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Combined use of CYFRA 21-1 and CA 125 predicts survival of patients with metastatic NSCLC and stable disease in IMpower150.
Mang, Anika; Zou, Wei; Rolny, Vinzent; Reck, Martin; Cigoianu, Daniel; Schulze, Katja; Holdenrieder, Stefan; Socinski, Mark A; Shames, David S; Wehnl, Birgit; Patil, Namrata S.
Afiliação
  • Mang A; Roche Diagnostics GmbH, Penzberg, Germany.
  • Zou W; Oncology Biomarkers Development, Genentech, San Francisco, CA, USA.
  • Rolny V; Roche Diagnostics GmbH, Penzberg, Germany.
  • Reck M; Lung Clinic Grosshansdorf, Airway Research Center North, German Center of Lung Research, Grosshansdorf, Germany.
  • Cigoianu D; Roche Diagnostics International, Rotkreuz, Switzerland.
  • Schulze K; Oncology Biomarkers Development, Genentech, San Francisco, CA, USA.
  • Holdenrieder S; Institute of Laboratory Medicine, German Heart Centre Munich, Technical University of Munich, Munich, Germany.
  • Socinski MA; Adventhealth Cancer Institute, Orlando, FL, USA.
  • Shames DS; Oncology Biomarkers Development, Genentech, San Francisco, CA, USA.
  • Wehnl B; Roche Diagnostics GmbH, Penzberg, Germany.
  • Patil NS; Oncology Biomarkers Development, Genentech, San Francisco, CA, USA.
Tumour Biol ; 46(s1): S177-S190, 2024.
Article em En | MEDLINE | ID: mdl-37545290
BACKGROUND: Patients with non-small cell lung cancer (NSCLC) and stable disease (SD) have an unmet clinical need to help guide early treatment adjustments. OBJECTIVE: To evaluate the potential of tumor biomarkers to inform on survival outcomes in NSCLC SD patients. METHODS: This post hoc analysis included 480 patients from the IMpower150 study with metastatic NSCLC, treated with chemotherapy, atezolizumab and bevacizumab combinations, who had SD at first CT scan (post-treatment initiation). Patients were stratified into high- and low-risk groups (overall survival [OS] and progression-free survival [PFS] outcomes) based on serum tumor biomarker levels. RESULTS: The CYFRA 21-1 and CA 125 biomarker combination predicted OS and PFS in patients with SD. Risk of death was ~4-fold higher for the biomarker-stratified high-risk versus low-risk SD patients (hazard ratio [HR] 3.80; 95% confidence interval [CI] 3.02-4.78; p < 0.0001). OS in patients with the low- and high-risk SD was comparable to that in patients with the CT-defined partial response (PR; HR 1.10; 95% CI 0.898-1.34) and progressive disease (PD) (HR 1.05; 95% CI 0.621-1.77), respectively. The findings were similar with PFS, and consistent across treatment arms. CONCLUSIONS: Biomarker testing shows potential for providing prognostic information to help direct treatment in NSCLC patients with SD. Prospective clinical studies are warranted.ClinicalTrials.gov: NCT02366143.
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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 Tipo de estudo: Prognostic_studies / Risk_factors_studies 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 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Tumour Biol Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha
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