Ovarian Cancer Subcommittee

Purpose
The NRG Oncology Ovarian Cancer Subcommittee’s purpose is to improve the lives of patients with ovarian cancer by designing and conducting practice-changing multi-institutional clinical trials and translational research. This committee focuses on developing and testing innovative advanced surgical, radiation oncology, and systemic (including chemotherapy, and other targeted / biologic therapies) technologies for patients with gynecologic ovarian malignancies. Additionally, the committee is committed to identifying and rectifying disparities in patient outcomes within this population.

The goals of this committee include developing national and international priorities, goals and initiatives for the management of ovarian cancer; developing and managing currently active and developing NRG clinical trials on the prevention, diagnosis and treatment of ovarian cancers; and, fostering the advancement of promising therapeutics in development and exploring potential translational research and biomarker development for incorporation into future clinical trials. This committee strives to develop and implement standardized procedures needed to design and conduct a research protocol within the NRG while identifying potential barriers and potential solutions to improve enrollment to NRG clinical trials in ovarian cancers, including fostering international collaboration. This committee meets four times a year, twice in-person and twice virtually.

Ovarian Cancer Subcommittee Leadership

Chair

Kathleen Moore, MD, MS

Vice Chair

Joyce Liu, MD, MPH

Committee Members

    TR Representatives

    • Rebecca Arend
    • Elizabeth Swisher

    Core Members

    • Sarah Adams
    • Miriam AlHilli
    • Michael Birrer
    • Stephanie Blank
    • Michael Bookman
    • Justin Bottsford-Miller
    • Lindsay W. Brubaker
    • Yovanni Casablanca
    • Robert Coleman
    • Keiichi Fujiwara
    • Melissa Geller
    • Andrea Jewell
    • Tamara Kalir
    • Kidong Kim
    • Katherine Kurnit
    • Carrie Langstraat
    • Jayanthi Lea
    • Jung-Min Lee
    • Robin Lockhorst
    • Haider Mahdi
    • Gina Mantia-Smaldone
    • Merry Markham
    • Daniela Matei
    • Georgia McCann
    • Carolyn Muller
    • John Nakayama
    • Matthew Oliver
    • David O'Malley
    • Brian Orr
    • Kathryn Pennington
    • Leslie Randall
    • Debra Richardson
    • Sang Young Ryu
    • Angeles Alvarez Secord
    • Mark Shahin
    • Chrisann Winslow

    General Members

    • Vaagn Andikyan
    • Kian Behbakht
    • Erin Bishop
    • Sara Bouberhan
    • Stephen H. Bush II
    • Guilherme Henrique Cantuaria
    • Michael Carney
    • John Chan
    • Deidre Cleary
    • Lauren Cobb
    • Amaranta Craig
    • Marta Crispens
    • Lauren Dockery
    • Nicole Eiseler
    • Tony Eng
    • Evelyn Fleming
    • Katherine Fuh
    • Anne Gabel
    • Whitney Graybill
    • Jean Hansen
    • Ellen Hartenbach
    • Nadia Ismiil
    • Eleftheria Kalogera
    • Michael Kelly
    • Byoung-Gie Kim
    • Charles Landen
    • Ying Liu
    • Colleen McCormick
    • Arwa Mohammad
    • Deborah Moore
    • Mark Morgan
    • Robert Morris
    • Mary Mullen
    • Christa Nagel
    • Matthew T Oliver
    • Brian Orr
    • Jeong-Yeol Park
    • Clarissa Polen-De
    • Rebecca L. Porter
    • Jianyu Rao
    • Maria Reyes
    • Colleen Rivard
    • John Schorge
    • William Tew
    • Diogo Torres
    • John Veena
    • Katrina Wade
    • Saravut Weroha
    • Ira Winer
    • Kristen Zeligs
    • Wenxin Zheng
    • Oliver Zivanovic
    • Emese Zsiros

    Patient Representatives

    Katheen Gavin

    Alexi Wright

    Nurse/DM Representatives

    Mary Smrekar

    Liz Swords


     

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    Study Title Status Phase Disease Category Disease Site
    NRG-GY033A Phase II Study of Androgen Receptor (AR) Inhibition by Darolutamide in combination with Leuprolide Acetate and Exemestane in Recurrent Adult-Type Ovarian Granulosa Cell Tumors
    Temporarily Closed to AccrualIIGynecologic [GY]Ovarian
    EAY191-N4 Molecular Analysis for Combination Therapy Choice (ComboMATCH) EAY191-N4: A Randomized Trial of Selumetinib and Olaparib or Selumetinib Alone in Patients with Recurrent or Persistent RAS Pathway Mutant Ovarian and Endometrial Cancers - A ComboMATCH Treatment Trial

