News_addition_layout

ADDITION OF BEVACIZUMAB TO CAPECITABINE IMPROVES PROGRESSION-FREE SURVIVAL IN ELDERLY PATIENTS Key Points:
• The addition of bevacizumab to capecitabine significantly prolonged progression-free survival in elderly
patients with previously untreated metastatic colorectal cancer who were not considered candidates for
oxaliplatin- or irinotecan-based chemotherapy.
• No difference in overall survival was observed between the two groups.
• Adverse events were more common with bevacizumab/capecitabine.
Elderly patients are often underepresented in clinical trials of metastatic colorectal cancer. In a phase III study (AVEX trial) reported in The Lancet Oncology, David Cunningham, MD, of Royal Marsden Hospital in London and colleagues
assessed the addition of bevacizumab (Avastin) to capecitabine in patients aged ≥ 70 years with previously untreated metastatic colorectal cancer who were not considered candidates for oxaliplatin- or irinotecan-based chemotherapy. The bevacizumab/capecitabine combination significantly improved progression-free survival and was associated with more frequent adverse events than capecitabine alone.
Study Details
In this international open-label trial, 280 patients were randomly assigned to receive capecitabine 1,000 mg/m2 orally twice a day on days 1 to 14 alone (n = 140) or with bevacizumab 7.5 mg/kg intravenously on day 1 (n = 140) given every 3 weeks until disease progression, unacceptable toxic effects, or withdrawal of consent. The primary endpoint was progression-free Median ages were 76 years in the combination group (61% ≥ 75 years) and 77 years in the capecitabine-alone group (67% ≥ 75 years), and 60% of patients in both groups were male. The groups were generally well matched for baseline charac- teristics, although more patients in the combination group had undergone surgical resection of the primary tumor (74% vs 64%), received previous adjuvant treatment (completed more than 6 months before the start of study treatment) (32% vs 19%), and been treated with radiotherapy (12% vs 6%).
Prolonged Progression-Free Survival
Median follow-up was 24.8 months for the combination group and 21.6 months for the capecitabine-alone group.
Progression-free survival was significantly longer with bevacizumab/capecitabine (median 9.1 vs 5.1 months, hazard ratio [HR] = 0.53, P < .0001). Progression-free survival was 66.7% vs 44.2% at 6 months, 34.8% vs 10.3% at 12 months, and 16.2% vs 3.6% at 18 months. Exploratory subgroup analyses of progression-free survival were consistent with the overall findings. Analysis by age suggested improved outcomes with the combination in patients aged 70 to 74 years (HR = 0.52, 95% confidence interval [CI] = 0.32–0.83), 75 to 79 years (HR = 0.60, 95% CI = 0.40–0.89), and ≥ 80 years (HR = 0.36, More patients in the combination group achieved response (19% vs 10%, P = .04) and disease control (74% vs 58%, P = .01), with duration of response being similar in the two groups (median 9.0 vs 9.4 months).
Overall Survival Outcomes
Median overall survival did not differ significantly in the combination vs capecitabine-alone groups (20.7 vs 16.8 months, HR = 0.79, P = .18). Overall survival was 73.6% vs 60.0% at 1 year and 44.3% vs 35.1% at 2 years. The proportions of patients who had subsequent treatment after progression were similar in the two groups, including treatment with fluoropy- rimidine monotherapy (17% vs 18%), bevacizumab (6% vs 8%), irinotecan doublets (6% vs 3%), oxaliplatin doublets (2% vs 1%), cetuximab (Erbitux; 3% vs 1%), and panitumumab (Vectibix; 1% vs 4%).
Adverse Events
Treatment-related adverse events of grade 3 or higher occurred in 40% of patients in the combination group and 22% of patients in the capecitabine-alone group, and treatment-related serious adverse events occurred in 14% and 8%, respec- tively. The most common grade 3 or higher adverse events of special interest for bevacizumab or chemotherapy were hand-foot syndrome (16% vs 7%), diarrhea (7% vs 7%), and venous thromboembolic events (8% vs 4%). Treatment-related deaths occurred in 3.7% of patients in the combination group and 2.9% in the capecitabine-alone group.
The most common adverse event of any grade of special interest for bevacizumab was hemorrhage (25% vs 7%). Adverse events led to dose interruption or modification in 55% of combination patients vs 43% of capecitabine patients and The investigators concluded, “Our data suggest that bevacizumab plus capecitabine represents an additional therapeutic option in elderly patients with metastatic colorectal cancer, particularly in those who are unsuitable for upfront oxaliplatin- based or irinotecan-based combination regimens.” The study was funded by F Hoffmann-La Roche.

Source: http://www.giscad.org/pdf/ADDITION.pdf

exeter.k12.pa.us

A. Biological Chemistry(though water is the universal medium for life on earth, living organisms are made of chemicals based mostly on the element a. contain Carbon. total of 6e-, 2 in 1st shel , 4 in 2nd that holds 8 i. Carbon has 4 valence electrons that can join with an electron from another atom to form a strong covalent bond-usual y with C, H, O, or N ex/ CH4 (methane) ii. Carbon can

Accord national médico-mutualiste 2009-2010

Accord national médico-mutualiste 2009–2010 ACCORD NATIONAL MEDICO-MUTUALISTE 2009–2010 En vertu des articles 26, 50 et 51 de la loi relative à l’assurance obligatoire soins de santé et indemnités, coordonnée le 14 juillet 1994, la Commission nationale médico-mutualiste (dénommée ci-après CNMM), sous la Présidence de M. Johan DE COCK, a conclu le 17 décembre 2008, l’accord

Copyright ©2018 Drugstore Pdf Search