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Safety and efficacy of netupitant/palonosetron and dexamethasone in classical Hodgkin's lymphoma patients with inadequate chemotherapy-induced nausea and vomiting prophylaxis with palonosetron and dexamethasone: a single-center real-life experience.
Zilioli, Vittorio R; Muzi, Cristina; Minga, Periana; Codega, Paolo; Crucitti, Lara; Meli, Erika; Esposito, Anna; Panico, Claudia; Rusconi, Chiara; Cairoli, Roberto.
Afiliación
  • Zilioli VR; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Muzi C; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Minga P; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Codega P; Medical Affairs Department, Italfarmaco SpA, Cinisello Balsamo, Italy.
  • Crucitti L; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Meli E; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Esposito A; Pharmacy, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Panico C; Pharmacy, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Rusconi C; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Cairoli R; Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Int J Hematol Oncol ; 9(1): IJH23, 2020 Feb 28.
Article en En | MEDLINE | ID: mdl-32382409
ABSTRACT
We analyzed safety of NEPA (netupitant/palonosetron) and dexamethasone (NEPA+DEX) for the management of chemotherapy-induced nausea and vomiting (CINV) in classical Hodgkin's lymphoma patients that experienced CINV with a prophylaxis with palonosetron (PALO + DEX). In a retrospective, monocentric, noncomparative study, we analyzed adverse events and CINV grading in patients who switched from PALO + DEX to NEPA + DEX. Among 32 patients treated with ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) during the study period, 47% did not properly control CINV with PALO + DEX and were shifted to NEPA + DEX. Among these, 53.3% properly controlled CINV is for all the remaining chemotherapy cycles. We did not observe an increase of adverse events after switching to NEPA. In our study, NEPA did not show drug-drug interaction with ABVD (doxorubicin, bleomycin, vinblastine, dacarbazinechemotherapy agents and NEPA administration was well tolerated with mild and transient adverse events.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Int J Hematol Oncol Año: 2020 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Int J Hematol Oncol Año: 2020 Tipo del documento: Article País de afiliación: Italia