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Identifying MSI Status From ctDNA in Chinese Patients With Refractory Advanced Solid Tumors

Identifying Microsatellite Instability Status From Circulating Tumor DNA in Chinese Patients With Refractory Advanced Solid Tumors: a Large Molecular Epidemiological Investigation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03596593
Acronym
IMPACT
Enrollment
8000
Registered
2018-07-24
Start date
2018-07-11
Completion date
2020-06-30
Last updated
2018-07-24

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

Conditions

Solid Tumor

Keywords

Solid tumor, China, MSI, ctDNA

Brief summary

This is a molecular epidemiological investigation aiming to identify microsatellite instability status from circulating tumor DNA in Chinese patients with refractory advanced solid tumors.

Detailed description

This study is conducted in Chinese patients with advanced refractory metastatic solid tumors. A total of 8-10 mL of blood will be collected from eligible patients and used for extracting circulating tumor DNA. Blood-MSI status will be tested based on SPANOM technique developed by 3D Medicines Inc. Shanghai, China. Patients are encouraged to provide tissues collected from progressive disease for tissue-MSI testing (not required for inclusion).

Interventions

DIAGNOSTIC_TESTSPANOM (identifying MSI status from ctDNA)

SPANOM technique, which has been developed by 3D Medicines Inc. Shanghai, China and made it possible to identify MSI status from blood samples, will be used in patients with refractory advanced solid tumors.

Sponsors

Peking University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female, age≥18 years old. 2. Confirmed malignant solid tumor by histopathology or cytopathology. 3. Colorectal cancer: progression after second-line therapy. Non-colorectal cancer: progression after first-line therapy. 4. Time duration from the last time of anti-cancer treatment to blood sample collection for MSI testing ≥ two weeks or five times half-life period of anti-cancer drugs 5. Signed the informed consent with name and time.

Exclusion criteria

1. Hematological malignancy 2. Patients who received immuotherapies. 3. Patients who received blood transfusion within one month before blood collection. 4. Pregnancy.

Design outcomes

Primary

MeasureTime frame
Incidence of MSI-H across different cancer types in Chinese patientsTwo years

Secondary

MeasureTime frameDescription
Incidence of Lynch syndrome across different cancer typesTwo years
Concordance between blood-MSI and corresponding tissue-MSI statusTwo yearsIn patients who are able to provide tumor tissue samples, concordance between blood-MSI status by SPANOM technique and tissue-MSI status by polymerase chain reaction (PCR) method will be calculated. DNA extracted from each tumor tissue will be amplified by standard PCR using six microsatellite loci: NR-21, BA-26, NR-27, BA-25, NR-24, MONO-27. Tumors are designated MSI-H if more than two loci were instable, MSI-L if one locus is instable, and MSS if all loci are stable.

Countries

China

Contacts

Primary ContactShen Lin, Professor
Linshenpku@163.com010-88196561
Backup ContactJian Li, Professor
oncogene@163.com010-88196561

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026