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Application of MRI in Identifying Myelosuppression Risk of Neoadjuvant Chemoradiotherapy for Rectal Cancer

Application of MRI Quantitative Parameters in Identifying Myelosuppression Risk of Neoadjuvant Chemoradiotherapy for Rectal Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04970498
Enrollment
120
Registered
2021-07-21
Start date
2021-02-01
Completion date
2022-10-31
Last updated
2021-07-21

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

Conditions

Rectal Cancer Stage II, Rectal Cancer Stage III

Keywords

Rectal Cancer, Myelosuppression, magnetic resonance imaging, IDEAL-IQ

Brief summary

Rectal cancer patients who received neoadjuvant chemoradiotherapy in Peking University Third Hospital in 2021 are divided into acute myelosuppression group, chronic myelosuppression group and normal group. The differences of magnetic resonance parameters between the groups were compared. The risk identification model of acute and chronic myelosuppression after neoadjuvant chemoradiotherapy was established by clinical risk factors and quantitative parameters of magnetic resonance imaging, and the prediction efficiency of the model was evaluated.

Detailed description

The patients with locally advanced rectal cancer diagnosed in Peking University Third Hospital and undergoing neoadjuvant chemoradiotherapy were collected. The basic information of patients (including age, sex, BMI, TNM stage of rectal cancer (T2, T3 stage)) was collected. The blood routine was collected before radiotherapy, 1 week, 2 weeks and 90 days after radiotherapy. MRI including T1WI, DWI sequence and IDEAL-IQ sequence before radiotherapy, 1-2 weeks after radiotherapy and 90 days after radiotherapy were performed, and the corresponding parameters were obtained. The white blood cell values and quantitative parameters of magnetic resonance (including T1WI, DWI signal intensity (b = 1000) and proton density fat fraction (PDFF) of sacrilium and proximal femur were collected. Patients were divided into acute myelosuppression group and non-acute myelosuppression group according to blood routine results 14 days after radiotherapy, and chronic myelosuppression group and non-chronic myelosuppression group according to blood routine results 90 days after radiotherapy. The magnetic resonance parameters difference between 1-2 weeks after radiotherapy and before radiotherapy, and the magnetic resonance parameters difference between 90 days after radiotherapy and before radiotherapy were calculated. By comparing the differences of clinical risk factors and quantitative parameters of MRI between the two groups, the meaningful variables were screened out, and the risk identification model of acute and chronic myelosuppression was established.

Interventions

DIAGNOSTIC_TESTMRI

MRI including T1WI, DWI sequence and IDEAL-IQ sequence before radiotherapy, 1-2 weeks after radiotherapy and 90 days after radiotherapy were performed

DIAGNOSTIC_TESTblood routine test

The blood routine was collected before radiotherapy, 1 week, 2 weeks and 90 days after radiotherapy.

Sponsors

Peking University Third Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* From February 2021 to August 2022, patients with locally advanced rectal cancer were treated with neoadjuvant chemoradiotherapy in the Third Hospital of Peking University. * There were blood routine before radiotherapy, 1 week, 2 weeks and 90 days after radiotherapy, and MRI examination including routine MRI sequence and IDEAL-IQ sequence before radiotherapy, 1-2 weeks and 90 days after radiotherapy. * Each patient used the same chemotherapy regimen.

Exclusion criteria

* Patients with metabolic bone diseases such as hyperparathyroidism and Cushing's syndrome. * Patients with history of pelvic radiotherapy or systemic chemotherapy. * Patients with leukocytes below 4.0×10\^9/L or long-term severe anemia before radiotherapy. * Patients with tumor bone metastases; patients with pelvic trauma, fracture, and infectious diseases.

Design outcomes

Primary

MeasureTime frameDescription
Changes of IDEAL-IQ sequence of MRI1-2 weeks after radiotherapyThe differences of PDFF(%) between the acute myelosuppression group and no suppression group
Changes of T1WI sequence of MRI1-2 weeks after radiotherapyThe differences of T1WI signal intensity(IU) between the acute myelosuppression group and no suppression group
Changes of DWI sequence of MRI1-2 weeks after radiotherapyThe differences of DWI signal intensity(IU)between the acute myelosuppression group and no suppression group
Changes of ADC map of MRI1-2 weeks after radiotherapyThe differences of ADC value(mm\^2/s) between the acute myelosuppression group and no suppression group

Countries

China

Contacts

Primary Contact宁 朗, Professor
13501241339@126.com13501241339
Backup ContactNing 朗, Professor
13501241339@126.com13501241339

Outcome results

None listed

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