TPS®
Combating Cancer with TPS®
TPS® is a tumor activity marker assay used to support prognosis, treatment monitoring, and patient follow-up for various epithelial cancers, including breast, colorectal, ovarian, and prostate cancer.
TPS® measures soluble fragments of cytokeratin 18, which is over-expressed in epithelial cells and particularly in many types of cancer. This information is crucial for early detection of cancer recurrence and the quick assessment of treatment efficacy.
The tumor marker TPS® is a reliable indicator of tumor cell activity particularly useful in patient management for different carcinomas. Compared with conventional tumor mass markers, the activity marker TPS® provides the clinician with earlier signals about the course of the disease. TPS® is particularly useful in treatment monitoring and surveillance of patients with epithelial cell carcinomas e.g. breast, prostate, and ovarian cancer.
The TPS® ELISA only for China is manufactured and distributed by IDL Biotech.
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Clinical evaluation
TPS® ELISA assay is a valuable tumor marker for epithelial cancer, generating clinical information in breast and prostate cancer but also valuable in other forms of epithelial cell tumors such as colorectal and ovarian cancer.
References for TPS®
TPS® general
1. Barak V., et al. Clinical utility of cytokeratins as tumor markers. Clin Biochem 2004; 37:529-540
TPS® in breast
3. Ahn S.K., et al. Preoperative serum tissue polypeptide-specific antigen is a valuable prognostic marker in breast cancer. Int J Cancer. 2013; 132:875-881
TPS® in prostate
4. Kil P.J., et al. Tissue polypeptide specific (TPS) determination before and during intermittant maximal androgen blockade in patients with prostatic carcinoma. Euro Urol. 2003; 43:31-38
TPS® in ovarian
5. Van Dalen A., et al. Significance of serum CA125 and TPS antigen levels for detemination of overall survival after three chemotherapy courses in ovarian cancer patients during long-term follow-up. Eur J Gynaec Oncol. 2009; 30:609-615
MonoTotal®
For high sensitivity in NSCLC
MonoTotal® is a quantitative immunoassay that specifically measures defined epitopes on cytokeratin 19, 8, and 18. The test result is directly proportional to the concentration of soluble cytokeratin fragments in serum. An elevated level of soluble cytokeratin fragments in patient samples is an indication of epithelial tumor cell activity.
Lung cancer is the most frequently diagnosed cancer and the leading cause of cancer mortality worldwide. Patients may suffer from one of two cancer types: Non-Small Cell Lung Cancer (NSCLC), or the less common, Small-Cell Lung Cancer (SCLC).
Cancer biomarkers are effective for prognostic evaluation and monitoring of disease. MonoTotal® is a sensitive and efficient tool for managing patients with Non-Small Cell Lung Cancer (NSCLC).
With MonoTotal®, physicians receive an early indication of disease status, measured in terms of tumor cell activity rather than more conventional tumor burden measurements. MonoTotal® provides the physician with a reliable monitoring aid for disease progression and treatment in lung cancer patients.
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Clinical evaluation
MonoTotal® correlates well with tumor cell activity and the extent of the disease. Studies published during the last years show that MonoTotal®has a strong association with clinical response in patients. MonoTotal®demonstrates high sensitivity in patients with NSCLC, independent of histotype. The overall sensitivity is about 70-75%, at 95% specificity, and correlates well with tumor cell activity and the extent of the disease.
References for MonoTotal®
1. Barak, V. et al. Clinical utility of cytokeratin as a tumor marker. Clin Biochem. 2004;37:529-540.
4. Kim, DW. et al. Evaluation of usefulness for MonoTotal™ in non-small cell lung cancer. J Nucl Med Tech. 2009;13:171-174.
5. Wojcik, E. et al. Evaluation of the diagnostic utility of MonoTotal® in lung cancer patients. J Lab Diagn. 2009; 45:75-80.
6. Topolcan, O. et al. (Abstract). MonoTotal® – prognosis and therapy control in patients with non small cell lung cancer (NSCLC). XIIth International Symposium on Biology and Clinical Usefulness of Tumor Markers, February 4-7, 2009, Barcelona, Spain.
UBC®
UBC® ELISA for Bladder Cancer detection
UBC® is an immunoassay for both primary diagnosis and monitoring of bladder cancer. The test specifically measures soluble fragments of cytokeratin 8 and 18 in urine samples. Elevated amounts of cytokeratin protein fragments are present in the urine of many individuals with bladder cancer, even at the early stages of the disease.
UBC® is available in ELISA and Rapid format.
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Clinical evaluation
UBC® assay is a valuable tumor marker for epithelial cancer, generating clinical information in bladder cancer.
References
Onkologi
Diagnostik för onkologi
Cancer är en av de vanligaste dödsorsakerna i världen, trots att kunskapen ökar. För att förbättra behandlingen av cancerpatienter finns det ett tydligt behov av effektiva diagnostikverktyg för att fånga upp dessa viktiga kliniska data.
Bakteriologi
Ett effektivt tyfusprov
Tyfoidfeber är en vatten- och livsmedelsburen infektionssjukdom som orsakas av bakterien, Salmonella enterica. IDL Biotechs produkt TUBEX® TF, är ett snabbt och känsligt in vitro-diagnostiskt test för detektion av akut tyfoidfeber.
Investerare
Vi är noterade på NASDAQ First North Growth Market.
Vi vill vara det självklara valet inom vårt segment på de marknader där vi är etablerade. Marknaden för våra produkter är stor och vi är en mindre aktör med en betydande tillväxtpotential än så länge. IDL Diagnostics är unikt för ett bolag av den här storleken.
