Therapeutic advances in anaplastic thyroid cancer: a current perspective.
Shikha SainiKiara TullaAjay V MakerKenneth D BurmanBellur S PrabhakarPublished in: Molecular cancer (2018)
Thyroid cancer incidence is increasing at an alarming rate, almost tripling every decade. In 2017, it was the fifth most common cancer in women. Although the majority of thyroid tumors are curable, about 2-3% of thyroid cancers are refractory to standard treatments. These undifferentiated, highly aggressive and mostly chemo-resistant tumors are phenotypically-termed anaplastic thyroid cancer (ATC). ATCs are resistant to standard therapies and are extremely difficult to manage. In this review, we provide the information related to current and recently emerged first-line systemic therapy (Dabrafenib and Trametinib) along with promising therapeutics which are in clinical trials and may be incorporated into clinical practice in the future. Different categories of promising therapeutics such as Aurora kinase inhibitors, multi-kinase inhibitors, epigenetic modulators, gene therapy using oncolytic viruses, apoptosis-inducing agents, and immunotherapy are reviewed. Combination treatment options that showed synergistic and antagonistic effects are also discussed. We highlight ongoing clinical trials in ATC and discuss how personalized medicine is crucial to design the second line of treatment. Besides using conventional combination therapy, embracing a personalized approach based on advanced genomics and proteomics assessment will be crucial to developing a tailored treatment plan to improve the chances of clinical success.
Keyphrases
- combination therapy
- clinical trial
- gene therapy
- small molecule
- clinical practice
- gene expression
- oxidative stress
- dna methylation
- cancer therapy
- randomized controlled trial
- radiation therapy
- cell death
- risk factors
- type diabetes
- metabolic syndrome
- mass spectrometry
- young adults
- smoking cessation
- pregnant women
- cell proliferation
- bone marrow
- phase ii
- single cell
- locally advanced
- skeletal muscle
- open label
- pregnancy outcomes
- study protocol
- cell cycle arrest
- label free
- lymph node metastasis
- pi k akt