Epithelial ovarian cancer: A case report

• Published in: Experimental and therapeutic medicine Vol. 8; no. 5; pp. 1535 - 1538
• Main Authors: GAO, JIANYUAN, FANG, HAIYING, WANG, XIAOMING, WU, LIPING, ZHANG, RONGHUAI, HAN, YAJUN
• Format: Journal Article
• Language: English
• Published: Greece D.A. Spandidos 01.11.2014; Spandidos Publications; Spandidos Publications UK Ltd
• Subjects: Abdomen; bevacizumab; Cancer; Cancer therapies; carboplatin; Care and treatment; Case reports; Case studies; Chemotherapy; Development and progression; Diagnosis; Drug dosages; Drug therapy; Health aspects; Immunotherapy; massive pleural effusions; Metastasis; Monoclonal antibodies; Ovarian cancer; Pain; Patients; Pulmonary arteries; recurrent epithelial ovarian cancer; Surgery; Targeted cancer therapy; China; United States > US; bevacizumab; recurrent epithelial ovarian cancer; massive pleural effusions; chemotherapy; carboplatin
• ISSN: 1792-0981; 1792-1015
• DOI: 10.3892/etm.2014.1970

An 82-year-old female was diagnosed with ovarian cancer in May 2004. Following gynecological surgery, pathological evaluation showed stage IIIC epithelial ovarian cancer. From June 2004 to January 2005, the patient received six cycles of conventional treatment combined with intravenous paclitaxel (Taxol®) and cisplatin. The patient developed abdominal distension and experienced a gradual deterioration in health during 2007, with admission to The First Affiliated Hospital in May 2007. The patient presented with severe abdominal distension and breathing difficulty on May 15 and appeared to be in critical condition. Ultrasound examination revealed massive ascites and left-side pleural effusion. Thoracentesis and abdominocentesis were performed, and 300 mg carboplatin was administered intraperitoneally on May 19, followed by a second abdominocentesis on May 21. However, these treatments did not alleviate the symptoms, and 200 mg bevacizumab was administered by intravenous infusion on May 27. The condition of the patient gradually improved and 400 mg bevacizumab was administered by intravenous infusion every two weeks from June 9. From December, the dosage of bevacizumab was reduced to 200 mg every two weeks. In addition, 300 mg carboplatin was administered intraperitoneally on November 4 and intraperitoneal carboplatin chemotherapy was repeated thereafter. The patient exhibited disease-free survival until July 2009, at which time disease progression was observed and the cancer recurred in August 2009. The patient died of multiple organ failure in September 2009. Bevacizumab rapidly eliminated the patient's massive ascites and pleural effusion, and achieved an effect that was not possible with other treatments. Therefore, bevacizumab is an effective therapy for late-stage relapse and refractory ovarian cancer.