Devi R Nandini, Menon Abhilash, Shenoy Praveen K, Avaronnan Manuprasad, Shahana Sherin, George Allwin
Department of Clinical Hematology and Medical Oncology, Malabar Cancer Centre - Post Graduate Institute of Oncology Sciences and Research, Thalassery, IND.
Department of Medical Oncology, Aster MIMS Hospital, Kannur, IND.
Cureus. 2024 Nov 6;16(11):e73171. doi: 10.7759/cureus.73171. eCollection 2024 Nov.
Introduction The majority of the patients with advanced-stage epithelial ovarian cancer relapse within three years of standard first-line treatment. Access to novel therapies like poly ADP-ribose polymerase (PARP) inhibitors and antiangiogenic agents is limited in low- and middle-income countries. Oral metronomic therapy (OMT) may be an effective alternative treatment option in resource-limited settings. Materials and methods A retrospective study was conducted among patients with epithelial ovarian cancer who received OMT. OMT consisted of cyclophosphamide 50mg per day and tamoxifen 40mg per day which was administered continuously until unacceptable toxicity or progression was reached. OMT was given to patients with relapsed ovarian cancer and to those newly diagnosed ovarian cancer patients who were unfit for cytoreductive surgery and/or standard first-line intravenous platinum-based chemotherapy. All patients who received OMT at our center between 01-01-2017 and 31-12-2021 were included for analysis. Relevant details, as needed for the study, were collected from medical records. SPSS version 24 (IBM Corp., Armonk, NY) was used for statistical analysis. Results A total of 61 patients received OMT during the study period. The median age at diagnosis of ovarian cancer was 59 years. The median age at the start of OMT was 61 years. The majority (n= 37, 60.7%) had high-grade serous carcinoma subtype. A total of 52 patients received OMT in the relapse setting while nine received it in the first-line setting. Among relapsed ovarian cancer patients, 13 patients (21.3%) experienced platinum-sensitive relapse, 16 patients (26.2%) experienced partial platinum-sensitive relapse, and 23 patients (37.7%) experienced platinum-resistant disease. The mean duration of treatment with OMT was 7.8 months. The clinical benefit rate was 59% and the overall response rate was 22.9%. Ca-125 response was seen in 40.4% of patients. The median PFS for the overall group was 6.7 months. Median PFS was longer in patients with Ca-125 response and platinum-sensitive relapse. Only five patients (8.1%) had significant toxicity. Conclusion OMT is a safe and effective palliative treatment option for epithelial ovarian cancer, worth consideration in low- and middle-income countries.
大多数晚期上皮性卵巢癌患者在标准一线治疗的三年内复发。在低收入和中等收入国家,获得聚ADP核糖聚合酶(PARP)抑制剂和抗血管生成药物等新型疗法的机会有限。口服节拍器疗法(OMT)可能是资源有限环境中一种有效的替代治疗选择。
对接受OMT的上皮性卵巢癌患者进行了一项回顾性研究。OMT包括每天50毫克环磷酰胺和每天40毫克他莫昔芬,持续给药直至出现不可接受的毒性或病情进展。OMT用于复发性卵巢癌患者以及那些不适合进行细胞减灭术和/或标准一线静脉铂类化疗的新诊断卵巢癌患者。纳入了2017年1月1日至2021年12月31日期间在本中心接受OMT的所有患者进行分析。根据研究需要,从病历中收集相关细节。使用SPSS 24版(IBM公司,纽约州阿蒙克)进行统计分析。
在研究期间共有61名患者接受了OMT。卵巢癌诊断时的中位年龄为59岁。开始OMT时的中位年龄为61岁。大多数(n = 37,60.7%)为高级别浆液性癌亚型。共有52名患者在复发情况下接受了OMT,而9名患者在一线治疗中接受了OMT。在复发性卵巢癌患者中,13名患者(21.3%)经历了铂敏感复发,16名患者(26.2%)经历了部分铂敏感复发,23名患者(37.7%)经历了铂耐药疾病。OMT的平均治疗持续时间为7.8个月。临床获益率为59%,总体缓解率为22.9%。40.4%的患者出现Ca-125反应。整个组的中位无进展生存期(PFS)为6.7个月。Ca-125反应和铂敏感复发患者的中位PFS更长。只有5名患者(8.1%)有明显毒性。
OMT是上皮性卵巢癌一种安全有效的姑息治疗选择,在低收入和中等收入国家值得考虑。