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The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size

INTRODUCTION: At present, there is no approved medical treatment option for patients with non-functioning pituitary adenoma. A number of open-label studies suggest that treatment with somatostatin analogues may prevent tumour progression. In vivo somatostatin receptor imaging using (68)Ga-DOTATATE P...

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Autores principales: Boertien, Tessel M, Drent, Madeleine L, Booij, Jan, Majoie, Charles B L M, Stokkel, Marcel P M, Hoogmoed, Jantien, Pereira, Alberto, Biermasz, Nienke R, Simsek, Suat, Groote Veldman, Ronald, Tanck, Michael W T, Fliers, Eric, Bisschop, Peter H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430490/
https://www.ncbi.nlm.nih.gov/pubmed/32792446
http://dx.doi.org/10.1136/bmjopen-2020-038250
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author Boertien, Tessel M
Drent, Madeleine L
Booij, Jan
Majoie, Charles B L M
Stokkel, Marcel P M
Hoogmoed, Jantien
Pereira, Alberto
Biermasz, Nienke R
Simsek, Suat
Groote Veldman, Ronald
Tanck, Michael W T
Fliers, Eric
Bisschop, Peter H
author_facet Boertien, Tessel M
Drent, Madeleine L
Booij, Jan
Majoie, Charles B L M
Stokkel, Marcel P M
Hoogmoed, Jantien
Pereira, Alberto
Biermasz, Nienke R
Simsek, Suat
Groote Veldman, Ronald
Tanck, Michael W T
Fliers, Eric
Bisschop, Peter H
author_sort Boertien, Tessel M
collection PubMed
description INTRODUCTION: At present, there is no approved medical treatment option for patients with non-functioning pituitary adenoma. A number of open-label studies suggest that treatment with somatostatin analogues may prevent tumour progression. In vivo somatostatin receptor imaging using (68)Ga-DOTATATE PET (PET, positron emission tomography) could help in preselecting patients potentially responsive to treatment. Our aim is to investigate the effect of the somatostatin analogue lanreotide as compared with placebo on tumour size in patients with a (68)Ga-DOTATATE PET-positive non-functioning pituitary macroadenoma (NFMA). METHODS AND ANALYSIS: The GALANT study is a multicentre, randomised, double-blind, placebo-controlled trial in adult patients with a suprasellar extending NFMA. Included patients undergo a (68)Ga-DOTATATE PET/CT of the head and tracer uptake is assessed after coregistration with pituitary MRI. Forty-four patients with a (68)Ga-DOTATATE PET-positive NFMA are randomised in a 1:1 ratio between lanreotide 120 mg or placebo, both administered as subcutaneous injections every 28 days for 72 weeks. The primary outcome is the change in cranio-caudal tumour diameter on pituitary MRI after treatment. Secondary outcomes are change in tumour volume, time to tumour progression, change in quality of life and number of adverse events. Final results are expected in the second half of 2021. ETHICS AND DISSEMINATION: The study protocol has been approved by the Medical Research Ethics Committee of the Academic Medical Centre (AMC) of the Amsterdam University Medical Centres and by the Dutch competent authority. It is an investigator-initiated study with financial support by Ipsen Farmaceutica BV. The AMC, as sponsor, remains owner of all data. Results will be submitted for publication in a peer-reviewed journal. TRIAL REGISTRATION NUMBER: NL5136 (Netherlands Trial Register); pre-recruitment.
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spelling pubmed-74304902020-08-24 The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size Boertien, Tessel M Drent, Madeleine L Booij, Jan Majoie, Charles B L M Stokkel, Marcel P M Hoogmoed, Jantien Pereira, Alberto Biermasz, Nienke R Simsek, Suat Groote Veldman, Ronald Tanck, Michael W T Fliers, Eric Bisschop, Peter H BMJ Open Diabetes and Endocrinology INTRODUCTION: At present, there is no approved medical treatment option for patients with non-functioning pituitary adenoma. A number of open-label studies suggest that treatment with somatostatin analogues may prevent tumour progression. In vivo somatostatin receptor imaging using (68)Ga-DOTATATE PET (PET, positron emission tomography) could help in preselecting patients potentially responsive to treatment. Our aim is to investigate the effect of the somatostatin analogue lanreotide as compared with placebo on tumour size in patients with a (68)Ga-DOTATATE PET-positive non-functioning pituitary macroadenoma (NFMA). METHODS AND ANALYSIS: The GALANT study is a multicentre, randomised, double-blind, placebo-controlled trial in adult patients with a suprasellar extending NFMA. Included patients undergo a (68)Ga-DOTATATE PET/CT of the head and tracer uptake is assessed after coregistration with pituitary MRI. Forty-four patients with a (68)Ga-DOTATATE PET-positive NFMA are randomised in a 1:1 ratio between lanreotide 120 mg or placebo, both administered as subcutaneous injections every 28 days for 72 weeks. The primary outcome is the change in cranio-caudal tumour diameter on pituitary MRI after treatment. Secondary outcomes are change in tumour volume, time to tumour progression, change in quality of life and number of adverse events. Final results are expected in the second half of 2021. ETHICS AND DISSEMINATION: The study protocol has been approved by the Medical Research Ethics Committee of the Academic Medical Centre (AMC) of the Amsterdam University Medical Centres and by the Dutch competent authority. It is an investigator-initiated study with financial support by Ipsen Farmaceutica BV. The AMC, as sponsor, remains owner of all data. Results will be submitted for publication in a peer-reviewed journal. TRIAL REGISTRATION NUMBER: NL5136 (Netherlands Trial Register); pre-recruitment. BMJ Publishing Group 2020-08-13 /pmc/articles/PMC7430490/ /pubmed/32792446 http://dx.doi.org/10.1136/bmjopen-2020-038250 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Diabetes and Endocrinology
Boertien, Tessel M
Drent, Madeleine L
Booij, Jan
Majoie, Charles B L M
Stokkel, Marcel P M
Hoogmoed, Jantien
Pereira, Alberto
Biermasz, Nienke R
Simsek, Suat
Groote Veldman, Ronald
Tanck, Michael W T
Fliers, Eric
Bisschop, Peter H
The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
title The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
title_full The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
title_fullStr The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
title_full_unstemmed The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
title_short The GALANT trial: study protocol of a randomised placebo-controlled trial in patients with a (68)Ga-DOTATATE PET-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
title_sort galant trial: study protocol of a randomised placebo-controlled trial in patients with a (68)ga-dotatate pet-positive, clinically non-functioning pituitary macroadenoma on the effect of lanreotide on tumour size
topic Diabetes and Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430490/
https://www.ncbi.nlm.nih.gov/pubmed/32792446
http://dx.doi.org/10.1136/bmjopen-2020-038250
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