The significance of upfront autologous stem cell transplantation for high‐intermediate/high‐risk stage IV diffuse large B‐cell lymphoma

Author:

Koviazin Aleksei K.12ORCID,Filatova Larisa V.123ORCID,Zyuzgin Ilia S.1,Artemyeva Anna S.4,Poliatskin Ilia L.4,Burda Darya S.4,Volchenkov Stanislav A.1ORCID,Elkhova Svetlana S.1ORCID,Semiglazova Tatiana Yu.23ORCID

Affiliation:

1. Department of Hematology and Chemotherapy with Intensive Care Unit NMRC of Oncology n.a. N.N.Petrov of MoH of Russia, Federal State Budgetary Institution “Petrov National Medical Cancer Research Centre” of the Ministry of Health of the Russian Federation Saint‐Petersburg Russian Federation

2. Department of Innovative Methods in Therapeutic Oncology and Rehabilitation NMRC of Oncology n.a. N.N.Petrov of MoH of Russia, Federal State Budgetary Institution “Petrov National Medical Cancer Research Centre” of the Ministry of Health of the Russian Federation Saint‐Petersburg Russian Federation

3. Department of Oncology Federal State Budgetary Educational Institution of Higher Education “North‐Western State Medical University named after I.I. Mechnikov” of the Ministry of Health of the Russian Federation Saint‐Petersburg Russian Federation

4. Laboratory of Tumor Morphology Federal State Budgetary Institution “Petrov National Medical Cancer Research Centre” of the Ministry of Health of the Russian Federation Saint‐Petersburg Russian Federation

Abstract

AbstractBackgroundDiffuse large B‐cell lymphoma (DLBCL) is the most common (30%–35%) type of B‐cell lymphoma. Only about 60% of all newly diagnosed advanced‐stage DLBCL can be completely treated with x6 R‐CHOP. High‐dose chemotherapy (HDCT) followed by autologous hematopoietic stem cell transplantation in the first remission (upfront auto‐HSCT) can serve as an option to improve a prognosis in these patients.AimsThis trial aimed to improve prognosis in DLBCL by upfront auto‐HSCT.Methods and ResultsA group of 105 patients: DLBCL NOS, age 18–65, stage IV, IPI ≥2, CR/PR after x6 R‐CHOP/DA‐EPOCH‐R from 2010 to 2019 at NMRC of Oncology named after N.N.Petrov of MoH of Russia was retrospectively analyzed. The HSCT group included patients with upfront HDCT followed by auto‐HSCT (n = 35). The control group included patients with non‐invasive follow‐up after induction (n = 70). Primary endpoint was progression‐free survival (PFS). Secondary endpoints were overall survival (OS), response rate and relapse rate. The 3‐year OS (p = .013) and 3‐year PFS (p = .033) were significantly higher in the HSCT group. The 3‐year OS was decreased by the occurrence of relapse (p ≤ .001) and weight loss (B‐symptom) (p = .04). DEL was the negative prognostic factor for 3‐year PFS in all patients (p = .001) and control group (p = .001). DA‐EPOCH‐R significantly increased the 3‐year PFS (p = .041).ConclusionUpfront HDCT followed by auto‐HSCT can increase 3‐year OS and PFS and improve prognosis in DLBCL NOS, age 18–65, stage IV, IPI ≥2 patients.

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference57 articles.

1. National Cancer Institute.Surveillance Epidemiology and End Results (SEER) Program. Accessed February 11 2022.seer.cancer.gov

2. Autologous Bone Marrow Transplantation as Compared with Salvage Chemotherapy in Relapses of Chemotherapy-Sensitive Non-Hodgkin's Lymphoma

3. Diffuse Large B-Cell Lymphoma

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