Clinical Trials Logo

Clinical Trial Summary

Bevacizumab in combination with chemotherapy represents a standard of care for first-line treatment in patients with advanced colorectal cancer. Molecular predictive factors for bevacizumab efficacy have not yet been identified therefore selection of patients more likely to benefit from such a treatment approach is not possible. Retrospective analyses suggested that LDH serum levels may influence the clinical activity of anti-angiogenetic drugs. Primary aim of our clinical trial will be to prospectively ascertain whether bevacizumab in combination with chemotherapy has an improved clinical activity in patients with high LDH serum levels compared to patients with normal LDH serum levels


Clinical Trial Description

The VEGF-driven tumour pathway has been demonstrated to represent a novel therapeutic target for an innovative class of antineoplastic agents. Among these antiangiogenetic-targeted treatment modalities the anti-VEGF monoclonal antibody bevacizumab has become a new standard of care for first-line treatment of metastatic colorectal cancer. The biological link between hypoxia, LDH levels and the tumour-driven angiogenesis pathway through the abnormal activation of the hypoxia Inducible factor 1 α (HIF1-α) is well established. HIF1-α is a key transcription factor that up-regulates a series of genes involved in glycolytic metabolism, angiogenesis, cell survival and erythropoiesis Accordingly to this biological assumption Azuma et al (Azuma et al 2007) demonstrated that high LDH serum levels were associated with tumour over-expression of VEGFA and VEGFR-1. As a clinical consequence it has been speculated that LDH levels may represent an indirect indicator of activated tumour angiogenesis and ultimately of worse prognosis We previously analysed the role of LDH pre-treatment serum levels in colorectal cancer patients receiving first-line bevacizumab in metastatic colorectal cancer treated with first-line bevacizumab were eligible. A control group including all consecutive patients treated with chemotherapy alone was also considered. Pre-treatment LDH serum levels were collected for all cases ;


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01853813
Study type Interventional
Source Gruppo Italiano per lo studio dei Carcinomi dell'Apparato Digerente
Contact
Status Completed
Phase Phase 2
Start date May 2013
Completion date July 2015

See also
  Status Clinical Trial Phase
Completed NCT01570452 - Matrilysin Expression in Different Stages of Colorectal Tumors N/A
Active, not recruiting NCT04304209 - Pd1 Antibody Sintilimab ± Chemoradiotherapy for Locally Advanced Rectal Cancer Phase 2
Active, not recruiting NCT04398446 - Effect of Hemp-CBD on Patients With CIPN Phase 2
Recruiting NCT04486378 - A Phase II Clinical Trial Comparing the Efficacy of RO7198457 Versus Watchful Waiting in Patients With ctDNA-positive, Resected Stage II (High Risk) and Stage III Colorectal Cancer Phase 2
Recruiting NCT04264676 - Study of Oral Metronidazole on Postoperative Chemotherapy in Colorectal Cancer Phase 2
Recruiting NCT06314958 - Stage II/III Colorectal Cancer Recurrence
Recruiting NCT06342440 - Early Detection of Advanced Adenomas and Colorectal Cancer
Recruiting NCT05898789 - Virtual Rehabilitation for Cancer Survivors N/A
Recruiting NCT04813627 - Epidemiological Study to Monitor Study Participants With Resected Stage II (High Risk) or Stage III Colorectal Cancer for Circulating Tumor DNA Before, During and After Their Treatment With Adjuvant Chemotherapy
Not yet recruiting NCT05131243 - the Role of ctDNA in Predicting the Recurrence Risk of Colorectal Cancer N/A
Recruiting NCT06076811 - DANISH.MRD: Danish Assessment of Minimal Residual Disease by Liquid Biopsies
Recruiting NCT06342401 - Early Onset Colorectal Cancer Detection
Completed NCT06271980 - Early-Onset Colorectal Cancer Recurrence