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. 2021 Nov;100(11):2733-2744.
doi: 10.1007/s00277-021-04650-5. Epub 2021 Sep 3.

The role of autologous stem cell transplantation (ASCT) in aggressive B-cell lymphomas: real-world data from a retrospective single-center analysis

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The role of autologous stem cell transplantation (ASCT) in aggressive B-cell lymphomas: real-world data from a retrospective single-center analysis

Ramona Wullenkord et al. Ann Hematol. 2021 Nov.

Abstract

Patients with high-risk or relapsed aggressive B-cell lymphomas are characterized by poor prognosis. High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) can induce durable remissions in these patients and is potentially curative. Two hundred forty-seven patients with aggressive B-cell lymphomas treated with high-dose chemotherapy and ASCT, either as consolidation after first-line therapy or after salvage therapy for relapsed disease, between 2002 and 2019 at the University Hospital Muenster, were analyzed. The median follow-up of surviving patients was 36 months (range 0-163). Progression-free survival (PFS) and overall survival (OS) after 3 years was 63% and 68%, respectively. After ASCT, 28% of all patients experienced a relapse. The cumulative incidence of non-relapse mortality at day 100 after ASCT was 4%. Multivariate analysis identified remission status at ASCT, age at ASCT, and the numbers of infused CD34+ cells as independent prognostic factors for both PFS and OS. Patients with mantle cell lymphoma (MCL) or primary CNS lymphoma (PCNSL) treated with ASCT in first-line had a superior OS and PFS when compared to patients treated with ASCT in relapsed disease. For patients with diffuse large B-cell lymphoma (DLBCL) and Hodgkin lymphoma (HL), early relapse (< 12 months) after first-line therapy showed a trend towards an inferior PFS and OS. Deaths after ASCT were predominantly caused by lymphoma relapse and/or progression (64%) or due to infections (23%). In conclusion, high-dose chemotherapy followed by ASCT in the era of novel targeted agents remains a feasible and effective approach for patients with high-risk or relapsed aggressive B-cell lymphomas. Remission status and age at ASCT, and the number of infused stem cells were of prognostic relevance.

Keywords: Aggressive B-cell lymphoma; Autologous stem cell transplantation; DLBCL; HL; MCL; PCNSL; Prognostic factors.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Kaplan–Meier survival estimates showing overall survival (OS) for a DLBCL patients, b Hodgkin lymphoma patients, c mantle cell lymphoma patients, and d primary CNS lymphoma patients. OS curves stratified by time of relapse (< 12 months vs. ≥ 12 months) after first-line treatment in the e de novo DLBCL and f Hodgkin lymphoma subcohorts. Conditional OS by line of therapy of ASCT (first-line [1st line] vs. at relapse) for the g mantle cell lymphoma and h primary CNS lymphoma subcohorts
Fig. 2
Fig. 2
Kaplan–Meier survival estimates showing progression-free (PFS) for a DLBCL patients, b Hodgkin lymphoma patients, c mantle cell lymphoma patients, and d primary CNS lymphoma patients. PFS by time of relapse (< 12 months vs. ≥ 12 months) after first-line treatment for patients with e de novo DLBCL and f for patients with Hodgkin lymphoma. PFS by line of therapy of ASCT (first-line [1st line] vs. at relapse) for g patients with mantle cell lymphoma and h patients with primary CNS lymphoma subcohorts
Fig. 3
Fig. 3
Kaplan–Meier survival estimates showing progression-free survival and overall survival stratified by ab age at ASCT and cd remission status at ASCT

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