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Sharing real-world experiences to optimize the management of olaparib toxicities: a practical guidance from an Italian expert panel

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ARTICLE DOWNLOAD

Sharing real-world experiences to optimize the management of olaparib toxicities: a practical guidance from an Italian expert panel

10$

Domenica Lorusso, Alessandra Bologna, Sabrina Chiara Cecere, Elisabetta De Matteis, Giusy Scandurra, Claudio Zamagni, Valentina Arcangeli, Fabrizio Artioli, Mariangela Bella, Giusi Blanco, Cinzia Cardalesi, Clelia Casartelli, Rocco De Vivo, Marilena Di Napoli, Emanuele Baldo Gisone, Rossella Lauria, Alberto Andrea Lissoni, Vera Loizzi, Elena Maccaroni, Giorgia Mangili, Claudia Marchetti, Francesca Martella, Emanuele Naglieri, Veronica Parolin, Giusy Ricciardi, Graziana Ronzino, Vanda Salutari, Giovanna Scarfone, Simona Secondino, Ilaria Spagnoletti, Giulia Tasca, Germana Tognon & Valentina Guarneri -Show fewer authors 

Abstract

Olaparib is the first poly(ADP-ribose) polymerase inhibitor approved as maintenance therapy of recurrent ovarian cancer (OC) patients with a BRCA mutation. To achieve the maximum clinical benefit, adherence to olaparib must be persistent. However, in clinical practice, this is challenged by the frequent suboptimal management of toxicities. In view of the expanding use of olaparib also in Italy, physicians must learn how to adequately and promptly manage drug toxicities not to unnecessarily interrupt or reduce the dose. The experts agreed that nausea,vomiting, anemia, and fatigue are the most frequent events experienced by OC patients on olaparib, and that these toxicities usually develop early during treatment, are mainly of grade 1–2 and transient and can be managed with simple non-pharmacological interventions. By sharing their real-world experiences, the panel prepared, for each toxicity, an algorithm organized by grade and besides the procedures indicated in the local label, included supportive care interventions based also on nutritional and lifestyle modifications and psycho-oncology consultation. Moreover, in view of the tablet entry into the Italian market, the full and reduced dosages of capsules and tablets were compared. This practical guidance is intended to be a tool to support especially less-experienced physicians in the management of these complex patients, with the aim to help preventing the worsening of patients’ conditions and the unnecessary interruption/reduction of olaparib dosage, which may jeopardize treatment efficacy.

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Year 2020
Language English
Format PDF
DOI 10.1007/s00520-020-05320-4