Fisch Michael J, Grabner Michael, Mytelka Daniel S, Raval Amit D, Bowman Lee, Kern David M, Churchill Collin, Singer Joseph, Wetmore Stewart, Barron John, Eleff Michael
AIM Specialty Health, Chicago, IL, USA.
HealthCore, Inc., Wilmington, DE, USA.
Cancer Manag Res. 2020 Mar 3;12:1535-1541. doi: 10.2147/CMAR.S222925. eCollection 2020.
Choosing chemotherapy for metastatic colorectal cancer (mCRC) requires balancing clinical effectiveness and risk of complications. This study characterized real-world inpatient/emergency department (ED) hospitalizations during first-line chemotherapy among individuals with mCRC.
This retrospective cohort study used data from medical and pharmacy claims. All patients had mCRC with ≥1 claim for ≥1 of the 5 most frequently utilized first-line chemotherapy agents (fluorouracil, oxaliplatin, bevacizumab, irinotecan, capecitabine). The main outcome was all-cause hospitalizations (inpatient or ED setting) identified from claims via ICD-9/10-CM coding from index date until 30 days after the end of first-line chemotherapy or last available data.
A total of 717 individuals (mean age 55 years; 58% male; ECOG 0/1/2+/missing in 44%/39%/6%/11%; median follow-up 116 days) met study criteria. Thirty-four distinct chemotherapy regimens were used. Overall, 40% of patients had ≥1 hospitalization (n=285; total 415 hospitalizations); 12% (n=85) had ≥2 hospitalizations. The median time to first hospitalization was 52 days; median inpatient length of stay was 4 days; infections/neutropenia (21%) and bowel-related complications (17%) were the most common issues associated with inpatient hospitalizations. In univariate analyses, insurance plan type, geographical location, ECOG, and renal disease were associated with hospitalization. In multivariable analyses, ECOG ≥1 was associated with a 67% increase (p<0.01) in the odds of hospitalization vs ECOG= 0.
Approximately 40% of patients with mCRC were hospitalized during the study period. Hospital stays were typically short. Further research is needed to determine how many of these hospitalizations may be avoidable. We also observed a large amount of variation in regimens used in the first-line setting.
为转移性结直肠癌(mCRC)选择化疗方案需要平衡临床疗效和并发症风险。本研究对mCRC患者一线化疗期间的真实世界住院/急诊就诊情况进行了特征描述。
这项回顾性队列研究使用了医疗和药房理赔数据。所有患者均患有mCRC,且针对5种最常用的一线化疗药物(氟尿嘧啶、奥沙利铂、贝伐单抗、伊立替康、卡培他滨)中的至少1种有≥1次理赔记录。主要结局是从索引日期至一线化疗结束后30天或最后可用数据期间,通过ICD-9/10-CM编码从理赔记录中识别出的全因住院(住院或急诊就诊)情况。
共有717名个体(平均年龄55岁;58%为男性;东部肿瘤协作组[ECOG]评分为0/1/2 + /缺失的比例分别为44%/39%/6%/11%;中位随访时间116天)符合研究标准。使用了34种不同的化疗方案。总体而言,40%的患者有≥1次住院(n = 285;共415次住院);12%(n = 85)的患者有≥2次住院。首次住院的中位时间为52天;中位住院天数为4天;感染/中性粒细胞减少(21%)和肠道相关并发症(17%)是与住院相关的最常见问题。在单因素分析中,保险计划类型、地理位置、ECOG评分和肾脏疾病与住院有关。在多变量分析中,与ECOG = 0相比,ECOG≥1与住院几率增加67%相关(p < 0.01)。
在研究期间,约40%的mCRC患者住院。住院时间通常较短。需要进一步研究以确定这些住院中有多少是可以避免的。我们还观察到一线治疗方案存在大量差异。