Critical questions in ovarian cancer research and treatment: Report of an American Association for Cancer Research Special Conference.
PARP inhibitors
drug resistance
early detection
heterogeneity
immunotherapy
metabolism
microenvironment
ovarian cancer
prevention
Journal
Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236
Informations de publication
Date de publication:
15 06 2019
15 06 2019
Historique:
received:
24
08
2018
revised:
17
12
2018
accepted:
19
12
2018
pubmed:
6
3
2019
medline:
25
3
2020
entrez:
6
3
2019
Statut:
ppublish
Résumé
Substantial progress has been made in understanding ovarian cancer at the molecular and cellular level. Significant improvement in 5-year survival has been achieved through cytoreductive surgery, combination platinum-based chemotherapy, and more effective treatment of recurrent cancer, and there are now more than 280,000 ovarian cancer survivors in the United States. Despite these advances, long-term survival in late-stage disease has improved little over the last 4 decades. Poor outcomes relate, in part, to late stage at initial diagnosis, intrinsic drug resistance, and the persistence of dormant drug-resistant cancer cells after primary surgery and chemotherapy. Our ability to accelerate progress in the clinic will depend on the ability to answer several critical questions regarding this disease. To assess current answers, an American Association for Cancer Research Special Conference on "Critical Questions in Ovarian Cancer Research and Treatment" was held in Pittsburgh, Pennsylvania, on October 1-3, 2017. Although clinical, translational, and basic investigators conducted much of the discussion, advocates participated in the meeting, and many presentations were directly relevant to patient care, including treatment with poly adenosine diphosphate ribose polymerase (PARP) inhibitors, attempts to improve immunotherapy by overcoming the immune suppressive effects of the microenvironment, and a better understanding of the heterogeneity of the disease.
Identifiants
pubmed: 30835824
doi: 10.1002/cncr.32004
pmc: PMC6557260
mid: NIHMS1033147
doi:
Substances chimiques
Antineoplastic Agents
0
Poly(ADP-ribose) Polymerase Inhibitors
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
1963-1972Subventions
Organisme : NCI NIH HHS
ID : P50 CA159981
Pays : United States
Organisme : NICHD NIH HHS
ID : K12 HD000849
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA217685
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA010815
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA138835
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA163377
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA200462
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA174904
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA195670
Pays : United States
Organisme : Cancer Research UK
ID : 15601
Pays : United Kingdom
Organisme : NCI NIH HHS
ID : R01 CA202919
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA083639
Pays : United States
Organisme : Medical Research Council
ID : G0902418
Pays : United Kingdom
Informations de copyright
© 2019 American Cancer Society.
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