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HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors

BACKGROUND: Nearly 30% of neuroendocrine tumors (NETs) have evidence of immunohistochemical (IHC) expression of estrogen (ER) and/or progesterone (PR) receptors. Therefore, targeting ER/PR may offer an effective NET-directed treatment to select patients. METHODS: We conducted a multicenter Simon two...

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Autores principales: Barros, Milton J., Strosberg, Jonathan, Al-Toubah, Taymeyah, de Jesus, Victor Hugo F., Durant, Lais, Mello, Celso A., Felismino, Tiago C., De Brot, Louise, Taboada, Rodrigo G., Donadio, Mauro D., Riechelmann, Rachel P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387775/
https://www.ncbi.nlm.nih.gov/pubmed/37529158
http://dx.doi.org/10.1177/17588359231186041
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author Barros, Milton J.
Strosberg, Jonathan
Al-Toubah, Taymeyah
de Jesus, Victor Hugo F.
Durant, Lais
Mello, Celso A.
Felismino, Tiago C.
De Brot, Louise
Taboada, Rodrigo G.
Donadio, Mauro D.
Riechelmann, Rachel P.
author_facet Barros, Milton J.
Strosberg, Jonathan
Al-Toubah, Taymeyah
de Jesus, Victor Hugo F.
Durant, Lais
Mello, Celso A.
Felismino, Tiago C.
De Brot, Louise
Taboada, Rodrigo G.
Donadio, Mauro D.
Riechelmann, Rachel P.
author_sort Barros, Milton J.
collection PubMed
description BACKGROUND: Nearly 30% of neuroendocrine tumors (NETs) have evidence of immunohistochemical (IHC) expression of estrogen (ER) and/or progesterone (PR) receptors. Therefore, targeting ER/PR may offer an effective NET-directed treatment to select patients. METHODS: We conducted a multicenter Simon two-stage single-arm phase II trial of tamoxifen in patients with metastatic, progressive NETs. Eligible patients had positive IHC expression of ER and/or PR ⩾ 1%. Prior therapy with somatostatin analogs was required for progressing/functioning cases. Main exclusion criterion was aggressive disease requiring cytotoxic therapy. The primary end point was disease control rate (DCR) at week 24 by Response Evaluation Criteria in Solid Tumors version 1.1. We planned to enroll 23 patients in the first stage, to reach a DCR at week 24 of 70% (versus 50%); if ⩾12 patients reached the primary end point, a total of 37 would be included. RESULTS: From February 2019 to February 2022, 23 out of 59 patients were eligible and enrolled: 15 (65%) were females; the most common sites were pancreas (11; 48%) and small bowel (6; 26%). In all, 13 patients (56.5%) had G2 NETs. At a median follow-up of 27 months, 13 patients (56.5%) had stable disease at week 24 and median progression-free survival (PFS) was 7.9 months [interquartile range (IQR): 3.7–12.1]. The best response was stable disease in 13 patients, with most patients experiencing minor tumor growth. Median PFS times were not significantly different according to ER/PR < or ⩾30% (p = 0.49) or ER versus PR expression (p = 0.19). One patient experienced grade 2 constipation. CONCLUSION: Tamoxifen for ER-/PR-positive NETs patients is safe but offers modest antitumor effects. TRIAL REGISTRY NAME: Study of Tamoxifen in Well Differentiated Neuroendocrine Tumors and Hormone Receptor Positive Expression (HORMONET). URL: https://clinicaltrials.gov/ct2/show/NCT03870399?term=03870399&draw=2&rank=1 REGISTRATION NUMBER: NCT03870399
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spelling pubmed-103877752023-08-01 HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors Barros, Milton J. Strosberg, Jonathan Al-Toubah, Taymeyah de Jesus, Victor Hugo F. Durant, Lais Mello, Celso A. Felismino, Tiago C. De Brot, Louise Taboada, Rodrigo G. Donadio, Mauro D. Riechelmann, Rachel P. Ther Adv Med Oncol Advances in Diagnosis and Treatment of Neuroendocrine Neoplasms BACKGROUND: Nearly 30% of neuroendocrine tumors (NETs) have evidence of immunohistochemical (IHC) expression of estrogen (ER) and/or progesterone (PR) receptors. Therefore, targeting ER/PR may offer an effective NET-directed treatment to select patients. METHODS: We conducted a multicenter Simon two-stage single-arm phase II trial of tamoxifen in patients with metastatic, progressive NETs. Eligible patients had positive IHC expression of ER and/or PR ⩾ 1%. Prior therapy with somatostatin analogs was required for progressing/functioning cases. Main exclusion criterion was aggressive disease requiring cytotoxic therapy. The primary end point was disease control rate (DCR) at week 24 by Response Evaluation Criteria in Solid Tumors version 1.1. We planned to enroll 23 patients in the first stage, to reach a DCR at week 24 of 70% (versus 50%); if ⩾12 patients reached the primary end point, a total of 37 would be included. RESULTS: From February 2019 to February 2022, 23 out of 59 patients were eligible and enrolled: 15 (65%) were females; the most common sites were pancreas (11; 48%) and small bowel (6; 26%). In all, 13 patients (56.5%) had G2 NETs. At a median follow-up of 27 months, 13 patients (56.5%) had stable disease at week 24 and median progression-free survival (PFS) was 7.9 months [interquartile range (IQR): 3.7–12.1]. The best response was stable disease in 13 patients, with most patients experiencing minor tumor growth. Median PFS times were not significantly different according to ER/PR < or ⩾30% (p = 0.49) or ER versus PR expression (p = 0.19). One patient experienced grade 2 constipation. CONCLUSION: Tamoxifen for ER-/PR-positive NETs patients is safe but offers modest antitumor effects. TRIAL REGISTRY NAME: Study of Tamoxifen in Well Differentiated Neuroendocrine Tumors and Hormone Receptor Positive Expression (HORMONET). URL: https://clinicaltrials.gov/ct2/show/NCT03870399?term=03870399&draw=2&rank=1 REGISTRATION NUMBER: NCT03870399 SAGE Publications 2023-07-29 /pmc/articles/PMC10387775/ /pubmed/37529158 http://dx.doi.org/10.1177/17588359231186041 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Advances in Diagnosis and Treatment of Neuroendocrine Neoplasms
Barros, Milton J.
Strosberg, Jonathan
Al-Toubah, Taymeyah
de Jesus, Victor Hugo F.
Durant, Lais
Mello, Celso A.
Felismino, Tiago C.
De Brot, Louise
Taboada, Rodrigo G.
Donadio, Mauro D.
Riechelmann, Rachel P.
HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
title HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
title_full HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
title_fullStr HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
title_full_unstemmed HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
title_short HORMONET: a phase II trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
title_sort hormonet: a phase ii trial of tamoxifen for estrogen/progesterone receptor-positive neuroendocrine tumors
topic Advances in Diagnosis and Treatment of Neuroendocrine Neoplasms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387775/
https://www.ncbi.nlm.nih.gov/pubmed/37529158
http://dx.doi.org/10.1177/17588359231186041
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