Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee, USA
Department of Gynecology and Obstetrics, Gynecologic Oncology, Leuven Cancer Institute, Catholic University Leuven, Leuven, Belgium.
Int J Gynecol Cancer. 2023 Jan 3;33(1):1-9. doi: 10.1136/ijgc-2022-003947.
The impact of blood transfusion on ovarian cancer survival is uncertain.
To investigate whether peri-operative blood transfusion negatively impacted progression-free survival, overall survival, and quality of life in patients with advanced ovarian cancer.
We performed an ancillary analysis of the European Organization for Research and Treatment (EORTC) 55971 phase III trial, in which patients were randomized to primary debulking surgery versus neoadjuvant chemotherapy. Patients included in the per-protocol analysis were categorized by receipt of a transfusion.
612 of 632 (97%) of patients had adequate data for analysis. Of those, 323 (53%) received a transfusion. The transfusion cohort was more likely to have had better Word Health Organization (WHO) performance status, serous histology, undergone primary debulking surgery, and received more aggressive surgery, with higher rates of no gross residual disease. Median overall survival was 34.0 vs 35.2 months in the no transfusion and transfusion cohorts (p=0.97). The adjusted HR for death was 1.18 (95% CI 0.94 to 1.48) in favor of the transfusion cohort. Median progression-free survival was 13.6 vs 12.6 months in the no transfusion and transfusion cohorts (p=0.96). The adjusted HR for progression was 1.14 (95% CI 0.91 to 1.43). There were no significant differences in global quality of life, fatigue, dyspnea, or physical functioning between the two cohorts at baseline or at any of the four assessment times. Grade 3 and 4 surgical site infections were more common in the transfusion cohort.
Transfusion did not negatively impact progression-free survival or overall survival; however, it was associated with increased peri-operative morbidity without improvements in quality of life.
输血对卵巢癌生存的影响尚不确定。
研究围手术期输血是否会对晚期卵巢癌患者的无进展生存期、总生存期和生活质量产生负面影响。
我们对欧洲癌症研究与治疗组织(EORTC)55971 期临床试验进行了辅助分析,该试验中患者被随机分为直接减瘤手术与新辅助化疗组。根据是否输血,对符合方案分析的患者进行分类。
在 632 例可评估患者中,有 612 例(97%)患者的数据足够用于分析。其中 323 例(53%)患者接受了输血。输血组更有可能具有更好的世界卫生组织(WHO)表现状态、浆液性组织学特征、接受直接减瘤手术以及接受更积极的手术,无肉眼残留疾病的比例更高。无输血组和输血组的中位总生存期分别为 34.0 个月和 35.2 个月(p=0.97)。输血组死亡的调整 HR 为 1.18(95%CI 0.94 至 1.48)。无输血组和输血组的中位无进展生存期分别为 13.6 个月和 12.6 个月(p=0.96)。进展的调整 HR 为 1.14(95%CI 0.91 至 1.43)。两组在基线或任何四个评估时间点,在整体生活质量、疲劳、呼吸困难或身体功能方面均无显著差异。输血组的 3 级和 4 级手术部位感染更为常见。
输血并未对无进展生存期或总生存期产生负面影响,但与围手术期发病率增加相关,而生活质量并未改善。