![]() | Mark F BradyNRG Oncology; Clinical Trial Development Division; Biostatistics & Bioinformatics; Roswell Park Comprehensive Cancer Center, Buffalo, NY. | NRG Oncology SDMC, CTD Division, ... |
KOL Resume for Mark F Brady
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2022 | NRG Oncology; Clinical Trial Development Division; Biostatistics & Bioinformatics; Roswell Park Comprehensive Cancer Center, Buffalo, NY. |
2021 | NRG Oncology SDMC, CTD Division, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States of America. Electronic address: |
2020 | Roswell Park Cancer Institute, Buffalo, NY; |
2019 | From the University of Texas M.D. Anderson Cancer Center, Houston (R.L.C., K.B.-E.); Women's Cancer Center of Nevada, Las Vegas (N.M.S.); NRG Oncology Statistical and Data Management Center, Roswell Park Cancer Institute, Buffalo (D.E., H.Q.H., M.F.B.), and Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York (P.S.) - both in New York; the University of Cincinnati, University of Cincinnati Cancer Institute, Cincinnati (T.J.H.); the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore (D.K.A.); Seoul National University College of Medicine (J.-W.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine (B.-G.K.), and Asan Medical Center, University of Ulsan College of Medicine (J.-H.N.), Seoul, and the Research Institute and Hospital, National Cancer Center, Goyang (S.-Y.P.) - all in South Korea; Saitama Medical University International Medical Center, Hidaka, Japan (K.F.); the University of Oklahoma Health Sciences Center, Oklahoma City (J.L.W., R.S.M.); National Surgical Adjuvant Breast and Bowel Project/NRG Oncology, U.S. Oncology Research, and Metro-Minnesota Community Oncology Research Consortium, Minneapolis (A.C.C.); Duke Cancer Institute, Duke University Medical Center, Durham, NC (A.A.S.); Abramson Cancer Center, University of Pennsylvania, Philadelphia (S.R.); Gynecologic Cancer Program, California Pacific-Palo Alto Medical Foundation, Sutter Research Institute, San Francisco (J.K.C.); Women and Infants Hospital, Providence, RI (P.D.); the University of Colorado School of Medicine, Aurora, and Denver Health Medical Center, Denver (S.A.D.); Ohio State University, Columbus (D.E.C.); and the University of California, Irvine, Orange (K.S.T.). NRG Oncology Statistical and Data Center, Roswell Park Cancer Institute, University of Buffalo, Buffalo, NY, USA 2 Roswell Park Cancer Institute, Buffalo, NY. |
2018 | NRG Statistical and Data Center, Roswell Park Cancer Institute, Buffalo, NY; |
2017 | GOG Foundation Statistical and Data Center, Roswell Park Cancer Institute, Buffalo. The NRG Oncology Statistical and Data Center, Roswell Park Cancer Center Institute, Buffalo, New York. University of Buffalo, Buffalo, NY, USA |
2016 | Statistical Office, NRG Oncology, Buffalo, New York From the California Pacific-Palo Alto Medical Foundation, Sutter Cancer Research Institute, San Francisco (J.K.C.); NRG Oncology-Gynecologic Oncology Group Statistics and Data Center, Roswell Park Cancer Institute, Buffalo, NY (M.F.B., H.H.); Massachusetts General Hospital, Boston (R.T.P., M.J.B.); University of Oklahoma, Oklahoma City (J.L.W.); Women and Infants Hospital, Providence, RI (P.A.D.S.); University of Pennsylvania (S.C.R.) and Fox Chase Cancer Center (L.P.M.) - both in Philadelphia; University of Colorado Cancer Center, Aurora (S.A.D.); University of Alabama at Birmingham, Birmingham (W.K.H.); James Cancer Center, Ohio State University, Columbus (D.M.O.); Minnesota Oncology/Hematology-Oncology Service, Edina (M.P.B.); Indiana University School of Medicine, Carmel (H.M.); and University of Arizona Cancer Center, Creighton University School of Medicine, and St. Joseph's Hospital and Medical Center (B.J.M.) - all in Phoenix. |
2015 | NRG Oncology Statistical Office, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY 14263, United States |
2014 | GOG Statistical and Data Center, Buffalo, NY |
