Gies Anton, Niedermaier Tobias, Gruner Laura Fiona, Heisser Thomas, Schrotz-King Petra, Brenner Hermann
Division of Preventive Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Im Neuenheimer Feld 460, D-69120 Heidelberg, Germany.
Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany.
Cancers (Basel). 2021 Feb 5;13(4):644. doi: 10.3390/cancers13040644.
Fecal immunochemical tests (FITs) are widely used for colorectal cancer (CRC) screening. The detection of early-stage cancer and advanced adenoma (AA), the most important premalignant lesion, is highly relevant to reducing CRC-related deaths. We aimed to assess sensitivity for the detection of CRC and AA stratified by tumor stage; number; size; histology of AA; and by location, age, sex, and body mass index (BMI).
Participants of screening colonoscopy ( = 2043) and newly diagnosed CRC patients ( = 184) provided a stool sample before bowel preparation or CRC surgery. Fecal hemoglobin concentration was determined in parallel by nine different quantitative FITs among 94 CRC patients, 200 AA cases, and 300 participants free of advanced neoplasm. Sensitivities were calculated at original cutoffs and at adjusted cutoffs, yielding 93% specificity among all FITs.
At adjusted cutoffs, UICC stage I cancers yielded consistently lower sensitivities (range: 62-68%) compared to stage II-IV cancers (range: 73-89%). An even stronger gradient was observed according to T status, with substantially lower sensitivities for T1 (range: 39-57%) than for T2-T4 cancers (range: 71-100%). Sensitivities for the detection of participants with multiple AAs ranged from 55% to 64% and were by up to 25% points higher than sensitivities for T1 cancers.
FITs detect stage I cancers and especially T1 cancers at substantially lower sensitivities than more advanced cancer stages. Participants with multiple AAs were detected with slightly lower sensitivities than stage I cancers and with even higher sensitivities than T1 cancers. Further research should focus on improving the detection of early-stage cancers.
粪便免疫化学检测(FITs)广泛用于结直肠癌(CRC)筛查。早期癌症以及最重要的癌前病变——高级别腺瘤(AA)的检测对于降低CRC相关死亡至关重要。我们旨在评估按肿瘤分期、数量、大小、AA组织学类型以及位置、年龄、性别和体重指数(BMI)分层的CRC和AA检测敏感性。
筛查结肠镜检查参与者(n = 2043)和新诊断的CRC患者(n = 184)在肠道准备或CRC手术前提供粪便样本。在94例CRC患者、200例AA病例和300例无高级别肿瘤的参与者中,通过9种不同的定量FITs平行测定粪便血红蛋白浓度。在原始临界值和调整后的临界值下计算敏感性,所有FITs的特异性均为93%。
在调整后的临界值下,与II-IV期癌症(范围:73-89%)相比,国际抗癌联盟(UICC)I期癌症的敏感性始终较低(范围:62-68%)。根据T分期观察到更强的梯度,T1期癌症的敏感性(范围:39-57%)明显低于T2-T4期癌症(范围:71-100%)。检测多个AA参与者的敏感性范围为55%至64%,比T1期癌症的敏感性高25个百分点。
FITs检测I期癌症,尤其是T1期癌症的敏感性明显低于更晚期的癌症阶段。检测多个AA参与者的敏感性略低于I期癌症,但高于T1期癌症。进一步的研究应侧重于提高早期癌症的检测率。