BACKGROUND: The CA-125 tumor marker has limitations when used to distinguish between benign and malignant ovarian masses. We therefore establish likelihood curves of six subgroups of ovarian pathology based on CA-125 and menopausal status. METHODS: This cross-sectional study conducted by the International Ovarian Tumor Analysis group involved 3,511 patients presenting with a persistent adnexal mass that underwent surgical intervention. CA-125 distributions for six tumor subgroups (endometriomas and abscesses, other benign tumors, borderline tumors, stage I invasive cancers, stage II-IV invasive cancers, and metastatic tumors) were estimated using kernel density estimation with stratification for menopausal status. Likelihood curves for the tumor subgroups were derived from the distributions. RESULTS: Endometriomas and abscesses were the only benign pathologies with median CA-125 levels above 20 U/mL (43 and 45, respectively). Borderline and invasive stage I tumors had relatively low median CA-125 levels (29 and 81 U/mL, respectively). The CA-125 distributions of stage II-IV invasive cancers and benign tumors other than endometriomas or abscesses were well separated; the distributions of the other subgroups overlapped substantially. This held for premenopausal and postmenopausal patients. Likelihood curves and reference tables comprehensibly show how subgroup likelihoods change with CA-125 and menopausal status. CONCLUSIONS AND IMPACT: Our results confirm the limited clinical value of CA-125 for preoperative discrimination between benign and malignant ovarian pathology. We have shown that CA-125 may be used in a different way. By using likelihood reference tables, we believe clinicians will be better able to interpret preoperative serum CA-125 results in patients with adnexal masses.
BACKGROUND: The CA-125 tumor marker has limitations when used to distinguish between benign and malignant ovarian masses. We therefore establish likelihood curves of six subgroups of ovarian pathology based on CA-125 and menopausal status. METHODS: This cross-sectional study conducted by the International Ovarian Tumor Analysis group involved 3,511 patients presenting with a persistent adnexal mass that underwent surgical intervention. CA-125 distributions for six tumor subgroups (endometriomas and abscesses, other benign tumors, borderline tumors, stage I invasive cancers, stage II-IV invasive cancers, and metastatic tumors) were estimated using kernel density estimation with stratification for menopausal status. Likelihood curves for the tumor subgroups were derived from the distributions. RESULTS:Endometriomas and abscesses were the only benign pathologies with median CA-125 levels above 20 U/mL (43 and 45, respectively). Borderline and invasive stage I tumors had relatively low median CA-125 levels (29 and 81 U/mL, respectively). The CA-125 distributions of stage II-IV invasive cancers and benign tumors other than endometriomas or abscesses were well separated; the distributions of the other subgroups overlapped substantially. This held for premenopausal and postmenopausal patients. Likelihood curves and reference tables comprehensibly show how subgroup likelihoods change with CA-125 and menopausal status. CONCLUSIONS AND IMPACT: Our results confirm the limited clinical value of CA-125 for preoperative discrimination between benign and malignant ovarian pathology. We have shown that CA-125 may be used in a different way. By using likelihood reference tables, we believe clinicians will be better able to interpret preoperative serum CA-125 results in patients with adnexal masses.
Authors: Ben Van Calster; Yvonne Vergouwe; Caspar W N Looman; Vanya Van Belle; Dirk Timmerman; Ewout W Steyerberg Journal: Eur J Epidemiol Date: 2012-10-07 Impact factor: 8.082
Authors: B Van Calster; K Van Hoorde; W Froyman; J Kaijser; L Wynants; C Landolfo; C Anthoulakis; I Vergote; T Bourne; D Timmerman Journal: Facts Views Vis Obgyn Date: 2015
Authors: Ben Van Calster; Kirsten Van Hoorde; Lil Valentin; Antonia C Testa; Daniela Fischerova; Caroline Van Holsbeke; Luca Savelli; Dorella Franchi; Elisabeth Epstein; Jeroen Kaijser; Vanya Van Belle; Artur Czekierdowski; Stefano Guerriero; Robert Fruscio; Chiara Lanzani; Felice Scala; Tom Bourne; Dirk Timmerman Journal: BMJ Date: 2014-10-15
Authors: Parsa Charkhchi; Cezary Cybulski; Jacek Gronwald; Fabian Oliver Wong; Steven A Narod; Mohammad R Akbari Journal: Cancers (Basel) Date: 2020-12-11 Impact factor: 6.639
Authors: A Sayasneh; L Wynants; J Preisler; J Kaijser; S Johnson; C Stalder; R Husicka; Y Abdallah; F Raslan; A Drought; A A Smith; S Ghaem-Maghami; E Epstein; B Van Calster; D Timmerman; T Bourne Journal: Br J Cancer Date: 2013-05-14 Impact factor: 7.640
Authors: A Testa; J Kaijser; L Wynants; D Fischerova; C Van Holsbeke; D Franchi; L Savelli; E Epstein; A Czekierdowski; S Guerriero; R Fruscio; F P G Leone; I Vergote; T Bourne; L Valentin; B Van Calster; D Timmerman Journal: Br J Cancer Date: 2014-06-17 Impact factor: 7.640
Authors: E M J Meys; L S Jeelof; N M J Achten; B F M Slangen; S Lambrechts; R F P M Kruitwagen; T Van Gorp Journal: Ultrasound Obstet Gynecol Date: 2017-06 Impact factor: 7.299