    Open to AccrualIIGynecologic [GY]Multiple
    NRG-GY029A Randomized Phase II trial comparing the combination of PI3K inhibitor Copanlisib (BAY 80-6946) and PARP inhibitor Olaparib (AZD2281) to standard chemotherapy in patients with recurrent platinum resistant ovarian, fallopian tube, or primary peritoneal cancer who have progressed through prior PARP inhibitor therapy

    Closed to AccrualIIGynecologic [GY]Ovarian
    NRG-GY027NRG-GY027: PHASE I/IB SAFETY AND PHARMACODYNAMIC STUDY OF NEOADJUVANT (NACT) PACLITAXEL AND CARBOPLATIN WITH IPATASERTIB AS INITIAL THERAPY OF OVARIAN CANCER PTMA 100805

    Open to AccrualIGynecologic [GY]Ovarian
    NRG-GY023A Randomized Phase II Trial of Triplet Therapy (A PD-L1 Inhibitor Durvalumab (MEDI4736) in Combination With Olaparib and Cediranib) Compared to Olaparib and Cediranib or Durvalumab (MEDI4736) and Cediranib or Standard of Care Chemotherapy in Women With Platinum-Resistant Recurrent Epithelial Ovarian Cancer, Primary Peritoneal or Fallopian Cancer Who Have Received Prior BevacizumabClosed to AccrualIIGynecologic [GY]Ovarian
    GOG-0268A Phase II Evaluation of Temsirolimus (CCI-779) (NCI Supplied Agent: 683864, IND #61010) in Combination with Carboplatin and Paclitaxel followed by Temsirolimus Consolidation as First-line Therapy in the Treatment of Clear Cell Carcinoma of the Ovary.Closed to AccrualIIGynecologic [GY]Ovarian
    GOG-0214Phase II Double Blind Randomized Trial Evaluating the Biologic Effect of Levonorgestrel on the Ovarian Epithelium in Women at High Risk for Ovarian Cancer (IND# 79,610)

