Kaparelou Maria, Liontos Michalis, Katsimbri Pelagia, Andrikopoulou Aggeliki, Papatheodoridi Alikistis, Kyriazoglou Anastasios, Bamias Aristotelis, Zagouri Flora, Dimopoulos Meletios Athanasios
Department of Clinical Therapeutics, Alexandra Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Rheumatology Unit, 4th Dept of Internal Medicine, ATTIKON University, Hospital, School of Medicine, National & Kapodistrain University of Athens, Athens, Greece.
Gynecol Oncol Rep. 2022 Mar 2;40:100953. doi: 10.1016/j.gore.2022.100953. eCollection 2022 Apr.
Joint manifestations are ill-defined adverse events that were frequently reported of bevacizumab in ovarian cancer patients. The aim of this study is to describe the incidence and severity of joint manifestations among bevacizumab treated patients as well as their relation to clinical outcomes.
Medical charts of all ovarian cancer patients that received bevacizumab from 2012 through 2017 were reviewed. Joint manifestations were staged. Kaplan-Meier Survival curves were generated; survival differences were estimated.
76 Patients diagnosed with stage III or IV ovarian cancer were included. 23 patients (30.3%) developed joint manifestations, 12 of them had Grade I, 4 Grade II and 7 Grade III. Only 3 patients developed arthritis. In 8 cases (34.8%) one joint was affected and in the remaining 15, multiple sites. Median number of bevacizumab cycles to arthralgia development was 7. 3 patients were managed with corticosteroids or methotrexate, all had grade 3 AEs. The remaining received common analgesics. Median duration of the AE was 4.8 months. 7 patients discontinued bevacizumab due to AE. In all but 3 patients AE was finally resolved. Median number of bevacizumab cycles received, frequency of treatment completion or treatment discontinuation due to disease progression did not differ significantly among patients that developed joint manifestations or not. Median PFS and median OS did not differ statistical significantly.
Joint manifestations are common AEs in bevacizumab treated ovarian cancer patients and led to treatment discontinuation in 9% of the patients. However, this has not adversely affected the clinical outcome of the patients. Further research is needed for the appropriate management of these patients.
关节表现是贝伐单抗治疗卵巢癌患者时经常报告的不明确不良事件。本研究的目的是描述接受贝伐单抗治疗的患者中关节表现的发生率和严重程度,以及它们与临床结局的关系。
回顾了2012年至2017年期间所有接受贝伐单抗治疗的卵巢癌患者的病历。对关节表现进行分期。绘制Kaplan-Meier生存曲线;估计生存差异。
纳入76例诊断为III期或IV期卵巢癌的患者。23例患者(30.3%)出现关节表现,其中12例为I级,4例为II级,7例为III级。仅3例患者发生关节炎。8例(34.8%)累及一个关节,其余15例累及多个部位。发生关节痛时贝伐单抗的中位疗程数为7个。3例患者接受了皮质类固醇或甲氨蝶呤治疗,均发生3级不良事件。其余患者接受普通镇痛药治疗。不良事件的中位持续时间为4.8个月。7例患者因不良事件停用贝伐单抗。除3例患者外,所有患者的不良事件最终均得到缓解。出现或未出现关节表现的患者接受贝伐单抗的中位疗程数、因疾病进展完成治疗或停止治疗的频率无显著差异。中位无进展生存期和中位总生存期无显著统计学差异。
关节表现是贝伐单抗治疗卵巢癌患者常见的不良事件,9%的患者因此停药。然而,这并未对患者的临床结局产生不利影响。需要进一步研究以对这些患者进行适当管理。