Magni M, Di Nicola M, Patti C, Scimè R, Mulè A, Rambaldi A, Intermesoli T, Viero P, Tarella C, Gueli A, Bergui L, Trentin L, Barzan A, Benedetti F, Ambrosetti A, Di Raimondo F, Chiarenza A, Parvis G, Billio A, Attolico I, Olivieri A, Montanari M, Carlo-Stella C, Matteucci P, Devizzi L, Guidetti A, Viviani S, Valagussa P, Gianni A M
Division of Medical Oncology, Bone Marrow Transplantation Unit, Fondazione IRCCS, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
Department of Hematology I, Azienda Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.
Bone Marrow Transplant. 2014 Apr;49(4):485-91. doi: 10.1038/bmt.2013.214. Epub 2014 Jan 20.
The importance of early therapy intensification in B-cell CLL (B-CLL) patients remains to be defined. Even though several studies have been published, no randomized trials comparing directly autologous stem cell transplant (ASCT) and the accepted conventional therapy (that is, rituximab, fludarabine and CY; R-FC) have been reported so far. To assess the benefit of a first-line aggressive therapy, we designed a multicenter, randomized, phase 3 trial comparing R-FC and high-dose chemotherapy supported by ASCT in patients under 65 years of age, with stage B(II) or C B-CLL. Primary end point was CR: 96 patients were enrolled (48 in each arm). On an intent-to-treat basis, the CR rates in the ASCT and R-FC arms were 62.5% and 58%, respectively. After 5 years of follow-up, PFS was 60.4% in the ASCT arm and 65.1% in the R-FC arm, time to progression 65.8 and 70.5%, and overall survival 88% vs 88.1%, respectively. Our trial demonstrates, for the first time in a randomized manner, that frontline ASCT does not translate into a survival advantage when compared with benchmark chemoimmunotherapy in B-CLL patients; the possibility of its clinical benefit in certain subgroups remains uncertain.
早期强化治疗在B细胞慢性淋巴细胞白血病(B-CLL)患者中的重要性仍有待确定。尽管已经发表了几项研究,但迄今为止,尚无直接比较自体干细胞移植(ASCT)和公认的传统疗法(即利妥昔单抗、氟达拉滨和环磷酰胺;R-FC)的随机试验报告。为了评估一线积极治疗的益处,我们设计了一项多中心、随机、3期试验,比较R-FC和在65岁以下、B(II)期或C期B-CLL患者中采用ASCT支持的大剂量化疗。主要终点是完全缓解(CR):共纳入96例患者(每组48例)。在意向性治疗基础上,ASCT组和R-FC组的CR率分别为62.5%和58%。经过5年的随访,ASCT组的无进展生存期(PFS)为60.4%,R-FC组为65.