A1 Refereed original research article in a scientific journal

Patient-reported outcomes in the subpopulation of patients with mismatch repair-deficient/microsatellite instability-high primary advanced or recurrent endometrial cancer treated with dostarlimab plus chemotherapy compared with chemotherapy alone in the ENGOT-EN6-NSGO/GOG3031/RUBY trial




AuthorsValabrega, Giorgio; Powell, Matthew A.; Hietanen, Sakari; Miller, Eirwen M.; Novak, Zoltan; Holloway, Robert; Denschlag, Dominik; Myers, Tashanna; Thijs, Anna M.; Pennington, Kathryn P.; Gilbert, Lucy; Fleming, Evelyn; Zub, Oleksandr; Landrum, Lisa M.; Ataseven, Beyhan; Gogoi, Radhika; Podzielinski, Iwona; Cloven, Noelle; Monk, Bradley J.; Sharma, Sudarshan; Herzog, Thomas J.; Stuckey, Ashley; Pothuri, Bhavana; Secord, Angeles Alvarez; Chase, Dana; Vincent, Veena; Meyers, Oren; Garside, Jamie; Mirza, Mansoor Raza; Black, Destin

PublisherBMJ PUBLISHING GROUP

Publishing placeLONDON

Publication year2024

JournalInternational Journal of Gynecological Cancer

Journal acronymINT J GYNECOL CANCER

Number of pages11

ISSN1048-891X

eISSN1525-1438

DOIhttps://doi.org/10.1136/ijgc-2024-005484

Web address https://ijgc.bmj.com/content/early/2024/09/25/ijgc-2024-005484

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/458612764


Abstract

Objective In the ENGOT-EN6-NSGO/GOG3031/RUBY trial, dostarlimab+carboplatin-paclitaxel demonstrated significant improvement in progression free survival and a positive trend in overall survival compared with placebo+carboplatin-paclitaxel, with manageable toxicity, in patients with primary advanced or recurrent endometrial cancer. Here we report on patient-reported outcomes in the mismatch repair-deficient/microsatellite instability-high population, a secondary endpoint in the trial.

Methods Patients were randomized 1:1 to dostarlimab+carboplatin-paclitaxel or placebo+carboplatin-paclitaxel every 3 weeks for 6 cycles followed by dostarlimab or placebo monotherapy every 6 weeks for <= 3 years or until disease progression. Patient-reported outcomes, assessed with the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 and Endometrial Cancer Module, were prespecified secondary endpoints. A mixed model for repeated measures analysis, a prespecified exploratory analysis, was conducted to generate least-squares means to compare between-treatment differences while adjusting for correlations across multiple time points within a patient and controlling for the baseline value. Results are provided with 2-sided, nominal p values.

Results Of 494 patients enrolled, 118 were mismatch repair-deficient/microsatellite instability-high. In this population, mean change from baseline to end of treatment showed visual improvements in global quality of life (QoL), emotional and social function, pain, and back/pelvis pain for dostarlimab+carboplatin-paclitaxel. Meaningful differences (least-squares mean [standard error]) favoring the dostarlimab arm were reported for change from baseline to end of treatment for QoL (14.7 [5.45]; p=0.01), role function (12.7 [5.92]); p=0.03), emotional function (14.3 [4.92]; p<0.01), social function (13.5 [5.43]; p=0.01), and fatigue (-13.3 [5.84]; p=0.03).

Conclusions Patients with mismatch repair-deficient/microsatellite instability-high primary advanced or recurrent endometrial cancer receiving dostarlimab+carboplatin-paclitaxel demonstrated improvements in several QoL domains over patients receiving placebo+carboplatin-paclitaxel. The observed improvements in progression free survival and overall survival while improving or maintaining QoL further supports dostarlimab+carboplatin-paclitaxel as a standard of care in this setting.

Trial registration ClinicalTrials.gov NCT03981796


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Funding information in the publication
This study (NCT03981796) was funded by GSK, Waltham, Massachusetts, USA.


Last updated on 2025-27-01 at 19:25