Time to treatment initiation and its impact on real-world survival in metastatic colorectal cancer and pancreatic cancer

被引:4
|
作者
Gbolahan, Olumide [1 ,2 ]
Hashemi-Sadraei, Neda [3 ]
Yash, Suri [1 ,2 ]
Williams, Grant [1 ,2 ]
Ramachandran, Rekha [4 ]
Kim, Young-il [4 ]
Paluri, Ravikumar [1 ,2 ,5 ]
Outlaw, Darryl [1 ,2 ]
El-Rayes, Bassel [6 ,7 ]
Nabell, Lisle [1 ,2 ]
机构
[1] Univ Alabama Birmingham, Birmingham Sch Med, NP 2540J,1802 6th Ave S, Birmingham, AL 35233 USA
[2] Univ Alabama Birmingham, ONeal Comprehens Canc Ctr, NP 2540J,1802 6th Ave S, Birmingham, AL 35233 USA
[3] Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA
[4] Univ Alabama Birmingham, Div Prevent Med, Sch Med, Birmingham, AL 35233 USA
[5] Wake Forest Sch Med, Winston Salem, NC USA
[6] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[7] Winship Canc Inst, Atlanta, GA USA
来源
CANCER MEDICINE | 2023年 / 12卷 / 03期
关键词
colorectal neoplasms; decision making; outcome assessment; pancreatic neoplasms; time-to-treatment; ADJUVANT CHEMOTHERAPY; DUCTAL ADENOCARCINOMA; INSURANCE STATUS; DELAY; DISPARITIES; CARE; BEVACIZUMAB; MORTALITY; CETUXIMAB; OUTCOMES;
D O I
10.1002/cam4.5133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Given the dearth of data regarding the time to treatment initiation (TTI) in the palliative setting, and its impact on survival outcomes, we sought to determine TTI in a real-world cohort of metastatic colorectal cancer (mCRC) and metastatic pancreatic cancer (mPC) patients and evaluate the impact of TTI on real-world survival outcomes. Methods We collected survival and treatment data for mCRC and mPC from the Flatiron Health electronic health records (EHR) derived database. We divided TTI into 3 categories: < 2 weeks, 2-< 4 weeks, and 4-8 weeks, from diagnosis to first-line therapy. Outcome measures were median TTI, real-world overall survival (RW-OS) based on TTI categories by Kaplan-Meier method, and impact of TTI on survival using cox proportional hazard models. Results Among 7108 and 3231 patients with mCRC and mPC treated within 8 weeks of diagnosis, the median TTI were 28 days and 20 days. Median RW-OS for mCRC was 24 months; 26.9 months versus 22.6 and 18.05 months in the 4-8-week, 2-< 4 week (control) and < 2-week groups, respectively (p < 0.0001). For mPC, median RW-OS was 8 months, without significant difference in RW-OS among the groups (p = 0.05). The 4-8-week group was associated with lower hazard of death (HR 0.782, 95% CI 0.73-0.84, p < 0.0001) and the < 2-week group was associated with a higher hazard of death (HR 1.26, 95% CI 1.15-1.38, p < 0.0001) in mCRC. The 4-8-week group was associated with lower hazard of death for mPC (HR 0.88, 95% CI 0.8-0.97, p = 0.0094). Conclusion In a real-world cohort of patients treated within 8 weeks of diagnosis, and with the limitations of a retrospective study, later TTI did not have a negative impact on survival outcomes in mCRC and mPC.
引用
收藏
页码:3488 / 3498
页数:11
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