Department of Hematology, Huadong Hospital Affiliated with Fudan University, Shanghai, China.
Front Immunol. 2024 May 10;15:1382189. doi: 10.3389/fimmu.2024.1382189. eCollection 2024.
There was little evidence of autologous stem cell transplantation (ASCT) as consolidation therapy after remission of induction for patients with Peripheral T-cell lymphoma (PTCL). In this study, we conducted a comparative analysis of real-world survival outcomes between consolidation therapy and observation in patients with PTCL.
A total of 92 patients with peripheral T-cell lymphoma (PTCL) who were admitted to the Department of Hematology, Huadong Hospital Affiliated with Fudan University from January 2013 to April 2019 were divided into two groups based on whether they were treated with high-dose therapy (HDT) followed by autologous hematopoietic stem cell transplantation (ASCT): ASCT as consolidation therapy (n=30) and observation (n=62). Clinical characteristics, treatment patterns, and survival outcomes were analyzed between the two groups. Univariate and Cox multivariate regression analyses were also performed to detect prognostic factors of survival.
With a median follow-up time of 41 months, the median overall survival (OS) of peripheral T-cell lymphoma patients treated with ASCT was not reached; the median progression-free survival (PFS) was 77.0 months, which was much higher than that of patients without ASCT (<0.003 for OS, p=0.015 for PFS). Subgroup analysis found that patients with high risks benefited more from ASCT. Combination with hemophagocytic lymphohistiocytosis (HLH) (<0.001), clinical stage more than III (=0.014), IPI score above 3 (=0.049), and bone marrow involvement (=0.010) were the independent prognostic factors significantly associated with worse OS and PFS. Additionally, pegylated liposomal doxorubicin (PLD)-containing chemotherapy regimen could bring a higher overall response rate (ORR) and prolong the survival of patients with PTCL who underwent ASCT.
ASCT may improve the long-term survival of patients with PTCL as consolidation therapy after achieving complete or partial remission of induction treatment, particularly for those with high risks. The chemotherapy regimen containing pegylated liposomal doxorubicin may induce deeper remission than traditional doxorubicin in PTCL. It is crucial to identify the specific groups most likely to benefit from upfront ASCT.
在诱导缓解后,自体造血干细胞移植(ASCT)作为巩固治疗在外周 T 细胞淋巴瘤(PTCL)患者中几乎没有证据。在这项研究中,我们对接受巩固治疗与观察治疗的 PTCL 患者的真实世界生存结局进行了比较分析。
纳入 2013 年 1 月至 2019 年 4 月在复旦大学附属华山医院血液科就诊的 92 例外周 T 细胞淋巴瘤(PTCL)患者,根据是否接受大剂量化疗(HDT)联合自体造血干细胞移植(ASCT)作为巩固治疗分为两组:ASCT 巩固治疗组(n=30)和观察组(n=62)。比较两组患者的临床特征、治疗模式和生存结局。采用单因素和 Cox 多因素回归分析检测生存的预后因素。
中位随访时间为 41 个月,ASCT 巩固治疗组患者的中位总生存(OS)未达到,中位无进展生存(PFS)为 77.0 个月,显著高于未接受 ASCT 巩固治疗组(OS:P<0.003,PFS:P=0.015)。亚组分析发现,高危患者从 ASCT 巩固治疗中获益更多。与 OS 相关的独立预后因素包括合并噬血细胞性淋巴组织细胞增生症(HLH,P<0.001)、临床分期Ⅲ期以上(P=0.014)、国际预后指数(IPI)评分>3 分(P=0.049)和骨髓累及(P=0.010)。此外,含脂质体阿霉素(PLD)的化疗方案可提高接受 ASCT 的 PTCL 患者的总缓解率(ORR)并延长其生存。
ASCT 可改善诱导缓解后完全或部分缓解的 PTCL 患者的长期生存,尤其对高危患者有益。含 PLD 的化疗方案在 PTCL 中可能比传统阿霉素诱导更深层次的缓解。确定最有可能从 upfront ASCT 中获益的特定患者群体至关重要。