In the single-arm non-interventional OTILIA study, patients with newly diagnosed International Federation of Gynecology and Obstetrics (FIGO) stage IIIB–IV ovarian cancer received bevacizumab (15 mg/kg every 3 weeks for up to 15 months) and standard carboplatin–paclitaxel. The primary aim was to assess safety and progression-free survival (PFS). Subgroup analyses according to age were prespecified. The analysis population included 824 patients (453 aged <70 years, 371 aged ≥70 years). At data cutoff, the median bevacizumab duration was 13.8 months. Grade ≥3 adverse events (AEs), serious AEs, and AEs leading to bevacizumab discontinuation were more common in older than younger patients, whereas treatment-related AEs were less common. Median ...
Background: In the PAOLA-1/ENGOT-ov25 primary analysis, maintenance olaparib plus bevacizumab demons...
<p><strong>Background: </strong>in advanced ovarian cancer, over the last 10 years no studies have d...
Background: PAOLA-1/ENGOT-ov25 (NCT02477644) demonstrated a significant progression-free survival (P...
International audienceIntroduction: Bevacizumab-containing therapy is considered a standard-of-care ...
The aim of this study was to assess the safety and efficacy of extending bevacizumab therapy beyond ...
Objective Two randomized phase III trials demonstrated the efficacy and safety of combining bevacizu...
Objective: Because elderly patients with ovarian cancer are underrepresented in randomized studies, ...
Claudia Marchetti, Ludovico Muzii, Alessia Romito, Pierluigi Benedetti Panici Department of Gynecol...
Summary Background: The ICON7 trial previously reported improved progression-free survival in women...
Objective To explore the clinical and biological prognostic factors for advanced ovarian cancer pati...
BACKGROUND: The AURELIA trial demonstrated significantly improved progression-free survival (PFS) wi...
(1) Background: We investigated survival outcomes following first-line chemotherapy before and after...
Platinum-based standard chemotherapy improves survival of ovarian cancer (OC), but the five-year sur...
Objective: In the randomized phase 3 ICON7 trial (ISRCTN91273375), adding bevacizumab to chemotherap...
BACKGROUND: Platinum-based standard chemotherapy improves survival of ovarian cancer (OC), but the f...
Background: In the PAOLA-1/ENGOT-ov25 primary analysis, maintenance olaparib plus bevacizumab demons...
<p><strong>Background: </strong>in advanced ovarian cancer, over the last 10 years no studies have d...
Background: PAOLA-1/ENGOT-ov25 (NCT02477644) demonstrated a significant progression-free survival (P...
International audienceIntroduction: Bevacizumab-containing therapy is considered a standard-of-care ...
The aim of this study was to assess the safety and efficacy of extending bevacizumab therapy beyond ...
Objective Two randomized phase III trials demonstrated the efficacy and safety of combining bevacizu...
Objective: Because elderly patients with ovarian cancer are underrepresented in randomized studies, ...
Claudia Marchetti, Ludovico Muzii, Alessia Romito, Pierluigi Benedetti Panici Department of Gynecol...
Summary Background: The ICON7 trial previously reported improved progression-free survival in women...
Objective To explore the clinical and biological prognostic factors for advanced ovarian cancer pati...
BACKGROUND: The AURELIA trial demonstrated significantly improved progression-free survival (PFS) wi...
(1) Background: We investigated survival outcomes following first-line chemotherapy before and after...
Platinum-based standard chemotherapy improves survival of ovarian cancer (OC), but the five-year sur...
Objective: In the randomized phase 3 ICON7 trial (ISRCTN91273375), adding bevacizumab to chemotherap...
BACKGROUND: Platinum-based standard chemotherapy improves survival of ovarian cancer (OC), but the f...
Background: In the PAOLA-1/ENGOT-ov25 primary analysis, maintenance olaparib plus bevacizumab demons...
<p><strong>Background: </strong>in advanced ovarian cancer, over the last 10 years no studies have d...
Background: PAOLA-1/ENGOT-ov25 (NCT02477644) demonstrated a significant progression-free survival (P...