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Titel: Ramucirumab in combination with dacarbazine in patients with progressive well-differentiated metastatic pancreatic neuroendocrine tumors (RamuNET) : study protocol for a multicenter single-arm trial
Autor(en): Krug, SebastianIn der Gemeinsamen Normdatei der DNB nachschlagen
Kegel, Thomas
Gress, Thomas MathiasIn der Gemeinsamen Normdatei der DNB nachschlagen
Rinke, AnjaIn der Gemeinsamen Normdatei der DNB nachschlagen
Apostolidis, LeonidasIn der Gemeinsamen Normdatei der DNB nachschlagen
Jann, HenningIn der Gemeinsamen Normdatei der DNB nachschlagen
König, Alexander
Hörsch, DieterIn der Gemeinsamen Normdatei der DNB nachschlagen
Schrader, JörgIn der Gemeinsamen Normdatei der DNB nachschlagen
Ettrich, Thomas J.In der Gemeinsamen Normdatei der DNB nachschlagen
Richter, Michael
Steighardt, Jörg
Michl, PatrickIn der Gemeinsamen Normdatei der DNB nachschlagen
Erscheinungsdatum: 2021
Art: Artikel
Sprache: Englisch
Zusammenfassung: Background: Cytotoxic chemotherapy combinations and targeted agents represent established treatment concepts in advanced pancreatic neuroendocrine tumors (PNETs). However, response rates, side effects and outcome data strongly vary among these therapeutic approaches. Head-to-head comparisons between chemo- and molecular therapies are missing and secondary resistances frequently occur. The RamuNET trial aims to identify the effectiveness of dual treatment with DTIC and ramucirumab in progressive advanced PNET patients. Methods: The RamuNET study is an investigator-initiated multicenter prospective single-arm trial to evaluate the efficacy of ramucirumab in combination with dacarbazine (DTIC) over a period of at least 6 months. Patients with progressive well-differentiated and metastatic pancreatic neuroendocrine tumors are eligible. The study aims to include 45 patients over a period of 24 months with a minimum follow-up of 24 months. The primary endpoint is disease control after 6 months. Secondary endpoints include progression-free survival, biochemical response, overall survival, quality of life and toxicity. Based on the hypothesis that 80% of the patients can achieve a disease control after 6 months, the sample size calculation follows an exact binomial single-stage design. H0: p < =p0 = 60% versus H1: p > =p1 = 80%, alpha = 0.05, beta = 0.1. Discussion: This study investigates a new therapeutic approach using the combination of cytotoxic and targeted antiangiogenic therapy in advanced PNET. If positive, this trial will be the basis for a randomized two-arm study to investigate the combination of ramucirumab and DTIC against other established therapies in PNET.
URI: https://opendata.uni-halle.de//handle/1981185920/59067
http://dx.doi.org/10.25673/57116
Open-Access: Open-Access-Publikation
Nutzungslizenz: (CC BY 4.0) Creative Commons Namensnennung 4.0 International(CC BY 4.0) Creative Commons Namensnennung 4.0 International
Sponsor/Geldgeber: Publikationsfonds MLU
Journal Titel: BMC cancer
Verlag: BioMed Central
Verlagsort: London
Band: 21
Originalveröffentlichung: 10.1186/s12885-021-08900-7
Enthalten in den Sammlungen:Open Access Publikationen der MLU

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