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Evaluation of Thymidine Kinase Activity in the Serum of Patients With Solid Tumors

H

Hadassah Medical Center

Status

Unknown

Conditions

Solid Tumors

Study type

Observational

Funder types

Other

Identifiers

NCT01050413
044108-HMO-CTL

Details and patient eligibility

About

This study aimed to evaluate serum thymidine kinase 1 (TK1) activity as a marker for solid tumors and more specifically in: preoperative testing for prediction of disease recurrence and survival; follow-up after surgical removal of the original tumor for early detection of disease recurrence and in monitoring therapy as a surrogate marker of tumor response.

Full description

Thymidine kinase 1 (TK1) is a metabolic enzyme catalyzing the ATP-dependent phosphorylation of thymidine to thymidine monophosphate followed by its utilization in DNA synthesis. It has been demonstrated that activity of TK1 in the serum of cancer patients corresponds to the amount of dividing tumor cells. Several clinical investigations clearly showed that abnormal TK1 levels indicate tumor growth. In breast cancer, serum TK1 was shown to predict increased risk of recurrence following surgery and may be a good marker for monitoring the response to therapy. The measurements of TK1 were useful as a prognostic and monitoring factor in patients with NSCLC. Unfortunately, all previously used assays measuring TK1 activity showed relatively low analytical sensitivity. Recently, the novel high sensitive non-radioactive TK1 assay (DiviTum) has been developed. With this assay tumour growth may be detected at an earlier stage of disease and smaller amounts of residual disease may be detected during and after therapy.

Enrollment

300 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with colon, breast, prostate and lung cancer before and during treatment

Exclusion criteria

  • pregnant women;
  • patients with generalized CMV and HZV infections;
  • patients with severe rheumatoid arthritis

Trial design

300 participants in 1 patient group

1
Description:
colon cancer, prostate cancer, lung cancer, ovarian cancer

Trial contacts and locations

1

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Central trial contact

Hadas Lemberg, PhD; Tamar Peretz, MD

Data sourced from clinicaltrials.gov

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