<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(19)</volume><submitter>Camus V</submitter><pubmed_abstract>Primary mediastinal B-cell lymphoma (PMBL) is a rare type of aggressive lymphoma typically affecting young female patients. The first-line standard of care remains debated. We performed a large multicenter retrospective study in 25 centers in France and Belgium to describe PMBL patient outcomes after first-line treatment in real-life settings. A total of 313 patients were enrolled and received rituximab (R) plus ACVBP (doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone) (n = 180) or CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) delivered every 14 days (R-CHOP14, n = 76) or 21 days (R-CHOP21, n = 57) and consolidation strategies in modalities that varied according to time and institution, mainly guided by positron emission tomography. Consolidation autologous stem cell transplantation was performed for 46 (25.6%), 24 (31.6%), and 1 (1.8%) patient in the R-ACVBP, R-CHOP14, and R-CHOP21 groups, respectively (P &lt; .001); only 17 (5.4%) patients received mediastinal radiotherapy. The end-of-treatment complete metabolic response rates were 86.3%, 86.8%, and 76.6% (P = .23) in the R-ACVBP, R-CHOP14, and R-CHOP21 groups. The median follow-up was 44 months, and the R-ACVBP, R-CHOP14, and R-CHOP21 three-year progression-free survival probabilities were 89.4% (95% confidence interval [CI], 84.8-94.2), 89.4% (95% CI, 82.7-96.6), and 74.7% (95% CI, 64-87.1) (P = .018). A baseline total metabolic tumor volume (TMTV) ≥360 cm3 was associated with a lower progression-free survival (hazard ratio, 2.18; 95% CI, 1.05-4.53). Excess febrile neutropenia (24.4% vs 5.3% vs 5.3%; P &lt; .001) and mucositis (22.8% vs 3.9% vs 1.8%; P &lt; .001) were observed with R-ACVBP compared with the R-CHOP regimens. Patients with PMBL treated with dose-dense immunochemotherapy without radiotherapy have excellent outcomes. R-ACVBP acute toxicity was higher than that of R-CHOP14. Our data confirmed the prognostic importance of baseline TMTV.</pubmed_abstract><journal>Blood advances</journal><pagination>3862-3872</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8679665</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Outcomes after first-line immunochemotherapy for primary mediastinal B-cell lymphoma: a LYSA study.</pubmed_title><pmcid>PMC8679665</pmcid><pubmed_authors>Lequesne J</pubmed_authors><pubmed_authors>Tardy M</pubmed_authors><pubmed_authors>Decazes P</pubmed_authors><pubmed_authors>Lazarovici J</pubmed_authors><pubmed_authors>Bernard S</pubmed_authors><pubmed_authors>Maisonneuve H</pubmed_authors><pubmed_authors>Chauchet A</pubmed_authors><pubmed_authors>Moles-Moreau MP</pubmed_authors><pubmed_authors>Houot R</pubmed_authors><pubmed_authors>Berriolo-Riedinger A</pubmed_authors><pubmed_authors>Gauthier M</pubmed_authors><pubmed_authors>Becker S</pubmed_authors><pubmed_authors>Willaume A</pubmed_authors><pubmed_authors>Antier C</pubmed_authors><pubmed_authors>Le Du K</pubmed_authors><pubmed_authors>Bailly S</pubmed_authors><pubmed_authors>Lebras L</pubmed_authors><pubmed_authors>Jardin F</pubmed_authors><pubmed_authors>Damaj G</pubmed_authors><pubmed_authors>Rossi C</pubmed_authors><pubmed_authors>Durot E</pubmed_authors><pubmed_authors>Sesques P</pubmed_authors><pubmed_authors>Monjanel H</pubmed_authors><pubmed_authors>Haioun C</pubmed_authors><pubmed_authors>Bonnet C</pubmed_authors><pubmed_authors>Besson C</pubmed_authors><pubmed_authors>Laribi K</pubmed_authors><pubmed_authors>Tilly H</pubmed_authors><pubmed_authors>Choquet S</pubmed_authors><pubmed_authors>Tonnelet D</pubmed_authors><pubmed_authors>Traverse-Glehen A</pubmed_authors><pubmed_authors>Camus V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes after first-line immunochemotherapy for primary mediastinal B-cell lymphoma: a LYSA study.</name><description>Primary mediastinal B-cell lymphoma (PMBL) is a rare type of aggressive lymphoma typically affecting young female patients. The first-line standard of care remains debated. We performed a large multicenter retrospective study in 25 centers in France and Belgium to describe PMBL patient outcomes after first-line treatment in real-life settings. A total of 313 patients were enrolled and received rituximab (R) plus ACVBP (doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone) (n = 180) or CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) delivered every 14 days (R-CHOP14, n = 76) or 21 days (R-CHOP21, n = 57) and consolidation strategies in modalities that varied according to time and institution, mainly guided by positron emission tomography. Consolidation autologous stem cell transplantation was performed for 46 (25.6%), 24 (31.6%), and 1 (1.8%) patient in the R-ACVBP, R-CHOP14, and R-CHOP21 groups, respectively (P &lt; .001); only 17 (5.4%) patients received mediastinal radiotherapy. The end-of-treatment complete metabolic response rates were 86.3%, 86.8%, and 76.6% (P = .23) in the R-ACVBP, R-CHOP14, and R-CHOP21 groups. The median follow-up was 44 months, and the R-ACVBP, R-CHOP14, and R-CHOP21 three-year progression-free survival probabilities were 89.4% (95% confidence interval [CI], 84.8-94.2), 89.4% (95% CI, 82.7-96.6), and 74.7% (95% CI, 64-87.1) (P = .018). A baseline total metabolic tumor volume (TMTV) ≥360 cm3 was associated with a lower progression-free survival (hazard ratio, 2.18; 95% CI, 1.05-4.53). Excess febrile neutropenia (24.4% vs 5.3% vs 5.3%; P &lt; .001) and mucositis (22.8% vs 3.9% vs 1.8%; P &lt; .001) were observed with R-ACVBP compared with the R-CHOP regimens. Patients with PMBL treated with dose-dense immunochemotherapy without radiotherapy have excellent outcomes. R-ACVBP acute toxicity was higher than that of R-CHOP14. Our data confirmed the prognostic importance of baseline TMTV.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-09T07:05:58.035Z</modification><creation>2022-02-11T14:38:08.455Z</creation></dates><accession>S-EPMC8679665</accession><cross_references><pubmed>34461634</pubmed><doi>10.1182/bloodadvances.2021004778</doi></cross_references></HashMap>