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Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study

PURPOSE: Restoration of iodine incorporation (redifferentiation) by MAPK inhibition was achieved in previously radioiodine-refractory, unresectable thyroid carcinoma (RR-TC). However, results were unsatisfactory in BRAF(V600E)-mutant (BRAF-MUT) RR-TC. Here we assess safety and efficacy of redifferen...

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Autores principales: Weber, Manuel, Kersting, David, Riemann, Burkhard, Brandenburg, Tim, Führer-Sakel, Dagmar, Grünwald, Frank, Kreissl, Michael C., Dralle, Henning, Weber, Frank, Schmid, Kurt Werner, Herrmann, Ken, Jentzen, Walter, Grafe, Hong, Rischpler, Christoph, Theurer, Sarah, Bockisch, Andreas, Nagarajah, James, Fendler, Wolfgang P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527501/
https://www.ncbi.nlm.nih.gov/pubmed/35594174
http://dx.doi.org/10.1158/1078-0432.CCR-22-0437
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author Weber, Manuel
Kersting, David
Riemann, Burkhard
Brandenburg, Tim
Führer-Sakel, Dagmar
Grünwald, Frank
Kreissl, Michael C.
Dralle, Henning
Weber, Frank
Schmid, Kurt Werner
Herrmann, Ken
Jentzen, Walter
Grafe, Hong
Rischpler, Christoph
Theurer, Sarah
Bockisch, Andreas
Nagarajah, James
Fendler, Wolfgang P.
author_facet Weber, Manuel
Kersting, David
Riemann, Burkhard
Brandenburg, Tim
Führer-Sakel, Dagmar
Grünwald, Frank
Kreissl, Michael C.
Dralle, Henning
Weber, Frank
Schmid, Kurt Werner
Herrmann, Ken
Jentzen, Walter
Grafe, Hong
Rischpler, Christoph
Theurer, Sarah
Bockisch, Andreas
Nagarajah, James
Fendler, Wolfgang P.
author_sort Weber, Manuel
collection PubMed
description PURPOSE: Restoration of iodine incorporation (redifferentiation) by MAPK inhibition was achieved in previously radioiodine-refractory, unresectable thyroid carcinoma (RR-TC). However, results were unsatisfactory in BRAF(V600E)-mutant (BRAF-MUT) RR-TC. Here we assess safety and efficacy of redifferentiation therapy through genotype-guided MAPK-modulation in patients with BRAF-MUT or wildtype (BRAF-WT) RR-TC. PATIENTS AND METHODS: In this prospective single-center, two-arm phase II study, patients received trametinib (BRAF-WT) or trametinib + dabrafenib (BRAF-MUT) for 21 ± 3 days. Redifferentiation was assessed by (123)I-scintigraphy. In case of restored radioiodine uptake, (124)I-guided (131)I therapy was performed. Primary endpoint was the redifferentiation rate. Secondary endpoints were treatment response (thyroglobulin, RECIST 1.1) and safety. Parameters predicting successful redifferentiation were assessed using a receiver operating characteristic analysis and Youden J statistic. RESULTS: Redifferentiation was achieved in 7 of 20 (35%) patients, 2 of 6 (33%) in the BRAF-MUT and 5 of 14 (36%) in the BRAF-WT arm. Patients received a mean (range) activity of 300.0 (273.0–421.6) mCi for (131)I therapy. Any thyroglobulin decline was seen in 57% (4/7) of the patients, RECIST 1.1 stable/partial response/progressive disease in 71% (5/7)/14% (1/7)/14% (1/7). Peak standardized uptake value (SUV(peak)) < 10 on 2[(18)F]fluoro-2-deoxy-D-glucose (FDG)-PET was associated with successful redifferentiation (P = 0.01). Transient pyrexia (grade 3) and rash (grade 4) were noted in one patient each. CONCLUSIONS: Genotype-guided MAPK inhibition was safe and resulted in successful redifferentiation in about one third of patients in each arm. Subsequent (131)I therapy led to a thyroglobulin (Tg) decline in more than half of the treated patients. Low tumor glycolytic rate as assessed by FDG-PET is predictive of redifferentiation success. See related commentary by Cabanillas et al., p. 4164
