Fremont-Smith Maurice, Marino James, Griffin Bryan, Spencer Lynn, Bolick David
SeaCoast Pathology, 1 Hampton Road, Suite 108, Exeter, NH 03833, USA.
Cancer. 2004 Oct 25;102(5):269-79. doi: 10.1002/cncr.20599.
Split-sample clinical trials for liquid-based Papanicolaou (Pap) smears demonstrated that the liquid-based Pap smear was a safe and effective replacement for the conventional Pap smear. However, clinical intended use of liquid-based technology employs direct-to-vial collection methods. The current study compared the cytologic detection rates of the liquid-based Pap smear with conventional Pap smears in a direct-to-vial study performed at three clinical sites.
Data from 58,580 prospective SurePath slides and 58,988 historic conventional slides were collected. Results were statistically compared with regard to disease prevalence and adequacy to include biopsy follow-up data for conventional and SurePath tests.
The SurePath method was found to provide a statistically significantly greater detection rate for clinically important categories of high-grade squamous intraepithelial lesion (HSIL+) and low-grade squamous intraepithelial lesion (LSIL+) (64% and 107%, respectively; P < 0.00001 for each lesion) compared with conventional slides. The clinical significance of increased cytologic detection using SurePath was supported by biopsy data that essentially demonstrated concordance with regard to biopsy interpretation for HSIL+ (P = 0.9105 at Site 1; P = 1.0000 at Site 2; and P = 1.0000 at Site 3) and LSIL+ (P = 0.6966 at Site 1; P = 0.8052 at Site 2; and P = 1.00 at Site 3). The detection rate of atypical squamous cells of undetermined significance (ASCUS+) was found to be significantly increased (75.12%; P < 0.00001). A statistically significantly lower proportion of unsatisfactory slides using the SurePath test compared with conventional slides was noted (-58%; P < 0.00001). The ASCUS/LSIL+ ratio was found to be reduced overall when using SurePath (-28.9%), regardless of whether the study sites were combined or considered individually. The rate of false-negative results noted with SurePath (10.43%) and conventional slides (12.97%) was essentially equivalent.
The SurePath Pap smear was found to outperform conventional slides in the detection of HSIL+ and LSIL+ cytologic lesions of the cervix and reduced the number of unsatisfactory diagnoses. The HSIL+ advantage for SurePath is not limited to HSIL but appears to extend to carcinoma as well.
液基巴氏涂片的分样本临床试验表明,液基巴氏涂片是传统巴氏涂片安全有效的替代品。然而,液基技术的临床预期用途采用直接采集到保存瓶的方法。本研究在三个临床地点进行的直接采集到保存瓶的研究中,比较了液基巴氏涂片与传统巴氏涂片的细胞学检出率。
收集了58580份前瞻性SurePath玻片和58988份历史传统玻片的数据。对疾病患病率和充分性进行了统计学比较,包括传统检查和SurePath检查的活检随访数据。
与传统玻片相比,发现SurePath方法在临床上重要的高级别鳞状上皮内病变(HSIL+)和低级别鳞状上皮内病变(LSIL+)类别中的检出率在统计学上显著更高(分别为64%和107%;每种病变P<0.00001)。活检数据支持了使用SurePath增加细胞学检出的临床意义,这些数据基本上表明在HSIL+(第1个地点P = 0.9105;第2个地点P = 1.0000;第3个地点P = 1.0000)和LSIL+(第1个地点P = 0.6966;第2个地点P = 0.8052;第3个地点P = 1.00)的活检解读方面具有一致性。意义不明确的非典型鳞状细胞(ASCUS+)的检出率显著增加(75.12%;P<0.00001)。与传统玻片相比,使用SurePath检测不满意玻片的比例在统计学上显著更低(-58%;P<0.00001)。无论研究地点是合并还是单独考虑,使用SurePath时ASCUS/LSIL+比率总体上降低(-28.9%)。SurePath(10.43%)和传统玻片(12.97%)的假阴性结果率基本相当。
发现SurePath巴氏涂片在检测宫颈HSIL+和LSIL+细胞学病变方面优于传统玻片,并减少了不满意诊断的数量。SurePath在HSIL+方面的优势不仅限于HSIL,似乎也扩展到了癌。