Adherence to CheckMate 577 Within a Community Health Care System in the First 2 Years After Approval

John M. Campbell MD , Brian E. Louie MD , Peter T. White MD , Eric Vallières MD , Alexander S. Farivar MD , Adam J. Bograd MD
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Abstract

Background

CheckMate 577 demonstrated a significant benefit with adjuvant nivolumab for those with residual disease after esophagectomy following chemoradiation, resulting in subsequent Food and Drug Administration approval and guideline inclusion. We analyzed adherence to this recommendation in a nontrial setting and assessed for factors associated with noncompliance within our health care system.

Methods

We performed a cross-sectional analysis of patients with esophageal cancer within a multistate community health care system between February 2021 and December 2022. Patients with resected residual disease following induction chemoradiation were included. Patients were assigned to categories of those offered nivolumab and those not, then assessed for demographic, socioeconomic, or clinical factors associated with nonadherence. Area Deprivation Index was used as surrogate for socioeconomic status. Patients completing year-long nivolumab were then compared with those discontinuing prematurely for factors associated with noncompletion.

Results

Of the 73 patients eligible for nivolumab, 67 (92%) were offered therapy. Not being offered nivolumab was associated with receiving care from medical oncologists located in more disadvantaged communities. Of patients offered nivolumab, 57 of 67 (85%) initiated treatment. Year-long immunotherapy was completed by 25 (48%) patients. Patients with node-positive disease were more likely to have completed year-long nivolumab.

Conclusions

In the first 2 years after CheckMate 577, results within our health care system suggest high clinician adherence to and patient acceptance of adjuvant immunotherapy with decreased adoption in more socioeconomically challenged oncology offices. In addition, compliance with the year-long adjuvant regimen mirrored clinical trial results. These results warrant further validation in a more diverse, less affluent population.
在获得批准后的头两年内,在社区卫生保健系统内遵守CheckMate 577
背景:checkmate 577显示,对于那些放化疗后食管切除术后残留疾病患者,辅助nivolumab具有显著的益处,随后获得了美国食品和药物管理局(fda)的批准和指南的纳入。我们分析了在非试验环境下对该建议的依从性,并评估了在我们的卫生保健系统中与不依从性相关的因素。方法:我们对2021年2月至2022年12月期间多州社区卫生保健系统内的食管癌患者进行了横断面分析。包括诱导放化疗后切除残留病变的患者。患者被分配到接受纳武单抗治疗和不接受纳武单抗治疗的类别,然后评估与不依从性相关的人口统计学、社会经济或临床因素。区域剥夺指数作为社会经济地位的替代指标。完成一年纳武单抗治疗的患者与因未完成相关因素而过早停止治疗的患者进行比较。结果在符合nivolumab治疗条件的73例患者中,67例(92%)接受了治疗。不提供纳武单抗与接受来自弱势社区的内科肿瘤学家的护理有关。在给予纳武单抗的患者中,67例中有57例(85%)开始治疗。25例(48%)患者完成了为期一年的免疫治疗。淋巴结阳性疾病患者更有可能完成一年的纳武单抗治疗。结论:在CheckMate 577项目实施后的前2年,美国医疗保健系统的结果表明,临床医生对辅助免疫治疗的依从性和患者接受度较高,但在社会经济困难的肿瘤诊所,辅助免疫治疗的接受度有所下降。此外,对为期一年的辅助治疗方案的依从性反映了临床试验结果。这些结果值得在更多样化、不那么富裕的人群中进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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