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Biomarkers for Predicting Neoadjuvant Chemoradio-resistance for Middle-low Advanced Rectal Cancer

Identification of Tissue Biomarkers for Predicting Neoadjuvant Chemoradio-resistance in Patients With Middle-low Local Advanced Rectal Cancer.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03573791
Enrollment
152
Registered
2018-06-29
Start date
2018-05-21
Completion date
2028-05-21
Last updated
2026-08-18

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

Conditions

Cancer of Rectum, Cancer of the Rectum, Neoplasms, Rectal, Rectal Cancer, Rectal Tumors, Rectum Cancer, Rectum Neoplasms

Brief summary

Neoadjuvant therapy has been widely applied to locally advanced rectal cancer. However, about 50% of patients receiving this therapy do not respond well as evidenced by the fact that their T or N stages are not effectively decreased judged by postoperative pathological examination. The purpose of this trail is to identify the biomarkers (from within patients' tumor mass before neoadjuvant therapy) to predict resistance to neoadjuvant therapy. These biomarkers can help stratify neoadjuvant-resistant patients towards surgery while avoiding unnecessary chemoradio-based neoadjuvant therapy.

Detailed description

According to postoperative pathological examination results, all participants will be divided into two groups: complete response (ypT0N0) and poor response (\>ypT1-2N0). Differentially expressed genes between complete response and poor response will be analyzed. A scoring formula will be established based on the results. Tumor tissue samples are collected before neoadjuvant therapy and will be analyzed via RNA sequencing.

Interventions

None listed

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Histopathology proved to be adenocarcinoma of the rectum. * The edge of tumor is within 12cm of anus margin. * According to the eighth edition of AJCC TNM staging standard ,that staging for Ⅱ-Ⅲ period, as T3-T4, N0 or any T, N1-2. * There is no history of chemotherapy, radiotherapy or immunotherapy before neoadjuvant therapy. * Understand and agree to sign the informed consent for the study.

Exclusion criteria

* With intestinal obstruction or impending obstruction, or perforation. * With other malignancies occurred within 5 years.

Design outcomes

Primary

MeasureTime frameDescription
Comparing gene expression differences between poor response group and complete response group by using RNA sequencing.6 monthsUsing RNA-seq sequencing method to obtain the whole genome transcription profiles of the poor response group and complete response group, and compare the gene expression differences between these two groups.

Secondary

MeasureTime frameDescription
Overall survival(OS)3 yearsThe total survival time of the participants from joining the group to the death. If the death time is unknown, the relevant participants will be excluded for analysis.
Progression Free Survival(PFS)3 yearsThe time period that from participants joining the groups to the progression of disease(recurrence or metastasis) or death of any cause.

Countries

China

Contacts

CONTACTZheng Wang, MD/PhD
zhengwang@hust.edu.cn+86 27 85726612
STUDY_CHAIRZheng Wang, MD/PhD

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026