2013 | Gynecology Oncology Group Statistical and Data Center, Roswell Park Cancer Institute, Elm and Carlton Streets, 14221, Buffalo, NY, USA Roswell Park Cancer Institute, Buffalo, NY |
2012 | The Fox Chase Cancer Center, Philadelphia; The Gynecologic Oncology Group Statistical and Data Center, Roswell Park Cancer Institute, Buffalo, NY; The Arizona Cancer Center, Tucson; The University of Chicago, Chicago; Creighton University School of Medicine at St. Joseph's Hospital and Medical Center, Phoenix, AZ; The University of Oklahoma Health Sciences Center, Oklahoma City; Wake Forest University School of Medicine, Winston-Salem, NC; James Cancer Hospital at Ohio State University, Hilliard; Seattle Cancer Care Alliance, Seattle; Minnesota Oncology and Hematology, Minneapolis; Harvard Medical School and Massachusetts General Hospital, Boston; and North Shore–Long Island Jewish Health System, New Hyde Park, NY |
2011 | Gynecologic Oncology Group Statistical & Data Center, Roswell Park Cancer Institute, Buffalo, NY 14263-0001, USA |
2010 | *National Cancer Institute of Canada Clinical Trials Group (NCIC CTG), Kingston, Ontario, Canada; †Gynecologic Oncology Group (GOG), Philadelphia, PA; ‡AGO-OVAR-Arbeitsgemeinschaft Gynaekologische Onkologie Studiengruppe Ovarialkarzinom, Wiesbaden, Germany; §Université Paris Descartes, AP-HP, Hôpital Hôtel-Dieu, Paris, France; ∥Medical Research Council, London, UK; ¶Scottish Gynaecological Cancer Trials Group, Glasgow, UK; and **IEO-Istituto Europeo di Oncologia, Milan, Italy. Fox Chase Cancer Center, Philadelphia, PA; Gynecologic Oncology Group, Buffalo, NY; Arizona Cancer Center, Tucson, AZ; University of Oklahoma Health Sciences Center, Oklahoma City, OK; The Brody School of Medicine, Greenville, NC; James Cancer Hospital, The Ohio State University, Hilliard, OH; University of California, Irvine Medical Center, Orange, CA; Seattle Cancer Care Alliance, Seattle, WA; Minnesota Oncology and Hematology, Minneapolis, MN; Stony Brook University, Stony Brook, NY Gynecologic Oncology Group Statistical and Data Center, Roswell Park Cancer Institute, Buffalo, New York |
2009 | University of Minnesota School of Medicine, Minneapolis, MN From the Fox Chase Cancer Center, Philadelphia, PA SUNY Buffalo, Buffalo, NY; Roswell Park Cancer Institute, Buffalo, NY Franklin Square Hospital Baltimore, MD |
2008 | Affiliations of authors: MRC Clinical Trials Unit, London, UK (MKBP, MS, RL, RK, AMS, WQ, PR); Institute of Psychiatry, King’s College London, London, UK (FMSB); NCIC Clinical Trials Group, Queen's University, Kingston, Ontario, Canada (EE); School of Public Health and Health Professions, University at Buffalo, Buffalo, NY (MB); CR-UK Institute for Cancer Studies, University of Birmingham, Birmingham, UK (NJ); Fox Chase Cancer Center, Philadelphia, PA (MAB) |
2007 | Gynecologic Oncology Group Statistical Center, Buffalo, NY From the Division of Solid Tumor Oncology, Department of Medical Oncology, Memorial Sloan-Kettering Cancer Center, New York Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, Oklahoma City, OK University of Arizona Cancer Center, Tucson, AZ and the M.D. Anderson Cancer Center, Houston, TX |
2006 | Vanderbilt University Medical Center, Nashville, TN Fred Hutchinson Cancer Research Center, Seattle, WA; Arizona Cancer Center, Tucson, AZ; University of California Irvine, Irvine, CA; GOG Statistical and Data Center, Buffalo, NY; M. D. Anderson Cancer Center, Houston, TX Southwest Oncology Group Statistical Office, Seattle, WA |
2004 | MetroHealth Medical Center, Cleveland, OH; Tufts-New England Medical Center, Hartford, CT; Gynecology Oncology Group, Buffalo, NY; Duke University Medical center, Durham, NC; Medical Center of Pennsylvania, Hershey, PA; University of Pennsylvania, Philadelphia, PA; Indiana University School of Medicine, Indianapolis, IN; Presbyterian St. Lukes Hospital, Chicago, IL From the Division of Oncology, Department of Medicine, University of Mississippi School of Medicine, Jackson, MS and Department of Pathology, University of California at Irvine, Orange, CA Wake Forest University School of Medicine, Winston-Salem, NC |
