甲氨蝶呤、氢化可的松、长春新碱、索布佐辛和依托泊苷是阿来珠单抗再治疗后CD52表达缺失的复发T细胞前淋巴细胞白血病的有效选择

IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL
JMA journal Pub Date : 2024-10-15 Epub Date: 2024-09-27 DOI:10.31662/jmaj.2024-0145
Shohei Ikeda, Manabu Suzuki, Masumi Sukegawa, Saburo Tsunoda, Masatsugu Ohta
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引用次数: 0

摘要

T细胞原淋巴细胞白血病(T-PLL)是一种罕见的侵袭性极强的成熟T细胞肿瘤。虽然抗CD52抗体阿仑妥珠单抗的反应率很高,但仅靠这种药物很难治愈该病。因此,建议符合条件的患者进行造血干细胞移植。然而,对于不符合造血干细胞移植条件的患者,几乎没有有效的挽救治疗方案。在本研究中,我们报告了一名复发或难治性T-PLL老年患者接受甲氨蝶呤、氢化可的松、长春新碱、索布佐辛和依托泊苷(MTX-HOPE)挽救治疗的病例。患者是一名 85 岁的老人。他接受了两次阿仑妥珠单抗治疗(初始治疗和复发时)以及环磷酰胺、长春新碱和氢化可的松化疗。此外,还根据之前的病例报告使用了新型治疗药物(venetoclax 和 tofacitinib)。然而,患者对所有治疗都产生了耐药性,肿瘤细胞也失去了CD52表达。我们使用了MTX-HOPE,患者存活了约8个月。虽然由于疾病进展而需要输红血,但治疗过程中未发现任何不良反应,而且患者在临终前仍能维持日常生活。MTX-HOPE是经典化疗药物的复方制剂,最初开发用于难治性淋巴瘤体弱患者的姑息化疗。据报道,MTX-HOPE 对 T 细胞肿瘤有效。严重的非血液学不良反应很少见,但骨髓抑制很常见。约半数患者出现 3-4 级中性粒细胞减少。因此,应对患者进行密切监测,尤其是在开始治疗时。必要时应考虑暂停治疗、调整给药间隔或使用 G-CSF。治疗间隔可以适当调整,因此是治疗难治性T-PLL的重要选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methotrexate, Hydrocortisone, Vincristine, Sobuzoxane, and Etoposide Is an Effective Option for Relapsed T-cell Prolymphocytic Leukemia with Loss of CD52 Expression after Retreatment with Alemtuzumab.

T-cell prolymphocytic leukemia (T-PLL) is a rare and highly aggressive mature T-cell neoplasm. Although the response rate to alemtuzumab, an anti-CD52 antibody, is high, it is difficult to cure the disease with this agent alone. Therefore, hematopoietic stem cell transplantation is recommended for eligible patients. However, there are few effective salvage therapy options for patients ineligible for hematopoietic stem cell transplantation. In this study, we report the case of an elderly patient with relapsed or refractory T-PLL who underwent salvage therapy with methotrexate, hydrocortisone, vincristine, sobuzoxane, and etoposide (MTX-HOPE). The patient was an 85-year-old man. He was administered alemtuzumab twice (at the time of initial treatment and relapse) and cyclophosphamide, vincristine, and hydrocortisone chemotherapy. Furthermore, novel therapeutic drugs (venetoclax and tofacitinib) were administered based on previous case reports. However, the patient was resistant to all treatments, and the tumor cells lost CD52 expression. We administered MTX-HOPE, and the patient survived for approximately 8 months. Although red blood transfusions were necessary because of disease progression, no adverse events were observed because of treatment, and the patient was able to maintain activities of daily living until immediately before death. MTX-HOPE is a combination of classical chemotherapy agents originally developed for palliative chemotherapy in frail patients with refractory lymphoma. MTX-HOPE has been reported to be effective against T-cell tumors. Severe nonhematologic adverse events are rarely reported; however, bone marrow suppression is commonly observed. Grade 3-4 neutropenia has been documented in approximately half of the patients. Therefore, patients should be closely monitored, particularly at the onset of therapy. Consideration should be given to suspending treatment, adjusting the administration interval, or administering G-CSF if necessary. The treatment interval can be appropriately adjusted, making it a valuable treatment option for refractory T-PLL.

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