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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03702868
Other study ID # SYSUCC-011
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date October 10, 2018
Est. completion date October 30, 2020

Study information

Verified date January 2021
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Breast cancer is the most common cause of cancer death in women. Adjuvant chemotherapy significantly reduces the risk of recurrence of high-risk breast cancer. However, about 30% of patients still have distant metastasis or local recurrence after chemotherapy. Moreover, 60% of patients had 3-4 degrees of adverse drug reactions during chemotherapy. The purpose of the study is to investigate relationship between gut microbiome and adjuvant chemotherapy in early breast cancer patients.


Description:

Breast cancer is the most common cause of cancer death in women. Adjuvant chemotherapy significantly reduces the risk of recurrence of high-risk breast cancer. However, about 30% of patients still have distant metastasis or local recurrence after chemotherapy. Moreover, 60% of patients had 3-4 degrees of adverse drug reactions during chemotherapy. The human gut microbiota have been considered the most important microecosystem living in symbiosis with the body. It is identified as a crucial determinant in cancer occurrence and development . Besides, Gut microbial alterations may influence the therapy efficacy and adverse drug event. We collect the fresh tail stool sample 24h before adjuvant chemotherapy and 24h after adjuvant chemotherapy then the composition of intestinal microbiota and subsequent short-term alterations are analysed by 16srRNA sequencing.The purpose of the study is to investigate relationship between gut microbiome and adjuvant chemotherapy in early breast cancer patients.


Recruitment information / eligibility

Status Terminated
Enrollment 226
Est. completion date October 30, 2020
Est. primary completion date October 30, 2020
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Histologically diagnosed stage I-III breast cancer; - Plan to receive adjuvant chemotherapy in our hospital; - Sign the informed consent; - Good compliance and willing to follow up. Exclusion Criteria: - Those who have started receiving adjuvant chemotherapy; - Chemotherapy contraindications;

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Sun Yat-sen University Cancer Center Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of chemotherapy related adverse reaction chemotherapy related adverse reaction are assessed by CTCAE protocol 1 years
Secondary disease free survival the length of time after surgery during which no breast cancer is found 5years
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