Cyramza (ramucirumab) vs Retsevmo (selpercatinib)

Cyramza (ramucirumab) vs Retsevmo (selpercatinib)

Cyramza (ramucirumab) and Retsevmo (selpercatinib) are targeted therapies used to treat different types of cancer, but their mechanisms of action and indications vary. Cyramza is a vascular endothelial growth factor (VEGF) receptor 2 antagonist, which can inhibit tumor angiogenesis and is approved for use in certain types of gastric, colorectal, lung, and liver cancers. In contrast, Retsevmo is a selective RET kinase inhibitor indicated for the treatment of specific thyroid cancers and non-small cell lung cancer (NSCLC) with RET gene alterations, making it essential for patients to have their tumor's genetic profile assessed to determine if Retsevmo is an appropriate treatment option.

Difference between Cyramza and Retsevmo

Metric Cyramza (ramucirumab) Retsevmo (selpercatinib)
Generic name ramucirumab selpercatinib
Indications Gastric cancer, non-small cell lung cancer, colorectal cancer, and hepatocellular carcinoma RET-altered thyroid cancers and non-small cell lung cancer
Mechanism of action Angiogenesis inhibitor by VEGFR-2 antagonism Kinase inhibitor targeting RET alterations
Brand names Cyramza Retsevmo
Administrative route Intravenous Oral
Side effects Hypertension, diarrhea, headache, and hematological abnormalities Increased liver enzymes, hypertension, dry mouth, diarrhea, and QT interval prolongation
Contraindications Hypersensitivity to ramucirumab or any component of the formulation Hypersensitivity to selpercatinib or any component of the formulation, QT prolongation
Drug class Monoclonal antibody, angiogenesis inhibitor Kinase inhibitor
Manufacturer Eli Lilly and Company Eli Lilly and Company

Efficacy

Cyramza (Ramucirumab) Efficacy in Lung Cancer

Cyramza (ramucirumab) is a vascular endothelial growth factor (VEGF) Receptor 2 antagonist that has been approved for use in the treatment of non-small cell lung cancer (NSCLC) in combination with docetaxel, after prior platinum-based chemotherapy has failed. Clinical trials have demonstrated that Cyramza, when added to docetaxel, can lead to an improvement in overall survival compared to docetaxel alone in patients with advanced or metastatic NSCLC. The REVEL trial, a pivotal phase III study, showed that patients receiving Cyramza plus docetaxel had a median overall survival of 10.5 months compared to 9.1 months in the placebo plus docetaxel group, which was statistically significant.

Furthermore, Cyramza has shown efficacy in increasing progression-free survival (PFS) and improving the objective response rate (ORR) in the same patient population. The REVEL trial reported a median PFS of 4.5 months with Cyramza plus docetaxel versus 3.0 months with placebo plus docetaxel. The ORR was also higher in the Cyramza group at 23% compared to 14% in the placebo group. These results support the use of Cyramza in combination with docetaxel for the second-line treatment of patients with NSCLC.

Retsevmo (Selpercatinib) Efficacy in Lung Cancer

Retsevmo (selpercatinib) is a selective RET kinase inhibitor approved for the treatment of adult patients with metastatic RET fusion-positive non-small cell lung cancer (NSCLC). Selpercatinib has shown significant efficacy in patients with RET fusion-positive NSCLC who are treatment-naive or have been previously treated with platinum chemotherapy. The LIBRETTO-001 trial, a multi-cohort, open-label, phase 1/2 study, demonstrated a robust response to selpercatinib in this patient population. The trial reported an ORR of 64% in previously treated patients and 85% in treatment-naive patients, indicating a high level of activity against RET-driven tumors.

In addition to high response rates, selpercatinib has also been associated with a durable response. The LIBRETTO-001 trial showed that the median duration of response (DoR) was not reached at the time of data cut-off, suggesting that the responses are long-lasting. Moreover, selpercatinib was effective in controlling brain metastases, which is a common and challenging complication in lung cancer. The intracranial ORR for patients with measurable brain metastases was 91%, highlighting the potential of selpercatinib to manage central nervous system involvement in RET fusion-positive NSCLC.

Regulatory Agency Approvals

Cyramza
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Retsevmo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Cyramza or Retsevmo today

If Cyramza or Retsevmo 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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