2003 | From the Fox Chase Cancer Center, Philadelphia, PA; Roswell Park Cancer Institute, Buffalo, NY; University of California Los Angeles Medical Center, Los Angeles, CA, Mayo Comprehensive Cancer Center, Rochester, MN; Walter Reed Army Medical Center, Washington, DC; Wake Forest University School of Medicine, Winston-Salem, NC; Indiana University School of Medicine, Indianapolis, IN; and the University of Arizona College of Medicine and Arizona Cancer Center, Tucson, AZ. Gynecologic Oncology Group Statistical and Data Center, Roswell Park Cancer Institute, Buffalo, New York, 14263 |
2001 | From the Department of Medicine, Washington University School of Medicine, St Louis, MO; Gynecologic Oncology Group, Roswell Park Cancer Institute, Buffalo, NY; Department of Obstetrics and Gynecology, Indiana University Medical Center, Indianapolis, IN; Section of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences, Oklahoma City, OK; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Case Western Reserve University, University... Gynecologic Oncology Group, Roswell Park Cancer Institute, Buffalo, New York, 14263 |
2000 | From the Departments of Medicine and Medical OncologyKaplan Cancer Center, New York University, New York; and Roswell Park Cancer Institute, Buffalo, NY; Department of Obstetrics and Gynecology, Louisiana State University Medical Center, New Orleans, LA; Division of Gynecologic Oncology, Indiana University Medical School, Indianapolis, IN; Department of Pathology, Columbus Cancer Council, James Cancer Hospital, Ohio State University, Columbus, OH; Section on Gynecologic Oncology, Wake Forest University... |
1999 | GOG Statistical Office, Roswell Park Cancer Institute, Buffalo, USA. From the Division of Oncology, University of Mississippi School of Medicine, Jackson, MS; Gynecologic Oncology Group, Roswell Park Cancer Institute, Buffalo, and Comprehensive Gynecology, Crouse Irving Memorial Hospital, Syracuse, NY; Department of Gynecologic Oncology, Division of Gynecologic Oncology, University of Alabama at Birmingham, Birmingham, AL; Bowman Gray School of Medicine, Carolina Gynecologic Oncology, Winston-Salem, and Division of Gynecologic Oncology, Department of Obstetrics and... |
1997 | Gynecologic Oncology Group Statistical Office, Roswell Park Cancer Center, Buffalo, |
1996 | Gynecologic Oncology Group Statistical Office, Roswell Park Cancer Institute, Buffalo, N.Y. (M.F.B.) |
1994 | New York and Buffalo, New York, Baltimore, Maryland, Winston-Salem, North Carolina, Charleston, South Carolina, Irvine and Los Angeles, California, and Boston, Massachusetts |
1993 | GOG Administrative Office, Suite 1945, 1234 Market Street, Philadelphia, PA 19107 University of Colorado School of Medicine and the Gynecology Tumor Service, St. Luke's Hospital, Denver, Colorado Roswell Park Cancer Institute, Buffalo, New York |
1992 | Section of Gynecologic Oncology, Department of Obstetrics and Gynecology (D.S.M.), University of Texas Southwestern Medical School, Dallas, Texas; Gynecologic Oncology Group (M.F.B.), Roswell Park Memorial Institute, Buffalo, New York; Department of Obstetrics and Gynecology, Section on Gynecologic Oncology (R.J.B.), Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina, U.S.A. From the Department of Anatomic Pathology (T.K., S.G.S.), George Washington University Medical Center, Washington, D.C.; The Milton S. Hershey Medical Center of the Pennsylvania State University (T.K.), Hershey, Pennsylvania; the Department of Obstetrics and Gynecology, University of Colorado School of Medicine, and Gynecology Tumor Service (F.J.M.), St. Luke's Hospital, Denver, Colorado; the Department of Pathology (A.M.), Rush-Presbyterian St. Luke's Medical Center, Chicago, Illinois; the Department of Pathology (B.F.), Duke University Medical Center, Durham, North Carolina; and the Gynecologic Oncology Group (M.F.B.), Roswell Park Cancer Institute, Buffalo, New York. |
