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Status unknownNCT00851604Updated Jun 3, 2010

ProGRP, CgA, NSE and TUM2-PK in in Patients With Neuroendocrine Tumors

An observational study in Neuroendocrine Tumors, sponsored by Hadassah Medical Organization. Status unknown at 1 site in Israel. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2010-06-03.

Sponsored by Hadassah Medical Organization · Observational

The sponsor has not verified this record recently (last verified May 2010), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years to 90 Years
Sex
All
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Study summary

The purpose of this study is to determine whether monitoring of levels of Serological Markers ProGRP, CgA, NSE and Pyruvate Kinase M2 are effective in the Evaluation of Diagnosis, Monitoring Therapeutic Effects and Predicting response to somatostatin analogues in Patients with Malignant Neuroendocrine Tumors.

Read the detailed description

Assessment of the anatomical spread and disease progression in neuroendocrine tumor patients has become an essential part of disease management, but sometimes in many patients difficult to be measured. Therefore, the evaluation of serum markers could represent a useful tool for monitoring the course of the disease and the response of patients to therapy or palliative treatment.Clinical data considers CgA and NSE as available today blood biomarkers for neuroendocrine tumors.Until now the usefulness of serum ProGRP as a clinical tumor marker has been evaluated mainly in Small Cell Lung Carcinoma, while its role in the management of NE tumors has not been elucidated.Available in the literature limited data suggests that ProGRP may be a potential tumor marker in NE tumors.

Pyruvate kinase type M2 is the key glycolytic regulator in tumor cells.It catalyzes the dephosphorylation of phosphoenolpyruvate to pyruvate with ATP production.The dimeric form of this enzyme (TUM2-PK) has been detected in the blood of patients with different cancers.High TUM2-PK expression was suggested to be an important element of tumor cell metabolism adaptation to an inadequate oxygen and nutrient supply.Recently, it has been shown that somatostatin and its structural analogues pass through cell membrane and actively bind to cytosolic TUM2-PK. In response to this binding TUM2-PK translocates into the nucleus and induce programmed cell death. It is suggested that TUM2-PK enzyme may contribute significantly to response of neuroendocrine tumors to somatostatin analogues.

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Conditions studied

  • Neuroendocrine Tumors

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Keywords

  • ProGRP
  • CgA
  • NSE
  • TUM2-PK
  • Neuroendocrine Tumors
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In context

Neuroendocrine Tumors

676 studies on the registry are indexed under Neuroendocrine Tumors; 169 are open to participants now.

This study's planned enrollment of 40 is below the median of 115 across 176 observational studies indexed under Neuroendocrine Tumors.

Browse Neuroendocrine Tumors studies →

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 659 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The patients with neuroendocrine tumors

Inclusion criteria

  • The patients at diagnosis of neuroendocrine tumors before therapy will be approached to participate in the study.
  • Older then 18 years old
  • Patients who agree to participate will receive a detailed explanation and sign an informed consent form.

Exclusion criteria

Exclusion Criteria:

  • Pregnant women
  • Coexistence of another primary malignant tumor other then neuroendocrine tumors
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (estimated)
Biospecimen retention
Samples without dna

Groups and cohorts

  • 1

    Patients with malignant neuroendocrine tumors

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Study locations

1 of 1 sites recruiting
  • Hadassah Medical Organization
    Jerusalem, 91120, Israel
    • Arik Tzukert, DMD · Contact · arik@hadassah.org.il · 6776095
    • Hadas Lemberg, PhD · Contact · lhadas@hadassah.org.il · 6777572
    • Benjamin Nisman, PhD · Sub investigator
    • Tamar Peretz, M.D., PhD · Sub investigator
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 3, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00851604
Lead sponsor
Hadassah Medical Organization
First posted
Feb 26, 2009
Start date
Mar 2009
Primary completion
Mar 2010 (estimated)
Completion
Jan 2011 (estimated)
Last update
Jun 3, 2010

Study contacts

Asher Salmon, M.D., Ph.D.
Contact
aysalmon@gmail.com
6778199 ext. 00 972 2
Hadas Lemberg, PhD
Contact
lhadas@hadassah.org.il
6777572 ext. 00 972 2
Asher Salmon, M.D.
principal investigator · Hadassah Medical Organization

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2010. You cannot join it, but the record below documents what was studied.

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