Burden Of Cancer Patients Research Articles

Microsatellite alterations in serum DNA of head and neck cancer patients.

Microsatellite DNA alterations are an integral part of neoplastic progression and are valuable as clonal markers for the detection of human cancers. Moreover, recent evidence suggests that senescent tumor cells may release DNA into the circulation, which is subsequently carried by and therefore enriched in the serum and plasma. We tested 21 patients with primary head and neck squamous cell carcinoma (HNSCC) by polymerase chain reaction (PCR)-based microsatellite analysis of DNA from lymphocytes and paired serum samples. Patients were scored for alterations as defined by the presence of new alleles (shifts) or loss of heterozygosity (LOH) in serum at each of 12 markers and then compared with primary tumor DNA. Six out of 21 patients (29%) were found to have one or more microsatellite alterations in serum precisely matching those in the primary tumors. All six patients had advanced disease (stage III or IV); five of these patients had nodal metastases, three later developed distant metastases, and four died of disease. Microsatellite analysis of serum represents a novel method for the detection of circulating tumor cell DNA. If these results are confirmed in larger studies, microsatellite markers may be useful in assessing tumor burden in cancer patients.

Lack of association of rheumatoid factor with either circulating immune complexes or tumor burden in cancer patients.

The frequency of rheumatoid factor (RF) seropositivity and the frequency of association of RF with immune complex (IC) elevation were determined in 72 patients with a variety of solid tumors, in 78 patients with IC-associated diseases, 27 patients with non-IC-associated diseases, and in 31 normal healthy controls. The frequency of RF positivity in cancer patients (31%) was virtually identical to that in patients with IC-associated diseases (28%), and did not differ significantly from that seen in patients with non-IC-associated disease (15%). Whereas IC elevation was clearly related to tumor progress, RF was not. RF and IC status also appeared to be unrelated to each other, not only in cancer patients, but in patients with other diseases as well. The results do not support the concept that RF reflects progressive tumor growth or an immune response to IgG-containing immune complexes.

Lack of association of rheumatoid factor with either circulating immune complexes or tumor burden in cancer patients

The frequency of rheumatoid factor (RF) seropositivity and the frequency of association of RF with immune complex (IC) elevation were determined in 72 patients with a variety of solid tumors, in 78 patients with IC-associated diseases, 27 patients with non-IC-associated diseases, and in 31 normal healthy controls. The frequency of RF positivity in cancer patients (31%) was virtually identical to that in patients with IC-associated diseases (28%), and did not differ significantly from that seen in patients with non-IC-associated disease (15%). Whereas IC elevation was clearly related to tumor progress, RF was not. RF and IC status also appeared to be unrelated to each other, not only in cancer patients, but in patients with other diseases as well. The results do not support the concept that RF reflects progressive tumor growth or an immune response to IgG-containing immune complexes.

Correlations among serum protein-bound carbohydrates, serum glycoproteins, lymphocyte reactivity, and tumor burden in cancer patients

Levels of glycoprotein-associated carbohydrates (neutral hexoses, hexosamine, sialic acid and fucose) were determined in the serum of patients with either local, regional or metastatic cancer, patients clinically cured of cancer, and controls (smokers and nonsmokers). Total protein-bound carbohydrates were compared with levels of 17 normal serum glycoproteins, carcinoembryonic antigen (CEA), and with lymphocyte reactivity to phytohemagglutin (PHA). Tumor burden was directly related to protein-bound carbohydrate levels in patient groups. Levels of bound carbohydrates reflect the sum of all the changes in serum glycoproteins, but primarily changes in the acute-phase proteins (alpha 1-acid glycoprotein, alpha 1-antitrypsin, haptoglobin, ceruloplasmin) found in the alpha-globulin fraction of serum. Increases in protein-bound carbohydrates in tumor-bearers were not related to increases in CEA. Increased levels of the acute-phase proteins occurred in individuals with depressed in vitro lymphocyte reactivity to PHA. A significant positive correlation was found between lymphocyte reactivity and level of alpha 2HS-glycoprotein. The results suggest that serum protein-bound carbohydrates or glycoproteins may be of adjunctive value is assessing tumor burden and immune reactivity in cancer patients.