1.Role of frontline autologous stem cell transplantation in young, high-risk diffuse large B-cell lymphoma patients.
Jae Ho YOON ; Jong Wook KIM ; Young Woo JEON ; Sung Eun LEE ; Ki Seong EOM ; Yoo Jin KIM ; Seok LEE ; Hee Je KIM ; Chang Ki MIN ; Jong Wook LEE ; Woo Sung MIN ; Chong Won PARK ; Seok Goo CHO
The Korean Journal of Internal Medicine 2015;30(3):362-371
BACKGROUND/AIMS: Several studies have demonstrated the effect of autologous hematopoietic stem cell transplantation (auto-HSCT) as a salvage treatment for patients with relapsed diffuse large B-cell lymphoma (DLBCL). However, the role of auto-HSCT as a frontline treatment has not been fully investigated in the rituximab era. We validated the age-adjusted International Prognostic Index (aaIPI) score for high-risk DLBCL patients and identified a possible role for frontline auto-HSCT. METHODS: We recommended frontline auto-HSCT for high-risk DLBCL patients who satisfied the criteria of both a higher Ann-Arbor stage (III to IV) and an elevated lactate dehydrogenase (LDH) level at diagnosis with an aaIPI score > or = 2. From 2006 to 2011, among the 150 DLBCL patients aged < or = 60 years who were treated with six cycles of rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP), 23 high-risk patients with a complete response (CR) were treated with auto-HSCT. For comparison, we selected 35 well-matched high-risk patients with CR who completed R-CHOP treatment alone. In addition, there were 81 low-risk patients and 11 refractory patients. RESULTS: DLBCL patients with an aaIPI score > or = 2 showed inferior overall survival (OS; p = 0.040) and progression-free survival (PFS; p = 0.007) compared to the aaIPI score 0 to 1. Between the two treatment arms among the high-risk DLBCL patients, the clinical parameters were not different. The high-risk group treated with frontline auto-HSCT showed similar OS (p = 0.392) and PFS (p = 0.670) to those in the low-risk group. Thus, frontline auto-HSCT showed superior PFS (p = 0.004), but only a trend towards favorable OS (p = 0.091) compared to R-CHOP alone. CONCLUSIONS: We identified the possible role of frontline auto-HSCT for high-risk DLBCL with a higher stage (III to IV) and elevated LDH level.
Adolescent
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Adult
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Age Factors
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Antibodies, Monoclonal, Murine-Derived/therapeutic use
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Antineoplastic Combined Chemotherapy Protocols/therapeutic use
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Biomarkers, Tumor/blood
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Chemotherapy, Adjuvant
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Cyclophosphamide/therapeutic use
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Disease Progression
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Disease-Free Survival
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Doxorubicin/therapeutic use
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Female
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Humans
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Kaplan-Meier Estimate
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L-Lactate Dehydrogenase/blood
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Lymphoma, Large B-Cell, Diffuse/blood/mortality/pathology/*surgery
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Male
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Middle Aged
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Neoadjuvant Therapy
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Neoplasm Staging
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Predictive Value of Tests
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Prednisone/therapeutic use
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Proportional Hazards Models
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Reproducibility of Results
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Risk Assessment
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Risk Factors
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*Stem Cell Transplantation
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Time Factors
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Transplantation, Autologous
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Treatment Outcome
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Up-Regulation
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Vincristine/therapeutic use
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Young Adult