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Completed

NCT Number: NCT02248012

Everolimus and Temozolomide in Advanced Gastroenteropancreatic Neuroendocrine Carcinoma (G3)

To study the efficacy of everolimus combined with temozolomide as first-line treatment in advanced gastroenteropancreatic neuroendocrine carcinoma with a Ki67 of 20-55%, measured as disease control rate (non-progressive disease) at 6 months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Haukeland University Hospital

Bergen, 5021, Norway

About this study

Guidelines for treating advanced gastroenteropancreatic neuroendocrine carcinomas (GEP-NECs) advocate the use of combination chemotherapy with a platinum-based chemotherapy combined with etoposide. No other regimen has consistently shown a benefit over this combination. NECs do not respond to treatments usually applied in other neuroendocrine tumours such as somatostatin analogues and interferon. In contrast to metastatic neuroendocrine tumours with a low Ki67, debulking surgery and surgery for liver metastasis is generally not recommended. Cisplatin /carboplatin and etoposide is established as standard treatment of advanced disease based on two small retrospective studies showing a response rate between 41- 67% and median survival of 15-19 months. In the current trial we propose an alternative treatment for a subgroup of patients with GEP-NEC based on new data, with the intention to improve response rates and clinical benefit rate without increasing toxicity

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Histologically proven neuroendocrine carcinoma with a Ki67 of 20-55%.Primary gastroenteropancreatic tumor or cancer of unknown primary where metastases are mainly abdominalMeasurable disease according to RECIST by CT/MR

General conditions:

  • >18 years;
  • WHO/ECOG performance status 0-1.
  • Adequate haematological, renal and hepatic functions:
  • Written informed consent prior to inclusion

Prior therapy:

  • No prior chemotherapy treatment for advanced disease.
  • Adjuvant chemotherapy must have ended > 6 months before inclusion.

Prior or current history:

  • No curatively resectable disease;
  • No other serious illness or medical conditions (including: unstable angina, myocardial infarction within 6 months, unstable diabetes, immune suppression )

Concomitant treatments :

  • No concomitant (or within 4 weeks before inclusion) administration of any other experimental drug;
  • No other concurrent anti-cancer therapy.

Other :

  • Not pregnant or breast feeding. Fertile patients must use adequate contraceptives and fertile females must have a negative pregnancy test.

Treatment and study plan

Everolimus , temozolomide

Drug

Primary outcomes

  1. Disease control rate

    Time frame: 6 months

Secondary outcomes

  1. Number of patients with adverse events

    Time frame: During treatment + 30 days

    Especially number of patients with grade 3-4 toxicity.

Other outcomes

  1. Time (months) from start of study treatment to death (survival)

    Time frame: Average 14 months

    Patients alive at 18 months after last patient entered into the study will be censored.

Sponsors and collaborators

Lead sponsor

Haukeland University Hospital

Other

Collaborators

  • Aarhus University Hospital
  • Copenhagen University Hospital, Denmark
  • Rigshospitalet, Denmark
  • Sahlgrenska University Hospital
  • Skane University Hospital
  • Ullevaal University Hospital
  • Uppsala University Hospital

Registry information

Official study title

Everolimus and Temozolomide as 1-line Treatment in Advanced Gastroenteropancreatic Neuroendocrine Carcinoma (G3) With a Ki67 of 20-55%

Important dates

Study start
2014
Primary completion
2018
Study completion
2019
First posted
Sep 25, 2014
Registry last updated
Dec 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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