Cetin Taha Enes, Sutcuoglu Osman, Akdogan Orhun, Savas Gozde, Günel Nazan, Uner Aytug, Ozdemir Nuriye, Ozet Ahmet, Yazici Ozan
Department of Internal Medicine, Gazi University, Ankara, Turkey.
Department of Medical Oncology, Gazi University, Ankara, Turkey.
BMC Cancer. 2025 Jul 1;25(1):1111. doi: 10.1186/s12885-025-14513-1.
This study aims to determine the 30-day mortality rate following intravenous systemic anticancer therapies (SACT) and to compare mortality rates between different therapeutic modalities, including immunotherapy, monoclonal antibodies, and chemotherapy.
A retrospective analysis was conducted on cancer patients who received intravenous SACT between January 1, 2022, and December 31, 2022. Patient data, including demographics, cancer types, treatment details, and mortality outcomes, were collected from hospital records. The primary endpoint was 30-day mortality following the last dose of SACT.
Among the 1,937 patients included, the overall 30-day mortality rate post-SACT was 7%. Significant factors affecting 30-day mortality included Eastern Cooperative Oncology Group (ECOG) performance status, body mass index (BMI), and smoking status. In Non-Stage 4 treated patients, a higher ECOG score was significantly associated with increased mortality. In Stage 4 treated patients, both a higher ECOG score and a lower BMI were independent predictors of increased mortality. Additionally, receiving Stage 4 treatment and being an active smoker significantly increased mortality risk in patients with gastrointestinal and breast cancers.
Monitoring 30-day mortality post-SACT is essential for improving oncological care quality. Identifying and addressing modifiable risk factors and carefully selecting patients for modern oncological treatments can help reduce mortality rates. Further prospective studies are warranted to explore the impact of immunotherapy on short-term mortality in diverse cancer populations.
本研究旨在确定静脉全身抗癌治疗(SACT)后的30天死亡率,并比较不同治疗方式(包括免疫疗法、单克隆抗体和化疗)之间的死亡率。
对2022年1月1日至2022年12月31日期间接受静脉SACT的癌症患者进行回顾性分析。从医院记录中收集患者数据,包括人口统计学信息、癌症类型、治疗细节和死亡结果。主要终点是最后一剂SACT后的30天死亡率。
在纳入的1937例患者中,SACT后30天的总死亡率为7%。影响30天死亡率的显著因素包括东部肿瘤协作组(ECOG)体能状态、体重指数(BMI)和吸烟状况。在非4期治疗患者中,较高的ECOG评分与死亡率增加显著相关。在4期治疗患者中,较高的ECOG评分和较低的BMI都是死亡率增加的独立预测因素。此外,接受4期治疗和当前吸烟者在胃肠道癌和乳腺癌患者中显著增加死亡风险。
监测SACT后的30天死亡率对于提高肿瘤护理质量至关重要。识别并解决可改变的风险因素,以及为现代肿瘤治疗仔细挑选患者,有助于降低死亡率。有必要进行进一步的前瞻性研究,以探讨免疫疗法对不同癌症人群短期死亡率的影响。