Carreras Enric, Rosiñol Laura, Terol Maria José, Alegre Adrián, de Arriba Felipe, García-Laraña José, Bello José Luis, García Raimundo, León Angel, Martínez Rafael, Peñarrubia M Jesús, Poderós Concha, Ribas Paz, Ribera Josep Maria, San Miguel Jesús, Bladé Joan, Lahuerta Juan José
Haematology Department of Hospital Clínic, Barcelona, Spain.
Biol Blood Marrow Transplant. 2007 Dec;13(12):1448-54. doi: 10.1016/j.bbmt.2007.08.002.
Veno-occlusive disease of the liver (VOD) is a potentially severe complication of high-dose cytoreductive therapy (HDT) used for stem cell transplantation (SCT). This complication is uncommon after HDT for autologous SCT (ASCT) in patients with multiple myeloma (MM). The Spanish Myeloma Group/PETHEMA conducted a study (MM2000) for patients with newly diagnosed MM consisting of induction with alternating VBMCP/VBAD chemotherapy followed by intensification with busulfan/melphalan (Bu/MEL) with a second high-dose therapy procedure in patients not achieving at least near-complete remission with the first procedure. After 2 years of the trial, a number of episodes resembling classical VOD but with a late onset were recognized. Consequently, the protocol was modified, and Bu/MEL was replaced by melphalan 200 mg/m(2) (MEL-200). Three years later, after a total of 734 patients had undergone first autologous SCT, the incidence and characteristics of VOD episodes were analyzed in the whole series. Nineteen cases of VOD (8%) were observed among the first 240 patients receiving Bu/MEL, whereas only 2 (0.4%) were observed among the 494 patients treated with MEL-200 (P < .0001). VOD manifestations in the Bu/MEL group appeared at a median of 29 days (range, 3-57 days) after ASCT. Mortality directly attributable to VOD was 2% in the Bu/MEL group and 0.2% in the MEL-200 group (P = .026). This high incidence of severe VOD probably had a multifactorial origin (busulfan followed by melphalan and previous use of BCNU). This observation should be kept in mind when designing future trials for the treatment of MM.
肝静脉闭塞病(VOD)是用于干细胞移植(SCT)的大剂量细胞减灭疗法(HDT)的一种潜在严重并发症。这种并发症在多发性骨髓瘤(MM)患者进行自体SCT(ASCT)的HDT后并不常见。西班牙骨髓瘤研究组/PETHEMA针对新诊断的MM患者开展了一项研究(MM2000),包括采用VBMCP/VBAD交替化疗进行诱导治疗,随后用白消安/美法仑(Bu/MEL)进行强化治疗,对于首次治疗未达到至少接近完全缓解的患者进行第二次大剂量治疗。试验进行2年后,发现了一些类似典型VOD但起病较晚的病例。因此修改了方案,将Bu/MEL替换为美法仑200mg/m²(MEL - 200)。三年后,在总共734例患者接受首次自体SCT后,分析了整个系列中VOD发作的发生率和特征。在接受Bu/MEL治疗的前240例患者中观察到19例VOD(8%),而在接受MEL - 200治疗的494例患者中仅观察到2例(0.4%)(P <.0001)。Bu/MEL组的VOD表现出现在ASCT后的中位时间为29天(范围3 - 57天)。Bu/MEL组中直接归因于VOD的死亡率为2%,MEL - 200组为0.2%(P =.026)。这种严重VOD的高发生率可能有多种因素(白消安后接美法仑以及先前使用过卡莫司汀)。在设计未来MM治疗试验时应牢记这一观察结果。