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Glucose metabolic activity measured by [18F]-fluoro-2-deoxy-glucose positron emission tomography (FDG-PET) has shown prognostic value in multiple malignancies, but results are often confounded by the inclusion of patients with various disease stages and undergoing various therapies.
The size and extent of LGE have shown prognostic value in patients with chronic myocardial infarction, suspected coronary artery disease, and clinically unrecognized myocardial infarction.
Intraoperative measurement of CEA mRNA in venous blood by RT-PCR has shown prognostic value in detecting disease recurrence, especially in patients with high-stage disease [ 39, 40].
In other studies however, semi-quantitative PET measures such as SUVmax have shown prognostic value in many cancer types using multiple radiotracers [ 38].
Lack of relationship between markers of angiogenesis and clinicopathological features has been observed in other studies, but most reports have shown prognostic value of increased MVD and/or presence of LVI [ 12, 24, 28- 31, 40- 44].
A number of previous studies have shown prognostic value of genomic alterations in CC such as loss of 11p and 18q and over expression of EGFR with poor prognosis, and 9p loss with metastasis [ 9, 41].
Similar(50)
Conclusions Our studied did not show prognostic value with low levels of serum IgG within 24 hours from SS or SSh onset.
50, 51 Low TS expression from pretherapeutic biopsies showed prognostic value with respect to impaired CSS.
HER2 amplification showed prognostic value in subgroups of patients, as well as Topo2a.
Several biomarkers have failed to show prognostic value when externally validated in an independent cohort.
High CD44 and CD133 expression showed prognostic value for worse patient survival (P=0.014 and P=0.019, respectively).
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