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Journal ArticleDOI

Tumor markers (CEA, CA 125, CYFRA 21-1, SCC and NSE) in patients with non-small cell lung cancer as an aid in histological diagnosis and prognosis: Comparison with the main clinical and pathological prognostic factors

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TLDR
All tumor markers showed a clear relationship with tumor stage and histology and therefore enabled a better histological diagnosis and helped in the diagnosis of non-small cell lung cancer.
Abstract
CEA, CA 125, SCC, CYFRA 21-1 and NSE were prospectively studied in 211 patients with non-small cell lung cancer and compared with clinical parameters (age, sex, Karnofsky Index, symptoms and smoking status), histopathological parameters (stage, histology, tumor size and nodal involvement), biological parameters (LDH and albumin) and the therapy used (surgery, chemotherapy or radiotherapy). Tumor marker sensitivity was CYFRA 21-1: 76%, CA 125: 55%, CEA: 52%, SCC: 33% and NSE: 22%. One of the tumor markers was abnormally high in 87% of the patients with locoregional disease and in 100% of the patients with metastases. Except for NSE, all tumor markers showed a clear relationship with tumor stage and histology and therefore enabled a better histological diagnosis. Abnormal CEA serum levels were mainly found in adenocarcinomas, CA 125 in large-cell lung cancers (LCLC) and adenocarcinomas and SCC in squamous tumors. Eighty-five percent of the patients with SCC levels >2 ng/ml had squamous tumors. Likewise, CA 125 levels <60 U/ml or CEA <10 ng/ml excluded adenocarcinoma or LCLC with a probability of 82 and 91%, respectively.

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Journal ArticleDOI

Breath gas aldehydes as biomarkers of lung cancer.

TL;DR: Sensitivity and specificity of this method were comparable to the diagnostic certitude of conventional serum markers and CT imaging and noninvasive recognition of lung malignancies may be realized if analytical skills, biochemical knowledge and medical expertise are combined into a joint effort.
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Clinical utility of cytokeratins as tumor markers.

TL;DR: The clinical value of determining soluble cytokeratins protein fragments in body fluids lies in the early detection of recurrence and the fast assessment of the efficacy of therapy response in epithelial cell carcinomas.
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Label-free photoelectrochemical immunoassay for CEA detection based on CdS sensitized WO3@BiOI heterostructure nanocomposite.

TL;DR: The obtained label-free PEC immunosensor showed an excellent PEC performance toward CEA detection and showed a satisfied result in human serum sample analysis.
Journal ArticleDOI

Six-Color Time-Resolved Förster Resonance Energy Transfer for Ultrasensitive Multiplexed Biosensing

TL;DR: The multiplexed FRET biosensor offers clinically relevant detection limits in the low picomolar concentration range for all five markers, thus providing an effective early screening tool for lung cancer with the possibility of distinguishing small-cell from non-small-cell lung carcinoma.
References
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Book ChapterDOI

Nonparametric Estimation from Incomplete Observations

TL;DR: In this article, the product-limit (PL) estimator was proposed to estimate the proportion of items in the population whose lifetimes would exceed t (in the absence of such losses), without making any assumption about the form of the function P(t).
Book ChapterDOI

Regression Models and Life-Tables

TL;DR: The analysis of censored failure times is considered in this paper, where the hazard function is taken to be a function of the explanatory variables and unknown regression coefficients multiplied by an arbitrary and unknown function of time.
Journal ArticleDOI

Polychemotherapy in advanced non small cell lung cancer: a meta-analysis.

TL;DR: A reduction in mortality during the first 6 months with polychemotherapy is shown, although small, and this increase in survival, together with an improved quality of life, suggests that polyChemotherapy should be recommended for patients with non-resectable non small cell lung cancer.
Journal ArticleDOI

An Evaluation of the Carcinoembryonic Antigen (CEA) Test for Monitoring Patients With Resected Colon Cancer

TL;DR: Carcinoembryonic antigen testing was most sensitive for hepatic or retroperitoneal metastasis and relatively insensitive for local, pulmonary, or peritoneal involvement and cancer cures attributable to CEA monitoring are, at best, infrequent.
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