Impact of operative start time on surgical outcomes in patients undergoing primary cytoreduction for advanced ovarian cancer

被引:20
|
作者
Tanner, Edward J. [1 ]
Long, Kara C. [1 ]
Zhou, Qin [2 ]
Brightwell, Rachel M. [1 ]
Gardner, Ginger J. [1 ]
Abu-Rustum, Nadeem R. [1 ]
Leitao, Mario M., Jr. [1 ]
Sonoda, Yukio [1 ]
Barakat, Richard R. [1 ]
Iasonos, Alexia [2 ]
Chi, Dennis S. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Gynecol Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Biostat, New York, NY 10065 USA
关键词
Cytoreductive surgery; Advanced ovarian cancer; Operative start time; QUALITY-IMPROVEMENT; SLEEP-DEPRIVATION; SURGERY; SURVIVAL; MORBIDITY; PERFORMANCE; CARCINOMA; DISEASE; PART;
D O I
10.1016/j.ygyno.2012.04.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives. To evaluate the impact of operative start time (OST) on surgical outcomes in patients with advanced ovarian cancer. Methods. All stage IIIB-IV serous ovarian cancer patients who underwent primary surgery at our institution from 1/01 to 1/10 were identified. Fourteen factors were evaluated for an association with surgical outcomes including OST and OR tumor index (1 point each for carcinomatosis and/or bulky [>= 1 cm] upper abdominal disease). Univariate logistic regression considering within-surgeon clustering was performed for cytoreduction to <= 1 cm versus > 1 cm residual disease. In patients with <= 1 cm residual disease, univariate logistic regression considering within-surgeon clustering was performed for 1-10 mm residual disease versus complete gross resection (CGR, 0 mm residual). A multivariate logistic model was developed based on univariate analysis results in the <= 1 cm residual disease cohort. Results. Of 422 patients, residual disease was: 0 mm, 144 (34.1%); 1-10 mm, 175 (41.5%); > 10 mm, 103 (23.3%). OST was not associated with cytoreduction to <= 1 cm residual disease on univariate analysis. In the <= 1 cm residual disease cohort, albumin, CA-125, ascites, ASA score, stage, OR tumor index, and OST were associated with CGR on univariate analysis. Earlier OSTs were associated with increased rates of CGR. On multivariate analysis, CA-125 was independently associated with CGR. OST was associated with CGR in patients with an OR tumor index of 2 but not an OR tumor index < 2. Conclusions. OST was not associated with cytoreduction to <= 1 cm residual disease in patients with advanced serous ovarian cancer. In the cohort of patients with <= 1 cm residual disease, later OSTs were associated with reduced rates of CGR in patients with greater tumor burden. (c) 2012 Elsevier Inc. All rights reserved.
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页码:58 / 63
页数:6
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