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结直肠癌基因转诊:我们做得够吗?

Colorectal cancer genetic referral: Are we doing enough?

作者信息

Broyles Whitnee C, Narvekar Priyanka, Lee Hanjoo, Fleshman James W, Fichera Alessandro, Wells Katerina K O

机构信息

Department of Surgery, Baylor University Medical Center, Dallas, Texas, USA.

Texas A&M School of Medicine, Baylor University Medical Center, Dallas, Texas, USA.

出版信息

Proc (Bayl Univ Med Cent). 2024 Feb 8;37(2):250-254. doi: 10.1080/08998280.2024.2303529. eCollection 2024.

Abstract

PURPOSE

Guidelines are published for referral to genetic counseling and multigene panel genetic testing for colorectal cancer. We hypothesize that these guidelines are not recognized in practice, resulting in the underreferral of patients to genetic counseling. We aimed to investigate the clinical impact of these guidelines.

METHODS

This was a retrospective cohort study conducted using a single academic-institution colorectal cancer patient registry. The registry included all patients ≥18 years old with a pathologic diagnosis of colon cancer, rectal cancer, or polyposis from January 2018 to January 2020 with complete chart data to determine inclusion into the genetic referral cohort.

RESULTS

Out of 225 colon cancer patients, 92 met criteria for referral to genetic testing, but only 56 patients obtained referral and 39 completed testing. For rectal cancer, 29 out of 127 patients met criteria for referral, but only 11 obtained referral and 8 completed testing. Actionable variants, defined as pathogenic or likely pathogenic, were identified in 18 colon cancer and 5 rectal cancer patients. Age made a significant difference in the referral rate for colon cancer ( = 0.02) but not rectal cancer ( > 0.05).

CONCLUSION

Our study demonstrates poor adherence to guideline-based genetic testing. These data emphasize the need for more consistent referral to genetic testing for diagnosis of underlying inherited cancer syndromes.

摘要

目的

发布了关于转诊进行结直肠癌遗传咨询和多基因panel基因检测的指南。我们推测这些指南在实际应用中未得到认可,导致患者转诊至遗传咨询的比例不足。我们旨在调查这些指南的临床影响。

方法

这是一项回顾性队列研究,使用单一学术机构的结直肠癌患者登记系统进行。该登记系统纳入了2018年1月至2020年1月期间所有年龄≥18岁、经病理诊断为结肠癌、直肠癌或息肉病且有完整病历数据的患者,以确定是否纳入遗传转诊队列。

结果

在225例结肠癌患者中,92例符合基因检测转诊标准,但只有56例患者获得转诊,39例完成检测。对于直肠癌,127例患者中有29例符合转诊标准,但只有11例获得转诊,8例完成检测。在18例结肠癌患者和5例直肠癌患者中鉴定出可操作的变异,定义为致病性或可能致病性变异。年龄对结肠癌的转诊率有显著影响(=0.02),但对直肠癌没有显著影响(>0.05)。

结论

我们的研究表明对基于指南的基因检测的依从性较差。这些数据强调需要更一致地转诊进行基因检测,以诊断潜在的遗传性癌症综合征。

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