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Breakthrough Symptoms Remain an Unmet Need in Symptomatic Patients With Neuroendocrine Tumors and Carcinoid Syndrome.
Liu, Eric; Hoffman, Kathleen D; Murfin, Gary; Eccard, Hannah.
Affiliation
  • Liu E; From the Neuroendocrine Institute, Rocky Mountain Cancer Centers and Presbyterian/St Luke's, Denver, CO.
Pancreas ; 52(1): e70-e74, 2023 01 01.
Article de En | MEDLINE | ID: mdl-37378902
OBJECTIVES: The aims of the study were to assess the effects of breakthrough carcinoid syndrome symptoms on well-being in neuroendocrine tumor (NET) patients insufficiently controlled on long-acting somatostatin analog (SSA) and to assess patient experience with treatment options, physician communication, and disease information sources. METHODS: This study surveyed US NET patients from 2 online communities, experiencing at least one symptom, by utilizing a 64-item questionnaire. RESULTS: One hundred patients participated: 73% female, 75% age 56 to 75 years, and 93% White. Primary tumor distribution was as follows: gastrointestinal NET (n = 55), pancreatic NET (n = 33), lung NET (n = 11), and other NET (n = 13). All patients were actively treated with one long-acting SSA and experiencing breakthrough symptoms: diarrhea, flushing, or other (13% experienced one, 30% two, 57% greater than two). More than one third of treated patients experienced carcinoid-related symptoms daily. Sixty percent of respondents reported not having short-acting "rescue" treatment available, impacting well-being though anxiety or depression (45%), trouble exercising (65%), sleeping (57%), employment (54%), and maintaining friendships (43%). CONCLUSIONS: Breakthrough symptoms remain an unmet need, even in treated patients with NETs. Though still relying on physicians, NET patients are now also using the Internet. Improved awareness of optimal SSA use may improve syndrome control.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeur carcinoïde / Tumeurs neuroendocrines / Tumeurs de l'intestin / Syndrome carcinoïde malin Type d'étude: Diagnostic_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Pancreas Sujet du journal: GASTROENTEROLOGIA Année: 2023 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeur carcinoïde / Tumeurs neuroendocrines / Tumeurs de l'intestin / Syndrome carcinoïde malin Type d'étude: Diagnostic_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Pancreas Sujet du journal: GASTROENTEROLOGIA Année: 2023 Type de document: Article Pays de publication: États-Unis d'Amérique