Dreger P, von Neuhoff N, Kuse R, Sonnen R, Glass B, Uharek L, Bartels H, Löffler H, Schmitz N
Second Department of Medicine, University of Kiel, Germany.
Ann Oncol. 1997 Apr;8(4):401-3. doi: 10.1023/a:1008251301319.
Mantle cell lymphoma (MC) is not curable with conventional chemotherapy. To improve the prognosis of patients with this disease, we prospectively studied an intensive sequential therapy consisting of the Dexa-BEAM regimen (dexamethasone, BCNU, etoposide, ara-C, melphalan) followed by myeloablative therapy with autologous stem cell reinfusion.
Nine consecutive patients with stage III/IV MC were included. Two had untreated disease, four were in first remission, whereas three had more advanced disease. All patients underwent one to two cycles of Dexa-BEAM chemotherapy to reduce the tumor load and to mobilize peripheral blood progenitor cells (PBPC). Subsequently, patients were treated with high-dose radiochemotherapy followed by PBPC reinfusion and were prospectively analyzed for residual disease by clinical methods as well as by PCR amplification clonal CDRIII rearrangements.
With an overall response rate of 100%, the initial Dexa-BEAM cycles effectively reduced the tumor load. All patients proceeded to high-dose therapy and subsequent stem cell rescue. Engraftment was prompt, and procedure-related deaths did not occur. With a median follow-up of 12 (3-33) months post transplant, all patients are alive in continuing clinical and molecular remission.
Sequential intensive therapy consisting of Dexa-BEAM and high-dose radiochemotherapy appears to be a highly effective treatment for patients with MC. However, the data are still preliminary, and larger patient numbers and a longer follow-up are required.
套细胞淋巴瘤(MC)无法通过传统化疗治愈。为改善该疾病患者的预后,我们前瞻性地研究了一种强化序贯疗法,该疗法由地塞米松-卡莫司汀、依托泊苷、阿糖胞苷、美法仑(Dexa-BEAM)方案(地塞米松、卡莫司汀、依托泊苷、阿糖胞苷、美法仑)组成,随后进行自体干细胞回输的清髓性治疗。
纳入9例连续的III/IV期MC患者。2例为初治患者,4例处于首次缓解期,而3例病情更为进展。所有患者接受1至2个周期的Dexa-BEAM化疗以降低肿瘤负荷并动员外周血祖细胞(PBPC)。随后,患者接受高剂量放化疗,接着进行PBPC回输,并通过临床方法以及PCR扩增克隆性CDRIII重排对残留疾病进行前瞻性分析。
初始的Dexa-BEAM周期总体缓解率为100%,有效降低了肿瘤负荷。所有患者均接受了高剂量治疗及随后的干细胞救援。造血重建迅速,且未发生与治疗相关的死亡。移植后中位随访时间为12(3 - 33)个月,所有患者均存活,处于持续的临床和分子缓解状态。
由Dexa-BEAM和高剂量放化疗组成的序贯强化疗法似乎是治疗MC患者的一种高效疗法。然而,数据仍属初步,需要更大规模的患者群体和更长时间的随访。