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1.
Ann Oncol ; 5(7): 623-6, 1994 Sep.
Article in English | MEDLINE | ID: mdl-7993838

ABSTRACT

BACKGROUND: Recently, the ganglioside Fucosyl-GM1 (FucGM1) has been described as a possible new tumour marker for small-cell lung cancer (SCLC). FucGM1 has been detected in 75% to 90% of SCLC tumours by immunohistochemical analysis and in about 50% of sera from SCLC patients. Neuron-specific enolase (NSE) is a glycolytic enzyme which is expressed in the majority of SCLC tumours and patient sera. PATIENTS AND METHODS: Sera from 156 patients with SCLC were analyzed for FucGM1 with a scintillation proximity assay (SPA), which is a simple and sensitive analysis. Sera were analyzed before the initiation of chemotherapy, and twenty patients were monitored during and after treatment. The concentration of FucGM1 was compared to the tumour marker NSE and related to clinical data and survival. RESULTS: Sixty-three per cent of the patients were positive for FucGM1. The concentrations did not correlate with NSE or clinical data including stage of disease, organ site of metastases or ABO blood group status. Nor did the expression of FucGM1 correlate with survival. As a monitor of clinical response, a correlation was found in 8 out of 20 patients. Eighty-four per cent of the patients were positive for NSE; and 97% were positive for either FucGM1 or NSE. CONCLUSION: We conclude that FucGM1 does not have a clinical role as a tumour marker for patients with SCLC at diagnosis or during treatment.


Subject(s)
Biomarkers, Tumor/blood , Carcinoma, Small Cell/diagnosis , G(M1) Ganglioside/analogs & derivatives , Lung Neoplasms/diagnosis , Phosphopyruvate Hydratase/blood , Adult , Aged , Female , G(M1) Ganglioside/blood , Humans , Male , Middle Aged , Predictive Value of Tests , Radioimmunoassay , Scintillation Counting
2.
Cancer Detect Prev ; 18(3): 221-9, 1994.
Article in English | MEDLINE | ID: mdl-8076384

ABSTRACT

The ganglioside fucosyl-GM1 (FucGM1) has been suggested as a marker for small-cell lung cancer (SCLC). Immunohistochemical analyses have shown the expression of the ganglioside in tumors in 75 to 90% of patients with SCLC. We have demonstrated that the ganglioside is shedded from SCLC cells both in vitro and in vivo, and that the antigen can be detected in sera from SCLC patients by an immunochemical analysis. The FucGM1 antigen has recently been shown to act as a target for antibody-dependent cellular cytotoxicity. This may provide a rationale for developing immunotherapy against SCLC. We used an immunoassay based on the scintillation proximity assay to analyze the concentrations of FucGM1 in sera from 112 SCLC patients, 21 patients with non-SCLC, 4 patients with other cancer forms, and 20 healthy controls. Sera were collected at the time of diagnosis before initiation of chemotherapy. The expression of FucGM1 was related to age, sex, blood group of the patient, and to the stage of disease and organ site involvement of metastases. The sera of 50% of the patients with SCLC were positive for FucGM1, and 12 of 21 sera from non-SCLC patients were markedly elevated. In SCLC sera, the concentration of FucGM1 in positive sera ranged from 7 to more than 3000 ng/ml FucGM1. None of 20 controls were positive. FucGM1 correlated to organ site involvement of metastases (p = 0.0016). The ganglioside was detected both at significantly higher concentrations (p = 0.0005) and in significantly more patients (p = 0.0026) with metastases to both the liver and bone marrow, compared to patients with metastases to the liver only.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Biomarkers, Tumor/blood , Carcinoma, Small Cell/blood , G(M1) Ganglioside/analogs & derivatives , Lung Neoplasms/blood , Bone Marrow , Carcinoma, Small Cell/mortality , Carcinoma, Small Cell/secondary , Female , Follow-Up Studies , G(M1) Ganglioside/blood , Humans , Liver Neoplasms/blood , Liver Neoplasms/secondary , Lung Neoplasms/mortality , Male , Middle Aged , Survival Rate
3.
Int J Health Plann Manage ; 8(4): 275-94, 1993.
Article in English | MEDLINE | ID: mdl-10134931

ABSTRACT

This article examines a specific management reform at three hospitals in a Danish county. Management reform at the hospital level implies a decentralization of responsibility and power to the departmental level. Along with increased responsibility and power, departments get the message: keep your budgets and keep your output level. This preliminary analysis indicates that departmental budgets can be a way of containing costs in clinical departments. Non-staff expenditures especially are subjected to reductions. The system still seems to 'favour' doctors and nurses, but less than in a system with traditional budgetary institutions. The behaviour of the top-management teams shows that the output constraint is not seriously meant. Departments are allowed to reduce capacity, with declining output, with the knowledge of the top-management team. The declining output makes it easier to departments ceteris paribus to keep within their budgets. And that makes it easier for the top-management team to keep the overall hospital budget. The obligation to keep the overall hospital budget is thus an important criterion of success in the eyes of the political masters of hospitals.


Subject(s)
Budgets/trends , Financial Management, Hospital/trends , Hospital Departments/economics , Hospital Restructuring/economics , Hospitals, County/organization & administration , Budgets/statistics & numerical data , Cost Savings/statistics & numerical data , Cost Savings/trends , Decision Making, Organizational , Denmark , Efficiency, Organizational , Health Services Research , Hospital Costs/statistics & numerical data , Hospital Costs/trends , Hospital Departments/trends , Hospitals, County/economics , Institutional Management Teams , Interdepartmental Relations
4.
Glycoconj J ; 9(6): 331-5, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1339041

ABSTRACT

We here report an enzyme linked immunosorbent assay (ELISA) and a scintillation proximity assay (SPA) for detection of the ganglioside FucGM1 in sera from small cell lung cancer (SCLC) patients. The SPA was more sensitive and reproducible than the ELISA. In this assay, monoclonal antibodies specific for FucGM1 were bound to SPA particles and incubated with labelled FucGM1 and 100 microliters test-serum overnight, and counted in a beta-counter. The sensitivity was 0.2 ng. Seven out of twenty sera from SCLC patients were positive, whereas none of twenty sera from healthy individuals were positive for FucGM1. The SPA was more sensitive than the previously reported HPTLC as well as a direct ELISA.


Subject(s)
Carcinoma, Small Cell/blood , G(M1) Ganglioside/analogs & derivatives , Lung Neoplasms/blood , Carbohydrate Sequence , Carcinoma, Small Cell/diagnosis , Enzyme-Linked Immunosorbent Assay , G(M1) Ganglioside/blood , Humans , Hybridomas , Immunoassay , Lung Neoplasms/diagnosis , Molecular Sequence Data , Prognosis , Scintillation Counting , Sensitivity and Specificity , Tumor Cells, Cultured
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