Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer

BACKGROUND: Influences of CMF (cyclophosphamide, methotrexate,5-fluorouracil) chemotherapy on blood coagulation were investigated in 30 patients receiving adjuvant chemotherapy and in 30 patients receiving chemotherapy for metastatic breast cancer. METHODS: In plasma samples of 60 patients (median a...

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Main Author: Petrović Dragana
Format: Article
Language:English
Published: Institute of Oncology, Sremska Kamenica, Serbia 2002-01-01
Series:Archive of Oncology
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0354-7310/2002/0354-73100202061P.pdf
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spelling doaj-55d1a26f7e3e47b78e8dcc54cd4883312020-11-24T21:16:22ZengInstitute of Oncology, Sremska Kamenica, SerbiaArchive of Oncology0354-73102002-01-01102616610.2298/AOO0202061PEffect of CMF-chemotherapy on blood coagulation in patients with breast cancerPetrović DraganaBACKGROUND: Influences of CMF (cyclophosphamide, methotrexate,5-fluorouracil) chemotherapy on blood coagulation were investigated in 30 patients receiving adjuvant chemotherapy and in 30 patients receiving chemotherapy for metastatic breast cancer. METHODS: In plasma samples of 60 patients (median age 49.5), we evaluated the following parameters 1)Markers of in vivo clotting activation thrombin-antithrombin complex (ELISA) and D-dimer (ELISA), 2) Natural anticoagulants (protein C [PC] and antithrombin III [AT III] by chromogenic methods). The coagulation studies were performed at the beginning and at the end of the first cycle of CMF protocol. RESULTS: Before CMF therapy, significant difference was observed between patients with early stage and patients with metastatic breast cancer in the PC (p<0.01), AT III (p<0.01) and TAT (p<0.01) levels. After CMF therapy, patients with stage II (adjuvant) disease manifested a significant decrease in the level of PC and AT III activity (p<0.01) and an increase in TAT level (p<0.01). In patients with disseminated breast cancer CMF therapy provoked an increased level of TAT and D-dimer with a decreased activity of protein C and antithrombin III. There was significant difference in value of TAT, D- dimer, protein C and antithrombin III between the patients with adjuvant and metastatic breast cancer patients after CMF chemotherapy CONCLUSION: Our results suggest that the application of cytotoxic therapy provokes hypercoagulable condition in breast cancer patients. This effect should be considered when chemotherapy is employed in advanced cancer patients at high risk for thrombosis, or in patients with other risk factors. http://www.doiserbia.nb.rs/img/doi/0354-7310/2002/0354-73100202061P.pdfbreast neoplasmsblood coagulationantineoplastic agents
collection DOAJ
language English
format Article
sources DOAJ
author Petrović Dragana
spellingShingle Petrović Dragana
Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer
Archive of Oncology
breast neoplasms
blood coagulation
antineoplastic agents
author_facet Petrović Dragana
author_sort Petrović Dragana
title Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer
title_short Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer
title_full Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer
title_fullStr Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer
title_full_unstemmed Effect of CMF-chemotherapy on blood coagulation in patients with breast cancer
title_sort effect of cmf-chemotherapy on blood coagulation in patients with breast cancer
publisher Institute of Oncology, Sremska Kamenica, Serbia
series Archive of Oncology
issn 0354-7310
publishDate 2002-01-01
description BACKGROUND: Influences of CMF (cyclophosphamide, methotrexate,5-fluorouracil) chemotherapy on blood coagulation were investigated in 30 patients receiving adjuvant chemotherapy and in 30 patients receiving chemotherapy for metastatic breast cancer. METHODS: In plasma samples of 60 patients (median age 49.5), we evaluated the following parameters 1)Markers of in vivo clotting activation thrombin-antithrombin complex (ELISA) and D-dimer (ELISA), 2) Natural anticoagulants (protein C [PC] and antithrombin III [AT III] by chromogenic methods). The coagulation studies were performed at the beginning and at the end of the first cycle of CMF protocol. RESULTS: Before CMF therapy, significant difference was observed between patients with early stage and patients with metastatic breast cancer in the PC (p<0.01), AT III (p<0.01) and TAT (p<0.01) levels. After CMF therapy, patients with stage II (adjuvant) disease manifested a significant decrease in the level of PC and AT III activity (p<0.01) and an increase in TAT level (p<0.01). In patients with disseminated breast cancer CMF therapy provoked an increased level of TAT and D-dimer with a decreased activity of protein C and antithrombin III. There was significant difference in value of TAT, D- dimer, protein C and antithrombin III between the patients with adjuvant and metastatic breast cancer patients after CMF chemotherapy CONCLUSION: Our results suggest that the application of cytotoxic therapy provokes hypercoagulable condition in breast cancer patients. This effect should be considered when chemotherapy is employed in advanced cancer patients at high risk for thrombosis, or in patients with other risk factors.
topic breast neoplasms
blood coagulation
antineoplastic agents
url http://www.doiserbia.nb.rs/img/doi/0354-7310/2002/0354-73100202061P.pdf
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