The Emergence of RAS Mutations in Metastatic Colorectal Cancer Patients Receiving Cetuximab Treatment

Colorectal Cancer Clinical Trial

Official title:

A Non-interventional Uncontrolled Multicenter Study to Investigate the Emergence of RAS Resistance Mutations in RAS Wild Type mCRC Patients Receiving First Line Cetuximab Treatment

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03401957
• Other study ID #: EC1060904
• Status: Recruiting
• Phase: N/A
• First received: January 10, 2018
• Last updated: January 10, 2018
• Start date: January 2018
• Est. completion date: January 2022

Study information

• Verified date: January 2018
• Source: National Health Research Institutes, Taiwan
• Contact: Shang Hung Chen, M.D.
• Phone: +886-6-7000123
• Email: bryanchen[@]nhri.org.tw
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

To evaluate the emergence of RAS mutation in patients with metastatic colorectal cancer, circulating free DNA will be analyzed using mass spectrometric genotyping in subjects during cetuximab treatment. The hypothesis of this study is that acquired RAS mutation is responsible for the resistance to cetuximab treatment in wild-type colorectal cancer. The usefulness of liquid biopsy to monitor dynamic genetic alterations in colorectal cancer during treatment will also be investigated in this study.

Description:

This is a single arm, non-interventional, uncontrolled, multicenter study in metastatic colorectal cancer patients receiving cetuximab-based infusional 5-FU regimen as 1st line treatment. Patients who are pathologically diagnosed as metastatic colorectal cancer with RAS wild type genotyping will be recruited in this study. Patients enrolled will be those for whom it is planned to treat their colorectal cancer with a cetuximab-based infusional 5-FU regimen according to the locally approved label. Cetuximab-based treatment is anticipated to be continued until disease progression, intolerable toxic effects, or withdrawal of consent occurs. Blood samples from patients enrolled in this study will be collected before the start of cetuximab-based chemotherapy, and every 3 months during the 1st line treatment with the cetuximab-based regimen. Blood sampling is also required at 2-3 weeks after disease progression following cetuximab treatment and after disease progression on 2nd line treatment. The blood samples will be sent to a central laboratory at the Taipei Institute of Pathology and evaluated for RAS genotype, using MassARRAY technique. The objectives of this study are described as follows.

Primary objective:

To observe the percentage of detected RAS mutations (circulating DNA) during 1st line cetuximab exposure in Taiwanese patients.

Secondary objective:

1. To observe the time to onset of detected RAS mutation in circulating DNA.

2. To observe the quantification mutation load change under treatment.

3. To evaluate clinical response and resection rate of metastases with 1st line cetuximab exposure.

4. To evaluate treatment duration with 1st line cetuximab.

5. To investigate the correlation between the occurrence and levels of acquired RAS mutations post-cetuximab treatment and clinical outcomes (progression free survival and overall survival).

6. To calculate total 1st line cetuximab exposure dosage.

7. To investigate correlation between the irinotecan or oxaliplatin dosage and acquired resistance.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: January 2022
• Est. primary completion date: January 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 90 Years

Eligibility

Inclusion Criteria:

1. Patients with histologically proven metastatic colorectal cancer for whom treatment with cetuximab in 1st line setting, is planned as part of routine clinical practice, as per the locally approved label and the best scientific information; the decision to prescribe cetuximab is at the sole discretion of the investigator. The choice of standard chemotherapy regimen for 1st line treatment of colorectal cancer is also at the sole discretion of the Investigator, based upon routine clinical practice.

2. Patients aged 20 years and above.

3. Patients who are molecularly diagnosed as having RAS wild-type mCRC.

4. Patients who are willing to provide blood samples during the study

5. Patients who are willing, and able and give, signed informed consent.

Exclusion Criteria:

1. Patients having a history of prior exposure to any anti-EGFR therapy.

2. Contra-indications to cetuximab as per locally approved label.

Related Conditions & MeSH terms

• Colorectal Cancer
• Colorectal Neoplasms
• Drug Resistance
• Mass Spectrometry
• RAS-RAF Pathway Deregulation

Intervention

Drug:
• Cetuximab
Cetuximab-based infusional 5-FU regimen as the 1st line treatment.

Diagnostic Test:
• liquid biopsy
The blood samples taken from subjects will be evaluated for RAS genotype using MassARRAY technique.

Locations

Country	Name	City	State
Taiwan	Kaohsiung Medical University Chung-Ho Memorial Hospital	Kaohsiung
Taiwan	National Cheng Kung University Hospital	Tainan
Taiwan	Cathay General Hospital	Taipei
Taiwan	Taipei Veterans General Hospital	Taipei

Sponsors (5)

Lead Sponsor	Collaborator
National Health Research Institutes, Taiwan	Cathay General Hospital, Kaohsiung Medical University Chung-Ho Memorial Hospital, National Cheng-Kung University Hospital, Taipei Veterans General Hospital, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of detected circulating DNA RAS mutations during 1st line cetuximab exposure.	Percentage of detected RAS mutations during cetuximab treatment.	9 months
Secondary	Time to onset of newly detected circulating DNA RAS mutation.	Time duration between the start of cetuximab treatment and newly detection of RAS mutation.	9 months
Secondary	Mutation load (percentage of detected mutated alleles) until disease progression.	Percentage of detected mutated alleles at disease progression.	9 months
Secondary	Percentage of detected RAS mutations at the time of progression.	Percentage of detected RAS mutations at the time of progression.	9 months
Secondary	Clinical response rate by the investigator's judgement based on RECIST criteria.	Response rate of tumor after cetuximab treatment.	9 months
Secondary	Resection rate of liver or lung metastases.	Resection rates of metastases after cetuximab treatment.	9 months
Secondary	Duration of treatment with cetuximab in 1st line treatment.	Time duration of cetuximab as the 1st line treatment.	9 months
Secondary	Total accumulated dosage of cetuximab in 1st line treatment.	Total accumulated dosage of cetuximab in 1st line treatment.	9 months
Secondary	Progression-free survival from start of 1st line treatment with cetuximab.	The time duration of subjects between the inclusion in the study and disease progression.	9 months
Secondary	Overall survival from the start of 1st line treatment with cetuximab.	The time duration of subjects between the inclusion in the study and death.	24 months