Is autologous hematopoietic stem cell transplantation as consolidation therapy superior to chemotherapy alone in newly diagnosed intermediate-high risk DLBCL patients?

Abstract Introduction Diffuse large B-cell lymphoma (DLBCL) is the most common type of aggressive B-cell lymphoma. Due to the use of Rituximab, the prognosis for DLBCL has significantly improved. However, in patients with intermediate-high risk International Prognostic Index (IPI) scores (i.e., IPI ≥ 3) —a widely accepted tool for risk stratification—are prone to early relapse or disease progression, resulting in poor long-term outcomes. The therapeutic value of autologous hematopoietic stem cell transplantation (ASCT) as consolidation therapy compared to chemotherapy alone remains controversial in younger patients with high-risk DLBCL who achieve first-line remission. Aim We conducted a retrospective study to evaluate the prognostic impact of first-line ASCT versus chemotherapy alone in newly diagnosed DLBCL patients with high-risk IPI scores (≥3). Propensity score matching(PSM) was employed to balance baseline characteristics between treatment groups. Methods A retrospective analysis was conducted on newly diagnosed DLBCL patients with IPI scores ≥3 treated at Beijing 6 Medical Center between March 2014 and March 2023. Among 194 eligible patients, 104 received ASCT following first-line remission induction (transplant group), while 90 were treated with chemotherapy alone or combined with radiotherapy (non-transplant group). To minimize baseline imbalances, a 1:1 PSM was performed based on age. Results Among the 194 patients, 102 were male patients and 92 were female, yielding a male-to-female ratio of 1.11:1. The median age was 53(22-69)years. Among these patients, 116 patients had an IPI score of 3, while 78 had scores of 4-5. A total of 51 pairs of DLBCL patients were successfully matched for data analysis, and the baseline characteristics of the two groups well balanced consistent after matching. After PSM the 1-,3-,and 5-year progression-free survival(PFS) rates for the transplant group and non-transplant group were 95.7%、86.8%、80.2% vs 77.8%、68.0%、60.6%, respectively. The Log-rank test showed a statistically significant difference in the overall PFS between the two groups (P<0.05). The 1-,3-,and 5-year overall survival(OS)rates for the transplant group and non-transplant group were 97.8%、91.0%、84.5% vs 98.0%、77.6%、71.3%, respectively. The Log-rank test showed no statistically significant difference in the overall OS between the two groups (P>0.05) Based on 194 patients, univariate analysis identified auto-HSCT, old age, high-risk IPI score, and elevated LDH as significant predictors of PFS (P<0.05), with auto-HSCT acting as a protective factor. Conversely, old age, high-risk IPI, and elevated LDH were associated with prognostic factors. For OS, auto-HSCT, old age, IPI score 5, and elevated LDH showed significant associations (P<0.05), where auto-HSCT remained protective. After excluding variables with >30% missing data, variables with P<0.2 in univariate analysis were included in multivariate modeling. Auto-HSCT retained its independent protective effect on PFS (P<0.05), while elevated LDH remained an independent adverse prognostic indicator (P<0.05). Multivariate analysis confirmed age and elevated LDH as the sole independent predictors of OS (P<0.05). Post-PSM subgroup analysis demonstrated that auto-HSCT significantly improved PFS across all patient subgroups. Notably, patients with IPI score 3(HR = 0.12, 95% CI: 0.01–0.92, P = 0.041), non-GCB subtype(HR = 0.31, 95% CI: 0.11–0.89, P = 0.029), or elevated LDH(HR = 0.36, 95% CI: 0.14–0.95, P = 0.039) exhibited markedly enhanced PFS benefits from auto-HSCT compared to the non-transplant cohort. Trends toward improved PFS were observed in patients with CD5 positivity(HR = 0.18, 95% CI: 0.02–1.33, P = 0.093), double-expression(HR = 0.34, 95% CI: 0.09–1.27, P = 0.107), bone marrow involvement(HR = 0.32, 95% CI: 0.10–1.06, P = 0.063), or ≥1 extra-nodal sites(HR = 0.43, 95% CI: 0.17–1.07, P = 0.070). Additionally, auto-HSCT demonstrated a trend toward improved OS in patients with IPI score 3(HR = 0.16, 95% CI: 0.02–1.28, P = 0.084). Conclusion Thus, ASCT represents a promising consolidation strategy that significantly improves PFS in specific subgroups of DLBCL patients with intermediate-high or high risk. Its potential benefits in OS deserve further validation.

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Journal
Blood
Published
2025-11-03
DOI
https://doi.org/10.1182/blood-2025-1888
Primary Topic
Lymphoma Diagnosis and Treatment
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article

Is autologous hematopoietic stem cell transplantation as consolidation therapy superior to chemotherapy alone in newly diagnosed intermediate-high risk DLBCL patients?

Zhenling Li, Junli Chen, Lan Ma, Wanling Sun et al.
Blood
Lymphoma Diagnosis and Treatment
article

Is autologous hematopoietic stem cell transplantation as consolidation therapy superior to chemotherapy alone in newly diagnosed intermediate-high risk DLBCL patients?

