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The Clinical Efficacy of Chemotherapy Determined by Histoculture Drug Response Assays in Patients with Colorectal Cancer

The Multicenter, Prospective, Randomized Controlled Clinical Study of Chemotherapy Determined by Histoculture Drug Response Assays in Patients with Colorectal Cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022033
Enrollment
Unknown
Registered
2019-03-21
Start date
2014-02-03
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

Colorectal cancer

Interventions

The Drug-sensitive group:Patients were regarded as sensitive to at least one kind of the drug in vitro HDRA assay
The Drug-resistant group:Patients who were diagnosed as resistant to all agents of their chemotherapy regiments in vitro HDRA assay
The Drug-empirical group:Patients who just underwent chemotherapy empirically without the direction of HDRA

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The enrolled patients should possess complete bone marrow function (neutrophils=1.5×10^3/µl, platelets=100×10^3/µl, and Hb=100 g/l), prothrombin time, liver and renal function (serum bilirubin=1.5×upper normal limit, aspartate aminotransferase [AST] and alanine aminotransferase [ALT]=1.5×upper normal limit and serum creatinine=1.5×upper normal limit). ^

Exclusion criteria

Exclusion criteria: (1) history of chemotherapy or radiotherapy before this study; (2) multiple primary tumors; (3) cachexia or important organ dysfunction; (4) history of myocardial infarction or severe unstable angina or congestive heart failure; (5) infectious disease or psychosis; (6) allergy to chemotherapeutic agents; (7) hereditary nonpolyposis CRC and familial adenomatous polyposis.

Design outcomes

Primary

MeasureTime frame
in vitro-in vivo correlations;

Secondary

MeasureTime frame
the overall survival time (OS);the progression-free survival time(PFS);

Countries

China

Contacts

Public ContactFu Liwu

Sun Yat-sen University Cancer Center

fulw@mail.sysu.edu.cn+86 020 87343163

Outcome results

None listed

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