(Secondary) solid tumors in thyroid cancer patients treated with the multi-kinase inhibitor sorafenib may present

Tatiana C Schneider1,2, Ellen Kapiteijn1, Tom van Wezel2

  • 1Department of Clinical Oncology, Leiden University Medical Center, Leiden, The Netherlands.

BMC Cancer
|January 21, 2016
PubMed
Abstract

Insights

Sorafenib treatment for thyroid cancer may lead to secondary non-cutaneous tumors, potentially causing misdiagnosis. Further research is needed to confirm sorafenib

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Sorafenib is a multikinase tyrosine kinase inhibitor (TKI) targeting BRAF, VEGFR, and RET.
  • It exhibits anti-angiogenic and pro-apoptotic effects in various solid tumors.
  • A known side effect of sorafenib is the development of cutaneous squamous tumors.

Observation:

  • Three patients with advanced, radioactive iodine-refractory papillary thyroid cancer treated with sorafenib developed secondary non-cutaneous lesions.
  • Lesions included squamous cell carcinoma (SCC) of the tongue, lung adenocarcinoma, and cricoid SCC.
  • Further analysis revealed the lung and cricoid tumors were recurrent thyroid cancer.

Findings:

  • Sorafenib may induce metaplasia or clonal divergence in metastatic thyroid cancer.
  • This phenomenon can lead to diagnostic misclassification of recurrent or metastatic disease.
  • Sorafenib may also be implicated in the tumorigenesis of secondary non-cutaneous SCC.

Implications:

  • Clinicians should consider the potential for sorafenib-induced tumor changes and misdiagnosis.
  • The findings suggest a need for careful histopathological evaluation in patients on sorafenib.
  • Larger studies are warranted to confirm sorafenib's role in secondary non-cutaneous tumor development.

Related Concept Videos

Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.9K
Treatment Resistent Cancers02:56

Treatment Resistent Cancers

1.5K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
9.1K