Zhenling Li, Junli Chen, Lan Ma, Wanling Sun, Shuozi Liu, Hongmei Jing, Min Wang, Hui Liu, Shan Gao, Li Bao, Jiefei Bai, Huang Wenrong
article en

Abstract

Abstract Introduction Diffuse large B-cell lymphoma (DLBCL) is the most common type of aggressive B-cell lymphoma. Due to the use of Rituximab, the prognosis for DLBCL has significantly improved. However, in patients with intermediate-high risk International Prognostic Index (IPI) scores (i.e., IPI ≥ 3) —a widely accepted tool for risk stratification—are prone to early relapse or disease progression, resulting in poor long-term outcomes. The therapeutic value of autologous hematopoietic stem cell transplantation (ASCT) as consolidation therapy compared to chemotherapy alone remains controversial in younger patients with high-risk DLBCL who achieve first-line remission. Aim We conducted a retrospective study to evaluate the prognostic impact of first-line ASCT versus chemotherapy alone in newly diagnosed DLBCL patients with high-risk IPI scores (≥3). Propensity score matching(PSM) was employed to balance baseline characteristics between treatment groups. Methods A retrospective analysis was conducted on newly diagnosed DLBCL patients with IPI scores ≥3 treated at Beijing 6 Medical Center between March 2014 and March 2023. Among 194 eligible patients, 104 received ASCT following first-line remission induction (transplant group), while 90 were treated with chemotherapy alone or combined with radiotherapy (non-transplant group). To minimize baseline imbalances, a 1:1 PSM was performed based on age. Results Among the 194 patients, 102 were male patients and 92 were female, yielding a male-to-female ratio of 1.11:1. The median age was 53(22-69)years. Among these patients, 116 patients had an IPI score of 3, while 78 had scores of 4-5. A total of 51 pairs of DLBCL patients were successfully matched for data analysis, and the baseline characteristics of the two groups well balanced consistent after matching. After PSM the 1-,3-,and 5-year progression-free survival(PFS) rates for the transplant group and non-transplant group were 95.7%、86.8%、80.2% vs 77.8%、68.0%、60.6%, respectively. The Log-rank test showed a statistically significant difference in the overall PFS between the two groups (P<0.05). The 1-,3-,and 5-year overall survival(OS)rates for the transplant group and non-transplant group were 97.8%、91.0%、84.5% vs 98.0%、77.6%、71.3%, respectively. The Log-rank test showed no statistically significant difference in the overall OS between the two groups (P>0.05) Based on 194 patients, univariate analysis identified auto-HSCT, old age, high-risk IPI score, and elevated LDH as significant predictors of PFS (P<0.05), with auto-HSCT acting as a protective factor. Conversely, old age, high-risk IPI, and elevated LDH were associated with prognostic factors. For OS, auto-HSCT, old age, IPI score 5, and elevated LDH showed significant associations (P<0.05), where auto-HSCT remained protective. After excluding variables with >30% missing data, variables with P<0.2 in univariate analysis were included in multivariate modeling. Auto-HSCT retained its independent protective effect on PFS (P<0.05), while elevated LDH remained an independent adverse prognostic indicator (P<0.05). Multivariate analysis confirmed age and elevated LDH as the sole independent predictors of OS (P<0.05). Post-PSM subgroup analysis demonstrated that auto-HSCT significantly improved PFS across all patient subgroups. Notably, patients with IPI score 3(HR = 0.12, 95% CI: 0.01–0.92, P = 0.041), non-GCB subtype(HR = 0.31, 95% CI: 0.11–0.89, P = 0.029), or elevated LDH(HR = 0.36, 95% CI: 0.14–0.95, P = 0.039) exhibited markedly enhanced PFS benefits from auto-HSCT compared to the non-transplant cohort. Trends toward improved PFS were observed in patients with CD5 positivity(HR = 0.18, 95% CI: 0.02–1.33, P = 0.093), double-expression(HR = 0.34, 95% CI: 0.09–1.27, P = 0.107), bone marrow involvement(HR = 0.32, 95% CI: 0.10–1.06, P = 0.063), or ≥1 extra-nodal sites(HR = 0.43, 95% CI: 0.17–1.07, P = 0.070). Additionally, auto-HSCT demonstrated a trend toward improved OS in patients with IPI score 3(HR = 0.16, 95% CI: 0.02–1.28, P = 0.084). Conclusion Thus, ASCT represents a promising consolidation strategy that significantly improves PFS in specific subgroups of DLBCL patients with intermediate-high or high risk. Its potential benefits in OS deserve further validation.

BloodVol. 146(Supplement 1)
Peking University (CN), China-Japan Friendship Hospital (CN), Chinese PLA General Hospital (CN), Beijing Jishuitan Hospital (CN), Beijing Xuanwu Traditional Chinese Medicine Hospital (CN), Beijing Hospital (CN), Peking University Third Hospital (CN)
Openalex Percentile: Top 46%
Lymphoma Diagnosis and Treatment
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