Retsevmo (selpercatinib) vs Exkivity (mobocertinib)

Retsevmo (selpercatinib) vs Exkivity (mobocertinib)

Retsevmo (selpercatinib) and Exkivity (mobocertinib) are both oral medications designed to target specific genetic mutations in cancer cells. Retsevmo is approved for the treatment of certain types of thyroid cancer and non-small cell lung cancer (NSCLC) with RET gene alterations, offering an option for patients with these specific genetic profiles. Exkivity, on the other hand, is approved for the treatment of NSCLC with EGFR Exon20 insertion mutations, providing a tailored therapy for patients with this distinct genetic change. It is essential for patients to undergo genetic testing to determine which medication is appropriate based on the specific mutation present in their cancer.

Difference between Retsevmo and Exkivity

Metric Retsevmo (selpercatinib) Exkivity (mobocertinib)
Generic name Selpercatinib Mobocertinib
Indications For the treatment of adult patients with metastatic RET fusion-positive non-small cell lung cancer (NSCLC), RET-mutant medullary thyroid cancer (MTC), and advanced or metastatic RET fusion-positive thyroid cancer. For the treatment of adult patients with locally advanced or metastatic NSCLC with epidermal growth factor receptor (EGFR) exon 20 insertion mutations.
Mechanism of action RET kinase inhibitor EGFR kinase inhibitor targeting exon 20 insertion mutations
Brand names Retsevmo Exkivity
Administrative route Oral Oral
Side effects Increased AST/ALT, increased blood glucose, decreased white blood cell count, decreased albumin, decreased calcium, dry mouth, diarrhea, increased creatinine, increased alkaline phosphatase, hypertension, fatigue, edema, rash, and constipation. Diarrhea, rash, nausea, stomatitis, vomiting, decreased appetite, paronychia, fatigue, dry skin, decreased weight, and cough.
Contraindications Hypersensitivity to selpercatinib or any of its excipients. Hypersensitivity to mobocertinib or any of its excipients.
Drug class Kinase inhibitor Kinase inhibitor
Manufacturer Eli Lilly and Company Takeda Pharmaceutical Company

Efficacy

Efficacy of Retsevmo (selpercatinib) in Lung Cancer

Retsevmo (selpercatinib) is a medication specifically approved for the treatment of non-small cell lung cancer (NSCLC) with a rearranged during transfection (RET) gene fusion, which is a less common driver mutation in lung cancer. Clinical trials have demonstrated significant efficacy of selpercatinib in patients with RET fusion-positive NSCLC. In a phase 1/2 trial, the overall response rate (ORR) was found to be approximately 64% among previously treated patients, and the median duration of response (DoR) was not reached, indicating sustained effectiveness. In treatment-naive patients, the ORR was even higher, reaching around 85%, showcasing selpercatinib's potential as a first-line treatment option for RET fusion-positive NSCLC.

Efficacy of Exkivity (mobocertinib) in Lung Cancer

Exkivity (mobocertinib) is an oral medication designed to target and inhibit epidermal growth factor receptor (EGFR) exon 20 insertion mutations in NSCLC. This mutation is associated with a subset of non-small cell lung cancers and has historically been challenging to treat with conventional EGFR inhibitors. In a pivotal phase 1/2 trial, mobocertinib demonstrated an ORR of 28% in patients with EGFR exon 20 insertion-positive metastatic NSCLC who had been previously treated with platinum-based chemotherapy. The median DoR was 17.5 months, indicating a durable response in a population with limited treatment options.

Both Retsevmo and Exkivity represent a significant advancement in the targeted therapy landscape for lung cancer, offering new avenues of treatment for patients with specific genetic alterations. Their approval by regulatory agencies is based on the positive outcomes from clinical trials, which highlight their efficacy in shrinking tumors and, in some cases, providing long-lasting responses. These therapies underscore the importance of genetic testing in NSCLC to identify appropriate candidates who may benefit from such targeted treatments.

While both medications have shown promise in their respective patient populations, it is essential to note that individual responses to treatment can vary. Ongoing research and post-marketing surveillance continue to provide additional data on the long-term efficacy and safety profiles of Retsevmo and Exkivity. Healthcare providers consider these factors, along with patient-specific characteristics, when determining the best treatment approach for lung cancer patients with these genetic alterations.

Regulatory Agency Approvals

Retsevmo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Exkivity
  • Food and Drug Administration (FDA), USA

Access Retsevmo or Exkivity today

If Retsevmo or Exkivity are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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