Carbonic anhydrase-9 expression levels and prognosis in human breast cancer: association with treatment outcome

Here, we set out to assess CA9 expression levels by real-time quantitative RT-PCR in breast cancer tissue samples obtained from 253 patients, and correlated those with relapse-free (RFS) survival. The median follow-up time was 75 months (range 2-168 months). CA9 expression was mainly found in high-g...

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Published inBritish journal of cancer Vol. 89; no. 2; pp. 271 - 276
Main Authors SPAN, P. N, BUSSINK, J, MANDERS, P, BEEX, Lvam, SWEEP, C. G. J
Format Journal Article
LanguageEnglish
Published Basingstoke Nature Publishing Group 21.07.2003
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Abstract Here, we set out to assess CA9 expression levels by real-time quantitative RT-PCR in breast cancer tissue samples obtained from 253 patients, and correlated those with relapse-free (RFS) survival. The median follow-up time was 75 months (range 2-168 months). CA9 expression was mainly found in high-grade, steroid receptor negative cancer tissues. CA9 levels were not significantly associated with RFS (P=0.926, hazard ratio (HR)=0.99, 95% CI=0.80-1.22) in the total cohort of 253 patients. In multivariate analysis with other clinicopathological factors, CA9 (P=0.018, HR=0.77, 95% CI=0.62-0.96), the interaction of adjuvant chemotherapy with CA9 (P=0.009, HR=1.31, 95% CI=1.07-1.61) and the interaction of adjuvant endocrine therapy with CA9 (P<0.001, HR=1.41, 95% CI=1.20-1.66) all contributed significantly to the final model. These results indicate that patients with low CA9 levels benefit more from adjuvant treatment than do patients with high levels. Thus, the determination of CA9 levels could aid in the selection of patients who will not benefit from adjuvant therapy, and whose prognosis will more likely improve with other treatment modalities.
AbstractList Here, we set out to assess CA9 expression levels by real-time quantitative RT–PCR in breast cancer tissue samples obtained from 253 patients, and correlated those with relapse-free (RFS) survival. The median follow-up time was 75 months (range 2–168 months). CA9 expression was mainly found in high-grade, steroid receptor negative cancer tissues. CA9 levels were not significantly associated with RFS ( P =0.926, hazard ratio (HR)=0.99, 95% CI=0.80–1.22) in the total cohort of 253 patients. In multivariate analysis with other clinicopathological factors, CA9 ( P =0.018, HR=0.77, 95% CI=0.62–0.96), the interaction of adjuvant chemotherapy with CA9 ( P =0.009, HR=1.31, 95% CI=1.07–1.61) and the interaction of adjuvant endocrine therapy with CA9 ( P <0.001, HR=1.41, 95% CI=1.20–1.66) all contributed significantly to the final model. These results indicate that patients with low CA9 levels benefit more from adjuvant treatment than do patients with high levels. Thus, the determination of CA9 levels could aid in the selection of patients who will not benefit from adjuvant therapy, and whose prognosis will more likely improve with other treatment modalities.
Here, we set out to assess CA9 expression levels by real-time quantitative RT-PCR in breast cancer tissue samples obtained from 253 patients, and correlated those with relapse-free (RFS) survival. The median follow-up time was 75 months (range 2-168 months). CA9 expression was mainly found in high-grade, steroid receptor negative cancer tissues. CA9 levels were not significantly associated with RFS (P=0.926, hazard ratio (HR)=0.99, 95% CI=0.80-1.22) in the total cohort of 253 patients. In multivariate analysis with other clinicopathological factors, CA9 (P=0.018, HR=0.77, 95% CI=0.62-0.96), the interaction of adjuvant chemotherapy with CA9 (P=0.009, HR=1.31, 95% CI=1.07-1.61) and the interaction of adjuvant endocrine therapy with CA9 (P<0.001, HR=1.41, 95% CI=1.20-1.66) all contributed significantly to the final model. These results indicate that patients with low CA9 levels benefit more from adjuvant treatment than do patients with high levels. Thus, the determination of CA9 levels could aid in the selection of patients who will not benefit from adjuvant therapy, and whose prognosis will more likely improve with other treatment modalities.
Author SPAN, P. N
MANDERS, P
BEEX, Lvam
SWEEP, C. G. J
BUSSINK, J
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Issue 2
Keywords Human
hypoxia
Relapse
Prognosis
Enzyme
Isozyme
breast neoplasms
quantitative real-time RT-PCR
Lyases
Malignant tumor
Real time
Polymerase chain reaction
Mammary gland diseases
survival analysis
Carbonate dehydratase
Mammary gland
Molecular biology
Carbon-oxygen lyases
Hydro-lyases
Quantitative analysis
Language English
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Snippet Here, we set out to assess CA9 expression levels by real-time quantitative RT-PCR in breast cancer tissue samples obtained from 253 patients, and correlated...
Here, we set out to assess CA9 expression levels by real-time quantitative RT–PCR in breast cancer tissue samples obtained from 253 patients, and correlated...
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proquest
crossref
pubmed
pascalfrancis
nature
SourceType Open Access Repository
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Publisher
StartPage 271
SubjectTerms Antigens, Neoplasm - analysis
Antineoplastic Agents, Hormonal - pharmacology
Biological and medical sciences
Biomarkers, Tumor - analysis
Breast cancer
Breast Neoplasms - pathology
Breast Neoplasms - therapy
Cancer research
Cancer therapies
Carbonic Anhydrase IX
Carbonic Anhydrases - analysis
Chemotherapy
Chemotherapy, Adjuvant
Clinical outcomes
Disease-Free Survival
DNA, Neoplasm
Drug Resistance, Neoplasm
Endocrine therapy
Endocrinology
Female
Follow-Up Studies
Gene Expression Regulation, Neoplastic
Gynecology. Andrology. Obstetrics
Humans
Hypoxia
Immunohistochemistry
Isoenzymes
Mammary gland diseases
Mastectomy, Modified Radical
Medical prognosis
Medical research
Medical sciences
Metastasis
Molecular and Cellular Pathology
Neoplasm Proteins - analysis
Oncology
Predictive Value of Tests
Prognosis
Radiotherapy, Adjuvant
Receptors, Steroid - analysis
Reverse Transcriptase Polymerase Chain Reaction
Surgery
Survival Analysis
Tumors
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  providerName: ProQuest
Title Carbonic anhydrase-9 expression levels and prognosis in human breast cancer: association with treatment outcome
URI http://dx.doi.org/10.1038/sj.bjc.6601122
https://www.ncbi.nlm.nih.gov/pubmed/12865916
https://www.proquest.com/docview/230015013
https://search.proquest.com/docview/73456304
https://pubmed.ncbi.nlm.nih.gov/PMC2394253
Volume 89
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