Enhancing radioiodine incorporation into radioiodine-refractory thyroid cancer with MAPK inhibition (ERRITI): A single-center prospective two-arm study Journal Article


Authors: Weber, M.; Kersting, D.; Riemann, B.; Brandenburg, T.; Führer-Sakel, D.; Grünwald, F.; Kreissl, M. C.; Dralle, H.; Weber, F.; Schmid, K. W.; Herrmann, K.; Jentzen, W.; Grafe, H.; Rischpler, C.; Theurer, S.; Bockisch, A.; Nagarajah, J.; Fendler, W. P.
Article Title: Enhancing radioiodine incorporation into radioiodine-refractory thyroid cancer with MAPK inhibition (ERRITI): A single-center prospective two-arm study
Abstract: 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 BRAFV600E-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 123I-scintigraphy. In case of restored radioiodine uptake, 124I-guided 131I 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 131I 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 (SUVpeak) < 10 on 2[18F]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 131I 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. ©2022 The Authors; Published by the American Association for Cancer Research.
Keywords: genetics; prospective study; prospective studies; protein kinase inhibitor; protein kinase inhibitors; radioactive iodine; iodine radioisotopes; fluorodeoxyglucose f 18; fluorodeoxyglucose f18; thyroid neoplasms; thyroglobulin; b raf kinase; thyroid tumor; proto-oncogene proteins b-raf; iodine-124; iodine-131; humans; human
Journal Title: Clinical Cancer Research
Volume: 28
Issue: 19
ISSN: 1078-0432
Publisher: American Association for Cancer Research  
Date Published: 2022-10-01
Start Page: 4194
End Page: 4202
Language: English
DOI: 10.1158/1078-0432.Ccr-22-0437
PUBMED: 35594174
PROVIDER: scopus
PMCID: PMC9527501
DOI/URL:
Notes: Editorial -- Export Date: 1 November 2022 -- Source: Scopus
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