Dtsch Med Wochenschr 2013; 138(01/02): 43-45
DOI: 10.1055/s-0032-1327370
Kommentar | Commentary
Onkologie
© Georg Thieme Verlag KG Stuttgart · New York

Sinn und Unsinn von Tumormarkern in der Krebsfrüherkennung

Biomarker screening for early detection of cancer
G. J. Wiedemann
1   Klinik für Innere Medizin, Gastroenterologie und Onkologie, Oberschwabenklinik, St. Elisabeth, Ravensburg
› Author Affiliations
Further Information

Publication History

29 July 2012

11 October 2012

Publication Date:
18 December 2012 (online)

Zusammenfassung

Serum-Biomarker sollten im Prinzip nur dann als Tumormarker bezeichnet werden, wenn ihr Nachweis beweisend für eine Tumordiagnose wäre. Wegen der zu geringen Spezifität und Sensitivität der heute verfügbaren Tumormarker sind diese entweder ungeeignet oder, unter bestimmten Prämissen, lediglich mit Einschränkungen geeignet zur Früherkennung von Tumoren (Screeninguntersuchungen). Die unreflektierte Bestimmung von Tumormarkern bei asymptomatischen Personen führt regelmäßig zu Überdiagnostik und Übertherapie. Unbestritten ist der Stellenwert bestimmter Biomarker in der Verlaufskontrolle und Differenzialdiagnose von Tumorerkrankungen.

Abstract

The question of when a certain concentration of a serum biomarker turns into a tumor marker, i. e. an objectively verifiable criterion for tumor diagnosis, leads to the analysis of the specificity (a measure of the proportion of correctly identified healthy individuals), sensitivity (a measure of the proportion of correctly recognized cancer patients), and precision (positive predictive value). Or in short: a tumor marker is specific if no healthy individual has one. This constitutes the problem: The serum concentrations of biomarkers of cancer patients and healthy subjects overlap. Healthy individuals occasionally have "tumor markers" and cancer patients in turn sometimes express inconspicuous biomarkers.

 
  • Literatur

  • 1 American Society of Clinical Oncology (ASCO). Update of recommendations for the use of tumor markers in breast cancer. JCO 2007; 25: 5287-5312
  • 2 Altekruse SF, Kosary C, Krapcho M et al. SEER cancer statistics review 1975-2007. Bethesda MD: National Cancer Institute; 2010
  • 3 Brett SA, Ablin RJ. Prostate-cancer screening\. What the U.S. preventive services left out. N Engl J Med 2011; 365: 1949-1951
  • 4 Buys SS, Partridge E, Black A et al. Effect of screening on ovarian cancer mortality: the prostate, lung, colorectal and ovarian (PLCO) cancer screening randomized controlled trial. JAMA 2011; 305: 2295-2303
  • 5 Hoffman RM. Screening for prostate cancer. N Engl J Med 2011; 365: 2013-9
  • 6 Holdenrieder S. Tumormarker. TumorDiagn u Ther 2011; 32: 52-56
  • 7 Jörgensen KJ, Götzsche PC. Overdiagnosis in publicly organized mammography screening programmes: systemic review of incidence trends. BMJ 2009; 339: 2587
  • 8 Longo DL. Tumor heterogeneity and personalized medicine. N Engl J Med 2012; 366: 956-7
  • 9 Marcus PM, Kramer BS. Screening for prostate cancer with prostate-specific antigen: What’s the evidence?. Alexandria, VA, USA: American Society of Clinical Oncology; Educational Book 2012 2012: 96-100
  • 10 Miller AB. New data on prostate-cancer mortality after PSA screening. N Engl J Med 2012; 366: 1047-8
  • 11 Schnipper LE, Smith TJ, Raghavan D et al. American Society of Clinical Oncology identifies five key opportunities to improve care and reduce costs: The top five list for oncology. J Clin Oncol 2012; 30: 1715-24
  • 12 Schröder FH, Hugosson J, Roobol MJ et al. Prostate-cancer mortality at 11 years of follow-up. N Engl J Med 2012; 366: 981-990
  • 13 Spix C, Blettner M. Screening. Dtsch Arztebl Int 2012; 109: 385-390
  • 14 Sterling RK, Wright EC, Morgan TR et al. Frequency of elevated hepatocellular carcinoma (HCC) biomarkers in patients with advanced hepatitis C. Am J Gastroenterol 2012; 107: 64-74
  • 15 Wilt TJ, Brawer M, Jones KM et al. Radical prostatectomy versus observation for localized prostate cancer. N Engl J Med 2012; 367: 203-213