Effects of newly developed chemotherapy regimens, comorbidities, chemotherapy-related toxicities on the changing patterns of the leading causes of death in elderly patients with colorectal cancer

被引:28
|
作者
Tong, L. [1 ,2 ]
Ahn, C. [2 ,3 ]
Symanski, E. [1 ,5 ]
Lai, D. [4 ,5 ]
Du, X. L. [1 ,6 ]
机构
[1] Univ Texas Sch Publ Hlth, Div Epidemiol Human Genet & Environm Sci, Houston, TX 77030 USA
[2] UT Southwestern Med Ctr, Dept Clin Sci, Dallas, TX USA
[3] UT Southwestern Med Ctr, Harold C Simmons Canc Ctr, Dallas, TX USA
[4] Univ Texas Sch Publ Hlth, Div Biostat, Houston, TX 77030 USA
[5] Univ Texas Sch Publ Hlth, Southwest Ctr Occupat & Environm Hlth, Houston, TX 77030 USA
[6] Univ Texas Sch Publ Hlth, Ctr Hlth Serv Res, Houston, TX 77030 USA
基金
美国医疗保健研究与质量局;
关键词
colorectal cancer; cause-specific death; newly developed chemotherapy regimens; comorbidity; chemotherapy-related toxicity; III COLON-CANCER; OLDER PATIENTS; CO-MORBIDITY; SURVIVAL; FLUOROURACIL; MORTALITY; DISEASE; ASSOCIATION; OXALIPLATIN; DISPARITIES;
D O I
10.1093/annonc/mdu131
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Abundant evidences have shown that newly developed chemotherapy regimens improved 5-year survival rate of colorectal cancer (CRC) patients over the past two decades. However, their impact on risk of death from leading causes among elderly patients is still poorly understood. Patients and methods: A retrospective cohort study of 69 718 elderly CRC patients with their first primary tumors in 1992-2009, identified from the 12 areas of Surveillance, Epidemiology, and End Results-Medicare linked database with their Medicare claims up to 2010. Multivariate Cox regression models were used to assess the effect of newly developed chemotherapy regimens, comorbidities, and chemotherapy related toxicities on cause-specific death and their temporal patterns among elderly CRC patients. Results: The leading causes of death among CRC patients were CRC, circulation disorders, and secondary cancers, which accounted for 51.4%, 25%, and 4.6% of all-cause death, respectively. Patients diagnosed in more recent diagnostic time periods were significantly less likely to die of CRC [period 2: 5-year hazard ratio = 0.94, 95% confidence interval (CI) 0.90-0.97; period 3: 0.86, 0.83-0.90], circulation disorders (period 2: 0.94, 0.88-1.00; period 3: 0.80, 0.75-0.87), and more likely to die of secondary cancer (period 3: 1.42, 1.20-1.68) compared with those diagnosed in period 1. Charlson comorbidities index and the selected pre-existing comorbidities were significantly associated with increased 5-year risk of death from all three leading causes. Both hematological and gastric toxicity were associated with reduced risk of death from CRC and circulation disorders. The association between diagnostic time period and risk reduction in death from CRC depended on chemotherapy treatment (P < 0.0001). Subgroup analyses showed that the chemotherapy-dependent significant risk reduction was seen in patients with stage II-III CRC, patients without comorbidities, and patients without toxicities (P < 0.0001 for all). Conclusion: The newly developed chemotherapy regimens were associated with the decreased risk of mortality from CRC.
引用
收藏
页码:1234 / 1242
页数:9
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