Emre Çakır
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Emre Çakır has a total of 33 co-authors. Here are the top co-authors by number of shared publications:
Atike Pınar Erdoğan
Department of Medical Oncology Manisa Celal Bayar University Faculty of Medicine. Manisa Turkey
1 shared publicationAtila Yıldırım
Department of Medical Oncology Karadeniz Technical University Faculty of Medicine Trabzon Turkey
1 shared publicationBülent Erdoğan
Department of Medical Oncology Trakya University Faculty of Medicine Edirne Turkey
1 shared publicationCanan Yıldız
Department of Medical Oncology Afyonkarahisar Health Sciences University Faculty of Medicine Afyon Turkey
1 shared publicationCemil Bilir
1 shared publication- Deniz Can Guven
Department of Medical Oncology, Hacettepe University Cancer Institute, 06230 Ankara, Turkey
1 shared publication
Latest Publications
- Open Access
- 6 August 2026
- Published by Wiley in International Journal of Cancer
Diabetes Increases Immunotherapy‐Related Toxicity but Not Efficacy in Metastatic Non‐Small Cell Lung Cancer: A Multicenter Retrospective Study
This multicenter retrospective study evaluated the impact of type 2 diabetes mellitus (DM) on clinical outcomes and immune‐related adverse events (irAEs) in 450 patients with metastatic non‐small cell lung cancer (NSCLC) treated with second‐line nivolumab at 17 centers between 2016 and 2024. Among these patients, 118 (26.2%) had DM. Baseline demographic and clinical characteristics, including age, sex, smoking status, ECOG performance status, histology, and PD‐L1 expression, were similar between patients with and without DM. Nivolumab demonstrated similar antitumor activity in both groups, with no significant differences in median progression‐free survival (PFS), overall survival (OS), or objective response rates. However, the incidence of Grade 3–4 irAEs was significantly higher in patients with DM. HbA1c levels were not associated with survival outcomes in univariate analyses, and metformin or insulin use did not affect PFS or OS among patients with DM. These findings indicate that DM does not compromise immunotherapy efficacy but is associated with a higher risk of severe toxicity. Clinicians should consider metabolic status and closely monitor patients with DM receiving immunotherapy. Further prospective studies are needed to clarify underlying mechanisms and optimize treatment strategies for this population.
- 6 August 2026
- Published by Wiley in International Journal of Cancer
Open AccessDiabetes Increases Immunotherapy‐Related Toxicity but Not Efficacy in Metastatic Non‐Small Cell Lung Cancer: A Multicenter Retrospective Study
This multicenter retrospective study evaluated the impact of type 2 diabetes mellitus (DM) on clinical outcomes and immune‐related adverse events (irAEs) in 450 patients with metastatic non‐small cell lung cancer (NSCLC) treated with second‐line nivolumab at 17 centers between 2016 and 2024. Among these patients, 118 (26.2%) had DM. Baseline demographic and clinical characteristics, including age, sex, smoking status, ECOG performance status, histology, and PD‐L1 expression, were similar between patients with and without DM. Nivolumab demonstrated similar antitumor activity in both groups, with no significant differences in median progression‐free survival (PFS), overall survival (OS), or objective response rates. However, the incidence of Grade 3–4 irAEs was significantly higher in patients with DM. HbA1c levels were not associated with survival outcomes in univariate analyses, and metformin or insulin use did not affect PFS or OS among patients with DM. These findings indicate that DM does not compromise immunotherapy efficacy but is associated with a higher risk of severe toxicity. Clinicians should consider metabolic status and closely monitor patients with DM receiving immunotherapy. Further prospective studies are needed to clarify underlying mechanisms and optimize treatment strategies for this population.
- 27 March 2021
- Published by Academician Publishing
- p. 165-174
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