Drugs

Bevacizumab solution

 On August 14, 2014, the U. S. Food and Drug Administration approved bevacizumab solution for intravenous infusion (Avastin, Genentech, Inc.) for the treatment of persistent, recurrent or metastatic cervical cancer, in combination with paclitaxel and cisplatin or paclitaxel and topotecan.    

The approval is based on the results of an international, randomized, four-arm, two-by-two factorial design trial with two primary comparisons of overall survival (OS).  The first comparison was between bevacizumab plus chemotherapy versus chemotherapy alone.  The second comparison of OS was between the platinum doublet versus the non-platinum doublet chemotherapy irrespective of addition of  bevacizumab.
 
The trial enrolled 452 patients: 227 patients were assigned to receive chemotherapy and bevacizumab, and 225 patients were assigned to receive chemotherapy alone. The chemotherapy could be either paclitaxel in combination with cisplatin or paclitaxel in combination with topotecan.
 
Treatment continued until disease progression, unacceptable toxicity, and/or consent withdrawal.  All enrolled patients had GOG performance status of 0 or 1, 80% had received prior radiation and 74% had received prior chemotherapy concurrent with radiation.
 
The key efficacy assessment in the first primary comparison of OS demonstrated a statistically significant improvement in patients who received bevacizumab and chemotherapy compared to those who received chemotherapy alone (HR=0.74; 95% CI: 0.58, 0.94; p= 0.013, log-rank test).  The median survival of patients who received bevacizumab and chemotherapy was 16.8 months (95% CI: 14.1, 19) compared to 12.9 months (95% CI: 10.9, 15) for those receiving chemotherapy alone.  
 
For the second primary comparison of OS, the paclitaxel plus topotecan with or without bevacizumab arms did not demonstrate an improvement in OS compared to the paclitaxel plus cisplatin with or without bevacizumab arms [HR 1.15 (95% CI: 0.91, 1.46)]. However, the HRs for addition of bevacizumab to either chemotherapy regimen were similar (HR 0.72 for paclitaxel/cisplatin and HR 0.76 for paclitaxel/topotecan). The results suggest that the regimen of paclitaxel with topotecan plus bevacizumab is an acceptable alternative for women with advanced cervical cancer who are not candidates for platinum treatment.
 
The most common adverse reactions (greater than or equal to 20%) in patients treated with bevacizumab and chemotherapy were fatigue, decreased appetite, hypertension, hyperglycemia, hypomagnesemia, urinary tract infection, headache and decreased weight. Gastrointestinal perforations were reported in 3.2% of bevacizumab-treated patients, all of whom had prior pelvic radiation. Gastrointestinal‑vaginal fistulae occurred in 8.2% of bevacizumab‑treated patients and 0.9% in control patients, all of whom also had prior pelvic radiation.  In addition to gastrointestinal perforation and fistulae, several other grade 3 or greater adverse reactions were also more common in patients receiving chemotherapy plus bevacizumab, including venous thromboembolic events, hemorrhage, hypertension, proteinuria, and wound healing complications.  
 
The recommended dose of Avastin is 15 mg/kg every three weeks as an intravenous infusion administered in combination with one of the following chemotherapy regimens: paclitaxel and cisplatin, or paclitaxel and topotecan. The dosing regimens used in the clinical trial were as follows and repeated every 21 days:
 
  • Day 1: paclitaxel 135 mg/m2 IV over 24 hours, Day 2: cisplatin 50 mg/m2 IV plus bevacizumab;

      or Day 1: paclitaxel 175 mg/m2 IV over 3 hours, Day 2: cisplatin 50 mg/m2 IV plus bevacizumab;

      or Day 1: paclitaxel 175 mg/m2 IV over 3 hours plus cisplatin 50 mg/m2 IV plus bevacizumab

  • Day 1: paclitaxel 175 mg/m2 over 3 hours plus bevacizumab, Days 1-3: topotecan 0.75 mg/m2 over 30 minutes.
 
Full prescribing information, including clinical trial information, safety, dosing, drug-drug interactions and contraindications is available at:
 
Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System by completing a form online at http://www.fda.gov/medwatch/report.htm, by faxing (1-800-FDA-0178) or mailing the postage-paid address form provided online, or by telephone (1-800-FDA-1088).
 
 

 

 

Page Last Updated: 09/01/2015
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