The Gynecological Cancers Program includes 59 members (25 primary, 34 associate) from 15 departments, reflecting a 25% increase over the last 6 years. The program is led by Dr. Karen Lu (prevention studies and translational research), with co-leaders Dr. Anil Sood (basic science mechanistic studies and translational research) and Dr. Robert Coleman (developmental therapeutics and clinical trials). The major scientific goal of the program is to advance knowledge of gynecologic cancers and translate this knowledge to the cure and prevention of these diseases. To achieve this goal, the program has 4 themes that focus on 1) biology of therapeutic targets in gynecologic cancers; 2) developmental therapeutics; 3) health services research, quality improvement, and surgical outcomes; and 4) prevention and early detection. These, in turn, are paired with 4 specific aims.
Specific Aim 1 : To understand the mechanisms of tumor growth and metastasis in gynecologic cancers in order to identify novel molecular targets and inform future clinical studies;
Specific Aim 2 : To improve gynecologic cancer treatment by using a translational research platform that enables rapid clinical evaluation of biologics and immunotherapeutics, effect on molecular targets, and tumor adaptive responses;
Specific Aim 3 : To integrate patient-reported outcomes, quality improvement, and health services research into developmental therapeutics and surgical trials;
Specific Aim 4 : To reduce the incidence and mortality of gynecologic cancers by identifying innovative strategies for early detection and prevention. The annual direct cost peer-reviewed funding totals $4.4M, including the MD Anderson SPORE in Uterine Cancer, MD Anderson SPORE in Ovarian Cancer, a U01 EDRN-CVC for Early Detection of Ovarian Cancer, and U10 NRG Oncology Operations. Of the total peer-reviewed funding, $3.5M (80%) is from NCI grants. Since the last submission, the program has published 854 papers: 431 (50%) represent intra-programmatic collaborations, 216 (25%) represent inter- programmatic collaborations, and 619 (72%) represent inter-institutional collaborations. Thirty-eight percent of publications were in journals with IF >5, and 12% appeared in journals with IF >10, including Cancer Cell, J Clin Oncol, Lancet Oncol, and J Clin Invest. Program members utilize all 14 Shared Resources. During the last grant period, the program launched several high-impact initiatives, including the Ovarian Cancer Moon Shot and HPV Cancers Moon Shot. Accomplishments include the ?scope and score? algorithm to improve rates of achieving R0 (no gross residual disease) for ovarian cancer cytoreductive surgery and studies identifying mechanisms of adaptive response. A phase III clinical trial (GOG-0213) of bevacizumab added to standard chemotherapy followed by bevacizumab maintenance therapy showed improved overall survival in recurrent platinum-sensitive high-grade serous ovarian cancer. A CA125-based algorithm for ovarian cancer screening detected stage 1-2 disease in 70% of laparotomies, with a positive predictive value of 55%.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016672-44
Application #
9997823
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
44
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
DUNS #
800772139
City
Houston
State
TX
Country
United States
Zip Code
77030
Boddu, Prajwal; Masarova, Lucia; Verstovsek, Srdan et al. (2018) Patient characteristics and outcomes in adolescents and young adults with classical Philadelphia chromosome-negative myeloproliferative neoplasms. Ann Hematol 97:109-121
Casasent, Anna K; Schalck, Aislyn; Gao, Ruli et al. (2018) Multiclonal Invasion in Breast Tumors Identified by Topographic Single Cell Sequencing. Cell 172:205-217.e12
Noh, Hyangsoon; Zhao, Qingnan; Yan, Jun et al. (2018) Cell surface vimentin-targeted monoclonal antibody 86C increases sensitivity to temozolomide in glioma stem cells. Cancer Lett 433:176-185
Hutcheson, Katherine A; Barrow, Martha P; Plowman, Emily K et al. (2018) Expiratory muscle strength training for radiation-associated aspiration after head and neck cancer: A case series. Laryngoscope 128:1044-1051
Zhao, Jun; Xiao, Zhilan; Li, Tingting et al. (2018) Stromal Modulation Reverses Primary Resistance to Immune Checkpoint Blockade in Pancreatic Cancer. ACS Nano 12:9881-9893
Akhtari, Mani; Milgrom, Sarah A; Pinnix, Chelsea C et al. (2018) Reclassifying patients with early-stage Hodgkin lymphoma based on functional radiographic markers at presentation. Blood 131:84-94
Barua, Souptik; Solis, Luisa; Parra, Edwin Roger et al. (2018) A Functional Spatial Analysis Platform for Discovery of Immunological Interactions Predictive of Low-Grade to High-Grade Transition of Pancreatic Intraductal Papillary Mucinous Neoplasms. Cancer Inform 17:1176935118782880
Ma, Junsheng; Chan, Wenyaw; Tilley, Barbara C (2018) Continuous time Markov chain approaches for analyzing transtheoretical models of health behavioral change: A case study and comparison of model estimations. Stat Methods Med Res 27:593-607
Bayraktar, Recep; Ivan, Cristina; Bayraktar, Emine et al. (2018) Dual Suppressive Effect of miR-34a on the FOXM1/eEF2-Kinase Axis Regulates Triple-Negative Breast Cancer Growth and Invasion. Clin Cancer Res 24:4225-4241
Parra, Edwin R; Villalobos, Pamela; Mino, Barbara et al. (2018) Comparison of Different Antibody Clones for Immunohistochemistry Detection of Programmed Cell Death Ligand 1 (PD-L1) on Non-Small Cell Lung Carcinoma. Appl Immunohistochem Mol Morphol 26:83-93

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