What does a CA (Cancer Antigen) 125 level of 174 indicate?

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CA-125 Level of 174 U/mL: Clinical Interpretation and Management

A CA-125 level of 174 U/mL is elevated above the standard threshold of 35 U/mL and requires further evaluation with imaging (CT or transvaginal ultrasound with Doppler) to assess for ovarian malignancy, though this level can occur in both benign and malignant conditions. 1

Understanding the Significance of This Level

Malignancy Risk Assessment

  • CA-125 has 98.5% specificity for ovarian cancer in women over 50 years when elevated above 35 U/mL, making this level concerning enough to warrant thorough investigation 2
  • However, CA-125 detects only 50% of stage I ovarian cancers, so sensitivity for early disease is limited 2
  • The level of 174 U/mL falls in an intermediate range where both benign and malignant conditions are possible 3, 4
  • Epithelial ovarian cancer is present in approximately 85% of patients with advanced disease who have elevated CA-125, but only 50% of early-stage cases show elevation 5

Benign Conditions That Can Cause This Level

CA-125 levels can exceed 1,000 U/mL in benign conditions, so a level of 174 U/mL does not automatically indicate malignancy 6, 3:

  • Endometriosis and adenomyosis are common causes of moderate CA-125 elevation 7, 6, 8
  • Pelvic inflammatory disease can elevate CA-125 2, 7
  • Benign ovarian cysts (particularly complex cysts with septations) 2, 7
  • Menstruation and pregnancy (physiologic elevations) 8, 9
  • Ascites from any cause (including cirrhosis) elevates CA-125, even in men 7
  • Pleural effusion or peritonitis 3

Immediate Next Steps

Required Imaging Evaluation

Obtain CT scan of abdomen and pelvis with contrast OR transvaginal ultrasound with color/power Doppler to characterize any pelvic masses 1:

  • Look for complex ovarian masses with solid and cystic components, internal echoes, septations, papillary projections, ascites, or peritoneal metastases 2
  • Color or power Doppler is essential to differentiate true solid components from debris and assess vascular patterns 2
  • MRI with IV contrast is superior to CT for characterizing indeterminate adnexal masses if ultrasound findings are unclear 2

Additional Laboratory Testing

Measure CEA and CA 19-9 in addition to CA-125 to help distinguish primary ovarian tumors from gastrointestinal metastases 5:

  • A CA-125/CEA ratio >25 favors ovarian origin over gastrointestinal origin 5
  • If CEA or CA 19-9 is elevated, consider endoscopy to exclude gastrointestinal primary malignancy 5
  • In young women, measure alpha-fetoprotein and beta-HCG to exclude germ cell tumors 1

Interpretation Based on Clinical Context

Postmenopausal Women

  • Any persistent ovarian mass in postmenopausal women warrants closer evaluation, as functional cysts should not occur after menopause 2
  • Small cysts (<5 cm) with normal CA-125 have significantly lower malignancy risk, but a CA-125 of 174 U/mL changes this assessment 2
  • Surgical evaluation is typically indicated for postmenopausal women with elevated CA-125 and ovarian masses 2

Premenopausal Women

  • Consider menstrual cycle timing, as CA-125 can be elevated during menstruation 8, 9
  • Endometriosis is a common cause of moderate CA-125 elevation in this population 7, 6
  • Repeat CA-125 in 2-3 weeks if initial imaging is negative to confirm persistence and calculate rate of progression 1

Monitoring Strategy If Imaging Is Negative

If imaging shows no evidence of malignancy but CA-125 remains elevated 1:

  • Repeat CA-125 in 2-3 weeks to confirm the increase and calculate doubling time 1
  • Progressive elevation over time, even within normal range initially, warrants further evaluation 2
  • Use the same laboratory and test method for all serial measurements to ensure consistency 1
  • Median time from CA-125 elevation to clinical relapse is 2-6 months in patients with prior ovarian cancer 1

Critical Caveats

Limitations of CA-125

  • CA-125 alone cannot differentiate benign from malignant disease due to high false-positive rates 3, 4
  • Mucinous ovarian carcinomas show low CA-125 positivity (only 16%), so normal levels don't exclude this histology 9
  • No correlation exists between CA-125 level and clinical stage (FIGO) in ovarian cancer patients 9

When to Suspect Malignancy

High-risk imaging features that increase concern for malignancy 2:

  • Solid components >7 mm
  • Papillary projections
  • Thick septations (>3 mm)
  • Abnormal vascular patterns on Doppler
  • Ascites or peritoneal implants
  • Bilateral complex masses

The combination of elevated CA-125 AND concerning imaging features significantly increases malignancy risk and mandates surgical evaluation 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Risk Assessment for Ovarian Cancer

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

The Role of CA 125 as Tumor Marker: Biochemical and Clinical Aspects.

Advances in experimental medicine and biology, 2015

Guideline

Cancers Associated with Elevated CA-125 Levels

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Coding for Elevated Rheumatoid Factor and CA125

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

The CA 125 tumour-associated antigen: a review of the literature.

Human reproduction (Oxford, England), 1989

Research

[Significance of CA 125 antigen levels in patients with ovarian cancer].

Gan to kagaku ryoho. Cancer & chemotherapy, 1986

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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