首页> 外文期刊>International Journal of Hematology >Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL
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Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL

机译:改良的环磷酰胺,长春新碱,阿霉素和甲氨蝶呤(CODOX-M)/异环磷酰胺,依托泊苷和阿糖胞苷(IVAC)联合治疗或不联合利妥昔单抗治疗的成年伯基特淋巴瘤(BL)和B细胞淋巴瘤患者,无法分类,其特征介于两者之间弥漫性大B细胞淋巴瘤和BL

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摘要

The feasibility and efficacy of cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL (intermediate DLBCL/BL) have never been reported. The effects of adding rituximab to CODOX-M/IVAC have not been published either. Fifteen consecutive patients with a median age of 39 years were treated with modified CODOX-M/IVAC regimen (particularly, reducing the dose of methotrexate to 3 g/m2) with or without rituximab at our institution. Although all patients developed grade 4 neutropenia and grade 3/4 thrombocytopenia/anemia, 93% had febrile neutropenia, 60% showed transaminase elevation, and 40% had mucositis/stomatitis (all grade 3), there were no treatment-related deaths. Two of nine patients treated with rituximab developed biphasic late-onset neutropenia. Thirteen patients (87%) showed complete responses. The remaining two patients had refractory disease; one had presented with peritoneal dissemination and complex chromosomal abnormalities, while the other had double IGH–MYC and IGH–BCL2 translocations. The estimated 5-year overall and progression-free survival were 87% each, with a median follow-up of 74 months. In conclusion, our modified CODOX-M/IVAC regimen is well tolerated and highly effective in Japanese adult patients with BL and intermediate DLBCL/BL, warranting a larger study for confirmation.
机译:环磷酰胺,长春新碱,阿霉素和甲氨蝶呤(CODOX-M)/异环磷酰胺,依托泊苷和阿糖胞苷(IVAC)在日本成年Burkitt淋巴瘤(BL)和B细胞淋巴瘤患者中的可行性和有效性弥漫性大B细胞淋巴瘤和BL(中间DLBCL / BL)尚未见报道。尚未将利妥昔单抗添加至CODOX-M / IVAC的作用。连续15例中位年龄为39岁的患者接受改良的CODOX-M / IVAC方案(特别是将甲氨蝶呤的剂量降至3 g / m 2 ),无论是否接受利妥昔单抗。尽管所有患者均出现4级中性粒细胞减少和3/4级血小板减少症/贫血,但93%的患者出现发热性中性粒细胞减少症,60%的患者出现转氨酶升高,40%的患者出现粘膜炎/口腔炎(均为3级),但没有与治疗相关的死亡。接受利妥昔单抗治疗的9例患者中有2例发展为双相性迟发性中性粒细胞减少。 13名患者(87%)表现出完全缓解。其余两名患者患有难治性疾病。一个人出现了腹膜扩散和复杂的染色体异常,而另一个人出现了IGH-MYC和IGH-BCL2双重易位。估计的5年总体生存期和无进展生存期分别为87%,中位随访期为74个月。总之,我们改良的CODOX-M / IVAC方案在日本成人BL和中级DLBCL / BL患者中具有良好的耐受性和高效性,值得进行更大的研究证实。

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