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
Korch, Christopher; Hall, Erin M; Dirks, Wilhelm G et al. (2018) Authentication of M14 melanoma cell line proves misidentification of MDA-MB-435 breast cancer cell line. Int J Cancer 142:561-572
Lee, Jong-Ho; Liu, Rui; Li, Jing et al. (2018) EGFR-Phosphorylated Platelet Isoform of Phosphofructokinase 1 Promotes PI3K Activation. Mol Cell 70:197-210.e7
Brown, Justin C; Troxel, Andrea B; Ky, Bonnie et al. (2018) Dose-response Effects of Aerobic Exercise Among Colon Cancer Survivors: A Randomized Phase II Trial. Clin Colorectal Cancer 17:32-40
Zhang, Hong; Wang, Yirong; Li, Jun et al. (2018) Biosynthetic energy cost for amino acids decreases in cancer evolution. Nat Commun 9:4124
Vilar-Compte, Diana; Shah, Dimpy P; Vanichanan, Jakapat et al. (2018) Influenza in patients with hematological malignancies: Experience at two comprehensive cancer centers. J Med Virol 90:50-60
Bambhroliya, Arvind; Van Wyhe, Renae D; Kumar, Swaminathan et al. (2018) Gene set analysis of post-lactational mammary gland involution gene signatures in inflammatory and triple-negative breast cancer. PLoS One 13:e0192689
Koay, Eugene J; Lee, Yeonju; Cristini, Vittorio et al. (2018) A Visually Apparent and Quantifiable CT Imaging Feature Identifies Biophysical Subtypes of Pancreatic Ductal Adenocarcinoma. Clin Cancer Res 24:5883-5894
Jain, N; Zhu, H; Khashab, T et al. (2018) Targeting nucleolin for better survival in diffuse large B-cell lymphoma. Leukemia 32:663-674
Parker, Patricia A; Peterson, Susan K; Shen, Yu et al. (2018) Prospective Study of Psychosocial Outcomes of Having Contralateral Prophylactic Mastectomy Among Women With Nonhereditary Breast Cancer. J Clin Oncol 36:2630-2638
Fathi, Amir T; Erba, Harry P; Lancet, Jeffrey E et al. (2018) A phase 1 trial of vadastuximab talirine combined with hypomethylating agents in patients with CD33-positive AML. Blood 132:1125-1133

Showing the most recent 10 out of 12418 publications