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spelling pubmed-95275012023-01-05 Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study Weber, Manuel Kersting, David Riemann, Burkhard Brandenburg, Tim Führer-Sakel, Dagmar Grünwald, Frank Kreissl, Michael C. Dralle, Henning Weber, Frank Schmid, Kurt Werner Herrmann, Ken Jentzen, Walter Grafe, Hong Rischpler, Christoph Theurer, Sarah Bockisch, Andreas Nagarajah, James Fendler, Wolfgang P. Clin Cancer Res Clinical Trials: Targeted Therapy PURPOSE: Restoration of iodine incorporation (redifferentiation) by MAPK inhibition was achieved in previously radioiodine-refractory, unresectable thyroid carcinoma (RR-TC). However, results were unsatisfactory in BRAF(V600E)-mutant (BRAF-MUT) RR-TC. Here we assess safety and efficacy of redifferentiation therapy through genotype-guided MAPK-modulation in patients with BRAF-MUT or wildtype (BRAF-WT) RR-TC. PATIENTS AND METHODS: In this prospective single-center, two-arm phase II study, patients received trametinib (BRAF-WT) or trametinib + dabrafenib (BRAF-MUT) for 21 ± 3 days. Redifferentiation was assessed by (123)I-scintigraphy. In case of restored radioiodine uptake, (124)I-guided (131)I therapy was performed. Primary endpoint was the redifferentiation rate. Secondary endpoints were treatment response (thyroglobulin, RECIST 1.1) and safety. Parameters predicting successful redifferentiation were assessed using a receiver operating characteristic analysis and Youden J statistic. RESULTS: Redifferentiation was achieved in 7 of 20 (35%) patients, 2 of 6 (33%) in the BRAF-MUT and 5 of 14 (36%) in the BRAF-WT arm. Patients received a mean (range) activity of 300.0 (273.0–421.6) mCi for (131)I therapy. Any thyroglobulin decline was seen in 57% (4/7) of the patients, RECIST 1.1 stable/partial response/progressive disease in 71% (5/7)/14% (1/7)/14% (1/7). Peak standardized uptake value (SUV(peak)) < 10 on 2[(18)F]fluoro-2-deoxy-D-glucose (FDG)-PET was associated with successful redifferentiation (P = 0.01). Transient pyrexia (grade 3) and rash (grade 4) were noted in one patient each. CONCLUSIONS: Genotype-guided MAPK inhibition was safe and resulted in successful redifferentiation in about one third of patients in each arm. Subsequent (131)I therapy led to a thyroglobulin (Tg) decline in more than half of the treated patients. Low tumor glycolytic rate as assessed by FDG-PET is predictive of redifferentiation success. See related commentary by Cabanillas et al., p. 4164 American Association for Cancer Research 2022-10-03 2022-05-20 /pmc/articles/PMC9527501/ /pubmed/35594174 http://dx.doi.org/10.1158/1078-0432.CCR-22-0437 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
spellingShingle Clinical Trials: Targeted Therapy
Weber, Manuel
Kersting, David
Riemann, Burkhard
Brandenburg, Tim
Führer-Sakel, Dagmar
Grünwald, Frank
Kreissl, Michael C.
Dralle, Henning
Weber, Frank
Schmid, Kurt Werner
Herrmann, Ken
Jentzen, Walter
Grafe, Hong
Rischpler, Christoph
Theurer, Sarah
Bockisch, Andreas
Nagarajah, James
Fendler, Wolfgang P.
Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study
title Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study
title_full Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study
title_fullStr Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study
title_full_unstemmed Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study
title_short Enhancing Radioiodine Incorporation into Radioiodine-Refractory Thyroid Cancer with MAPK Inhibition (ERRITI): A Single-Center Prospective Two-Arm Study
title_sort enhancing radioiodine incorporation into radioiodine-refractory thyroid cancer with mapk inhibition (erriti): a single-center prospective two-arm study
topic Clinical Trials: Targeted Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527501/
https://www.ncbi.nlm.nih.gov/pubmed/35594174
http://dx.doi.org/10.1158/1078-0432.CCR-22-0437
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