Real-world practice patterns and outcomes for RAI-refractory differentiated thyroid cancer

Author:

Gianoukakis Andrew G1ORCID,Choe Jennifer H2,Bowles Daniel W3,Brose Marcia S4,Wirth Lori J5,Owonikoko Taofeek6,Babajanyan Svetlana7,Worden Francis P8

Affiliation:

1. The Lundquist Institute at Harbor-UCLA Medical Center, David Geffen School of Medicine at UCLA, Torrance, California, USA

2. Department of Medicine, Duke University Medical Center/Duke Cancer Institute, Durham, North Carolina, USA

3. Division of Medical Oncology, University of Colorado, Aurora, Colorado, USA

4. Department of Otorhinolaryngology: Head and Neck Surgery, Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania, USA

5. Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, USA

6. Winship Cancer Institute of Emory University, Atlanta, Georgia, USA

7. Bayer HealthCare Pharmaceuticals, Whippany, New Jersey, USA

8. Comprehensive Cancer Center, University of Michigan, Ann Arbor, Michigan, USA

Abstract

Background The optimal timing for initiating multi-kinase inhibitors (MKIs) in patients with radioactive iodine-refractory (RAI-R) differentiated thyroid cancer (DTC) remains unclear. Thus, we evaluated the real-world practice patterns and outcomes in asymptomatic patients with progressive RAI-R DTC (≥1 lesion ≥1 cm in diameter) in the USA (US population) and outside the USA (non-US population). Methods In this prospective, non-interventional, open-label study, eligible patients were chosen by treating physicians to receive MKI therapy (cohort 1) or undergo active surveillance (cohort 2) at study entry. Cohort 2 patients were allowed to transition to MKI therapy later. The primary endpoint was time to symptomatic progression (TTSP) from study entry. Data were compared descriptively. When endpoints were inestimable, 36-month rates were calculated. Results Of the 647 patients, 478 underwent active surveillance (cohort 2) and 169 received MKI treatment (cohort 1). Patients underwent surveillance at a higher rate in the US (92.6%) vs the non-US (66.9%) populations. Half of US and non-US patients who qualified for MKI treatment had initial American Thyroid Association (ATA) low-to-intermediate-risk disease. In cohort 2, the 36-month TTSP rates from study entry were 65.6% and 66.5% in the US and non-US populations, respectively. Cohort 2 patients treated later demonstrated 36-month TTSP rates of 30.8% and 55.8% in the US and non-US populations, respectively. Conclusions Active surveillance is a viable option for asymptomatic patients with progressive RAI-R DTC. However, early intervention with MKI therapy may be more suitable for others. Further research is needed to identify patients who are optimal for active surveillance. Registration NCT02303444.

Publisher

Bioscientifica

Subject

Endocrinology, Diabetes and Metabolism

Reference13 articles.

1. SEER cancer statistics review;Howlader,2020

2. Treatment strategies for radioactive iodine-refractory differentiated thyroid cancer;Worden,2014

3. Long-term outcome of 444 patients with distant metastases from papillary and follicular thyroid carcinoma: benefits and limits of radioiodine therapy;Durante,2006

4. Lenvatinib versus placebo in radioiodine-refractory thyroid cancer;Schlumberger,2015

5. Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial;Brose,2014

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