TY - JOUR
T1 - Serum mesothelin for diagnosing malignant pleural mesothelioma
T2 - an individual patient data meta-analysis
AU - Hollevoet, Kevin
AU - Reitsma, Johannes B
AU - Creaney, Jenette
AU - Grigoriu, Bogdan D
AU - Robinson, Bruce W
AU - Scherpereel, Arnaud
AU - Cristaudo, Alfonso
AU - Pass, Harvey I
AU - Nackaerts, Kristiaan
AU - Rodríguez Portal, José A
AU - Schneider, Joachim
AU - Muley, Thomas
AU - Di Serio, Francesca
AU - Baas, Paul
AU - Tomasetti, Marco
AU - Rai, Alex J
AU - van Meerbeeck, Jan P
PY - 2012
Y1 - 2012
N2 - PURPOSE: Mesothelin is currently considered the best available serum biomarker of malignant pleural mesothelioma. To examine the diagnostic accuracy and use of serum mesothelin in early diagnosis, we performed an individual patient data (IPD) meta-analysis.METHODS: The literature search identified 16 diagnostic studies of serum mesothelin, measured with the Mesomark enzyme-linked immunosorbent assay. IPD of 4,491 individuals were collected, including several control groups and 1,026 patients with malignant pleural mesothelioma. Mesothelin levels were standardized for between-study differences and age, after which the diagnostic accuracy and the factors affecting it were examined with receiver operating characteristic (ROC) regression analysis.RESULTS: At a common diagnostic threshold of 2.00 nmol/L, the sensitivities and specificities of mesothelin in the different studies ranged widely from 19% to 68% and 88% to 100%, respectively. This heterogeneity can be explained by differences in study population, because type of control group, mesothelioma stage, and histologic subtype significantly affected the diagnostic accuracy. The use of mesothelin in early diagnosis was evaluated by differentiating 217 patients with stage I or II epithelioid and biphasic mesothelioma from 1,612 symptomatic or high-risk controls. The resulting area under the ROC curve was 0.77 (95% CI, 0.73 to 0.81). At 95% specificity, mesothelin displayed a sensitivity of 32% (95% CI, 26% to 40%).CONCLUSION: In patients suspected of having mesothelioma, a positive blood test for mesothelin at a high-specificity threshold is a strong incentive to urge further diagnostic steps. However, the poor sensitivity of mesothelin clearly limits its added value to early diagnosis and emphasizes the need for further biomarker research.
AB - PURPOSE: Mesothelin is currently considered the best available serum biomarker of malignant pleural mesothelioma. To examine the diagnostic accuracy and use of serum mesothelin in early diagnosis, we performed an individual patient data (IPD) meta-analysis.METHODS: The literature search identified 16 diagnostic studies of serum mesothelin, measured with the Mesomark enzyme-linked immunosorbent assay. IPD of 4,491 individuals were collected, including several control groups and 1,026 patients with malignant pleural mesothelioma. Mesothelin levels were standardized for between-study differences and age, after which the diagnostic accuracy and the factors affecting it were examined with receiver operating characteristic (ROC) regression analysis.RESULTS: At a common diagnostic threshold of 2.00 nmol/L, the sensitivities and specificities of mesothelin in the different studies ranged widely from 19% to 68% and 88% to 100%, respectively. This heterogeneity can be explained by differences in study population, because type of control group, mesothelioma stage, and histologic subtype significantly affected the diagnostic accuracy. The use of mesothelin in early diagnosis was evaluated by differentiating 217 patients with stage I or II epithelioid and biphasic mesothelioma from 1,612 symptomatic or high-risk controls. The resulting area under the ROC curve was 0.77 (95% CI, 0.73 to 0.81). At 95% specificity, mesothelin displayed a sensitivity of 32% (95% CI, 26% to 40%).CONCLUSION: In patients suspected of having mesothelioma, a positive blood test for mesothelin at a high-specificity threshold is a strong incentive to urge further diagnostic steps. However, the poor sensitivity of mesothelin clearly limits its added value to early diagnosis and emphasizes the need for further biomarker research.
KW - Aged
KW - Biomarkers, Tumor
KW - Early Detection of Cancer
KW - Enzyme-Linked Immunosorbent Assay
KW - Female
KW - GPI-Linked Proteins
KW - Humans
KW - Male
KW - Mesothelioma
KW - Middle Aged
KW - Pleural Neoplasms
KW - Predictive Value of Tests
KW - Prognosis
KW - ROC Curve
KW - Regression Analysis
KW - Journal Article
KW - Meta-Analysis
KW - Research Support, N.I.H., Extramural
KW - Research Support, N.I.H., Intramural
KW - Research Support, Non-U.S. Gov't
KW - Review
U2 - 10.1200/JCO.2011.39.6671
DO - 10.1200/JCO.2011.39.6671
M3 - Article
C2 - 22412141
SN - 0732-183X
VL - 30
SP - 1541
EP - 1549
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 13
ER -