The Association Between Radiation Dermatitis and Skin Microbiome in Breast Cancer Patients

Sponsor
Fudan University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05032768
Collaborator
(none)
100
1
72
1.4

Study Details

Study Description

Brief Summary

The breast cancer patients who received radiotherapy after mastectomy and breast reconstruction will be enrolled. The skin microbiome before radiotherapy and its changes after radiotherapy will be analyzed systematically to find out whether the skin microbiome is associated with the severity of radiation dermatitis.

Condition or Disease Intervention/Treatment Phase
  • Radiation: post-operative radiotherapy

Detailed Description

Radiotherapy is an important treatment for breast cancer patients. About 95% of patients receiving radiotherapy will develop a degree of radiation dermatitis. Radiation dermatitis is usually limited to the site of radiation treatment. Symptoms vary and can range from itching, burning and pain to open or bleeding ulcers, which can greatly affect the quality of life of patients. Severe acute radiation dermatitis can lead to interruption or delay of treatment. At present, there is no standard for the prevention and treatment of radiation dermatitis. Our skin is home to millions of bacteria, fungi and viruses which compose the skin microbiota. Skin microbiota interacts with skin and affects physiology and immunity of the skin. Previous studies have reported the effects of radiotherapy on skin and immune system. However, so far, no studies have analyzed the effects of radiotherapy on skin microbiome and how skin microbiome affects the skin immune responses after radiotherapy. In this study, the breast cancer patients who received radiotherapy after mastectomy and breast reconstruction will be enrolled. The skin microbiome before radiotherapy and its changes after radiotherapy will be analyzed systematically to find out whether the skin microbiome is associated with the severity of radiation dermatitis. The long-term goal of this study is to deepen the understanding of the role of skin microbiome in the occurrence and development of radiation dermatitis, and provide a basis for subsequent exploration to reduce radiation dermatitis by regulating skin microecology.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Association Between Radiation Dermatitis and Skin Microbiome in Breast Cancer Patients Receiving Radiation After Mastectomy and Reconstructive Surgery
Actual Study Start Date :
Jan 1, 2021
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Severe radiation dermatitis

RTOG/EORTC grade 2 and above

Radiation: post-operative radiotherapy
Breast cancer patients who have received reconstructive surgery will receive post-operative radiotherapy.

No or mild radiation dermatitis

RTOG/EORTC grade 0 or 1

Radiation: post-operative radiotherapy
Breast cancer patients who have received reconstructive surgery will receive post-operative radiotherapy.

Outcome Measures

Primary Outcome Measures

  1. Skin microbiome differences between patients with and without >=2 acute radiation dermatitis [3 months]

    Acute radiation dermatitis will be graded per the Toxicity Criteria of the Radiation Therapy Oncology Group (RTOG)

Secondary Outcome Measures

  1. Skin microbiome differences between patients with and without >=2 late radiation dermatitis [5 years]

    Late radiation dermatitis will be graded per the Toxicity Criteria of the Radiation Therapy Oncology Group (RTOG)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Female patients

  2. Invasive breast cancer confirmed by pathology

  3. Underwent mastectomy and breast reconstruction

  4. Radiotherapy after breast reconstruction

  5. ECOG score 0-1

  6. Signed informed consent

Exclusion Criteria:
  1. Previous breast or chest radiotherapy

  2. Other serious skin diseases (systemic lupus erythematosus, skin sclerosis, et al) and cannot receive radiotherapy

  3. Pregnant women

  4. Patients who are unwilling or unable to receive regular follow-up.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fudan University Shanghai Cancer Center Shanghai Shanghai China 200032

Sponsors and Collaborators

  • Fudan University

Investigators

  • Principal Investigator: Xiaoli Yu, MD, Ph.D, Fudan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fudan University
ClinicalTrials.gov Identifier:
NCT05032768
Other Study ID Numbers:
  • FDRT-BC015
First Posted:
Sep 2, 2021
Last Update Posted:
Sep 2, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 2, 2021