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[用博纳吐单抗成功治疗难治性B淋巴细胞白血病合并恶性胸腔积液]

[Successful treatment with blinatumomab for refractory B lymphoblastic leukemia complicated with malignant pleural effusion].

作者信息

Kubota Saya, Fujiwara Yuki, Tobita Haruna, Inomata Tomoko, Asano Takeru, Kubonishi Shiro, Hiramatsu Yasushi

机构信息

Department of Hematology and Oncology, Japanese Red Cross Society Himeji Hospital.

出版信息

Rinsho Ketsueki. 2021;62(9):1393-1399. doi: 10.11406/rinketsu.62.1393.

Abstract

A 77-year-old man diagnosed with mixed-phenotype acute leukemia (MPAL (B/Myeloid), NOS) achieved complete remission (CR) after eight courses of hyper-CVAD/MA therapy. However, 6 months later, blasts were observed on peripheral blood smear, and bone marrow aspiration revealed that the disease had relapsed as B lymphoblastic leukemia (ALL). At this time, he had left pleural effusion. He received two courses of inotuzumab ozogamicin (InO) and achieved second hematological CR, but the left pleural effusion worsened over time, suggesting poor disease control. After changing the regimen to blinatumomab, aspiration biopsy cytology showed that the blasts in the pleural fluid disappeared and respiratory distress improved after one course of treatment. Flow cytometry results showed increased populations of CD3-positive T-cells, suggesting that blinatumomab may have migrated into the pleural fluid and exerted an antitumor effect. Although new ALL-specific antibody drugs, such as InO and blinatumomab, are expected to improve prognosis, only few reports have described their tissue migration. The difference between InO and blinatumomab in terms of efficacy of treating malignant pleural effusion remains unclear and should be explored in additional cases.

摘要

一名77岁男性被诊断为混合表型急性白血病(MPAL(B/髓系),未特指),在接受8个疗程的hyper-CVAD/MA治疗后达到完全缓解(CR)。然而,6个月后,外周血涂片观察到原始细胞,骨髓穿刺显示疾病复发为B淋巴细胞白血病(ALL)。此时,他出现了左侧胸腔积液。他接受了2个疗程的奥英妥珠单抗(InO)治疗并实现了第二次血液学CR,但随着时间的推移,左侧胸腔积液恶化,提示疾病控制不佳。在将治疗方案改为博纳吐单抗后,穿刺活检细胞学显示胸腔积液中的原始细胞消失,且经过1个疗程的治疗后呼吸窘迫症状有所改善。流式细胞术结果显示CD3阳性T细胞群体增加,提示博纳吐单抗可能已迁移至胸腔积液中并发挥了抗肿瘤作用。尽管新型ALL特异性抗体药物,如InO和博纳吐单抗,有望改善预后,但仅有少数报告描述了它们在组织中的迁移情况。InO和博纳吐单抗在治疗恶性胸腔积液疗效方面的差异仍不明确,应通过更多病例进行探索。

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