Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Department of Biostatistics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
JAMA Oncol. 2018 Feb 8;4(2):e173580. doi: 10.1001/jamaoncol.2017.3580.
Mismatch repair (MMR) deficiency of DNA has been observed in up to 15% of sporadic colorectal cancers (CRCs) and is a characteristic feature of Lynch syndrome, which has a higher incidence in young adults (age, <50 years) with CRC. Mismatch repair deficiency can be due to germline mutations or epigenetic inactivation, affects prognosis and response to systemic therapy, and results in unrepaired repetitive DNA sequences, which increases the risk of multiple malignant tumors.
To evaluate the utilization of MMR deficiency testing in adults with CRC and analyze nonadherence to long-standing testing guidelines in younger adults using a contemporary national data set to help identify potential risk factors for nonadherence to newly implemented universal testing guidelines.
DESIGN, SETTING, AND PARTICIPANTS: Adult (age, <30 to ≥70 years) and, of these, younger adult (<30 to 49 years) patients with invasive colorectal adenocarcinoma diagnosed between 2010 and 2012 and known MMR deficiency testing status were identified using the National Cancer Database. The study was conducted from March 16, 2016, to March 1, 2017.
Patient sociodemographic, facility, tumor, and treatment characteristics.
The primary outcome of interest was receipt of MMR deficiency testing. Multivariable logistic regression was used to identify independent predictors of testing in adult and/or young adult patients.
A total of 152 993 adults with CRC were included in the study (78 579 [51.4%] men; mean [SD] age, 66.9 [13.9] years). Of these patients, only 43 143 (28.2%) underwent MMR deficiency testing; the proportion of patients tested increased between 2010 and 2012 (22.3% vs 33.1%; P<.001). Among 17 218 younger adult patients with CRC, only 7422 (43.1%) underwent MMR deficiency testing; the proportion tested increased between 2010 and 2012 (36.1% vs 48.0%; P < .001). Irrespective of age, higher educational level (OR, 1.38; 95% CI, 1.15-1.66), later diagnosis year (OR, 1.81; 95% CI, 1.65-1.98), early stage disease (OR, 1.24; 95% CI, 1.18-1.30), and number of regional lymph nodes examined (≥12) (OR, 1.44; 95% CI, 1.34-1.55) were independently associated with MMR deficiency testing, whereas older age (OR, 0.31; 95% CI, 0.26-0.37); Medicare (OR, 0.89; 95% CI, 0.84-0.95), Medicaid (OR, 0.83; 95% CI, 0.73-0.93), or uninsured (OR, 0.78; 95% CI, 0.66-0.92) status; nonacademic vs academic/research facility type (OR, 0.44; 95% CI, 0.34-0.56); rectosigmoid or rectal tumor location (OR, 0.76; 95% CI, 0.68-0.86); unknown grade (OR, 0.61; 95% CI, 0.53-0.69); and nonreceipt of definitive surgery (OR, 0.33; 95% CI, 0.30-0.37) were associated with underuse of MMR deficiency testing.
Despite recent endorsement of universal use of MMR deficiency testing in patients with CRC and well-established guidelines aimed at high-risk populations, overall utilization of testing is poor and significant underuse of testing among young adults persists. Interventions tailored to groups at risk for nonadherence to guidelines may be warranted in the current era of universal testing.
在多达 15%的散发性结直肠癌 (CRC) 中观察到 DNA 错配修复 (MMR) 缺陷,这是林奇综合征的一个特征,林奇综合征在年轻成年人 (年龄 <50 岁) 中发病率较高。MMR 缺陷可能是由于种系突变或表观遗传失活引起的,会影响预后和对系统治疗的反应,并导致未修复的重复 DNA 序列增加,从而增加多种恶性肿瘤的风险。
评估 MMR 缺陷检测在 CRC 成年患者中的应用,并利用当代全国性数据集分析年轻患者不符合长期检测指南的情况,以帮助确定新实施的普遍检测指南不被遵守的潜在危险因素。
设计、地点和参与者:使用国家癌症数据库,确定 2010 年至 2012 年间诊断为侵袭性结直肠腺癌且已知 MMR 缺陷检测情况的成年 (年龄 <30 至 ≥70 岁) 和年轻 (<30 至 49 岁) 患者。研究于 2016 年 3 月 16 日至 2017 年 3 月 1 日进行。
患者的社会人口统计学、医疗机构、肿瘤和治疗特征。
主要观察结果是接受 MMR 缺陷检测。采用多变量逻辑回归分析方法确定成年和/或年轻患者接受检测的独立预测因素。
本研究共纳入 152993 例 CRC 成年患者 (78579 [51.4%] 为男性;平均 [标准差] 年龄为 66.9 [13.9] 岁)。其中仅 43143 (28.2%) 例患者接受了 MMR 缺陷检测;2010 年至 2012 年接受检测的患者比例有所增加 (22.3%比 33.1%;P<.001)。在 17218 例年轻 CRC 患者中,仅有 7422 (43.1%) 例接受了 MMR 缺陷检测;2010 年至 2012 年接受检测的患者比例有所增加 (36.1%比 48.0%;P < .001)。无论年龄大小,较高的教育水平 (比值比 [OR],1.38;95%置信区间 [CI],1.15-1.66)、较晚的诊断年份 (OR,1.81;95% CI,1.65-1.98)、早期疾病阶段 (OR,1.24;95% CI,1.18-1.30) 和检查的区域淋巴结数量 (≥12) (OR,1.44;95% CI,1.34-1.55) 与 MMR 缺陷检测独立相关,而年龄较大 (OR,0.31;95% CI,0.26-0.37);医疗保险 (OR,0.89;95% CI,0.84-0.95)、医疗补助 (OR,0.83;95% CI,0.73-0.93) 或无保险 (OR,0.78;95% CI,0.66-0.92) 状态;非学术与学术/研究机构类型 (OR,0.44;95% CI,0.34-0.56);直肠乙状结肠或直肠肿瘤位置 (OR,0.76;95% CI,0.68-0.86);未知的肿瘤分级 (OR,0.61;95% CI,0.53-0.69) 和未接受确定性手术 (OR,0.33;95% CI,0.30-0.37) 与 MMR 缺陷检测的使用不足相关。
尽管最近在 CRC 患者中支持普遍使用 MMR 缺陷检测,并且有明确的针对高危人群的指南,但检测的总体应用情况较差,年轻患者中检测的使用不足仍然存在。在当前普遍检测的时代,可能需要针对不符合指南的高危人群制定干预措施。