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Personalized use of irinotecan in colorectal cancer patients based on real world studies and pharmacogenomics

Personalized use of irinotecan in colorectal cancer patients based on real world studies and pharmacogenomics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073831
Enrollment
Unknown
Registered
2023-07-21
Start date
2022-10-12
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

colorectal cancer

Interventions

Wild-type group:None
Single heterozygous group:None
Mutant homozygous/double heterozygous group:None

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provincial People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Sign the informed consent; 2) Histopathological examination confirmed metastatic colorectal cancer; 3) Chemotherapy with irinotecan; 4) Age between 18-75 years old; 5) Physical condition score (ECOG) 0~2, estimated survival time =3 months; 6) Biochemical index requirements: bone marrow function (hemoglobin=10 g/dL, neutrophil count=1.5×10^9/L and platelets=100×10^9/L), renal function (serum creatinine=1.5×normal upper limit) and Liver function (serum creatinine and bilirubin < 1.5 x upper limit of normal and AST and ALT = 3 x upper limit of normal).

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Efficacy;The incidence of adverse events;

Secondary

MeasureTime frame
Progression Free Survival (PFS);Overall survival (OS);Duration of adverse reactions;

Countries

China

Contacts

Public ContactXia He

Sichuan Academy of Medical Sciences & Sichuan Provincial People’s Hospital

yaan_hbx@163.com+86 159 8227 4601

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026