Gutierrez Antonio, Rodriguez Jose, Martinez-Serra Jordi, Gines Jordi, Paredes Pilar, Garcia Florencia, Vercher Javier, Balanzat Josep, Del Campo Raquel, Galan Pilar, Morey Miguel, Sampol Antonia, Novo Andres, Bento Leyre, García Lucia, Bargay Joan, Besalduch Joan
Service of Hematology, Son Espases University Hospital, Palma de Mallorca, Spain.
Service of Pharmacy, Son Espases University Hospital, Palma de Mallorca, Spain.
Onco Targets Ther. 2014 Nov 13;7:2093-100. doi: 10.2147/OTT.S70264. eCollection 2014.
Most Hodgkin lymphomas (HL) can be cured with current strategies. However, one-third of the cases do not respond or relapse and need salvage regimens. We report the results of a retrospective study using the gemcitabine and oxaliplatinum (GemOx) regimen.
Patients who relapsed or failed to achieve complete response were eligible and received GemOx salvage therapy. To avoid selection bias and thus to overcome the retrospective nature of the study, all treated patients were included from the pharmacy database.
Between 2003-2013, 24 HL patients - relapsing (number [n]=12) or refractory (n=12) - were included, receiving a total of 26 induction treatments with GemOx. Mean previous regimens were 2.38 (42% relapsing after autologous transplantation). Median follow-up was 37 months, and 71% responded (38% of patients achieved complete response). The factors related to better progression-free survival were: B symptoms; response to GemOx; and consolidation with stem cell transplantation. Grades 1 and 2 neurological toxicity was present in 17% of patients. Hematological toxicity was common, with grades 3 and 4 neutropenia (25%) and thrombocytopenia (34%) observed. Progression-free survival was better in patients consolidated with stem cell transplantation. The peripheral blood stem cell collection after GemOx was successful for all candidates.
大多数霍奇金淋巴瘤(HL)患者可通过当前治疗策略治愈。然而,三分之一的病例无反应或复发,需要挽救性治疗方案。我们报告了一项使用吉西他滨和奥沙利铂(GemOx)方案的回顾性研究结果。
复发或未达到完全缓解的患者符合条件并接受GemOx挽救治疗。为避免选择偏倚,从而克服该研究的回顾性特点,所有接受治疗的患者均从药房数据库中选取。
2003年至2013年期间,纳入了24例HL患者——复发(n = 12)或难治性(n = 12)——共接受了26次GemOx诱导治疗。既往治疗方案的中位数为2.38(42%在自体移植后复发)。中位随访时间为37个月,71%的患者有反应(38%的患者达到完全缓解)。与无进展生存期较好相关的因素为:B症状;对GemOx的反应;以及干细胞移植巩固治疗。17%的患者出现1级和2级神经毒性。血液学毒性常见,观察到3级和4级中性粒细胞减少(25%)和血小板减少(34%)。接受干细胞移植巩固治疗的患者无进展生存期更好。GemOx治疗后外周血干细胞采集对所有候选者均成功。
1)GemOx方案对复发或难治性HL有效,毒性可控。2)未观察到动员失败情况。3)缓解后需要巩固治疗。4)其疗效和良好的毒性特征可能使HL多次复发时可进行多次给药。