Dynamics of the tumor marker (TM) cancer antigen 15.3 (CA 15.3) and its association with overall survival (OS) in patients (pts) with hormone-receptor (HR)-positive/HER2-negative advanced breast cancer (ABC) in a public oncologic institution of Peru.
Abstract
e13080 Background: CA 15.3 is a conventional TM commonly elevated in HR (+) /HER2 (-) ABC at diagnosis and is associated with a high burden of disease and shorter OS during follow-up for response to treatment. The aim of our study is to evaluate the association of elevated vs. normal CA15.3 at diagnosis with clinicopathological characteristics and OS. Methods: Retrospective and descriptive analysis were made between 2018-2024. The association of initial CA 15.3 levels (normal, elevated: ≥ 32.4 U/ml) with the qualitative variables was evaluated with Chi-square test. Effect of the variables that had a significant association with initial CA15.3 levels were estimated with logistic regression, through odds ratio (OR). Efficacy was measured as OS. A p < 0.05 value (SPSS) will be considered for a significant difference. Survival curves were constructed with the Kaplan-Meier method. Results: 127 female pts were included. Median age was 55 years old (45-63); 50% were postmenopausal and 42% had de novo disease at diagnosis. Most pts were in ECOG 0-1 (93%) and 79% were luminal B subtype. Regarding the first-line therapy, 80% used endocrine therapy (15% used also ribociclib) and the rest used chemotherapy. According site of metastases, 43% and 27% had visceral and bone metastases, respectively. Regarding number of metastases, 61%, 28% and 11% had 1, 2 and ≥ 3 metastases, respectively. 68% of pts had elevated CA 15.3 (median: 65.08) at diagnosis, and 68% had a persistently elevated final CA15.3 during follow-up (p < 0.001). Postmenopausal had more elevated CA 15.3 levels than premenopausal (p = 0.014). Also, pts with ≥ 2 metastases had more elevated CA 15.3 than 1 site (p = 0.013). After a median follow-up of 30 months (2-120), the median OS rates at 12, 36 and 48 months were estimated in 97%, 69% and 45%, respectively; with a median OS of 55 months. Pts with pretreatment normal CA 15.3 (65 vs. 41 months, p = 0.024), luminal B (p = 0.032) and normal last CA 15.3 had longer OS compared to those with persistently elevated CA 15.3 (p = 0.0036). Conclusions: Elevation of TM CA 15.3 is very common in Peruvian pts with ABC HR (+) /HER2 (-) at diagnosis and during follow-up. Postmenopausal status and ≥ 2 metastases are associated with raised CA15.3 at diagnosis. Pts with normal pretreatment baseline CA 15.3, luminal B and who have normal last CA15.3 have a longer OS compared to those with persistently elevated CA 15.3. Estimation of the effect of the characteristics under study on the likelihood of a high initial CA 15.3 level. Univariate Multivariate OR 95% CI p-value OR 95% CI p-value Age group (years) < 50 Ref. Ref. ≥ 50 3.02 1.26-8.14 0.019 3.27 1.33-9.03 0.014 Number of metastases 1 Ref. Ref. ≥ 2 2.53 1.18-5.49 0.017 2.72 1.24-6.10 0.013 OR: odds ratio; CI: confidence interval; Ref.: reference.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (15)
Guillermo Valencia
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Patricia Rioja
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Jessica Gabriela Meza
Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru
Claudia Castillo
3Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru
Armando Martin Sanchez Yarleque
Instituto Nacional de Enfermedades Neoplasicas, Surquillo, Lima, Peru
Raul Mantilla
Specialized Institute of Neoplastic Diseases Lima, Lima, Peru
Connie Antoinette Rabanal Carretero
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Karina Aliaga Llerena
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Zaida Morante
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Bruno Munante
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Hugo Fuentes
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Carlos Orlando Munive Huari
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Carlos Arturo Castaneda Altamirano
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Silvia P. Neciosup
Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru
Tatiana Vidaurre
2Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru