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Real-world practice patterns and outcomes for RAI-refractory differentiated thyroid cancer.
Gianoukakis, Andrew G; Choe, Jennifer H; Bowles, Daniel W; Brose, Marcia S; Wirth, Lori J; Owonikoko, Taofeek; Babajanyan, Svetlana; Worden, Francis P.
Affiliation
  • Gianoukakis AG; The Lundquist Institute at Harbor-UCLA Medical Center, David Geffen School of Medicine at UCLA, Torrance, California, USA.
  • Choe JH; Department of Medicine, Duke University Medical Center/Duke Cancer Institute, Durham, North Carolina, USA.
  • Bowles DW; Division of Medical Oncology, University of Colorado, Aurora, Colorado, USA.
  • Brose MS; Department of Otorhinolaryngology: Head and Neck Surgery, Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Wirth LJ; Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Owonikoko T; Winship Cancer Institute of Emory University, Atlanta, Georgia, USA.
  • Babajanyan S; Bayer HealthCare Pharmaceuticals, Whippany, New Jersey, USA.
  • Worden FP; Comprehensive Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.
Eur Thyroid J ; 13(1)2024 Feb 01.
Article in En | MEDLINE | ID: mdl-38096102
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Neoplasms / Adenocarcinoma Limits: Humans Language: En Journal: Eur Thyroid J Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Neoplasms / Adenocarcinoma Limits: Humans Language: En Journal: Eur Thyroid J Year: 2024 Document type: Article