National Institutes of Health, National Cancer Institute, Bethesda, MD, US.
Winship Cancer Institute, Biostatistics and Bioinformatics, Emory University, Atlanta, GA, US.
Eur J Haematol. 2021 Sep;107(3):301-310. doi: 10.1111/ejh.13649. Epub 2021 Jun 17.
While most patients with mantle cell lymphoma (MCL) receive therapy shortly after diagnosis, a subset of patients with indolent-behaving disease can safely defer treatment. In this subgroup, we evaluated the importance of treatment intensity in patients with MCL who defer initial therapy.
Out of 1134 patients with MCL from 12 academic centers, we analyzed 219 patients who initiated therapy at least 90 days after diagnosis. Patients who received induction with high-dose cytarabine and/or autologous stem cell transplantation (ASCT) in first remission were considered to have received intensive therapy (n = 88) while all other approaches were non-intensive (n = 131).
There was no difference in progression-free (PFS; P = .224) or overall survival (OS; P = .167) in deferred patients who received non-intensive vs. intensive therapy. Additionally, univariate and multivariate Cox proportional hazards models were performed for PFS and OS. Treatment at an academic center (HR 0.43, P = .015) was associated with improved OS in both univariate and multivariate models, while intensity of treatment was not associated with improved OS in either model.
These results indicate that intensified initial treatment is not associated with improved survival after deferring initial therapy, although prospective studies are needed to determine which of these patients with MCL may benefit from intensive therapy.
尽管大多数套细胞淋巴瘤 (MCL) 患者在确诊后不久即接受治疗,但有一部分惰性疾病患者可安全推迟治疗。在此亚组中,我们评估了在延迟初始治疗的 MCL 患者中,治疗强度的重要性。
在来自 12 个学术中心的 1134 例 MCL 患者中,我们分析了至少在诊断后 90 天开始治疗的 219 例患者。在首次缓解期接受高剂量阿糖胞苷和/或自体干细胞移植 (ASCT) 诱导治疗的患者被认为接受了强化治疗(n=88),而所有其他方法均为非强化治疗(n=131)。
在接受非强化治疗与强化治疗的延迟患者中,无进展生存期(PFS;P=0.224)或总生存期(OS;P=0.167)无差异。此外,还对 PFS 和 OS 进行了单变量和多变量 Cox 比例风险模型分析。在单变量和多变量模型中,在学术中心接受治疗(HR 0.43,P=0.015)与 OS 改善相关,而治疗强度与 OS 改善无关。
这些结果表明,在延迟初始治疗后,强化初始治疗并不能提高生存率,尽管需要前瞻性研究来确定哪些 MCL 患者可能从强化治疗中获益。