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Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
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Capmatinib successfully overcomes tepotinib-induced intolerable peripheral edema.

Kei Kunimasa1, Takahisa Kawamura1, Motohiro Tamiya1

  • 1Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.

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|October 25, 2021
PubMed
Summary

Tepotinib caused severe peripheral edema, but switching to capmatinib allowed continued treatment for metastatic non-small cell lung cancer with MET exon 14 skipping. This case highlights differing side effect profiles of MET inhibitors.

Keywords:
MET ex.14 skippingcapmatinibperipheral edematepotinib

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Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Capmatinib and tepotinib are FDA-approved MET inhibitors for metastatic non-small cell lung cancer (NSCLC) with MET exon 14 skipping.
  • Peripheral edema is a common adverse event associated with both capmatinib and tepotinib treatment.

Observation:

  • A patient experienced intolerable peripheral edema while receiving tepotinib.
  • The patient was successfully switched to capmatinib, allowing for continued treatment of their metastatic NSCLC.

Findings:

  • This case report is the first to demonstrate differential effects of two MET inhibitors, tepotinib and capmatinib, on the development of peripheral edema.
  • Switching between these MET inhibitors may be a viable strategy to manage treatment-related peripheral edema.

Implications:

  • This finding suggests that individual patient tolerance to specific MET inhibitors can vary regarding peripheral edema.
  • Management strategies for peripheral edema in patients receiving MET inhibitors may involve drug switching.
  • Further research is warranted to understand the mechanisms behind differential peripheral edema development and to establish unified management guidelines.