PRESTO 2: An International Survey to Evaluate Patients’ Injection Experiences with the Latest Devices/Formulations of Long-Acting Somatostatin Analog Therapies for Neuroendocrine Tumors or Acromegaly
Authors:
- Dermot O’tOoleDODermot O’tOole
- Pamela L. KunzPKPamela L. Kunz
- Susan M. WebbSWSusan M. Webb
- Grace GoldsteinGGGrace Goldstein
- Sheila KhawajaSKSheila Khawaja
- Mark McDonnellMMMark McDonnell
- Sandra BoiziauSBSandra Boiziau
- Delphine GueguenDGDelphine Gueguen
- Aude HouchardAHAude Houchard
- Antonio Ribeiro-OliveiraARAntonio Ribeiro-Oliveira
- Ally PrebtaniAPAlly Prebtani
- 11 December 2022
- journal article
- research article
- Published by Springer Nature in Advances in Therapy
- Vol. 40 (2) , 671-690
Abstract
Introduction Real-world data evaluating patients’ injection experiences using the latest devices/formulations of the long-acting (LA) somatostatin analogs (SSAs) lanreotide Autogel/Depot (LAN; Somatuline®) and octreotide LA release (OCT; Sandostatin®) are limited. Methods PRESTO 2 was a 2020/2021 e-survey comparing injection experience of adults with neuroendocrine tumors (NETs) or acromegaly treated with LAN prefilled syringe versus OCT syringe for > 3 months in Canada, Ireland, the UK and the USA (planned sample size, 304). Primary endpoint: the proportion of patients with injection-site pain lasting > 2 days after their most recent injection, analyzed using a multivariate logistic regression model. Secondary endpoints included interference with daily life due to injection-site pain and technical injection problems in patients with current SSA use for ≥ 6 months. Results There were 304 respondents (acromegaly, n = 85; NETs, n = 219; LAN, n = 168; OCT, n = 136; 69.2% female; mean age, 59.6 years). Fewer patients had injection-site pain lasting > 2 days after the most recent injection with LAN (6.0%) than OCT (22.8%); the odds of pain lasting > 2 days were significantly lower for LAN than OCT, adjusted for disease subgroup and occurrence of injection-site reactions (odds ratio [95% confidence interval]: 0.13 [0.06–0.30]; p < 0.0001). Injection-site pain interfered with daily life “a little bit” or “quite a bit” in 37.2% and 3.8% (LAN) versus 52.5% and 7.5% (OCT) of patients, respectively. Among patients with ≥ 6 months’ experience with current SSA (92.4% of patients), technical injection problems never occurred in 76.8% (LAN) and 42.9% (OCT) of patients. Conclusions Compared with OCT, significantly fewer patients using LAN had injection-site pain lasting > 2 days after their most recent injection. Also, fewer LAN-treated patients experienced technical problems during injection. These findings demonstrate the importance of injection modality for overall LA SSA injection experience for patients with acromegaly or NETs. Graphical abstractKeywords
Funding Information
- Ipsen
This publication has 19 references indexed in Scilit:
- A Consensus Statement on acromegaly therapeutic outcomesNature Reviews Endocrinology, 2018
- Neuroendocrine Tumors and Lanreotide Depot: Clinical Considerations and Nurse and Patient PreferencesClinical Journal of Oncology Nursing, 2016
- Acromegaly: clinical features at diagnosisPituitary, 2016
- Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegalyEuropean Journal of Endocrinology, 2016
- Lanreotide in Metastatic Enteropancreatic Neuroendocrine TumorsNew England Journal of Medicine, 2014
- World Medical Association Declaration of HelsinkiJAMA, 2013
- Evaluation of long-acting somatostatin analog injection devices by nurses: a quantitative studyMedical Devices: Evidence and Research, 2012
- Antiproliferative effect of somatostatin analogs in gastroenteropancreatic neuroendocrine tumorsWorld Journal of Gastroenterology, 2010
- AcromegalyNew England Journal of Medicine, 2006
- Development and Validation of the Patient Assessment of Chronic Illness Care (PACIC)Medical Care, 2005