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贝伐珠单抗联合化疗作为塞尔维亚队列中晚期卵巢癌的一线治疗。

Bevacizumab with Chemotherapy as a First-Line Treatment for Advanced Ovarian Cancer in a Serbian Cohort.

机构信息

Faculty of Medicine, University of Nis, 18000 Nis, Serbia.

Oncology Clinic, Clinical Center Nis, 18000 Nis, Serbia.

出版信息

Medicina (Kaunas). 2022 Apr 27;58(5):607. doi: 10.3390/medicina58050607.

DOI:10.3390/medicina58050607
PMID:35630024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9144683/
Abstract

: For stage IIIb-IV ovarian cancer, bevacizumab-containing treatment is considered the standard of care. The purpose of this study was to evaluate the efficacy of bevacizumab in combination with carboplatin and paclitaxel as a first-line treatment for advanced ovarian cancer. : Eligible patients had stage IIIc-IV ovarian cancer according to the International Federation of Gynecology and Obstetrics with no clinical signs or symptoms of gastrointestinal obstruction or a history of abdominal fistulae, gastrointestinal perforation, or intra-abdominal abscess or evidence of rectosigmoid involvement by pelvic examination, bowel involvement on computed tomography, or clinical symptoms of bowel obstruction in the previous 6 months. After debulking surgery, the patients received 175 mg/m paclitaxel and carboplatin (AUC 6) for the first six cycles and 7.5 mg/kg bevacizumab every three weeks up to 17 cycles until disease progression, unacceptable toxicity, or consent withdrawal. The primary endpoint was progression-free survival. The secondary endpoint was overall survival. : Between April 2017 and March 2020, 35 patients began study treatment. Bevacizumab was administered at 7.5 mg/kg in all the patients and for more than 7.5 months in 70% of them. The median progression-free survival was 20 months (95% CI: 16-23). The median overall survival was not reached. : This was, to our knowledge, the first trial in Serbia to show progression-free survival and overall survival of combination regimens in advanced ovarian cancer. Based on the observed progression-free survival, bevacizumab combined with chemotherapy should be considered as a standard option in advanced ovarian cancer.

摘要

对于 IIIb-IV 期卵巢癌,贝伐珠单抗联合治疗被认为是标准治疗方案。本研究旨在评估贝伐珠单抗联合卡铂和紫杉醇作为晚期卵巢癌一线治疗的疗效。

符合条件的患者为国际妇产科联合会(FIGO)分期为 IIIc-IV 期卵巢癌,无胃肠道梗阻的临床症状或体征,或无腹部瘘管、胃肠道穿孔或腹腔脓肿病史,或盆腔检查无直肠乙状结肠受累,计算机断层扫描(CT)无肠道受累,或在过去 6 个月内无肠道梗阻的临床症状。在肿瘤细胞减灭术后,患者接受了 175mg/m 紫杉醇和卡铂(AUC 6)治疗前 6 个周期,然后每 3 周给予 7.5mg/kg 贝伐珠单抗,最多 17 个周期,直至疾病进展、不可接受的毒性或同意退出。主要终点是无进展生存期。次要终点是总生存期。

2017 年 4 月至 2020 年 3 月,共有 35 例患者开始接受研究治疗。所有患者均给予 7.5mg/kg 贝伐珠单抗,其中 70%的患者接受贝伐珠单抗治疗超过 7.5 个月。中位无进展生存期为 20 个月(95%CI:16-23)。中位总生存期未达到。

据我们所知,这是塞尔维亚首例显示晚期卵巢癌联合方案无进展生存期和总生存期的试验。基于观察到的无进展生存期,贝伐珠单抗联合化疗应被视为晚期卵巢癌的标准治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/1fb380fe750f/medicina-58-00607-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/da74e87e2c1b/medicina-58-00607-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/8c65b7989ea9/medicina-58-00607-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/1fb380fe750f/medicina-58-00607-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/da74e87e2c1b/medicina-58-00607-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/8c65b7989ea9/medicina-58-00607-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/584a/9144683/1fb380fe750f/medicina-58-00607-g003.jpg

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