Adjuvant Chemoradiation Therapy for Cervical Cancer and Effect of Timing and Duration on Treatment Outcome

被引:27
作者
Jhawar, Sachin [1 ]
Hathout, Lara [1 ]
Elshaikh, Mohamed A. [2 ]
Beriwal, Sushil [3 ]
Small, William [4 ]
Mahmoud, Omar [1 ,5 ]
机构
[1] Rutgers State Univ, Canc Inst New Jersey, Dept Radiat Oncol, New Brunswick, NJ USA
[2] Henry Ford Hosp, Dept Radiat Oncol, Detroit, MI USA
[3] Univ Pittsburgh, Inst Canc, Dept Radiat Oncol, Pittsburgh, PA USA
[4] Loyola Univ, Dept Radiat Oncol, Chicago, IL 60611 USA
[5] Rutgers State Univ, New Jersey Med Sch, Dept Radiat Oncol, Newark, NJ USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2017年 / 98卷 / 05期
关键词
SQUAMOUS-CELL CARCINOMA; UTERINE CERVIX; TREATMENT TIME; HUMAN-PAPILLOMAVIRUS; POSTOPERATIVE RADIOTHERAPY; CONCURRENT CHEMOTHERAPY; RADICAL HYSTERECTOMY; RADIATION-THERAPY; REPOPULATION; PATTERNS;
D O I
10.1016/j.ijrobp.2017.03.045
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Worse treatment outcomes can be expected with prolongation of the overall treatment time (OTT) during definitive chemoradiation therapy (CRT) for cervical cancer. In the adjuvant setting, data on the relative importance of the OTT and the importance of RT and chemotherapy synchronization are scarce. Using the National Cancer Database, we evaluated the effect of these treatment variables on overall survival in the adjuvant CRT setting. Methods and Materials: The present analysis included nonmetastatic cervical cancer patients undergoing hysterectomy followed by adjuvant CRT. The proportional hazard model was used to estimate the effect of prognostic factors (age, comorbidity, race, tumor size, tumor grade, tumor histologic type, number of high-risk pathologic factors) and time-related variables (surgery to RT start interval [SR], OTT [RT start to end dates], package time [from diagnosis date to CRT end date] and optimum CRT synchronization [whether chemotherapy and RT start dates coincided]) on survival. Results: Of 3051 patients, 60% finished RT within 7 weeks and 85% received optimum CRT. Among other factors, univariate analysis identified longer OTT (hazards ratio [HR] 1.33; P<.001), longer SR (HR 1.17; P = .05), and nonoptimum CRT timing (HR 1.21; P = .04) as poor prognosticators. Of these factors, SR (HR 1.20; P = .04) and OTT (HR 1.21; P = .002) retained significance on multivariate analysis. An OTT >7 weeks remained a significant factor even after propensity score matching (PZ. 04). Conclusions: The results of our analysis suggest that prolongation of the adjuvant CRT duration >7 weeks is associated with poor survival and SR of <8 weeks should be attempted whenever clinically feasible. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1132 / 1141
页数:10
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