2024
Long-term follow-up of efficacy and safety of selinexor maintenance treatment in patients with TP53wt advanced or recurrent endometrial cancer: A subgroup analysis of the ENGOT-EN5/GOG-3055/SIENDO study
MAKKER, Vicky, Jose Alejandro PEREZ-FIDALGO, Giorgio VALABREGA, Erika HAMILTON, Toon Van GORP et. al.Základní údaje
Originální název
Long-term follow-up of efficacy and safety of selinexor maintenance treatment in patients with TP53wt advanced or recurrent endometrial cancer: A subgroup analysis of the ENGOT-EN5/GOG-3055/SIENDO study
Autoři
MAKKER, Vicky, Jose Alejandro PEREZ-FIDALGO, Giorgio VALABREGA, Erika HAMILTON, Toon Van GORP, Jalid SEHOULI, Klaudia REGINÁČOVÁ, Debra L RICHARDSON, Tamar PERRI, Amit M OZA, David S MILLER, Eva Maria Guerra ALÍA, Ugo De GIORGI, Stephanie HENRY, Daniel L SPITZ, Pauline WIMBERGER, Markéta BEDNAŘÍKOVÁ (203 Česká republika, domácí), Hye Sook CHON, Jerónimo MARTÍNEZ-GARCIA, Carmela PISANO, Jonathan S BEREK, Ignacio ROMERO, Giovanni SCAMBIA, Lorena FARIÑAS-MADRID, Joseph BUSCEMA, Fabienne SCHOCHTER, Kai LI, Pratheek KALYANAPU, Christopher J WALKER a Ignace VERGOTE
Vydání
Gynecologic Oncology, SAN DIEGO, ACADEMIC PRESS INC ELSEVIER SCIENCE, 2024, 0090-8258
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30214 Obstetrics and gynaecology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.700 v roce 2022
Organizační jednotka
Lékařská fakulta
UT WoS
001257369900001
Klíčová slova anglicky
Cancer biomarker; Endometrial neoplasm; Exportin 1 proteinp; 53 tumor-suppressor protein
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 12. 7. 2024 13:22, Mgr. Tereza Miškechová
Anotace
V originále
Objective To report long-term efficacy and safety of selinexor maintenance therapy in adults with TP53 wild-type (TP53wt) stage IV or recurrent endometrial cancer (EC) who achieved partial remission (PR) or complete remission (CR) following chemotherapy. Methods Analysis of the prespecified, exploratory subgroup of patients with TP53wt EC from the phase 3 SIENDO study was performed. Progression-free survival (PFS) benefit in patients with TP53wt EC and across other patient subgroups were exploratory endpoints. Safety and tolerability were also assessed. Results Of the 263 patients enrolled in the SIENDO trial, 113 patients had TP53wt EC; 70/113 (61.9%) had TP53wt/proficient mismatch repair (pMMR) EC, and 29/113 (25.7%) had TP53wt/deficient mismatch repair (dMMR) EC. As of April 1, 2024, the median PFS (mPFS) for TP53wt patients who received selinexor compared with placebo was 28.4 versus 5.2 months (36.8-month follow-up, HR 0.44; 95% CI 0.27–0.73). A benefit in mPFS was seen with selinexor versus placebo regardless of MMR status (patients with TP53wt/pMMR EC: 39.5 vs 4.9 months, HR 0.36; 95% CI 0.19–0.71; patients with TP53wt/dMMR EC: 13.1 vs 3.7 months, HR 0.49; 95% CI 0.18–1.34). Selinexor treatment was generally manageable, with no new safety signals identified. Conclusion In the phase 3 SIENDO study, selinexor maintenance therapy showed a promising efficacy signal and a manageable safety profile in the prespecified subgroup of patients with TP53wt EC who achieved a PR or CR following chemotherapy.