University of Alabama at Birmingham, Department of Obstetrics and Gynecology, Division of Gynecology Oncology, Birmingham, AL 35249, USA.
Gynecol Oncol. 2011 Sep;122(3):532-5. doi: 10.1016/j.ygyno.2011.05.023. Epub 2011 Jun 11.
Relative dose intensity (RDI) is the ratio of delivered dose intensity of chemotherapy to standard dose intensity. In this study, we sought to determine the prognostic significance of RDI in patients with epithelial ovarian cancer (EOC).
A retrospective analysis of chemotherapy naïve patients treated between 2001 and 2008 with intravenous taxane and platinum was performed. RDI was calculated as the delivered dose intensity (total dose delivered/total time of therapy) divided by standard dose intensity calculated for each regimen and compared to progression-free survival (PFS). Multivariate recursive partitioning survival analysis was utilized.
138 EOC patients completed initial taxane/platinum-based chemotherapy following surgical cytoreduction. The most common reasons for dose delays and reductions were thrombocytopenia (38%) and neutropenia (31%). 24% of treatment delays were due to social reasons such as transportation constraints or scheduling conflicts. The average RDI was 90% (range, 24-126%). The mean PFS was 31 months (range, 3-117). Patients that achieved an RDI between 70% and 110% had a mean PFS of 32 months compared to 20 months in patients with an RDI of <70% or >110% (p=0.046). 14 patients (10%) had a RDI of <70%.
RDI is a significant predictor of survival in patients with EOC. Effort should be made to achieve an RDI of at least 70%. Dose reductions and treatment delays could be minimized by utilizing prophylactic colony stimulating factors and educating patients about the importance of adhering to their treatment schedule.
相对剂量强度(RDI)是化疗实际给予剂量强度与标准剂量强度的比值。本研究旨在确定 RDI 对上皮性卵巢癌(EOC)患者的预后意义。
回顾性分析了 2001 年至 2008 年期间接受静脉紫杉醇和铂类化疗且无化疗史的患者。RDI 计算方法为实际给予的剂量强度(总剂量/治疗总时间)除以每种方案的标准剂量强度,并与无进展生存期(PFS)进行比较。采用多变量递归分区生存分析。
138 例 EOC 患者在肿瘤细胞减灭术后完成了初始紫杉醇/铂类化疗。剂量延迟和减少的最常见原因是血小板减少症(38%)和中性粒细胞减少症(31%)。24%的治疗延迟是由于交通限制或日程安排冲突等社会原因造成的。RDI 的平均值为 90%(范围为 24-126%)。平均 PFS 为 31 个月(范围为 3-117 个月)。RDI 为 70%至 110%之间的患者平均 PFS 为 32 个月,而 RDI<70%或>R110%的患者 PFS 为 20 个月(p=0.046)。14 例(10%)患者的 RDI<70%。
RDI 是 EOC 患者生存的重要预测因素。应努力实现至少 70%的 RDI。通过预防性使用集落刺激因子并教育患者按时治疗的重要性,可以最大限度地减少剂量减少和治疗延迟。