2019
DOI: 10.1016/j.ygyno.2018.10.023
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Novel treatment options in platinum-sensitive recurrent ovarian cancer: A review

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Cited by 31 publications
(32 citation statements)
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“…More specifically, PARP inhibitors (Olaparib) can be introduced as maintenance monotherapy in relapsed disease patients with BRCA mutation. Recently, SOLO-1 trial showed that among 391 patients with newly diagnosed advanced high-grade serous or endometrioid OC, primary peritoneal cancer, or fallopian-tube cancer (or a combination thereof) with a mutation in BRCA1, BRCA2, or both who underwent randomization, the use of maintenance therapy with olaparib provided a substantial benefit with regard to progression-free survival among women with newly diagnosed advanced OC and a BRCA1/2 mutation, with a 70% lower risk of disease progression or death with olaparib than with placebo during a 41 month follow-up period [4,20,21].…”
Section: Discussionmentioning
confidence: 99%
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“…More specifically, PARP inhibitors (Olaparib) can be introduced as maintenance monotherapy in relapsed disease patients with BRCA mutation. Recently, SOLO-1 trial showed that among 391 patients with newly diagnosed advanced high-grade serous or endometrioid OC, primary peritoneal cancer, or fallopian-tube cancer (or a combination thereof) with a mutation in BRCA1, BRCA2, or both who underwent randomization, the use of maintenance therapy with olaparib provided a substantial benefit with regard to progression-free survival among women with newly diagnosed advanced OC and a BRCA1/2 mutation, with a 70% lower risk of disease progression or death with olaparib than with placebo during a 41 month follow-up period [4,20,21].…”
Section: Discussionmentioning
confidence: 99%
“…For this reason, the 10 years aggressive ultraradical procedures are a common approach of such a lethal disease. Also, several trials are conducted regarding the new treatment options for recurrent OC [4,5].…”
Section: Introductionmentioning
confidence: 99%
“…Trebananib is a peptide that suppresses angiogenesis by inhibiting angiopoietin-1 and -2. Moreover, other treatment strategies involve PARP inhibitors (PARPi) which render PARP enzymes no more capable of performing DNA repair processes and ultimately leading to synthetic lethality [11]. These PARP inhibitors include olaparib (AZD2281), niraparib (MK4827), rucaparib (CO338, AGO14699, and PF01367338), veliparib (ABT-888) and talazoparib (BMN 673) [11].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, other treatment strategies involve PARP inhibitors (PARPi) which render PARP enzymes no more capable of performing DNA repair processes and ultimately leading to synthetic lethality [11]. These PARP inhibitors include olaparib (AZD2281), niraparib (MK4827), rucaparib (CO338, AGO14699, and PF01367338), veliparib (ABT-888) and talazoparib (BMN 673) [11]. However, it should be noted that that PARP inhibitors have mostly been successful and are approved for patients with platinum sensitive ovarian carcinoma rather than resistant disease [12].…”
Section: Introductionmentioning
confidence: 99%
“…The starting therapy relays on platinum drugs in combination with paclitaxel or doxorubicin. However, approximately 70% relapse due to insurgence of platinum drug resistance [13]. The resistant cancer type shows higher than normal levels of proteins involved in the replication pathways, including h TS, and cross-resistance with anti- h TS drugs [14,15,16] The above-mentioned anti- h TS drugs become ineffective.…”
Section: Introductionmentioning
confidence: 99%