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Bevacizumab in Patients With Hereditary Hemorrhagic Telangiectasia and Severe Hepatic Vascular Malformations and High Cardiac Output
- Source :
- JAMA. 307
- Publication Year :
- 2012
- Publisher :
- American Medical Association (AMA), 2012.
-
Abstract
- Context The only treatment available to restore normal cardiac output in patients with hereditary hemorrhagic telangiectasia (HHT) and cardiac failure is liver transplant. Anti–vascular endothelial growth factor treatments such as bevacizumab may be an effective treatment. Objectives To test the efficacy of bevacizumab in reducing high cardiac output in severe hepatic forms of HHT and to assess improvement in epistaxis duration and quality of life. Design, Setting, and Patients Single-center, phase 2 trial with national recruitment from the French HHT Network. Patients were 18 to 70 years old and had confirmed HHT, severe liver involvement, and a high cardiac index related to HHT. Intervention Bevacizumab, 5 mg per kg, every 14 days for a total of 6 injections. The total duration of the treatment was 2.5 months; patients were followed up for 6 months after the beginning of the treatment. Main Outcome Measure Decrease in cardiac output at 3 months after the first injection, evaluated by echocardiography. Results A total of 25 patients were included between March 2009 and November 2010. Of the 24 patients who had echocardiograms available for reread, there was a response in 20 of 24 patients with normalization of cardiac index (complete response [CR]) in 3 of 24, partial response (PR) in 17 of 24, and no response in 4 cases. Median cardiac index at beginning of the treatment was 5.05 L/min/m 2 (range, 4.1-6.2) and significantly decreased at 3 months after the beginning of the treatment with a median cardiac index of 4.2 L/min/m 2 (range, 2.9-5.2; P 2 ; range, 3.0-5.1). Among 23 patients with available data at 6 months, we observed CR in 5 cases, PR in 15 cases, and no response in 3 cases. Mean duration of epistaxis, which was 221 minutes per month (range, 0-947) at inclusion, had significantly decreased at 3 months (134 minutes; range, 0-656) and 6 months (43 minutes; range, 0-310) (P = .008). Quality of life had significantly improved. The most severe adverse events were 2 cases of grade 3 systemic hypertension, which were successfully treated. Conclusion In this preliminary study of patients with HHT associated with severe hepatic vascular malformations and high cardiac output, administration of bevacizumab was associated with a decrease in cardiac output and reduced duration and number of episodes of epistaxis. Trial Registration clinicaltrials.gov Identifier: NCT00843440
- Subjects :
- Male
medicine.medical_specialty
Cardiac output
Bevacizumab
Cardiac index
Angiogenesis Inhibitors
Antibodies, Monoclonal, Humanized
Vascular anomaly
Arteriovenous Malformations
Internal medicine
medicine
Humans
Prospective Studies
Cardiac Output
Prospective cohort study
Adverse effect
Telangiectasia
Heart Failure
business.industry
General Medicine
Middle Aged
medicine.disease
Surgery
Epistaxis
Treatment Outcome
Liver
Heart failure
Cardiology
Female
Telangiectasia, Hereditary Hemorrhagic
medicine.symptom
business
medicine.drug
Subjects
Details
- ISSN :
- 00987484
- Volume :
- 307
- Database :
- OpenAIRE
- Journal :
- JAMA
- Accession number :
- edsair.doi.dedup.....649430a4412b6535e39d1b402649e2c2
- Full Text :
- https://doi.org/10.1001/jama.2012.250