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A Surgical Window Trial Evaluating Medroxyprogesterone Acetate with or without Entinostat in Patients with Endometrial Cancer and Validation of Biomarkers of Cellular Response.
Duska, Linda R; Filiaci, Virginia L; Walker, Joan L; Holman, Laura L; Hill, Emily K; Moore, Richard G; Ring, Kari L; Pearl, Michael L; Muller, Carolyn Y; Kushnir, Christina L; Lankes, Heather A; Samuelson, Megan I; Carrick, Kelley S; Rajan, Anand; Rodgers, William H; Kohn, Elise C; Piekarz, Richard; Leslie, Kimberly K.
Afiliação
  • Duska LR; Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, University of Virginia School of Medicine, Charlottesville, Virginia. lduska@virginia.edu.
  • Filiaci VL; NRG Oncology SDMC, CTD Division, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
  • Walker JL; Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Holman LL; Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Hill EK; Department of Obstetrics and Gynecology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Moore RG; Department of Obstetrics and Gynecology, Wilmont Cancer Institute, University of Rochester Medical Center, Rochester, New York.
  • Ring KL; Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, University of Virginia School of Medicine, Charlottesville, Virginia.
  • Pearl ML; Department of Obstetrics, Gynecology and Reproductive Medicine, Division of Gynecologic Oncology, Stony Brook University Medical Center, Stony Brook, New York.
  • Muller CY; Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, University of New Mexico, Albuquerque, New Mexico.
  • Kushnir CL; Department of Obstetrics and Gynecology, Women's Cancer Center, Las Vegas, Nevada.
  • Lankes HA; NRG Oncology, Operations Center-Philadelphia East, Philadelphia, Pennsylvania.
  • Samuelson MI; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
  • Carrick KS; Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Rajan A; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Rodgers WH; Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Kohn EC; Department of Pathology, New York Hospital Queens, Weill Medical College of Cornell University, Flushing, New York.
  • Piekarz R; Cancer Therapy Evaluation Program, NCI, Rockville, Maryland.
  • Leslie KK; Cancer Therapy Evaluation Program, NCI, Rockville, Maryland.
Clin Cancer Res ; 27(10): 2734-2741, 2021 05 15.
Article em En | MEDLINE | ID: mdl-33766814
ABSTRACT

PURPOSE:

This surgical window of opportunity (window) study assessed the short-term effect of medroxyprogesterone acetate (MPA) alone versus MPA plus the histone deacetylase (HDAC) inhibitor entinostat on regulation of progesterone receptor (PR) in women with newly diagnosed endometrioid endometrial adenocarcinoma. PATIENTS AND

METHODS:

This multisite, randomized, open-label surgical window study treated women intramuscularly on day 1 with 400 mg MPA. Entinostat given 5 mg by mouth on days 1, 8, and 15 was randomly assigned with equal probability. Surgery followed on days 21-24. Pretreatment and posttreatment tissue was assessed for PR H-scores, Ki-67 levels, and histologic response.

RESULTS:

Fifty patients were accrued in 4 months; 22 and 20 participants had PR evaluable pretreatment and posttreatment slides in the MPA and MPA/entinostat arms, respectively. Median posttreatment PR H-scores were significantly lower than pretreatment H-scores in both arms but did not differ significantly (MPA 247 vs. 27, MPA/entinostat 260 vs. 23, respectively, P = 0.87). Decreased Ki-67 was shown in 90% treated with MPA/entinostat compared with 68% treated with MPA alone (P = 0.13). Median PR H-score decreases were larger when Ki-67 was decreased (208) versus not decreased (45). The decrease in PR pretreatment versus posttreatment was associated with loss of Ki-67 nuclear staining, consistent with reduced cellular proliferation (P < 0.008).

CONCLUSIONS:

This surgical window trial rapidly accrued in a multisite setting and evaluated PR as its primary endpoint and Ki-67 as secondary endpoint. Despite no immediate effect of entinostat on PR in this short-term study, lessons learned can inform future window and treatment trials.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias do Endométrio / Acetato de Medroxiprogesterona / Antineoplásicos Hormonais / Histerectomia Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Clin Cancer Res Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias do Endométrio / Acetato de Medroxiprogesterona / Antineoplásicos Hormonais / Histerectomia Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Clin Cancer Res Ano de publicação: 2021 Tipo de documento: Article