1990 | Gynecological Oncology Group, Philadelphia, Pennsylvania Gynecologic Oncology Group, Cancer Research Scientist, Roswell Park Memorial Institute, Buffalo, New YorkU.S.A. |
1984 | National Prostatic Cancer Project, Roswell Park Memorial Institute, Buffalo, New York |
Mark F Brady: Influence Statistics
Concept | World rank |
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institute genentech | #1 |
measurable complete response | #1 |
degree purpose | #1 |
paclitaxel death rate | #1 |
250 filgrastim | #1 |
ii26 | #1 |
ca125 regression | #1 |
iii92 | #1 |
cisplatin death rate | #1 |
individual trial manner | #1 |
cim stage | #1 |
cyclophosphamide cisplatin | #1 |
endpoints determination | #1 |
carboplatin 3 weeks | #1 |
probability neutropenic fever | #1 |
dose accompanied | #1 |
secondary surgical | #1 |
principles trial | #1 |
higher paclitaxel dose | #1 |
trial strength | #1 |
secondary surgical cytoreduction | #1 |
adjuvant cim wai | #1 |
auc cycles | #1 |
death rate paclitaxel | #1 |
suffering grade | #1 |
therapy longterm | #1 |
cisplatinifosfamide | #1 |
purpose gynecologic oncology | #1 |
filgrastim filgrastim dose | #1 |
race performance status | #1 |
paclitaxel probability | #1 |
cisplatinpaclitaxel | #1 |
gog trials | #1 |
manner principles | #1 |
median ca125 values | #1 |
cim101 | #1 |
175 250 | #1 |
filgrastim dose levels | #1 |
mesna cim | #1 |
paclitaxel 250 | #1 |
cisplatin cisplatin regimens | #1 |
considerations randomised | #1 |
patients prior platinum | #1 |
evidence individual trial | #1 |
clinical trial strength | #1 |
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Prominent publications by Mark F Brady
BACKGROUND: Platinum-based chemotherapy doublets are a standard of care for women with ovarian cancer recurring 6 months after completion of initial therapy. In this study, we aimed to explore the roles of secondary surgical cytoreduction and bevacizumab in this population, and report the results of the bevacizumab component here.
METHODS: The multicentre, open-label, randomised phase 3 GOG-0213 trial was done in 67 predominantly academic centres in the USA (65 centres), Japan (one ...
Known for Chemotherapy Bevacizumab | 3 Trial | Ovarian Cancer | Local Neoplasms | 6 Months |
BACKGROUND: A dose-dense weekly schedule of paclitaxel (resulting in a greater frequency of drug delivery) plus carboplatin every 3 weeks or the addition of bevacizumab to paclitaxel and carboplatin administered every 3 weeks has shown efficacy in ovarian cancer. We proposed to determine whether dose-dense weekly paclitaxel and carboplatin would prolong progression-free survival as compared with paclitaxel and carboplatin administered every 3 weeks among patients receiving and those not ...
Known for Ovarian Cancer | Paclitaxel Carboplatin | 3 Weeks | Patients Bevacizumab | Progressionfree Survival |
OBJECTIVE: The Gynecologic Oncology Group has divided patients with advanced epithelial ovarian cancer into those with optimal residual cancer, in which the maximum diameter of residual is < or = 1 cm, and suboptimal residual cancer, in which the residual disease is > 1 cm. Within the optimal group of patients there is a survival difference between patients with microscopic residual disease and those with any macroscopic disease < or = 1 cm. No analysis of the effect of various residual ...
Known for Residual Disease | Gynecologic Oncology | Epithelial Ovarian | Multivariate Analysis | Difference Survival |
BACKGROUND: Vascular endothelial growth factor is a key promoter of angiogenesis and disease progression in epithelial ovarian cancer. Bevacizumab, a humanized anti-vascular endothelial growth factor monoclonal antibody, has shown single-agent activity in women with recurrent tumors. Thus, we aimed to evaluate the addition of bevacizumab to standard front-line therapy.
