Lefrère F, Delmer A, Suzan F, Levy V, Belanger C, Djabarri M, Arnulf B, Damaj G, Maillard N, Ribrag V, Janvier M, Sebban C, Casasnovas R-O, Bouabdallah R, Dreyfus F, Verkarre V, Delabesse E, Valensi F, McIntyre E, Brousse N, Varet B, Hermine O
Service d'Hématologie Adultes, Hôpital Necker, Paris, France.
Leukemia. 2002 Apr;16(4):587-93. doi: 10.1038/sj.leu.2402406.
Mantle cell lymphoma (MCL) is a distinct clinico-pathological entity with a poor prognosis. We have conducted a prospective study in patients with MCL to evaluate a therapeutic strategy in which CHOP polychemotherapy was followed by DHAP if CHOP failed to induce complete remission. Responding patients then proceeded to an intensification therapy with autologous peripheral blood stem cell transplantation (APBSCT). Twenty-eight consecutive patients with newly diagnosed aggressive MCL were included. After four cycles of CHOP regimen, two complete responses (CR) were obtained (7%) and 14 (50%), five (18%) and seven (25%) patients achieved partial (PR), minor (MR) and no response, respectively (one patient died from septic complications during CHOP induction). The two patients in CR after CHOP underwent intensification with TBI, high-dose cyclophosphamide-etoposide and APBSCT. The other twenty-five patients received DHAP and in this group a response rate of 92% (21 CR (84%), two PR (8%)) was observed. Two patients had progressive disease. The twenty-three responding patients received high-dose therapy (TAM8 regimen: TBI-cytarabine-melphalan) followed by APBSCT. One of the two partial responding patients achieved CR after TAM8. After a median follow-up of 47.6 months (range, 14-70), seven patients have relapsed. Our data confirm that: (1) CHOP regimen induces a low CR rate in MCL; (2) CHOP plus DHAP appears to be much more efficient and allows a large proportion of patients to proceed to high-dose therapy in CR; (3) consolidation therapy including TBI and high-dose Arac-C followed by APBSCT may improve event-free survival.
套细胞淋巴瘤(MCL)是一种独特的临床病理实体,预后较差。我们对MCL患者进行了一项前瞻性研究,以评估一种治疗策略,即CHOP联合化疗失败后采用DHAP治疗。有反应的患者随后进行自体外周血干细胞移植(APBSCT)强化治疗。纳入了28例新诊断的侵袭性MCL连续患者。CHOP方案4个周期后,获得2例完全缓解(CR)(7%),14例(50%)、5例(18%)和7例(25%)患者分别达到部分缓解(PR)、微小缓解(MR)和无反应(1例患者在CHOP诱导期间死于败血症并发症)。CHOP后达到CR的2例患者接受了TBI、高剂量环磷酰胺-依托泊苷和APBSCT强化治疗。其他25例患者接受DHAP治疗,该组观察到的缓解率为92%(21例CR(84%),2例PR(8%))。2例患者疾病进展。23例有反应的患者接受了高剂量治疗(TAM8方案:TBI-阿糖胞苷-美法仑),随后进行APBSCT。2例部分缓解患者中的1例在TAM8后达到CR。中位随访47.6个月(范围14 - 70个月)后,7例患者复发。我们的数据证实:(1)CHOP方案在MCL中诱导的CR率较低;(2)CHOP加DHAP似乎更有效,且能使很大一部分患者在CR时进行高剂量治疗;(3)包括TBI和高剂量阿糖胞苷随后进行APBSCT的巩固治疗可能改善无事件生存期。