Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Biostatistics and Bioinformatics Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
JAMA Netw Open. 2024 Feb 5;7(2):e240044. doi: 10.1001/jamanetworkopen.2024.0044.
Hispanic and non-Hispanic Black patients receiving neoadjuvant therapy and surgery for locally advanced rectal cancer (LARC) achieve less favorable clinical outcomes than non-Hispanic White patients, but the source of this disparity is incompletely understood.
To assess whether racial and ethnic disparities in treatment outcomes among patients with LARC could be accounted for by social determinants of health and demographic, clinical, and pathologic factors known to be associated with treatment response.
DESIGN, SETTING, AND PARTICIPANTS: The National Cancer Database was interrogated to identify patients with T3 to T4 or N1 to N2 LARC treated with neoadjuvant therapy and surgery. Patients were diagnosed between January 1, 2004, and December 31, 2017. Data were culled from the National Cancer Database from July 1, 2022, through December 31, 2023.
Neoadjuvant therapy for rectal cancer followed by surgical resection.
The primary outcome was the rate of pathologic complete response (pCR) following neoadjuvant therapy. Secondary outcomes were rate of tumor downstaging and achievement of pN0 status.
A total of 34 500 patient records were reviewed; 21 679 of the patients (62.8%) were men and 12 821 (37.2%) were women. The mean (SD) age at diagnosis was 59.7 (12.0) years. In terms of race and ethnicity, 2217 patients (6.4%) were Hispanic, 2843 (8.2%) were non-Hispanic Black, and 29 440 (85.3%) were non-Hispanic White. Hispanic patients achieved tumor downstaging (48.9% vs 51.8%; P = .01) and pN0 status (66.8% vs 68.8%; P = .02) less often than non-Hispanic White patients. Non-Hispanic Black race, but not Hispanic ethnicity, was associated with less tumor downstaging (odds ratio [OR], 0.86 [95% CI, 0.78-0.94]), less frequent pN0 status (OR, 0.91 [95% CI, 0.83-0.99]), and less frequent pCR (OR, 0.81 [95% CI, 0.72-0.92]). Other factors associated with reduced rate of pCR included rural location (OR, 0.80 [95% CI, 0.69-0.93]), lack of or inadequate insurance (OR for Medicaid, 0.86 [95% CI, 0.76-0.98]; OR for no insurance, 0.65 [95% CI, 0.54-0.78]), and treatment in a low-volume center (OR for first quartile, 0.73 [95% CI, 0.62-0.87]; OR for second quartile, 0.79 [95% CI, 0.70-0.90]; OR for third quartile, 0.86 [95% CI, 0.78-0.94]). Clinical and pathologic variables associated with a decreased pCR included higher tumor grade (OR, 0.58 [95% CI, 0.49-0.70]), advanced tumor stage (OR for T3, 0.56 [95% CI, 0.42-0.76]; OR for T4, 0.30 [95% CI, 0.22-0.42]), and lymph node-positive disease (OR for N1, 0.83 [95% CI, 0.77-0.89]; OR for N2, 0.73 [95% CI, 0.65-0.82]).
The findings of this cohort study suggest that disparate treatment outcomes for Hispanic and non-Hispanic Black patients are likely multifactorial in origin. Future investigation into additional social determinants of health and biological variables is warranted.
接受新辅助治疗和手术的局部晚期直肠肿瘤(LARC)的西班牙裔和非西班牙裔黑人患者的临床结局不如非西班牙裔白人患者有利,但造成这种差异的原因尚不完全清楚。
评估 LARC 患者治疗结果中的种族和民族差异是否可以通过与治疗反应相关的健康和人口统计学、临床及病理因素的社会决定因素来解释。
设计、地点和参与者:国家癌症数据库被查询以确定接受新辅助治疗和手术的 T3 至 T4 或 N1 至 N2 LARC 患者。患者于 2004 年 1 月 1 日至 2017 年 12 月 31 日期间被诊断。数据于 2022 年 7 月 1 日至 2023 年 12 月 31 日从国家癌症数据库中提取。
直肠癌的新辅助治疗后行手术切除。
主要结局是新辅助治疗后病理完全缓解(pCR)的发生率。次要结局是肿瘤降期率和达到 pN0 状态的比例。
共回顾了 34500 份患者记录;21679 名患者(62.8%)为男性,12821 名(37.2%)为女性。诊断时的平均(SD)年龄为 59.7(12.0)岁。在种族和民族方面,2217 名患者(6.4%)为西班牙裔,2843 名(8.2%)为非西班牙裔黑人,29440 名(85.3%)为非西班牙裔白人。与非西班牙裔白人患者相比,西班牙裔患者的肿瘤降期(48.9% vs 51.8%;P = .01)和 pN0 状态(66.8% vs 68.8%;P = .02)较少发生。非西班牙裔黑人种族,但不是西班牙裔民族,与肿瘤降期(比值比[OR],0.86 [95%置信区间,0.78-0.94])、pN0 状态(OR,0.91 [95%置信区间,0.83-0.99])和 pCR 频率(OR,0.81 [95%置信区间,0.72-0.92])较低相关。其他与 pCR 发生率降低相关的因素包括农村地区(OR,0.80 [95%置信区间,0.69-0.93])、缺乏或保险不足(医疗补助的 OR,0.86 [95%置信区间,0.76-0.98];无保险的 OR,0.65 [95%置信区间,0.54-0.78])以及在低容量中心治疗(四分位第一的 OR,0.73 [95%置信区间,0.62-0.87];四分位第二的 OR,0.79 [95%置信区间,0.70-0.90];四分位第三的 OR,0.86 [95%置信区间,0.78-0.94])。与 pCR 降低相关的临床和病理变量包括肿瘤分级较高(OR,0.58 [95%置信区间,0.49-0.70])、肿瘤分期较晚(T3 的 OR,0.56 [95%置信区间,0.42-0.76];T4 的 OR,0.30 [95%置信区间,0.22-0.42])和淋巴结阳性疾病(N1 的 OR,0.83 [95%置信区间,0.77-0.89];N2 的 OR,0.73 [95%置信区间,0.65-0.82])。
这项队列研究的结果表明,西班牙裔和非西班牙裔黑人患者治疗结果的差异可能是多因素造成的。有必要进一步研究其他社会决定因素和生物学变量。