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CYFRA 21-1, CA 125 and CEA provide additional prognostic value in NSCLC patients with stable disease at first CT scan.
Muley, Thomas; Schneider, Mark A; Meister, Michael; Thomas, Michael; Heußel, Claus Peter; Kriegsmann, Mark; Holdenrieder, Stefan; Wehnl, Birgit; Rolny, Vinzent; Mang, Anika; Gerber, Rebecca; Herth, Felix.
Afiliação
  • Muley T; Translational Research Unit, Thoraxklinik, University Hospital, Heidelberg, Germany.
  • Schneider MA; Translational Lung Research Center, German Center for Lung Research (DZL), Heidelberg, Germany.
  • Meister M; Translational Research Unit, Thoraxklinik, University Hospital, Heidelberg, Germany.
  • Thomas M; Translational Lung Research Center, German Center for Lung Research (DZL), Heidelberg, Germany.
  • Heußel CP; Translational Research Unit, Thoraxklinik, University Hospital, Heidelberg, Germany.
  • Kriegsmann M; Translational Lung Research Center, German Center for Lung Research (DZL), Heidelberg, Germany.
  • Holdenrieder S; Translational Lung Research Center, German Center for Lung Research (DZL), Heidelberg, Germany.
  • Wehnl B; Department of Oncology, Thoraxklinik, University Hospital, Heidelberg, Germany.
  • Rolny V; Translational Lung Research Center, German Center for Lung Research (DZL), Heidelberg, Germany.
  • Mang A; Diagnostic and Interventional Radiology with Nuclear Medicine, Thoraxklinik, University Hospital, Heidelberg, Germany.
  • Gerber R; Diagnostic and Interventional Radiology, University Hospital, Heidelberg, Germany.
  • Herth F; Department of Pathology, Institute of Pathology, University Hospital, Heidelberg, Germany.
Tumour Biol ; 46(s1): S163-S175, 2024.
Article em En | MEDLINE | ID: mdl-37840516
ABSTRACT

BACKGROUND:

Serum tumor markers (STM) may complement imaging and provide additional clinical information for patients with non-small cell lung cancer (NSCLC).

OBJECTIVE:

To determine whether STMs can predict outcomes in patients with stable disease (SD) after initial treatment.

METHODS:

This single-center, prospective, observational trial enrolled 395 patients with stage III/IV treatment-naïve NSCLC; of which 263 patients were included in this analysis. Computed Tomography (CT) scans were performed and STMs measured before and after initial treatment (two cycles of chemotherapy and/or an immune checkpoint inhibitor or tyrosine kinase inhibitor); analyses were based on CT and STM measurements obtained at first CT performed after cycle 2 only PFS and OS were analyzed by Kaplan-Meier curves and Cox-proportional hazard models.

RESULTS:

When patients with SD (n = 100) were split into high- and low-risk groups based on CYFRA 21-1, CEA and CA 125 measurements using an optimized cut-off, a 4-fold increase risk of progression or death was estimated for high- vs low-risk SD patients (PFS, HR 4.17; OS, 3.99; both p < 0.0001). Outcomes were similar between patients with high-risk SD or progressive disease (n = 35) (OS, HR 1.17) and between patients with low-risk SD or partial response (n = 128) (PFS, HR 0.98; OS, 1.14).

CONCLUSIONS:

STMs can provide further guidance in patients with indeterminate CT responses by separating them into high- and low-risk groups for future PFS and OS events.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Queratina-19 / Neoplasias Pulmonares / Antígenos de Neoplasias Limite: Humans Idioma: En Revista: Tumour Biol Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Queratina-19 / Neoplasias Pulmonares / Antígenos de Neoplasias Limite: Humans Idioma: En Revista: Tumour Biol Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha