2016
DOI: 10.1093/annonc/mdw236
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Prognostic and predictive effects of primary versus secondary platinum resistance for bevacizumab treatment for platinum-resistant ovarian cancer in the AURELIA trial

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Cited by 31 publications
(11 citation statements)
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“…Based on previous studies, optimal debulking was defined as a maximum diameter of residual tumor after surgery of ≤2 cm 32 , 33 . Patients were defined as platinum-resistant if the disease progressed within 6 months after completing first-line platinum-based chemotherapy, while all other patients were defined as platinum-sensitive 34 . PNI was calculated according to the following formula: serum albumin (g/L) + 0.005 × lymphocyte count (per mm 3 ) in the peripheral blood 11 .…”
Section: Methodsmentioning
confidence: 99%
“…Based on previous studies, optimal debulking was defined as a maximum diameter of residual tumor after surgery of ≤2 cm 32 , 33 . Patients were defined as platinum-resistant if the disease progressed within 6 months after completing first-line platinum-based chemotherapy, while all other patients were defined as platinum-sensitive 34 . PNI was calculated according to the following formula: serum albumin (g/L) + 0.005 × lymphocyte count (per mm 3 ) in the peripheral blood 11 .…”
Section: Methodsmentioning
confidence: 99%
“…However, development of recurrent or drug‐resistant disease in most women necessitates the use of alternative strategies, such as dose‐dense therapy, aimed at improving both progression‐free survival and overall survival . To address the unmet need for novel strategies that deliver improved survival benefits, targeted agents are increasingly seen as an option for combination treatment with conventional cytotoxic chemotherapy …”
mentioning
confidence: 99%
“…(2)(3)(4)(5) To address the unmet need for novel strategies that deliver improved survival benefits, targeted agents are increasingly seen as an option for combination treatment with conventional cytotoxic chemotherapy. (6) Veliparib (ABT-888) is a potent, orally bioavailable poly (ADP-ribose) polymerase (PARP)-1/2 inhibitor that may increase the efficacy of chemotherapeutic regimens by delaying DNA repair after chemotherapy-induced damage. (7) In preclinical models, veliparib enhanced the activity of cisplatin, carboplatin and cyclophosphamide, whereas cell lines that quickly develop resistance to taxanes and carboplatin retained their sensitivity to veliparib, thus supporting the candidacy of this agent for the treatment of platinum-resistant or taxaneresistant ovarian cancer.…”
mentioning
confidence: 99%
“…The AURELIA trial, an exploratory analysis of the AUR-ELIA trial, and real-world evidence demonstrate the benefit of bevacizumab in PR-ROC settings [19][20][21]. They also support the panel recommendations on the addition of bevacizumab to single-agent chemotherapy (liposomal doxorubicin, topotecan, or paclitaxel) in recurrent ovarian cancer settings.…”
Section: Platinum-sensitive Recurrent Ovarian Cancer (Ps-roc) Settingsmentioning
confidence: 63%
“…Further analyses within the SPR and PPR subgroups revealed that the addition of bevacizumab conferred a numerically more pronounced PFS benefit in the SPR subgroup (HR 0.30) than in the PPR subgroup (HR 0.55; treatment-subgroup interaction p = 0.07). Similarly, for OS, a non-significant direction of effect was observed (p for interaction 0.18) [21].…”
Section: Platinum-sensitive Recurrent Ovarian Cancer (Ps-roc) Settingsmentioning
confidence: 91%