Prognostic Impact of Missed Chemotherapy Doses During Chemoradiation Therapy for Non-Small Cell Lung Cancer

被引:12
作者
Deek, Matthew P. [1 ]
Kim, Sinae [3 ,4 ]
Ahmed, Inaya [1 ]
Fang, Bruno S. [5 ]
Zou, Wei [1 ]
Malhotra, Jyoti [2 ]
Aisner, Joseph [2 ]
Jabbour, Salma K. [1 ]
机构
[1] Rutgers State Univ, Rutgers Canc Inst New Jersey, Rutgers Robert Wood Johnson Med Sch, Dept Radiat Oncol, New Brunswick, NJ USA
[2] Rutgers State Univ, Rutgers Canc Inst New Jersey, Rutgers Robert Wood Johnson Med Sch, Div Med Oncol, New Brunswick, NJ USA
[3] Rutgers Canc Inst New Jersey, Div Biometr, New Brunswick, NJ USA
[4] Rutgers State Univ, Sch Publ Hlth, Dept Biostat, Piscataway, NJ USA
[5] Reg Canc Care Associates LLC, Cent Jersey Div, East Brunswick, Jalisco, Mexico
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2018年 / 41卷 / 04期
关键词
missed chemotherapy; non-small cell lung cancer; chemoradiation therapy; toxicity; survival; PHASE-III TRIAL; RADIATION-THERAPY; TREATMENT TIME; LOCAL-CONTROL; ADJUVANT CHEMOTHERAPY; BREAST-CANCER; RADIOTHERAPY; CONCURRENT; CARCINOMA; INTERRUPTIONS;
D O I
10.1097/COC.0000000000000293
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective:The aim of this study is to investigate the impact of missed chemotherapy administrations (MCA) on the prognosis of non-small cell lung cancer (NSCLC) patients treated with definitive chemoradiation therapy (CRT).Materials and Methods:In total, 97 patients with NSCLC treated with definitive CRT were assessed for MCA due to toxicities. Logistic regression was used to determine factors associated with MCA. Kaplan-Meier curves, log-rank tests, and Cox Proportional Hazards models were conducted.Results:MCA occurred in 39% (n=38) of the patients. Median overall survival was 9.6 months for patients with MCA compared with 24.3 months for those receiving all doses (P=0.004). MCA due to decline in performance status was associated with the worst survival (4.6 mo) followed by allergic reaction (10.0 mo), hematologic toxicity (11 mo), and esophagitis (17.2 mo, P=0.027). In multivariate models, MCA was associated with higher mortality (hazard ratio, 1.97; P=0.01) and worse progression-free survival (hazard ratio, 1.96; P=0. 009).Conclusions:MCA correlated with worse prognosis and increased mortality. Methods to reduce toxicity may improve administration of all chemotherapy doses and increase overall survival in NSCLC treated with CRT.
引用
收藏
页码:362 / 366
页数:5
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