Development of a human herpesvirus 8-negative effusion-based lymphoma during treatment with dasatinib for chronic myeloid leukemia.

IF 0.9 Q4 HEMATOLOGY
Takahiro Suyama, Masao Hagihara, Naruaki Matsui, Rie Irie, Yoshiyuki Osamura, Tetsuo Sakai, Shouichi Watanabe, Shintarou Umemoto, Naoki Miyao
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引用次数: 1

Abstract

We present the case of an 85-year-old male patient diagnosed with human herpesvirus 8 (HHV8)-negative effusion-based lymphoma (EBL) that developed from long-lasting pleural effusion (PE) induced by dasatinib treatment for chronic myeloid leukemia (CML). After the onset of this disorder, dasatinib treatment was discontinued and drainage was performed to regress the effusion. The major molecular response (MMR) was thus lost. The patient did not tolerate nilotinib treatment, but bosutinib was successful in restoring MMR. During these clinical courses, the patient suffered from a recurrence of EBL, which was treated with rituximab-based chemotherapy. The PE sample just before the 3rd cycle of chemotherapy revealed the proliferation of CD57-positive T cells, along with the disappearance of lymphoma cells. Anti-tumor immunity may have been activated following the immunochemotherapy in the undisturbed immunological environment when both EBL and CML almost regressed. After four cycles of R-CVP therapy, the patient has been in remission for 16 months and no longer requires drainage.

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达沙替尼治疗慢性髓性白血病期间人类疱疹病毒8阴性积液性淋巴瘤的发展
我们报告一例85岁男性患者,诊断为人类疱疹病毒8 (HHV8)阴性积液性淋巴瘤(EBL),由达沙替尼治疗慢性髓性白血病(CML)引起的长期胸腔积液(PE)发展而来。发病后,停止达沙替尼治疗,引流以减少积液。因此,主要分子反应(MMR)丢失了。患者不能耐受尼罗替尼治疗,但博舒替尼成功地恢复了MMR。在这些临床过程中,患者出现EBL复发,并接受了基于利妥昔单抗的化疗。第3周期化疗前的PE标本显示cd57阳性T细胞增生,淋巴瘤细胞消失。在未受干扰的免疫环境下,当EBL和CML几乎消退时,免疫化疗可能激活了抗肿瘤免疫。经过4个周期的R-CVP治疗,患者病情缓解16个月,不再需要引流。
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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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