Comparison of plasma from healthy nonsmokers, smokers, and lung cancer patients: Pattern-based differentiation profiling of low molecular weight proteins and peptides by magnetic bead technology with MALDI-TOF MS

Biomarkers ◽  
2012 ◽  
Vol 17 (3) ◽  
pp. 223-230 ◽  
Author(s):  
Syed G. Musharraf ◽  
Naghma Hashmi ◽  
M. Iqbal Choudhary ◽  
Nadeem Rizvi ◽  
Ahmed Usman ◽  
...  
2002 ◽  
Vol 88 (08) ◽  
pp. 213-220 ◽  
Author(s):  
Ilene Weitz ◽  
Valerie Israel ◽  
James Waisman ◽  
Cary Presant ◽  
Leanne Rochanda ◽  
...  

SummaryTo evaluate the effect of standard chemotherapeutic regimens on the hemostatic profile of patients with breast and lung carcinoma; and to evaluate the effect of a single dose of a low molecular weight (LMW) heparin, dalteparin sodium, administered prior to the chemotherapy on markers of hemostatic activation.11 patients with breast cancer and 10 patients with lung cancer receiving systemic chemotherapy were studied. 10 breast cancer patients and 9 lung cancer patients completed at least 1 cycle of treatment and had all hemostatic studies. Patients had a complete hemostatic and prothrombotic profile performed at study initiation. Markers of hemostatic activation consisting of immunoassays for thrombin-antithrombin (TAT) complex and D-dimer were measured in plasma samples obtained prior to chemotherapy and at 1, 24 and 48 h after treatment. A 2500 U dose of dalteparin was given prior to the 2nd cycle of chemotherapy; 5000 U of dalteparin was given prior to the 4th treatment cycle.Chemotherapy resulted in statistically significant increases in TAT and D-dimer for the 1, 24 and 48 h plasma samples in both the breast and lung cancer patients for all cycles of chemotherapy given without LMW heparin. There were statistically significant increases in basal thrombin generation over the 4 cycles of treatment which was unrelated to active cancer. Both pretreatment doses of dalteparin effectively prevented increases in the markers of hemostatic activation. However, in the lung cancer patients, who had significantly increased basal thrombin generation, the 5000 U dose dalteparin was more effective.Chemotherapy results in significant hemostatic activation in patients with breast and lung cancer. The effect of treatment appears to be cumulative. A single dose of LMW heparin administered prior to therapy can suppress hemostatic activation.This project was funded by a grant from the Pharmacia corporation


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 1049-1049
Author(s):  
Khaleel Ashraf ◽  
Melissa Dillmon ◽  
Delicia Carey ◽  
Francisco Robert

Abstract Deep venous thrombosis (DVT) is a relatively common complication in patients with cancer. The occurrence of DVT may a play a role in the over all prognosis of these patients. We retrospectively reviewed a cohort of 276 patients with lung cancer of various histologies with regards to demographics, types of thrombosis and survival. These patients were followed in our clinic from 1997 to 2004. Median age of patients was 62 and the male to female ratio was 1.59 to 1. Small cell lung cancer (SCLC) was the histology among 39 patients (14 %) and non small cell lung cancer (NSCLC) among the remaining 237 patients (86 %). Among NSCLC, the distribution of various sub types was: 95(34 %) adenocarcinoma, 64(23 %) squamous cell, 5 (1%) large cells and 73(26%) non-small cell, not other wise specified. Metastatic disease was present in 28 % (67/237) of NSCLC and 51% (20/39) of SCLC patients. Most (83%) had an excellent performance status of 0 or 1 and only 27% had weight loss at the initial time of diagnosis. Among 276 patients, 44 (16 %) had DVT. Of these, 7 patients had DVT prior to the diagnosis of lung cancer. The remaining 37 (85 %) had DVT during the course of their lung cancer. Among patients with thrombosis, 17 patients (39 %) developed pulmonary thromboembolism (PTE). The incidence of thrombosis in SCLC (13 %) was not statistically different from NSCLC (16 %). However there was increased incidence of thrombosis among patients with adenocarcinoma or when histology was only characterized as non small cell, not other wise specified; 20% (34/168) compared to 9 % (10/108) among all other histological subtypes (P= 0.015). Among patients with metastatic disease, 18% (16/87) had DVT compared to 15% (28/189) in those with early stage disease (P= 0.451). The median survival (MS) of patients with SCLC and DVT was 10 months compared to those without DVT and SCLC of 16 months (P = 0.4135). The MS of patients with NSCLC and DVT was 16 months compared those without DVT and NSCLC of 21 months (P = 0.1262). There is only limited literature specifically looking at various factors affecting the incidence of and the prognostic value of DVT in patients with lung cancer. We found in this study that the incidence of DVT among lung cancer patients was 16 %. The incidence of DVT among lung cancer patients when histology was adenocarcinoma or when histology was only characterized as non small cell, not other wise specified was twice compared to other histologic sub types. In those who develop DVT associated with lung cancer, a very high proportion (39 %) developed PTE. Even with anticoagulation, the overall survival of those patients who developed DVT was shorter than those who did not develop DVT but the difference did not reach statistical significance. Most of our patients with lung cancer and DVT were treated with low molecular weight heparin and whether this aggressive anticoagulant approach provided additional anti neoplastic benefit is debatable. Currently there are therapeutic trials looking at the role of prophylactic use of low molecular weight heparins as a means to enhance the survival in patients with lung cancer.


Molecules ◽  
2017 ◽  
Vol 22 (10) ◽  
pp. 1712 ◽  
Author(s):  
Sergio Hernandez-Leon ◽  
Jose Sarabia-Sainz ◽  
Gabriela Montfort ◽  
Ana Guzman-Partida ◽  
Maria Robles-Burgueño ◽  
...  

Heterocycles ◽  
2012 ◽  
Vol 85 (4) ◽  
pp. 927 ◽  
Author(s):  
Masamichi Nakakoshi ◽  
Masayoshi Tsubuki ◽  
Natsumi Funakoshi ◽  
Hiroki Nakajima

2015 ◽  
Vol 50 (8) ◽  
pp. 1006-1012 ◽  
Author(s):  
Junji Mizukado ◽  
Hiroaki Sato ◽  
Liang Chen ◽  
Yasumasa Suzuki ◽  
Shogo Yamane ◽  
...  

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