    TerminatedIIGynecologic [GY]Ovarian
    GOG-0199Prospective Study of Risk-Reducing Salpingo-Oophorectomy and Longitudinal CA-125 Screening Among Women at Increased Genetic Risk of Ovarian Cancer
    TerminatedIGynecologic [GY]Ovarian
    NRG-GY021A Phase II Randomized Trial of Olaparib versus Olaparib plus Tremelimumab in Platinum-Sensitive Recurrent Ovarian CancerClosed to AccrualIIGynecologic [GY]Ovarian
    NRG-GY019A Randomized Phase III, Two-Arm Trial of Paclitaxel/Carboplatin/Maintenance Letrozole Versus Letrozole Monotherapy in Patients with Stage II-IV, Primary Low-Grade Serous Carcinoma of the Ovary or PeritoneumOpen to AccrualIIIGynecologic [GY]Ovarian
    NRG-GY014A Phase II Study of Tazemetostat (EPZ-6438) (IND # 138671) in Recurrent or Persistent Endometrioid or Clear Cell Carcinoma of the Ovary, and Recurrent or Persistent Endometrioid Endometrial AdenocarcinomaClosed to AccrualIIGynecologic [GY]Ovarian
    NRG-GY007STUDY STATUS = CLOSED A Phase I/II Study of Ruxolitinib with Front-Line Neoadjuvant and Post-Surgical Therapy in Patients with Advanced Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal CancerClosedI/IIGynecologic [GY]Ovarian
    GOG-9923A Phase I Study of Carboplatin/Paclitaxel/CTEP-Supplied Bevacizumab(NSC #704865, IND #7921)and CTEP-Supplied Agent ABT-888(NSC #737664,IND# 77840)in Newly Diagnosed Patients with Previously Untreated Epithelial Ovarian, Fallopian Tube or Primary PeritCancerTerminatedIGynecologic [GY]Ovarian
    GOG-0260A Phase II Evaluation of Elesclomol Sodium and Weekly Paclitaxel in the Treatment of Recurrent or Persistent Platinum-Resistant Ovarian, Fallopian Tube or Primary Peritoneal Cancer (IND 110072) (NCT# 00888615).TerminatedIIGynecologic [GY]Ovarian
    GOG-0186KA Randomized Phase II Study of NCI Supplied Cabozantinib (NSC #761968 IND #116059) versus weekly paclitaxel (NSC #673089) in the Treatment of Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal CancerTerminatedIIGynecologic [GY]Ovarian
    NRG-GY016A Phase II Study of MK-3475 (Pembrolizumab) (NSC #776864) + Epacadostat (NSC #766086) in Recurrent Clear Cell Carcinoma of the OvaryTerminatedIIGynecologic [GY]Ovarian
    NRG-GY001A Phase II Trial of Cabozantinib (XL-184) (NSC #761968) in Women with Recurrent, Clear Cell Carcinoma of the Ovary, Fallopian Tube, or PeritoneumTerminatedIIGynecologic [GY]Ovarian
    GOG-0213A Phase III Randomized Controlled Clinical Trial Of Carboplatin and Paclitaxel or  Gemcitabine) Alone or in Combination with Bevacizumab (NSC #704865, IND #113912) Followed by Bevacizumab and Secondary Cytoreductive Surgery in Platinum-Sensitive, Recurrenovarian, Peritoneal Primary and Fallopian Tube Cancer. NCI-Supplied Agents: Bevacizumab (NSC #704865, IND #113912) Closed to AccrualIIIGynecologic [GY]Ovarian
    NRG-GY005A Randomized Phase II/III study of the combination of Cediranib and Olaparib compared to Cediranib or Olaparib alone, or Standard of care chemotherapy in women with recurrent platinum-resistant or -refractory ovarian, fallopian tube, or primary peritoneal cancer (COCOS).Closed to AccrualII/IIIGynecologic [GY]Ovarian
    NRG-GY004A Phase III Study Comparing Single-Agent Olaparib or the Combination of Cediranib and Olaparib to Standard Platinum-Based Chemotherapy in Women with Recurrent Platinum-Sensitive Ovarian, Fallopian Tube, or Primary Peritoneal CancerClosed to AccrualIIIGynecologic [GY]Ovarian
    GOG-0239A Phase II Trial of AZD6244 (NSC #748727, IND #77782) in Women with Recurrent Low-Grade Serous Carcinoma of the Ovary or PeritoneumTerminatedIIGynecologic [GY]Ovarian
    NRG-GY003A Phase II Randomized Trial of Nivolumab with or without Ipilimumab in Patients with Persistent or Recurrent Epithelial Ovarian, Primary Peritoneal or Fallopian Tube CancerClosed to AccrualIIGynecologic [GY]Ovarian
    GOG-0225Can Diet and Physical Activity Modulate Ovarian or Primary Peritoneal Cancer Progression-Free Survival?Closed to AccrualIIIGynecologic [GY]Ovarian
    NRG-GY009A Randomized, Phase II/III Study of Pegylated Liposomal Doxorubicin and CTEP-Supplied Atezolizumab (IND #134427) Versus Pegylated Liposomal Doxorubicin, CTEP-Supplied Bevacizumab and CTEP-Supplied Atezolizumab Versus Pegylated Liposomal Doxorubicin and CTEP-Supplied Bevacizumab in Platinum Resistant Ovarian Cancer Closed to AccrualII/IIIGynecologic [GY]Ovarian
    GOG-0186HA Randomized Phase II Evaluation of Weekly Paclitaxel (NSC# 673089) versus Weekly Paclitaxel with Oncolytic Reovirus (Reolysin NSC # 729968, BB-IND #13370) in the Treatment of Recurrent or Persistent Ovarian, Fallopian Tube or Primary Peritoneal CancerTerminatedIIGynecologic [GY]Ovarian
    GOG-0281A Randomized Phase II/III Study to Assess the Efficacy of Trametinib (GSK 1120212) in Patients with Recurrent or Progressive Low-Grade Serous Ovarian Cancer or Peritoneal CancerClosed to AccrualII/IIIGynecologic [GY]Ovarian
    GOG-9928A Phase I study of the safety of intraperitoneal EGEN-001 (IL-12 plasmid formulated with PEG-PEI-Cholesterol lipopolymer) administered in combination with pegylated liposomal doxorubicin (PLD) in recurrent ovarian cancer patients. The purpose of this studtermine the safety of EGEN-001 IP plus PLD treatment in platinum-recurrent ovarian cancer patients.TerminatedIGynecologic [GY]Ovarian
    GOG-9924A Phase I Pharmacokinetic Study of Intraperitoneal CTEP-Supplied Agent Bortezomib (PS-341, NSC 681239, IND# 58443) and Carboplatin (NSC# 241240)in Patients with Persistent or Recurrent Ovarian, Fallopian Tube, or Primary Peritoneal CancerTerminatedIGynecologic [GY]Ovarian
    GOG-0280A Phase II Eval of the Poly(ADP-Ribose)Polymerase (PARP)-1 and -2 Inhibitor Veliparib (ABT-888)(NSC #737644) in the tx of Persistent or Recurrent Ovarian, Fallopian Tube or Primary Peritoneal Ca in Patients who carry a germline BRCA 1 or 2 Mutation  TerminatedIIGynecologic [GY]Ovarian
    RTOG-0724Phase III Randomized Study of Concurrent Chemotherapy and Pelvic Radiation Therapy with or without Adjuvant Chemotherapy in High-Risk Patients with Early-Stage Cervical Carcinoma Following Radical HysterectomyClosed to AccrualIIIGynecologic [GY]Ovarian

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