Real-life Experience With Rituximab-CHOP Every 21 or 14 Days in Primary Mediastinal Large B-cell Lymphoma

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3219445 59 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Real-life Experience With Rituximab-CHOP Every 21 or 14 Days in Primary Mediastinal Large B-cell Lymphoma
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Background/Aim: Primary mediastinal large Bcell lymphoma (PMLBCL) is an aggressive B-cell non- Hodgkin lymphoma (NHL), whose prognosis has greatly improved since the incorporation of the anti-CD20 monoclonal antibody rituximab into current therapeutic regimens. Evidence, however, on the optimal time interval between consecutive chemoimmunotherapy (CIT) cycles is still scarce. This study aimed to evaluate the efficacy outcomes of the more commonly administered 3-weekly regimens to the biweekly ones in a PMLBCL patients' population, who were mostly treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone every 21 days (R-CHOP-21) or R-CHOP-14. Patients and Methods: We retrospectively studied our cohort of consecutively treated PMLBCL patients, focusing on their treatment density, in order to determine possible differences in treatment outcomes. Results: CIT, in the form of both RCHOP- 21 as well as R-CHOP-14 (or similar regimens), is highly active in PMLBCL, with low rates of early treatment failure. In our cohort of patients, R-CHOP-14 did not result in a meaningful improvement of freedom from progression (FFP) or overall survival (OS). Conclusion: Both R-CHOP- 14 and R-CHOP-21 are probably equally effective in PMLBCL, yet further, prospective, randomized studies are warranted to clarify whether dose-dense regimens can be associated with better disease control and long-term results. © 2022 International Institute of Anticancer Research. All rights reserved.
Έτος δημοσίευσης:
2022
Συγγραφείς:
Karakatsanis, S.J.
Bouzani, M.
Symeonidis, A.
Angelopoulou, M.K.
Papageorgiou, S.G.
Michail, M.
Gainaru, G.
Kourti, G.
sachanas, S.
Kalpadakis, C.
Katodritou, E.
Leonidopoulou, T.
Kotsianidis, I.
Hatzimichael, E.
Kotsopoulou, M.
Dimou, M.
Variamis, E.
Boutsis, D.
Kanellias, N.
Dimopoulou, M.N.
Michali, E.
Karianakis, G.
Tsirkinidis, P.
Vadikolia, C.
Poziopoulos, C.
Pigaditou, A.
Vrakidou, E.
Economopoulos, T.
Kyriazopoulou, L.
Siakantaris, M.P.
Kyrtsonis, M.-C.
Anargyrou, K.
Papaioannou, M.
Hatjiharissi, E.
Vervessou, E.
Tsirogianni, M.
Palassopoulou, M.
Stefanoudaki, E.
Zikos, P.
Tsirigotis, P.
Tsourouflis, G.
Assimakopoulou, T.
Verrou, E.
Papadaki, H.
Lampropoulou, P.
Dimopoulos, M.-A.
Pappa, V.
Konstantopoulos, K.
Karmiris, T.
Roussou, P.
Panayiotidis, P.
Pangalis, G.A.
Vassilakopoulos, T.P.
Περιοδικό:
In vivo (Athens, Greece)
Εκδότης:
International Institute of Anticancer Research
Τόμος:
36
Αριθμός / τεύχος:
3
Σελίδες:
1302-1315
Λέξεις-κλειδιά:
antineoplastic agent; cyclophosphamide; doxorubicin; prednisone; rituximab; vincristine, B cell lymphoma; human; prospective study; retrospective study, Antineoplastic Combined Chemotherapy Protocols; Cyclophosphamide; Doxorubicin; Humans; Lymphoma, B-Cell; Prednisone; Prospective Studies; Retrospective Studies; Rituximab; Vincristine
Επίσημο URL (Εκδότης):
DOI:
10.21873/invivo.12831
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.