Tokyo 169-0073, Japan.

Department of Hematology, Toranomon Hospital, Toranomon, Minato, Tokyo 105-8470, Japan.

出版信息

Oncol Lett. 2017 Jun;13(6):4285-4289. doi: 10.3892/ol.2017.5989. Epub 2017 Apr 5.

DOI:10.3892/ol.2017.5989
PMID:28599428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5452986/
Abstract

A 35-year-old male was diagnosed with chronic myeloid leukemia in the chronic phase and was prescribed 100 mg daily dasatinib. However, dasatinib was discontinued due to thrombocytopenia, and within six months, the disease progressed to the lymphoid blastic phase. Hyper-cyclophosphamide, vincristine, adriamycin and dexamethasone chemotherapy combined with 140 mg dasatinib or 600 mg imatinib was prescribed. The two inhibitors were soon discontinued due to severe thrombocytopenia and jaundice, respectively. Myelosuppression persisted subsequent to the nadir. Bone marrow (BM) aspiration and biopsy revealed hypercellular marrow filled with blasts. Sequencing of the leukemia cells revealed overlapping peaks for the wild-type sequence and the T315I mutant sequence. The patient was treated with 500 mg bosutinib (which was later reduced to 300 mg) for pretransplant cytoreduction. After 5 months, the patient's spleen exhibited a reduction in volume and the percentage of blasts in the BM decreased from 96.1 to 17.5%. The patient successfully underwent cord blood transplantation. The patient has been disease-free for 5 months subsequent to transplantation. This case suggests that bosutinib may be effective for cytoreduction prior to stem cell transplantation, unless the leukemia cells consistently harbor the T315I mutation.

摘要

一名35岁男性被诊断为慢性期慢性髓性白血病,每日服用达沙替尼100毫克。然而,由于血小板减少症停用了达沙替尼,且在六个月内疾病进展至淋巴细胞母细胞期。给予了高剂量环磷酰胺、长春新碱、阿霉素和地塞米松化疗联合140毫克达沙替尼或600毫克伊马替尼治疗。两种抑制剂分别因严重血小板减少症和黄疸很快停用。骨髓抑制在最低点后持续存在。骨髓穿刺和活检显示骨髓细胞增多,充满原始细胞。白血病细胞测序显示野生型序列和T315I突变序列有重叠峰。患者接受500毫克博舒替尼治疗(后来减至300毫克)用于移植前细胞减灭。5个月后,患者脾脏体积缩小,骨髓中原始细胞百分比从96.1%降至17.5%。患者成功接受了脐血移植。移植后患者已无病生存5个月。该病例表明,博舒替尼可能对干细胞移植前的细胞减灭有效,除非白血病细胞持续携带T315I突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/d594490af749/ol-13-06-4285-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/020b85b5e172/ol-13-06-4285-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/83b9c1f7902a/ol-13-06-4285-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/848da8d4e0c8/ol-13-06-4285-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/d594490af749/ol-13-06-4285-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/020b85b5e172/ol-13-06-4285-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/83b9c1f7902a/ol-13-06-4285-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/848da8d4e0c8/ol-13-06-4285-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e8/5452986/d594490af749/ol-13-06-4285-g03.jpg

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