Rodríguez José, Conde Eulogio, Gutiérrez Antonio, Arranz Reyes, León Angel, Marín Julián, Bendandi Maurizio, Albo Carmen, Caballero María Dolores
Hospital Universitario Son Dureta, Palma, Spain.
Eur J Haematol. 2007 Jul;79(1):32-8. doi: 10.1111/j.1600-0609.2007.00856.x.
Retrospective data shows that peripheral T-cell lymphoma (PTCL) patients sensitive to conventional chemotherapy for aggressive lymphomas may respond better if this treatment is consolidated with frontline autologous stem cell transplantation (ASCT). Here, we present data from a prospective phase II trial of high-dose chemotherapy and ASCT as a frontline consolidation therapy for aggressive nodal PTCL.
This study involved 26 gallium-scan-positive patients with high-risk nodal PTCL [excluding anaplastic lymphoma kinase (ALK) positive]. Patients received three courses of MegaCHOP before they were evaluated, and those that were gallium-scan-negative at this stage then received another course of MegaCHOP and ASCT. Patients who remained gallium-scan-positive received two courses of an IFE regimen (ifosfamide 10 g/m(2), etoposide 150 mg/m(2)/12 h on days 1-3) and if they at least achieved PR, they then received the transplant.
Complete response (CR) was achieved by 12 patients (46%) after three courses of MegaCHOP and 12 patients received IFE as a salvage therapy. After the ASCT (n = 19), 89% of patients achieved CR. In contrast, six patients (23%) did not receive the transplant because of the progression of the disease (n = 5) or lethal toxicity (n = 1). One patient in first-line CR refused ASCT. After a median follow-up of 35 months, the overall survival (OS) and progression-free survival (PFS) at 3 yr was 73% and 53%, respectively. Moreover, the OS, PFS and disease-free survival (DFS) were 84%, 56% and 63%, respectively 2 yr after transplant in patients who received ASCT consolidation (n = 19).
Early salvage therapy for patients with high-risk aggressive nodal PTCL that do not achieve CR after three courses of chemotherapy and ASCT frontline consolidation for chemosensitive patients may improve treatment outcome.
回顾性数据显示,对侵袭性淋巴瘤常规化疗敏感的外周T细胞淋巴瘤(PTCL)患者,若采用一线自体干细胞移植(ASCT)巩固治疗,可能疗效更佳。在此,我们展示一项前瞻性II期试验的数据,该试验采用大剂量化疗和ASCT作为侵袭性淋巴结PTCL的一线巩固治疗。
本研究纳入26例经镓扫描呈阳性的高危淋巴结PTCL患者[不包括间变性淋巴瘤激酶(ALK)阳性患者]。患者在接受评估前接受三个疗程的MegaCHOP化疗,此时镓扫描呈阴性的患者再接受一个疗程的MegaCHOP化疗及ASCT。镓扫描仍呈阳性的患者接受两个疗程的IFE方案(异环磷酰胺10 g/m²,依托泊苷150 mg/m²,第1 - 3天每12小时一次),若至少达到部分缓解(PR),则接受移植。
三个疗程的MegaCHOP化疗后,12例患者(46%)达到完全缓解(CR),12例患者接受IFE作为挽救治疗。ASCT后(n = 19),89%的患者达到CR。相比之下,6例患者(23%)因疾病进展(n = 5)或致命毒性(n = 1)未接受移植。1例一线CR患者拒绝ASCT。中位随访35个月后,3年总生存期(OS)和无进展生存期(PFS)分别为73%和53%。此外,接受ASCT巩固治疗的患者(n = 19)移植后2年的OS、PFS和无病生存期(DFS)分别为84%、56%和63%。
对于三个疗程化疗后未达到CR的高危侵袭性淋巴结PTCL患者,早期挽救治疗以及对化疗敏感患者进行ASCT一线巩固治疗可能改善治疗效果。