Is C-Reactive Protein (CRP) elevated in common malignancies?

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Last updated: November 3, 2025View editorial policy

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CRP Elevation in Common Malignancies

Yes, CRP is frequently elevated in common malignancies, with solid tumors showing median CRP levels of approximately 46 mg/L, though considerable variability exists both within and across different cancer types. 1, 2, 3

Magnitude of CRP Elevation in Malignancy

  • Solid tumors demonstrate median CRP levels of 46 mg/L, which is substantially lower than bacterial infections (120 mg/L) but higher than cardiovascular disease (6 mg/L). 1, 2, 3

  • Approximately 33% of hospitalized cancer patients have CRP values less than 10 mg/L, indicating that normal or mildly elevated CRP does not exclude malignancy. 1

  • The degree of CRP elevation often parallels tumor progression and pathological stage, with preoperative CRP levels correlating with disease advancement in gastric cancer and other malignancies. 4

Prognostic Significance

  • Elevated preoperative CRP is a determinant predictor of lower survival rates in multiple cancer types including esophageal, colorectal, hepatocellular, pancreatic, bladder, renal, ovarian, and cervical cancers after surgical resection. 4

  • The modified Glasgow Prognostic Score (mGPS), which grades inflammatory response using CRP and albumin, is highly predictive of morbidity and mortality in cancer patients. 1

  • In patients with invasive breast cancer, CRP levels >3 mg/L at diagnosis confer a 1.7-fold increased risk of death compared to those with CRP <1 mg/L. 5

  • Individuals from the general population with CRP in the highest versus lowest quintile have a 1.3-fold increased risk of developing cancer of any type and a 2-fold increased risk of lung cancer. 5

Mechanistic Basis

  • CRP is produced by hepatocytes in response to inflammatory cytokines, particularly IL-6 and TNF-alpha, from the tumor microenvironment. 1, 4

  • Studies have identified associations between single-nucleotide polymorphisms in inflammatory genes (IL6, IL13, TNF-alpha, IL4, IL1B) and higher symptom burden in cancer patients. 1

  • The elevation reflects the chronic inflammatory state associated with malignancy, linking inflammation and cancer pathogenesis. 4, 6

Diagnostic Limitations

  • CRP has limited diagnostic accuracy for detecting secondary pleural malignancy, with sensitivity of 0.71 and specificity of only 0.56 at a cut-point of 35.5 mg/L. 1

  • The British Thoracic Society guideline states there is insufficient evidence to support using serum CRP to diagnose secondary pleural malignancy. 1

  • CRP is neither organ-specific nor tumor-specific, limiting its utility as a screening or diagnostic tool for malignancy. 7

Clinical Implications

  • In lung cancer patients receiving chemotherapy, a CRP cutoff value of ≥6.74 mg/dL can distinguish infection from malignancy-related elevation with 91.3% sensitivity and 86.6% specificity. 8

  • CRP measurement is simple, cheap, and available in daily practice, serving as an additional prognostic predictor for survival and post-treatment monitoring. 4

  • Baseline CRP might be a prognostic factor in oncological diseases, with normal levels at baseline correlating with longer overall survival in early-stage malignancies and lower levels predicting better prognosis in advanced stages. 6

Important Caveats

  • Multiple non-malignant factors influence CRP levels, including age, sex, race, body mass index, smoking, diet, sleep, and medication use. 1, 2

  • CRP values >10 mg/L are not always indicative of acute infection or malignancy alone—approximately 20% may be associated with smoking behavior and other lifestyle factors. 1

  • Single CRP measurements should be interpreted in clinical context rather than in isolation, as multiple conditions may coexist. 1, 3

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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