METHODS: In our double-blind, placebo-controlled, phase 3 trial, we randomly assigned eligible patients with newly ...
Known for Bevacizumab Cycles | Primary Treatment | Ovarian Cancer | Chemotherapy Placebo | Monoclonal Glandular |
BACKGROUND: On Aug 14, 2014, the US Food and Drug Administration approved the antiangiogenesis drug bevacizumab for women with advanced cervical cancer on the basis of improved overall survival (OS) after the second interim analysis (in 2012) of 271 deaths in the Gynecologic Oncology Group (GOG) 240 trial. In this study, we report the prespecified final analysis of the primary objectives, OS and adverse events.
METHODS: In this randomised, controlled, open-label, phase 3 trial, we ...
Known for Gynecologic Oncology | Advanced Cervical Cancer | Patients Chemotherapy | 3 Trial | Paclitaxel 175 |
IMPORTANCE: Germline mutations in BRCA1 and BRCA2 are relatively common in women with ovarian, fallopian tube, and peritoneal carcinoma (OC) causing a greatly increased lifetime risk of these cancers, but the frequency and relevance of inherited mutations in other genes is less well characterized.
OBJECTIVE: To determine the frequency and importance of germline mutations in cancer-associated genes in OC.
DESIGN, SETTING, AND PARTICIPANTS: A study population of 1915 woman with OC and ...
Known for Inherited Mutations | Ovarian Carcinoma | Brca1 Brca2 | Germline Dna | Rad51c Rad51d |
PURPOSE: To assess progression-free survival (PFS) and overall survival (OS) in patients with suboptimally debulked epithelial ovarian cancer receiving cisplatin (100 mg/m(2)) or 24-hour infusion paclitaxel (200 mg/m(2)) or the combination of paclitaxel (135 mg/m(2)) followed by cisplatin (75 mg/m(2)).
PATIENTS AND METHODS: After stratification for disease measurability, patients were randomized to receive six cycles of one of the treatments every 3 weeks. If measurable, complete ...
Known for Cisplatin Paclitaxel | Combination Therapy | Iii Randomized | Ovarian Cancer | Gynecologic Oncology |
PURPOSE: To compare progression-free survival (PFS), overall survival (OS) and toxicities of thalidomide versus tamoxifen and to evaluate serum vascular endothelial growth factor (VEGF) in biochemical-recurrent epithelial ovarian cancer, primary peritoneal cancer or fallopian tube carcinoma (EOC/PPC/FTC).
METHODS: Biochemical recurrence was defined as a rising CA-125 exceeding twice the upper limit of normal without evidence of disease as defined by RECIST 1.0 criteria. Women with FIGO ...
Known for Fallopian Tube | Growth Factor | Vascular Endothelial | Complete Response | Oral Aged Aged |
BACKGROUND: Secondary surgical cytoreduction in women with platinum-sensitive, recurrent epithelial ovarian, primary peritoneal, or fallopian-tube ("ovarian") cancer is widely practiced but has not been evaluated in phase 3 investigation.
METHODS: We randomly assigned patients with recurrent ovarian cancer who had received one previous therapy, had an interval during which no platinum-based chemotherapy was used (platinum-free interval) of 6 months or more, and had ...
Known for Secondary Surgical Cytoreduction | Recurrent Ovarian Cancer | Local Neoplasms | Patients Surgery | Platinumbased Chemotherapy |
Cyclophosphamide and Cisplatin Compared with Paclitaxel and Cisplatin in Patients with Stage III and Stage IV Ovarian Cancer
[ PUBLICATION ]
BACKGROUND: Chemotherapy combinations that include an alkylating agent and a platinum coordination complex have high response rates in women with advanced ovarian cancer. Such combinations provide long-term control of disease in few patients, however. We compared two combinations, cisplatin and cyclophosphamide and cisplatin and paclitaxel, in women with ovarian cancer.
METHODS: We randomly assigned 410 women with advanced ovarian cancer and residual masses larger than 1 cm after initial ...
