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Search / Trial NCT03656172

Interest of Reticulocyte Haemoglobin Content (RET-he) in Management of Functional Anemia for Patient With Solid Tumor

Launched by INSTITUT CANCEROLOGIE DE L'OUEST · Aug 30, 2018

Trial Information

Current as of August 02, 2025

Completed

Keywords

Anemia By Functional Martial Deficiency Ret He

ClinConnect Summary

Anemia is a common clinical situation in oncology. It contributes to the asthenia and thus to the decrease in the quality of life of the patient. In addition, it is considered an independent pejorative prognostic factor according to a literature review of 2001. An appropriate management of the latter is therefore paramount. To do this, it is necessary to successfully define its origins.

In 2014, RET-he was studied for the first time in the cancer patient. This analysis showed that there is a good negative predictive value of RET-he for a cut-off of 32 PG, i.e., that above this value the ir...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age ≥ 18 years.
  • Metastatic solid tumor or not.
  • * Anemia by functional martial deficiency (as defined in the NCCN2016 recommendations):
  • o Hb \< 11 g/DL, TSAT \< 20% and ferritinlike between 30 and 800 ng/ml
  • Initial assessment of anemia carried out at the laboratory of Biopathology of the ICO
  • Exclusion Criteria:
  • Patient with malignant hemopathy.
  • Patient with chronic renal failure with an estimation of renal filtration rate according to the formula CKD-EPI \< 60 ml/min/1.73 m².
  • Patient with vitamin B12 deficiency, folate deficiency, hemolysis and/or hemoglobinopathy.
  • Patient with active infection.
  • Patient with bone marrow tumor. Confirmation by a osteo-medullary biopsy (BOM) or a myelogram is not necessary to exclude the patient.
  • Patient who received ASE within two months prior to the initial blood test.
  • Patient who received iron (oral or injectable) in the two months preceding the initial blood test.
  • Patient who received a transfusion of globular pellets in the month preceding the initial blood test.

About Institut Cancerologie De L'ouest

The Institut de Cancérologie de l'Ouest (ICO) is a leading French cancer research and treatment center dedicated to advancing oncology through innovative clinical trials and multidisciplinary care. As a key player in the fight against cancer, ICO integrates cutting-edge research with clinical practice, focusing on personalized medicine and patient-centered approaches. With a commitment to improving patient outcomes, ICO collaborates with academic institutions and industry partners to develop novel therapies and enhance understanding of cancer biology. The institute's expertise spans various cancer types, making it a pivotal hub for oncological research and education in France and beyond.

Locations

Saint Herblain, , France

Patients applied

0 patients applied

Trial Officials

Mathilde DUPE, MD

Principal Investigator

Institut de Cancérologie de l'Ouest

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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