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dc.creatorVassilakopoulos T.P., Michail M., Papageorgiou S., Kourti G., Angelopoulou M.K., Panitsas F., Sachanas S., Kalpadakis C., Katodritou E., Leonidopoulou T., Kotsianidis I., Hatzimichael E., Kotsopoulou M., Dimou M., Variamis E., Boutsis D., Terpos E., Dimopoulou M.N., Karakatsanis S., Michalis E., Karianakis G., Tsirkinidis P., Vadikolia C., Poziopoulos C., Pigaditou A., Vrakidou E., Economopoulos T., Kyriazopoulou L., Siakantaris M.P., Kyrtsonis M.-C., Symeonidis A., Anargyrou K., Papaioannou M., Hatjiharissi E., Vervessou E., Tsirogianni M., Palassopoulou M., Gainaru G., Stefanoudaki E., Zikos P., Tsirigotis P., Tsourouflis G., Assimakopoulou T., Konstantinidou P., A. Papadaki H., Megalakaki K., Dimopoulos M.-A., Pappa V., Karmiris T., Roussou P., Panayiotidis P., Konstantopoulos K., Pangalis G.A.en
dc.date.accessioned2023-01-31T10:28:59Z
dc.date.available2023-01-31T10:28:59Z
dc.date.issued2021
dc.identifier10.1002/onco.13789
dc.identifier.issn10837159
dc.identifier.urihttp://hdl.handle.net/11615/80488
dc.description.abstractBackground: R-CHOP can cure approximately 75% of patients with primary mediastinal large B-cell lymphoma (PMLBCL), but prognostic factors have not been sufficiently evaluated yet. R-da- EPOCH is potentially more effective but also more toxic than R-CHOP. Reliable prognostic classification is needed to guide treatment decisions. Materials and Methods: We analyzed the impact of clinical prognostic factors on the outcome of 332 PMLBCL patients ≤65 years treated with R-CHOP ± radiotherapy in a multicenter setting in Greece and Cyprus. Results: With a median follow-up of 69 months, 5-year freedom from progression (FFP) was 78% and 5-year lymphoma specific survival (LSS) was 89%. On multivariate analysis, extranodal involvement (E/IV) and lactate dehydrogenase (LDH) ≥2 times upper limit of normal (model A) were significantly associated with FFP; E/IV and bulky disease (model B) were associated with LSS. Both models performed better than the International Prognostic Index (IPI) and the age-adjusted IPI by Harrel's C rank parameter and Akaike information criterion. Both models A and B defined high-risk subgroups (13%–27% of patients [pts]) with approximately 19%–23% lymphoma-related mortality. They also defined subgroups composing approximately one-fourth or one-half of the patients, with 11% risk of failure and only 1% or 4% 5-year lymphoma-related mortality. Conclusion: The combination of E/IV with either bulky disease or LDH ≥2 times upper limit of normal defined high-risk but not very-high-risk subgroups. More importantly, their absence defined subgroups comprising approximately one-fourth or one-half of the pts, with 11% risk of failure and minimal lymphoma-related mortality, who may not need more intensive treatment such as R-da-EPOCH. Implications for Practice: By analyzing the impact of baseline clinical characteristics on outcomes of a large cohort of patients with primary mediastinal large B-cell lymphoma homogeneously treated with R-CHOP with or without radiotherapy, we developed novel prognostic indices which can aid in deciding which patients can be adequately treated with R-CHOP and do not need more intensive regimens such as R-da-EPOCH. The new indices consist of objectively determined characteristics (extranodal disease or stage IV, bulky disease, and markedly elevated serum lactate dehydrogenase), which are readily available from standard initial staging procedures and offer better discrimination compared with established risk scores (International Prognostic Index [IPI] and age-adjusted IPI). © 2021 AlphaMed Pressen
dc.language.isoenen
dc.sourceOncologisten
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85108204012&doi=10.1002%2fonco.13789&partnerID=40&md5=813e1bfe07062447f9d4947e860c864d
dc.subjectcisplatinen
dc.subjectcyclophosphamide plus doxorubicin plus prednisolone plus rituximab plus vincristineen
dc.subjectcytarabineen
dc.subjectdexamethasoneen
dc.subjectdoxorubicinen
dc.subjectetoposideen
dc.subjectifosfamideen
dc.subjectlactate dehydrogenaseen
dc.subjectmethotrexateen
dc.subjectmethylprednisoloneen
dc.subjectmitoxantroneen
dc.subjectrituximaben
dc.subjectantineoplastic agenten
dc.subjectcyclophosphamideen
dc.subjectprednisoneen
dc.subjectrituximaben
dc.subjectvincristineen
dc.subjectadolescenten
dc.subjectadulten
dc.subjectanemiaen
dc.subjectArticleen
dc.subjectcancer mortalityen
dc.subjectcancer prognosisen
dc.subjectcancer recurrenceen
dc.subjectcancer specific survivalen
dc.subjectcontrolled studyen
dc.subjectDeauville 5 point scale scoreen
dc.subjectdiffuse large B cell lymphomaen
dc.subjectdrug megadoseen
dc.subjectfemaleen
dc.subjectfreedom from progressionen
dc.subjecthumanen
dc.subjectInternational Prognostic Indexen
dc.subjectlow risk patienten
dc.subjectlymphocytopeniaen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmediastinum lymph nodeen
dc.subjectoncological parametersen
dc.subjectpositron emission tomography-computed tomographyen
dc.subjectrisk factoren
dc.subjectserositisen
dc.subjecttreatment failureen
dc.subjectclinical trialen
dc.subjectmulticenter studyen
dc.subjectprognosisen
dc.subjectAdulten
dc.subjectAntineoplastic Combined Chemotherapy Protocolsen
dc.subjectCyclophosphamideen
dc.subjectDoxorubicinen
dc.subjectHumansen
dc.subjectLymphoma, Large B-Cell, Diffuseen
dc.subjectPrednisoneen
dc.subjectPrognosisen
dc.subjectRituximaben
dc.subjectVincristineen
dc.subjectJohn Wiley and Sons Incen
dc.titleIdentification of Very Low-Risk Subgroups of Patients with Primary Mediastinal Large B-Cell Lymphoma Treated with R-CHOPen
dc.typejournalArticleen


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