کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1965300 1538658 2015 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Personalized biomarkers to monitor disease progression in advanced non-small-cell lung cancer patients treated with icotinib
ترجمه فارسی عنوان
بیومارکرهای شخصی برای نظارت بر پیشرفت بیماری در بیماران مبتلا به سرطان پیشرفته غیر سلولی ریه که تحت درمان با ایکوتینیب قرار دارند
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
چکیده انگلیسی


• Three characteristic patterns of plasma IIRPCs are observed.
• Changes in the IIRPCs levels are closely associated with cancer development.
• The TLHIIR are closely associated with cancer development.
• The median TLHIIR is 22 weeks, lead time of 11 weeks relative to PFS.

BackgroundDisease-specific humoral immune response-related protein complexes in blood are associated with disease progression.MethodsThirty-one patients with stage IIIB and IV non-small-cell lung cancer (NSCLC) were administered with oral dose of icotinib hydrochloride (150 mg twice daily or 125 mg 3 times daily) for a 28-continuous-day cycle until diseases progressed or unacceptable toxicity occurred. The levels of immunoinflammation-related protein complexes (IIRPCs) in a series of plasma samples from 31 NSCLC patients treated with icotinib hydrochloride were determined by an optimized native polyacrylamide gel electrophoresis.ResultsThree characteristic patterns of the IIRPCs, named as patterns a, b, and c, respectively, were detected in plasma samples from 31 patients. Prior to the treatment, there were 18 patients in pattern a consisting of 5 IIRPCs, 9 in pattern b consisting of six IIRPCs, and 4 in pattern c without the IIRPCs. The levels of the IIRPCs in 27 patients were quantified. Our results indicate that the time length of humoral immune and inflammation response (TLHIIR) was closely associated with disease progression, and the median TLHIIR was 22.0 weeks, 95% confidence interval: 16.2 to 33.0 weeks, with a lead time of median 11 weeks relative to clinical imaging evidence confirmed by computed tomography or magnetic resonance imaging (the median progression-free survival, 34.0 weeks, 95% confidence interval: 27.9 to 49.0 weeks).ConclusionsThe complex relationships between humoral immune response, acquired resistance, and disease progression existed. Personalized IIRPCs could be indicators to monitor the disease progression.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Clinica Chimica Acta - Volume 440, 2 February 2015, Pages 44–48
نویسندگان
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