JEMPERLI + CP demonstrates a statistically significant (p<0.0001) and clinically meaningful PFS benefit vs placebo + CP in dMMR/MSI-H primary advanced or recurrent EC1,2
of endometrial cancers are dMMR/MSI-H3
dMMR/MSI-H is an important biomarker that can help to personalise endometrial cancer treatment4
Guidelines recommend testing patients with endometrial cancer for dMMR/MSI-H5,6
Do you have questions about how JEMPERLI can support your patients?
Indications
JEMPERLI is indicated in combination with platinum-containing chemotherapy for the treatment of adult patients with mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) primary advanced or recurrent endometrial cancer (EC) who are candidates for systemic therapy.
JEMPERLI is indicated as monotherapy for the treatment of adult patients with dMMR/MSI-H recurrent or advanced EC that has progressed on or following prior treatment with a platinumcontaining regimen.
Footnotes
CP, carboplatin/paclitaxel; dMMR, mismatch repair deficient; EC, endometrial cancer; MSI-H, microsatellite instability-high.
References
- Jemperli (dostarlimab) Summary of Product Characteristics, Great Britain. Accessed October 2023.
- Mirza MR, et al. Dostarlimab for primary advanced recurrent endometrial cancer. N Eng J Med. 2023;388(23):2145-2158
- Green AK, et al. A review of immune checkpoint blockade therapy in endometrial cancer. Am Soc Clin Oncol Educ Book. 2020;40:1-7
- Song Y, et al. Endometrial tumors with MSI-H and dMMR share a similar tumor immune microenvironment. Onco Targets Ther. 2021;14:4485-4497
- Oaknin A, et al. Endometrial Cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow up. Ann Oncol. 2022;33(9):860-8
- National Institute for Health and Care Excellence. DG42. Testing strategies for Lynch syndrome in people with endometrial cancer. October 2020. Available from https://www.nice.org.uk/guidance/dg42 Accessed October 2023
Adverse events should be reported.
Reporting forms and information can be found at: https://yellowcard.mhra.gov.uk/ (UK) or search for MHRA Yellow Card in the Google Play or Apple App store.
Adverse events should also be reported to GSK Limited on 0800 221 441 or uksafety@gsk.com
© 2022 GSK Group of Companies or its licensor. Trademarks are the property of their respective owners.
January 2023 ӏ PM-GB-DST-WCNT-230013 (V1.0)