Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0278488 (metastatic breast cancer)
 7,812 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Serum CEA levels were determined in 2095 patients following mastectomy for breast cancer by means of a double antibody 125 I-CEA-radioimmunoassay. 91% of 1462 patients free of metastases had normal levels less than or equal to 3 ng/ml (98% less than or equal to 5 ng/ml). In contrast, 54% of 633 patients with overt metastases had raised values greater than 3 ng/ml (43% greater than 5 ng/ml). The incidence of pathological levels was dependent on tumour burden and metastatic location rising from solitary lymph node disease (6% greater than 5 ng/ml) to skin, lung, bone, liver and multiple organ involvement (60%). CEA levels correlated weakly with total alkaline phosphatase and gamma-GT activities, but not with ESR or bilirubin levels. Of 531 patients followed after surgery and who had 3-18 serial determinations in 3-51 months, 46% without metastases had normal CEA levels as did 41% of 285 patients with metastases. Of the remaining 168 patients with elevated CEA levels, most showed a correlation between rising levels and disease progression, decreasing levels with remission and persistence of fluctuating levels with stationary disease. The CEA test is recommended as a valuable adjunct to monitor the clinical response to chemo/hormo/radiotherapy in metastatic breast cancer.
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PMID:Serial carcinoembryonic antigen (CEA) determinations in the management of metastatic breast cancer. 727 99

The role of blood tumour markers is established in the monitoring of response to systemic therapy for patients with metastatic breast cancer assessable by UICC criteria. This paper examines the use of marker measurements (in the form of a previously devised biochemical index score comprising CA15.3, CEA and ESR) in patients with metastatic lesions unassessable for response by UICC criteria. Of 218 patients with metastatic breast cancer treated over a 2-year period in the Nottingham Breast Unit, 43 patients (20%) had unassessable disease and 36 of them with blood marker results available were studied. Eighty-six per cent of patients were biochemically assessable. All patients who achieved biochemical response remained unassessable by UICC criteria. Twenty-two patients progressed initially or subsequently (after an initial biochemical response), either biochemically or by UICC criteria. Biochemical assessment completely paralleled UICC assessment in all eight patients who progressed by both assessments. Biochemical progression occurred ahead of UICC assessment in four of them with a median lead-time of 4.5 months. Biochemical assessment by blood tumour markers is useful in patients with metastatic breast cancer unassessable for response to systemic therapy. These findings need to be confirmed in a larger patient series.
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PMID:The use of blood tumour markers in the monitoring of metastatic breast cancer unassessable for response to systemic therapy. 1156 73

Measurement of remission and progression in metastatic breast cancer by the use of serum tumour markers is simple, objective, reproducible and cost effective. The most widely used markers are a MUC1 mucin (e.g. measured as CA15.3) and CEA. A combination of markers is more sensitive than using a single marker. When CA15.3, CEA and ESR are used as a panel of serum markers in monitoring therapeutic response, over 90% of patients are biochemically assessable. A biochemical index score comprising these three markers has been devised retrospectively, validated prospectively, in a single centre and in a multicentre study. Biochemical assessment by serum markers correlates with clinical/radiological (UICC) assessment and often pre-dates remission and progression shown by UICC criteria. It is also the only validated method in monitoring metastatic breast cancer with disease unassessable by UICC criteria (e.g. sclerotic bone metastases, irradiated lesions). Future studies should aim at incorporating new markers (e.g. serum c-erbB2, markers of bone metabolism) to tailor different clinical situations, and at exploiting the use of serum markers to direct systemic therapy.
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PMID:Objective measurement of remission and progression in metastatic breast cancer by the use of serum tumour markers. 1295 47

Lapatinib and tofacitinib are small-molecule kinase inhibitors approved for the treatment of advanced or metastatic breast cancer and rheumatoid arthritis, respectively. So far, the mechanisms which are responsible for their activities are not entirely understood. Here, we focus on the interaction of these drug molecules with phospholipid membranes, which has not yet been investigated before in molecular detail. Owing to their lipophilic characteristics, quantitatively reflected by large differences of the partition equilibrium between water and octanol phases (expressed by logP values), rather drastic differences in the membrane interaction of both molecules have to be expected. Applying experimental (nuclear magnetic resonance, fluorescence and ESR spectroscopy) and theoretical (molecular dynamics simulations) approaches, we found that lapatinib and tofacitinib bind to lipid membranes and insert into the lipid-water interface of the bilayer. For lapatinib, a deeper embedding into the membrane bilayer was observed than for tofacitinib implying different impacts of the molecules on the bilayer structure. While for tofacitinib, no influence to the membrane structure was found, lapatinib causes a membrane disturbance, as concluded from an increased permeability of the membrane for polar molecules. These data may contribute to a better understanding of the cellular uptake mechanism(s) and the side effects of the drugs.
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PMID:Interaction of the small-molecule kinase inhibitors tofacitinib and lapatinib with membranes. 3271 Aug 52