Liutkauskiene Sigita, Janciauskiene Rasa, Jureniene Kristina, Grizas Saulius, Malonyte Rasa, Juozaityte Elona
Oncology Institute of Lithuanian University of Health Sciences, Kaunas, Lithuania.
Institute of Biomedical Sciences of Lithuanian University of Health Sciences, Kaunas, Lithuania.
BMC Cancer. 2015 Mar 7;15:105. doi: 10.1186/s12885-015-1104-5.
Ovarian cancer is a common gynaecological malignancy still remaining a challenge to treat. The objective of this study was to evaluate the impact of platinum dose reduction and chemotherapy delays on progression free survival and overall survival in patients with stage III ovarian cancer and to analyze reasons for such chemotherapy scheme modifications.
Medical records of patients with FIGO stage III ovarian cancer were reviewed. Inclusion criteria involved FIGO stage III epithelial ovarian carcinoma; cytoreductive surgery performed and 6 courses of platinum-based chemotherapy completed; no neoadjuvant chemotherapy applied; and no history of previous malignancies. Progression free survival and overall survival were analyzed using Kaplan-Meier and Cox proportional hazards models.
Significant 3.3 times higher death risk in patients who experienced only chemotherapy delays compared with patients who did not experience any chemotherapy scheme modifications was established (HR = 3.3, 95% Cl: 1.2 - 8.5, p = 0.016). Increased death risk in patients who experienced only chemotherapy delays compared with patients who experienced both chemotherapy delays and platinum dose reduction was also established (HR = 2.3, 95% Cl: 1.1 - 4.8, p = 0.021). Main reasons for chemotherapy scheme modifications (in decreasing order) were the following: neutropenia, modifications with no objective medical reasons, renal disorders, anaemia, poor performance status, gastrointestinal symptoms and neuropathy. Overall survival in patients who experienced chemotherapy scheme modifications with no objective medical reasons was non-inferior than in patients who did not experience any chemotherapy scheme modifications.
Chemotherapy delays in patients with FIGO stage III ovarian cancer caused lower overall survival. The most common reason for chemotherapy scheme modifications was neutropenia.
卵巢癌是一种常见的妇科恶性肿瘤,其治疗仍然是一项挑战。本研究的目的是评估铂类药物剂量减少和化疗延迟对III期卵巢癌患者无进展生存期和总生存期的影响,并分析此类化疗方案调整的原因。
回顾了国际妇产科联盟(FIGO)III期卵巢癌患者的病历。纳入标准包括:FIGO III期上皮性卵巢癌;接受了肿瘤细胞减灭术并完成了6个疗程的铂类化疗;未应用新辅助化疗;且无既往恶性肿瘤病史。使用Kaplan-Meier法和Cox比例风险模型分析无进展生存期和总生存期。
与未经历任何化疗方案调整的患者相比,仅经历化疗延迟的患者死亡风险显著高出3.3倍(HR = 3.3,95%CI:1.2-8.5,p = 0.016)。与同时经历化疗延迟和铂类药物剂量减少的患者相比,仅经历化疗延迟的患者死亡风险也有所增加(HR = 2.3,95%CI:1.1-4.8,p = 0.021)。化疗方案调整的主要原因(按降序排列)如下:中性粒细胞减少、无客观医学原因的调整、肾脏疾病、贫血、身体状况差、胃肠道症状和神经病变。无客观医学原因而经历化疗方案调整的患者的总生存期不劣于未经历任何化疗方案调整的患者。
FIGO III期卵巢癌患者化疗延迟导致总生存期降低。化疗方案调整最常见的原因是中性粒细胞减少。