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Published in 2017 at "Scientific Reports"
DOI: 10.1038/s41598-017-07617-7
Abstract: Poly(ADP-ribose) polymerase (PARP) inhibitors represent a promising strategy toward the treatment of triple-negative breast cancer (TNBC), which is often associated to genomic instability and/or BRCA mutations. However, clinical outcome is controversial and no benefits have…
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Keywords:
negative breast;
breast cancer;
brca mutated;
brca ... See more keywords
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Published in 2023 at "Expert Review of Clinical Pharmacology"
DOI: 10.1080/17512433.2023.2188193
Abstract: ABSTRACT Introduction Poly-ADP-ribose polymerase inhibitors (PARPis) have emerged as a new class of therapeutic agents for breast cancer patients with breast cancer susceptibility gene (BRCA) mutations. However, the efficacy and toxicity of PARPis have not…
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Keywords:
brca mutated;
mutated breast;
breast cancer;
efficacy safety ... See more keywords
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Published in 2018 at "Annals of Oncology"
DOI: 10.1093/annonc/mdx639
Abstract: Background Preclinical evidence suggests a possible negative impact of deleterious BRCA mutations on female fertility. However, limited and rather conflicting clinical data are available. This study assessed the reproductive potential and performance of fertility preservation…
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Keywords:
breast cancer;
brca mutated;
performance;
cancer patients ... See more keywords
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Published in 2018 at "Molecular Cancer Therapeutics"
DOI: 10.1158/1535-7163.targ-17-a106
Abstract: Background: PARP inhibitors have demonstrated clinically meaningful increase in progression-free survival as a single agent in women with recurrent ovarian cancer following a response to platinum-based chemotherapy. However, there still needs more improvement in efficacy…
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Keywords:
inhibitor;
idx 1197;
brca mutated;
parp ... See more keywords
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Published in 2019 at "Cancer discovery"
DOI: 10.1158/2159-8290.cd-nb2019-030
Abstract: Niraparib showed promising signs of efficacy in the phase II GALAHAD trial of men with advanced prostate cancer whose tumors harbor mutations in the DNA damage-response pathway, especially among patients with gene defects in BRCA1…
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Keywords:
shrinks brca;
prostate tumors;
mutated prostate;
niraparib shrinks ... See more keywords
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Published in 2021 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2021.39.15_suppl.5518
Abstract: 5518Background: Niraparib has been approved for the maintenance treatment of patients with advanced ovarian, fallopian tube, or primary peritoneal cancer after front-line chemotherapy (CT) and in t...
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Keywords:
efficacy safety;
safety patients;
cancer;
niraparib efficacy ... See more keywords
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Published in 2022 at "Future oncology"
DOI: 10.2217/fon-2022-0206
Abstract: We reviewed clinical data for niraparib monotherapy in BRCA-mutated (BRCAm) epithelial ovarian cancer (OC), contextualizing results with data from other poly(ADP-ribose) polymerase inhibitors (PARPis). Niraparib reduced the likelihood of progression or death by 60% as…
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Keywords:
brca mutated;
niraparib treatment;
ovarian cancer;
clinical data ... See more keywords
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Published in 2022 at "Cancers"
DOI: 10.3390/cancers14164040
Abstract: Simple Summary BRCA-mutated high-grade epithelial ovarian cancers represent a specific subset of gynecological malignancies. Real-world comprehensive data have been elusive to date. As such, we conducted a comprehensive description of clinicopathological and therapeutical characteristics via…
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Keywords:
brca mutated;
high grade;
epithelial ovarian;
grade epithelial ... See more keywords
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Published in 2021 at "Molecular medicine reports"
DOI: 10.3892/mmr.2020.11713
Abstract: Loss‑of‑function BRCA mutations are frequent in high‑grade serous ovarian carcinoma. BRCA1 and ‑2 mutations lead to homologous recombination (HR) deficiency. Poly(ADP‑ribose) polymerases (PARP) are enzymes involved in DNA repair. PARP inhibitors (PARPi) lead to DNA damage accumulation in…
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Keywords:
mutated cancer;
brca mutated;
resistance;
tp53 mutations ... See more keywords