Jemperli (dostarlimab) vs Tivdak (tisotumab vedotin-tftv)

Jemperli (dostarlimab) vs Tivdak (tisotumab vedotin-tftv)

Jemperli (dostarlimab) is a PD-1 blocking antibody indicated for patients with mismatch repair-deficient (dMMR) recurrent or advanced endometrial cancer, as well as for other solid tumors with dMMR or high microsatellite instability (MSI-H) after prior treatment. Tivdak (tisotumab vedotin-tftv) is an antibody-drug conjugate targeted against tissue factor, approved for the treatment of recurrent or metastatic cervical cancer in patients who have undergone chemotherapy. The choice between Jemperli and Tivdak would depend on the specific type of cancer a patient has, its molecular profile, previous treatments, and the safety profile of each medication, which should be discussed with a healthcare provider.

Difference between Jemperli and Tivdak

Metric Jemperli (dostarlimab) Tivdak (tisotumab vedotin-tftv)
Generic name Dostarlimab Tisotumab vedotin-tftv
Indications Endometrial cancer, solid tumors with dMMR or MSI-H Recurrent or metastatic cervical cancer
Mechanism of action PD-1 blocking antibody Antibody-drug conjugate targeting tissue factor
Brand names Jemperli Tivdak
Administrative route Intravenous Intravenous
Side effects Fatigue, anemia, diarrhea, etc. Peripheral neuropathy, nausea, fatigue, etc.
Contraindications None known None known
Drug class Immune checkpoint inhibitor Antibody-drug conjugate
Manufacturer GlaxoSmithKline Seagen Inc. and Genmab

Efficacy

Efficacy of Jemperli (dostarlimab) in Gynecological Cancer

Jemperli (dostarlimab) is an anti-PD-1 monoclonal antibody used in the treatment of gynecological cancers, specifically for endometrial cancer. It has been approved for patients with mismatch repair deficient (dMMR) recurrent or advanced endometrial cancer that has progressed on or following prior treatment with a platinum-containing regimen. Clinical trials have demonstrated its efficacy in this patient population, with a significant proportion of patients achieving partial or complete responses to the therapy. The overall response rate and duration of response have been key metrics in assessing Jemperli's efficacy, indicating potential benefits for patients with limited treatment options.

Efficacy of Tivdak (tisotumab vedotin-tftv) in Gynecological Cancer

Tivdak (tisotumab vedotin-tftv) is a first-in-class antibody-drug conjugate targeting tissue factor, which is commonly expressed in various types of solid tumors, including gynecological cancers. It has been specifically approved for the treatment of recurrent or metastatic cervical cancer in patients who have progressed on or after chemotherapy. Clinical studies have shown that Tivdak can induce responses in a subset of patients with cervical cancer, with some patients experiencing a reduction in tumor size. The efficacy of Tivdak in this setting provides an important option for patients who have historically had very limited treatment choices.

Comparative Efficacy in Gynecological Cancers

While both Jemperli and Tivdak represent advances in the treatment of gynecological cancers, their efficacy must be understood within the context of the specific cancer types and patient populations they are approved to treat. Jemperli's efficacy has been demonstrated in endometrial cancer with dMMR, while Tivdak's efficacy has been shown in cervical cancer. Direct comparison of their efficacy is not straightforward due to differences in their mechanisms of action, the specific gynecological cancers they target, and the patient populations studied in clinical trials.

Conclusion

In conclusion, both Jemperli (dostarlimab) and Tivdak (tisotumab vedotin-tftv) have shown efficacy in treating certain types of gynecological cancers, offering hope to patients with these difficult-to-treat diseases. Jemperli has been effective for patients with dMMR endometrial cancer, while Tivdak has shown promise for patients with recurrent or metastatic cervical cancer. These therapies are important additions to the oncology arsenal, providing targeted treatment options that can lead to meaningful clinical outcomes for patients affected by these specific gynecological malignancies.

Regulatory Agency Approvals

Jemperli
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Tivdak
  • Food and Drug Administration (FDA), USA

Access Jemperli or Tivdak today

If Jemperli or Tivdak 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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