Background Painful mucositis is one of the most distressing toxicities of chemoradiotherapy (CRT) for head and neck cancer (HNC), with the characteristics of incidental predictable breakthrough pain (BTP) during swallowing. Fentanyl pectin nasal spray (FPNS) could be a good therapeutic option. Methods Patients were prospectively considered if receiving basal analgesic therapy with opiates for painful mucositis of grade ≥4 on a numerical rating scale from 0 to 10. They were offered FPNS 100 mcg before oral intake. When patients reached the effective dose, they evaluated the basal pain intensity before FPNS use and after 10, 20, 30 and 40 min. Results Seventeen HNC patients were offered FPNS before oral intake, with 15 patients completing treatment. Mean reduction of incidental BTP intensity after FPNS was 3.1 points (range 1.2-5.8). Mean time elapsed since FPNS use and highest pain reduction was 26 min. Conclusions FPNS demonstrated activity against BTP when swallowing in HNC patients. These data should be considered as hypothesis-generating.

Fentanyl pectin nasal spray as treatment for incident predictable breakthrough pain (BTP) in oral mucositis induced by chemoradiotherapy in head and neck cancer / P. Bossi, L. Locati, C. Bergamini, A. Mirabile, R. Granata, M. Imbimbo, C. Resteghini, L. Licitra. - In: ORAL ONCOLOGY. - ISSN 1368-8375. - 50:9(2014), pp. 884-887. [10.1016/j.oraloncology.2014.06.013]

Fentanyl pectin nasal spray as treatment for incident predictable breakthrough pain (BTP) in oral mucositis induced by chemoradiotherapy in head and neck cancer

A. Mirabile;C. Resteghini
Penultimo
;
L. Licitra
Ultimo
2014

Abstract

Background Painful mucositis is one of the most distressing toxicities of chemoradiotherapy (CRT) for head and neck cancer (HNC), with the characteristics of incidental predictable breakthrough pain (BTP) during swallowing. Fentanyl pectin nasal spray (FPNS) could be a good therapeutic option. Methods Patients were prospectively considered if receiving basal analgesic therapy with opiates for painful mucositis of grade ≥4 on a numerical rating scale from 0 to 10. They were offered FPNS 100 mcg before oral intake. When patients reached the effective dose, they evaluated the basal pain intensity before FPNS use and after 10, 20, 30 and 40 min. Results Seventeen HNC patients were offered FPNS before oral intake, with 15 patients completing treatment. Mean reduction of incidental BTP intensity after FPNS was 3.1 points (range 1.2-5.8). Mean time elapsed since FPNS use and highest pain reduction was 26 min. Conclusions FPNS demonstrated activity against BTP when swallowing in HNC patients. These data should be considered as hypothesis-generating.
Breakthrough pain (BTP); Chemo radiotherapy; Fentanyl pectin nasal spray; Head and neck cancer; Oral mucositis
Settore MED/06 - Oncologia Medica
2014
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/484648
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