Eric J. Sherman, MD, on Agents for Treating RET Fusion–Positive Thyroid Cancer

Video

Eric J. Sherman, MD, highlights several drugs that are being used to treat RET-positive thyroid cancer.

At the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting, CancerNetwork® sat down with Eric J. Sherman, MD, a medical oncologist at Memorial Sloan Kettering Cancer Center, who spotlighted agents that are currently used for the treatment of RET fusion–positive thyroid cancer. Although only a subset of patients with papillary thyroid cancer have disease that is driven by RET fusions, over half of all patients with medullary disease have RET mutations. Due to this, RET is believed to play an important role in the treatment of thyroid cancer

Transcript:

One of the things that we knew about for a long time is that a subset of thyroid cancers are driven by RET fusion genes [in papillary disease]. For medullary [disease], on other hand, probably about 55% or 60% are driven by RET mutations, either hereditary or somatic. We know RET plays a very important role in the treatment of thyroid cancers. A lot of the treatments that started out for medullary thyroid cancer were really based on the fact that certain drugs like cabozantinib [Cabometyx] and vandetanib [Caprelsa] targeted RET. Because of that, although these drugs hit many different targets, pretty good activity was seen and both vandetanib and cabozantinib got FDA approvals. [However], other drugs like sunitinib [Sutent], pazopanib [Votrient], and lenvatinib [Lenvima] were also shown to have reasonable activity, although they never went through randomized phase 3 studies.

Reference

Sherman EJ, Wirth LJ, Shah MH, et al. Selpercatinib efficacy and safety in patients with RET-altered thyroid cancer: a clinical trial update. J Clin Oncol. 2021;39(suppl 15):6073. doi:10.1200/JCO.2021.39.15_suppl.6073

Recent Videos
Jose Sandoval Sus, MD, discussed standard CAR T-cell therapies in patients across multiple high-risk lymphoma indications.
Elucidating nonresponses to bispecific T-cell engagers may be an important research consideration in the multiple myeloma field.
Barriers to access and financial toxicities are challenges that must be addressed for CAR T-cell therapies in LBCL, according to Jose Sandoval Sus, MD.
Fixed treatment durations with bispecific antibodies followed by observation may help in mitigating infection-related AEs, according to Shebli Atrash, MD.
Shebli Atrash, MD, stated that MRD should be considered carefully as an end point, given potential recurrence despite MRD negativity.
Data from the phase 3 DeLLphi-304 trial at ASCO 2025 revealed a survival advantage with tarlatamab vs chemotherapy in second-line ES-SCLC.
The FDA approval of tarlatamab in SCLC has received much press attention, according to Daniel R. Carrizosa, MD, MS.
The National ICE-T Conference may inspire future collaboration between community and academic oncologists in the management of different cancers.
One of the largest obstacles to tackle in the kidney cancer landscape will be translating the research on rare kidney cancer subtypes into clinical trials.
Long-term toxicities like infections and secondary primary malignancies remain a concern when sequencing novel agents for those with multiple myeloma.
Related Content