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
Haematology Department, Complejo Hospitalario Universitario de Albacete, Calle Hermanos Falcó 37, 02008 Albacete, Spain.
Nephrology Department, Hospital Universitario Reina Sofía, Murcia, Spain.
Ecancermedicalscience. 2021 Mar 22;15:1206. doi: 10.3332/ecancer.2021.1206. eCollection 2021.
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).
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).
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).
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.
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)。
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)。
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%。
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。