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Cervical Cancer PAX1 / JAM3 dual-gene methylation

CISCER®

Dual-gene methylation test, empowering cervical cancer prevention

PAX1/JAM3 dual-gene combined test using non-invasive cervical exfoliated cell sampling, accurately identifying CIN2+ high-grade lesions for precise triage.

NMPA Registration
国械注准 20233400253
Date Approved
2023
Clinical Data

Robust clinical data support

Based on multi-center registered clinical trials, sensitivity and specificity both reach industry-leading levels.

Sensitivity (CIN2+)89.60%
Registered clinical trial
Specificity96.50%
Registered clinical trial
Sensitivity (CIN3+)95.96%
Registered clinical trial
1,968cases
Registered clinical samples
Cervical exfoliated cells (non-invasive sampling)
Sample Type
Target Population

Who needs this test?

  • Precision triage for HPV-positive individuals
  • Women with mild cytological abnormalities (ASC-US)
  • Cervical cancer screening for postmenopausal women
  • Treatment response and recurrence monitoring for cervical lesions
Clinical Scenarios

How is it applied clinically?

  • Opportunistic and population-based cervical cancer screening
  • Colposcopy referral decisions after HPV-positive results
  • Post-treatment follow-up for high-grade cervical lesions
  • Women's health dual-screening programs at health checkup centers
Highlights

Why choose us

01

Dual-gene (PAX1/JAM3) combined test with superior performance

02

Supported by multi-center study data with 10,000+ paired cases

03

Recommended by multiple domestic and international expert consensus and guidelines

04

Ongoing nationwide multi-center real-world studies

Evidence

Cervical Cancer Related Publications

Standardized Application

Related Guidelines & Consensus