Suppr超能文献

血液癌症化疗方案的安全性比较:H-CVAD与GELA/BURKIMAB/PETHEMA LAL的毒性

Comparison in safety of chemotherapy protocols for blood cancers: toxicity of H-CVAD versus GELA/BURKIMAB/PETHEMA LAL.

作者信息

Marín-Sánchez Alberto, Martínez-Fernández Gonzalo, Gómez-Catalán Irene, Montoya-Morcillo Mari Carmen, Algarra Jesús Lorenzo, García Ángela Ibañez, Hernández-Fernández Francisco, Romero-Macías Juan Ramón

机构信息

Haematology Department, Complejo Hospitalario Universitario de Albacete, Calle Hermanos Falcó 37, 02008 Albacete, Spain.

Nephrology Department, Hospital Universitario Reina Sofía, Murcia, Spain.

出版信息

Ecancermedicalscience. 2021 Mar 22;15:1206. doi: 10.3332/ecancer.2021.1206. eCollection 2021.

Abstract

BACKGROUND AND OBJECTIVE

The Hyper-CVAD/Methotrexate-Cytarabine (H-CVAD/MTX-AraC) chemotherapy protocol has been one of the standard treatments for blood cancers, such as Mantle cell lymphoma (MCL), Burkitt's lymphoma (BL) and B-cell and T-cell acute lymphoblastic leukaemia (ALL). Due to high toxicity, it has been progressively replaced with new specific regimens with a better safety profile (GELA protocol for MCL, BURKIMAB for BL and PETHEMA for B-cell and T-cell ALL). The objective of this study is to analyse the toxicity and infectious complications of these therapeutic regimens, as well as the event free survival (EFS).

PATIENTS AND METHODS

This is a retrospective and descriptive observational study of 81 patients, comparing 42 patients treated with H-CVAD/MTX-AraC (group A) versus 39 patients treated with GELA/BURKIMAB/PETHEMA (group B).

RESULTS

All patients in group A developed pancytopenia, but in group B 74.4% neutropenia, 51.3% thrombocytopenia and 69.2% anaemia. The total number of infections in group A was higher than in group B: 154 versus 48, 3.67 versus 1.23 per patient and 0.59 versus 0.25 per cycle. Likewise, febrile neutropenia happened: 106 versus 21 cases, 2.52 versus 0.52 per patient and 0.41 versus 0.11 per cycle. EVS is higher in group B: 33% versus 79% (2-year), and 24% versus 69% (5-year).

CONCLUSIONS

Current therapeutic protocols have shown higher EFS due to better safety profile, with less haematological, neurological and haemorrhagic toxicity, as well as lower rates of infectious complications.

摘要

背景与目的

Hyper-CVAD/甲氨蝶呤-阿糖胞苷(H-CVAD/MTX-AraC)化疗方案一直是血液系统癌症的标准治疗方案之一,如套细胞淋巴瘤(MCL)、伯基特淋巴瘤(BL)以及B细胞和T细胞急性淋巴细胞白血病(ALL)。由于毒性高,它已逐渐被安全性更好的新的特异性方案所取代(MCL采用GELA方案,BL采用BURKIMAB方案,B细胞和T细胞ALL采用PETHEMA方案)。本研究的目的是分析这些治疗方案的毒性和感染并发症,以及无事件生存期(EFS)。

患者与方法

这是一项对81例患者的回顾性描述性观察研究,比较了42例接受H-CVAD/MTX-AraC治疗的患者(A组)与39例接受GELA/BURKIMAB/PETHEMA治疗的患者(B组)。

结果

A组所有患者均出现全血细胞减少,但B组有74.4%的患者出现中性粒细胞减少,51.3%的患者出现血小板减少,69.2%的患者出现贫血。A组的感染总数高于B组:分别为154次和48次,每位患者分别为3.67次和1.23次,每个周期分别为0.59次和0.25次。同样,发热性中性粒细胞减少的发生情况为:分别为106例和21例,每位患者分别为2.52例和0.52例,每个周期分别为0.41例和0.11例。B组的EVS更高:2年时分别为33%和79%,5年时分别为24%和69%。

结论

目前的治疗方案由于安全性更好,显示出更高的EFS,血液学、神经学和出血毒性更低,感染并发症发生率也更低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9275/8057780/ce31b5b19ab5/can-15-1206fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验