Rituximab and Chemotherapy for Newly Diagnosed Follicular Lymphoma: Real-World Report of Polish Lymphoma Research Group.


Journal

Chemotherapy
ISSN: 1421-9794
Titre abrégé: Chemotherapy
Pays: Switzerland
ID NLM: 0144731

Informations de publication

Date de publication:
2022
Historique:
received: 03 11 2021
accepted: 02 03 2022
pubmed: 7 3 2022
medline: 26 11 2022
entrez: 6 3 2022
Statut: ppublish

Résumé

Follicular lymphoma (FL) is the most common type of indolent B-cell lymphoma with a favorable prognosis in the majority of patients. The induction treatment is still based on rituximab and chemotherapy, though new anti-CD20 antibody and chemo-free regimen have been recently introduced. The aim of the study was to analyze the management, outcomes, and determinants of prognosis of newly diagnosed patients with FL in real-world experience. Data of consecutive patients diagnosed with FL in 5 years period (2011-2015) in three oncohematological centers were reviewed. Variables were compared using Mann-Whitney or χ2 test as appropriate, survival outpoints were calculated using Kaplan-Meier method. One hundred eighty-one patients were included in the study. The median patients' age at diagnosis was 56.6 years. Low histological grade (G1-G2) was found in 62.1% of patients and advanced clinical stage in 77.0% of patients. ECOG 0 performance status was observed in 57.1% of patients. The median follow-up was 5.91 years. Initially, 31.5% of the patients were qualified to watch-and-wait (W&W) strategy, and 84.0% of the whole patients' group received systemic treatment during the observation period. As induction treatment, 53.9% and 41.4% of patients received RCVP and RCHOP regimens, respectively; 39.8% received rituximab maintenance (RM) after first-line therapy. During follow-up, transformation to aggressive lymphoma occurred in 7.2% of patients. Median overall survival (OS) was not achieved, and median progression-free survival (PFS) was 8.28 years (95% CI; 7.35, NA), 19.6% of patients relapsed during 24 months from the start of the treatment (POD24). Median PFS for POD24 group was 1.1 years (95% CI; 0.56, 1.45) with a median OS longer than 8 years. ECOG 0, low PRIMA PI, and no POD24 were found as determinants of longer PFS and OS. Our data from clinical practice showed that rituximab and chemotherapy is still an effective method of FL treatment resulting in survival more than 8 years from diagnosis in most patients. RCVP protocol followed with RM is a reasonable choice for the first-line therapy especially in low/intermediate group of patients. The prognosis was significantly worse in patients with POD24. Therefore, searching for precise initial clinical and biological markers is warranted and development therapies to improve prognosis of POD24 patients.

Identifiants

pubmed: 35249035
pii: 000523921
doi: 10.1159/000523921
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Cyclophosphamide 8N3DW7272P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

201-210

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Ewa Paszkiewicz-Kozik (E)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Malgorzata Debowska (M)

Department of Computational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Nalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw, Poland.

Natalia Jakacka (N)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Martyna Kotarska (M)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Marcin Szymanski (M)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Kamil Wisniewski (K)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Agnieszka Konska (A)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Malgorzata Jarzembowska (M)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Joanna Drozd-Sokolowska (J)

Department of Hematology, Oncology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.

Joanna Romejko-Jarosinska (J)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Anna Szumera-Cieckiewicz (A)

Department of Diagnostic Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Department of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Grzegorz Rymkiewicz (G)

Flow Cytometry Laboratory, Department of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Bogna Ziarkiewicz-Wroblewska (B)

Department of Pathology, Warsaw Medical University Clinical Centre, Warsaw, Poland.

Ewa Lech-Maranda (E)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Jan Walewski (J)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Iwona Hus (I)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Department of Clinical Transplantology, Medical University of Lublin, Lublin, Poland.

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Classifications MeSH