Prognostic impact of elevated C-reactive protein and procalcitonin in patients with extensive-stage small cell lung cancer.

IF 1.8 4区 医学 Q3 ONCOLOGY Anti-Cancer Drugs Pub Date : 2024-11-27 DOI:10.1097/CAD.0000000000001670
İrfan Buğday, Mevlüde İnanç, Metin Özkan, Oktay Bozkurt, Ramazan Coşar, Sedat Tarik Firat, Emel Mutlu, Murat Eser, Ahmet Kürşad Dişli, Muhammet Cengiz
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Abstract

Small cell lung cancer (SCLC) constitutes around 15% of lung cancer cases and stands as the primary cause of cancer-related fatalities in men and the second leading cause in women globally. In this study, our objective was to evaluate the levels of C-reactive protein (CRP) and procalcitonin (PCT) in newly diagnosed extensive-stage SCLC patients without evidence of infection. We aimed to demonstrate that elevated CRP and PCT levels may not solely indicate infection but could also be elevated in malignancies. Furthermore, we sought to correlate these marker levels with patient and disease characteristics to elucidate the relationship between these inflammation markers and disease progression. A total of 115 patients who were pathologically and radiologically diagnosed with extensive-stage SCLC between January 2020 and December 2022 and who had received no prior treatment were included in the study. The Kaplan-Meier analysis revealed a median progression-free survival (PFS) of 7.46 months [95% confidence interval (CI), 6.85-8.07] and a median overall survival (OS) of 10.50 months (95% CI, 8.69-12.30) for all patients. In the group with elevated PCT, the median PFS was 6.73 months (95% CI, 3.92-9.54), whereas it was 7.86 months (95% CI, 7.13-8.59) in the group with normal PCT (P = 0.002). Similarly, the median OS was 9.10 months (95% CI, 5.61-12.58) in the elevated PCT group and 11.66 months (95% CI, 9.59-13.74) in the normal PCT group (P = 0.006). Patients with elevated procalcitonin (PRC) levels at the time of diagnosis exhibited shorter PFS and OS durations compared to patients with normal PRC levels. Furthermore, elevated CRP has also been demonstrated to correlate with poorer prognosis in extensive-stage SCLC.

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广泛期小细胞肺癌患者 C 反应蛋白和降钙素原升高的预后影响。
小细胞肺癌(SCLC)约占肺癌病例的 15%,是全球男性癌症相关死亡的主要原因,也是女性癌症相关死亡的第二大原因。在这项研究中,我们的目的是评估无感染证据的新诊断广泛期 SCLC 患者的 C 反应蛋白(CRP)和降钙素原(PCT)水平。我们的目的是证明,CRP 和 PCT 水平的升高可能并不仅仅表明感染,也可能在恶性肿瘤中升高。此外,我们还试图将这些标志物水平与患者和疾病特征相关联,以阐明这些炎症标志物与疾病进展之间的关系。本研究共纳入了115名在2020年1月至2022年12月期间经病理学和放射学诊断为广泛期SCLC且之前未接受过治疗的患者。卡普兰-梅耶尔分析显示,所有患者的中位无进展生存期(PFS)为7.46个月[95%置信区间(CI),6.85-8.07],中位总生存期(OS)为10.50个月(95% CI,8.69-12.30)。PCT 升高组的中位 PFS 为 6.73 个月(95% CI,3.92-9.54),而 PCT 正常组为 7.86 个月(95% CI,7.13-8.59)(P = 0.002)。同样,PCT 升高组的中位 OS 为 9.10 个月(95% CI,5.61-12.58),PCT 正常组为 11.66 个月(95% CI,9.59-13.74)(P = 0.006)。与PRC水平正常的患者相比,诊断时降钙素原(PRC)水平升高的患者的PFS和OS持续时间较短。此外,CRP升高也被证明与广泛期SCLC的不良预后相关。
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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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