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

Author:

Weber Manuel12ORCID,Kersting David12ORCID,Riemann Burkhard3,Brandenburg Tim24,Führer-Sakel Dagmar24,Grünwald Frank5,Kreissl Michael C.6ORCID,Dralle Henning7,Weber Frank7,Schmid Kurt Werner8,Herrmann Ken12,Jentzen Walter12,Grafe Hong12,Rischpler Christoph12ORCID,Theurer Sarah8,Bockisch Andreas12,Nagarajah James910ORCID,Fendler Wolfgang P.12

Affiliation:

1. 1Clinic for Nuclear Medicine, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

2. 2German Cancer Consortium (DKTK) partner site Essen, Essen, Germany.

3. 3Department of Nuclear Medicine, University Hospital Münster, Münster, Germany.

4. 4Department of Endocrinology and Metabolism, Division of Laboratory Research, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

5. 5Department of Nuclear Medicine, University Hospital Frankfurt, Frankfurt, Germany.

6. 6Clinic of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.

7. 7Department of General, Visceral and Transplantation Surgery, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

8. 8Institute of Pathology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

9. 9Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.

10. 10Department of Medical Imaging, Radboud University Medical Center, Nijmegen, Netherlands.

Abstract

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

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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