Known for Ovarian Cancer | Cisplatin Cyclophosphamide | Paclitaxel Women | Square Meter | Stage Iii |
OBJECTIVES: The coexistence of carcinomas of the endometrium and ovary occurs in about 10% of women with ovarian carcinoma. It is often unclear whether this represents synchronous primary tumors or metastasis from endometrium to ovary, or from ovary to endometrium; consequently, staging, therapy, and expected outcome are uncertain. The Gynecologic Oncology Group sought to study patients with simultaneously detected adenocarcinomas in the endometrium and ovary with disease grossly ...
Known for Ovarian Carcinomas | Gynecologic Oncology | Local Neoplasms | 5 Years | Simultaneously Detected |
Phase III Trial of Doxorubicin With or Without Cisplatin in Advanced Endometrial Carcinoma: A Gynecologic Oncology Group Study
[ PUBLICATION ]
PURPOSE: Doxorubicin and cisplatin have activity in endometrial carcinoma and at initiation of this study ranked as the most active agents. This trial of stage III, IV, or recurrent disease evaluated whether combining these agents increases response rate (RR) and prolongs progression-free survival (PFS) and overall survival (OS) over doxorubicin alone.
PATIENTS AND METHODS: Of 299 patients registered, 281 (94%) were eligible. Regimens were doxorubicin 60 mg/m(2) intravenously or ...
Known for Endometrial Carcinoma | Gynecologic Oncology | Doxorubicin Cisplatin | Phase Iii Trial | Single Agent |
Purpose: We hypothesized that mutations in homologous recombination repair (HRR) genes beyond BRCA1 and BRCA2 improve outcomes for ovarian carcinoma patients treated with platinum therapy and would impact the relative benefit of adding prolonged bevacizumab.Experimental Design: We sequenced DNA from blood and/or neoplasm from 1,195 women enrolled in GOG-0218, a randomized phase III trial in advanced ovarian carcinoma of bevacizumab added to carboplatin and paclitaxel. Defects in HRR were ...
Known for Ovarian Carcinoma | Homologous Recombination Genes | Bevacizumab Pfs | Hrr Mutations | Relative Benefit |
Phase II study of paclitaxel and valspodar (PSC 833) in refractory ovarian carcinoma: a gynecologic oncology group study.
[ PUBLICATION ]
PURPOSE: A phase II study was conducted to determine the efficacy of paclitaxel and valspodar (PSC 833) in patients with advanced epithelial ovarian cancer. Valspodar, a nonimmunosuppressive cyclosporine D analogue that reverses P-glycoprotein-mediated multidrug resistance, in combination with paclitaxel might be active in paclitaxel-resistant and refractory ovarian cancer.
PATIENTS AND METHODS: Patients received valspodar 5 mg/kg orally qid x 12 doses. Paclitaxel (70 mg/m(2) ...
Known for Patients Paclitaxel | Psc 833 | Multiple Drug Resistance | Neoplasm Female Humans | Gynecologic Oncology |
OBJECTIVE: Compared to 3 cycles, to determine if 6 cycles of adjuvant carboplatin (C) and paclitaxel (P) significantly lower the rate of recurrence in surgically staged patients with stage IA grade 3, IB grade 3, clear cell, IC, and completely resected stage II epithelial ovarian cancer (EOC); and to compare toxicities.
METHODS: Postoperatively, randomization was to either 3 or 6 cycles of chemotherapy consisting of P (175 mg/m2 over 3 h) and C (7.5 AUC over 30 min) every 21 days. ...
Known for Adjuvant Carboplatin | 6 Cycles | Ovarian Carcinoma | Recurrence Patients | Early Stage |
Key People For Ovarian Cancer
Mark F Brady:Expert Impact
Concepts for whichMark F Bradyhas direct influence:Ovarian cancer, Gynecologic oncology, Phase iii trial, Ovarian carcinoma, Phase iii, Primary therapy, Residual disease, Secondary surgical cytoreduction.
Mark F Brady:KOL impact
Concepts related to the work of other authors for whichfor which Mark F Brady has influence:Ovarian cancer, Neoadjuvant chemotherapy, Cytoreductive surgery, Fallopian tube, Antineoplastic agents, Uterine sarcoma.
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