Ketterer N, Salles G, Espinouse D, Dumontet C, Neidhardt-Berard E M, Moullet I, Bouafia F, Berger F, Felman P, Coiffier B
Service d'Hématologie, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, France.
Ann Oncol. 1997 Jul;8(7):701-4. doi: 10.1023/a:1008278605751.
Despite improved detection of mantle cell lymphoma (MCL), results of its treatment with conventional therapies remain disappointing and the survival rate poor. The role of high-dose chemotherapy has recently been investigated but no potential benefit has been clearly established. We report here our experience with MCL patients treated with intensive chemotherapy and autologous stem cell transplantation (ASCT).
Of the 16 MCL patients who received high-dose chemotherapy and ASCT beginning in 1989, six were treated in first-line and 10 in sensitive relapse. Twelve of 16 patients received regimens which included total body irradiation. All patients received peripheral blood stem cells (PBSC) with the exception of one, who underwent bone marrow transplantation.
Three patients died of toxic effects of treatment, Three months after transplant, seven achieved complete response, (CR) and two partial responses (PR), two were stable and two had progressed. With a median follow-up after transplant of 22 months, five of the six surviving patients were without progression, and three were in CR. The median times for event-free survival (EFS) and overall survival (OS) were, respectively, 249 and 317 days. The expected three-year EFS and OS were 24%. The median survival after diagnosis was only 29 months. None of the criteria appeared to be significantly associated with a better outcome, but first-line intensification and a short delay after initial diagnosis may be favorable.
In this study we were not able to confirm the hypothetical benefit of high-dose chemotherapy and PBSC transplantation in mantle cell lymphoma, even though this approach may be promising in a subgroup of patient.
尽管套细胞淋巴瘤(MCL)的检测方法有所改进,但传统疗法的治疗效果仍不尽人意,生存率较低。近期对大剂量化疗的作用进行了研究,但尚未明确其潜在益处。我们在此报告对接受强化化疗和自体干细胞移植(ASCT)的MCL患者的治疗经验。
1989年起,16例接受大剂量化疗和ASCT的MCL患者中,6例为一线治疗,10例为敏感复发后治疗。16例患者中有12例接受了包括全身照射的治疗方案。除1例接受骨髓移植的患者外,所有患者均接受外周血干细胞(PBSC)移植。
3例患者死于治疗毒性。移植后3个月,7例患者达到完全缓解(CR),2例部分缓解(PR),2例病情稳定,2例病情进展。移植后中位随访22个月,6例存活患者中有5例病情无进展,3例处于CR状态。无事件生存期(EFS)和总生存期(OS)的中位时间分别为249天和317天。预期的三年EFS和OS分别为24%。诊断后的中位生存期仅为29个月。没有任何标准似乎与更好的预后显著相关,但一线强化治疗和初次诊断后较短的延迟可能是有利的。
在本研究中,我们未能证实大剂量化疗和PBSC移植对套细胞淋巴瘤的假设益处,尽管这种方法在一部分患者中可能很有前景。