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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.
Valabrega, 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.
Afiliación
  • Valabrega G; Department of Oncology, Ordine Mauriziano Torino, University of Torino, Torino, Italy giorgio.valabrega@unito.it.
  • Powell MA; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Hietanen S; Department of Obstetrics and Gynecology, Turku University Hospital, Turku, Finland.
  • Miller EM; Division of Gynecologic Oncology, Western Pennsylvania Hospital, Allegheny Health Network, Pittsburgh, Pennsylvania, USA.
  • Novak Z; Department of Gynecology, Hungarian National Institute of Oncology, Budapest, Hungary.
  • Holloway R; AdventHealth Cancer Institute, Orlando, Florida, USA.
  • Denschlag D; Department of Obstetrics and Gynecology, Breast and Gynecologic Oncology Cancer Center, Hochtaunus-Kliniken Bad Homburg, Bad Homburg, Germany.
  • Myers T; Baystate Gynecologic Oncology, Springfield, Massachusetts, USA.
  • Thijs AM; Department of Gynecologic Oncology, Catharina Een Santeon Ziekenhuis, Eindhoven, Netherlands.
  • Pennington KP; University of Washington School of Medicine, Seattle, Washington, USA.
  • Gilbert L; Division of Gynecologic Oncology, McGill University Health Centre, Montreal, Quebec, Canada.
  • Fleming E; The Gerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada.
  • Zub O; Division of Gynecologic Oncology, Billings Clinic, Billings, Montana, USA.
  • Landrum LM; Ilan Bruchim Hillel Yaffe Medical Center, Hadera, Israel.
  • Ataseven B; Division of Gynecology Oncology, Indiana University Health and Simon Cancer Center, Indianapolis, Indiana, USA.
  • Gogoi R; AGO Study Group, Wiesbaden, Germany.
  • Podzielinski I; Evangelische Kliniken Essen-Mitte, Essen, Germany.
  • Cloven N; Medical School and University Medical Center OWL, Klinikum Lippe, Department of Gynecology, Gynecologic Oncology and Obstetrics, Bielefeld University, Detmold, Germany.
  • Monk BJ; Department of Gynecologic Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA.
  • Sharma S; Department of Gynecologic Oncology, Parkview Health, Fort Wayne, Indiana, USA.
  • Herzog TJ; Texas Oncology, Fort Worth, Texas, USA.
  • Stuckey A; GOG Foundation and the Division of Gynecologic Oncology, Florida Cancer Specialists and Research Institute, West Palm Beach, Florida, USA.
  • Pothuri B; Sharma Gynecology Oncology, Hinsdale, Illinois, USA.
  • Secord AA; Department of Obstetrics and Gynecology, University of Cincinnati Cancer Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Chase D; Department of Gynecologic Oncology, Women and Infants Hospital of Rhode Island, Providence, Rhode Island, USA.
  • Vincent V; GOG Foundation and the Departments of Obstetrics/Gynecology and Medicine and Division of Gynecologic Oncology, Laura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, New York, USA.
  • Meyers O; Gynecologic Oncology Program, Duke Cancer Institute, Durham, North Carolina, USA.
  • Garside J; Department of Obstetrics and Gynecology, David Geffen School of Medicine at the University of California Los Angeles, Los Angeles, California, USA.
  • Mirza MR; GSK, Bengaluru, India.
  • Black D; GSK, Collegeville, Pennsylvania, USA.
Int J Gynecol Cancer ; 2024 Sep 25.
Article en En | MEDLINE | ID: mdl-39322611
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 11 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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Int J Gynecol Cancer Asunto de la revista: GINECOLOGIA / NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Int J Gynecol Cancer Asunto de la revista: GINECOLOGIA / NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: Italia