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Protection of Cardiovascular Function With Crocin in BrEast Cancer Patients Undergoing Radiotherapy and Chemotherapy (ProtECtion)

Primary Purpose

Breast Cancer

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
crocin
Placebo
Sponsored by
Qilu Hospital of Shandong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breast Cancer focused on measuring Breast cancer, Cancer therapy-related cardiac dysfunction, Crocin, Echocardiography, Speckle tracking technology

Eligibility Criteria

25 Years - 80 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion criteria:

  1. Age 25-80 years old, female;
  2. Patients diagnosed with breast cancer by histopathology;
  3. Patients who plan to receive adjuvant radiotherapy/chemotherapy or combined adjuvant trastuzumab or pertuzumab targeted therapy;
  4. Patients who completed at least 6 cycles of treatment after enrollment;

Exclusion criteria:

  1. pregnant or breastfeeding women;
  2. Patients with poor echocardiographic image quality;
  3. Persistent atrial fibrillation and severe arrhythmia affect the collection and analysis of ultrasound data;
  4. Patients who are participating in other clinical studies.

Sites / Locations

  • Qilu Hospital of Shandong UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Crocin group

placebo group

Arm Description

The chemotherapy/radiotherapy protocols are made by oncologists adopted for patients depending on specific conditions , take saffron total glucosides tablets(provided by Reyoung Pharmaceutical Co., Ltd.) for 8 days during each chemotherapy (started on the 1st day before chemotherapy), 4 tablets/time, 3 times a day.

Undergoing chemotherapy/radiotherapy protocols as planned, take placebo piece during(the same appearance of crocin tablets, production unit:Reyoung Pharmaceutical Co., Ltd.) for 8 days during each chemotherapy (started on the 1st day before chemotherapy), 4 tablets/time, 3 times a day

Outcomes

Primary Outcome Measures

The change of LVEF measured by echocardiography
The differences between the two groups in the difference of LVEF measured by Echocardiography at the end of the experiment compared to that at the baseline.
The change of GLS measured by echocardiography
The differences between the two groups in the difference of GLS measured by Echocardiography at the end of the experiment compared to that at the baseline.

Secondary Outcome Measures

The incidences of the increase of serum troponin and/or NT-proBNP
Differences in the incidence rates of serum troponin exceeding the upper limit of normal value and NT-proBNP higher than the normal age reference value between the two groups during follow-up.
The incidences of chest tightness, chest pain and palpitation
The differences in the incidence of chest tightness, chest pain and palpitation between the two groups
The incidences of arrhythmia and ST-T changes
Differences between the two groups in the incidences of arrhythmia and ST-T changes displayed by dynamic electrocardiogram.
The differences of global circumferential strain, global radial strain, global area strain measured by echocardiography.
Differences between groups in the difference in global circumferential strain, global radial strain, global area strain measured by echocardiography at the end of the experiment compared to baseline.
The indexes of E, e', a', tricuspid regurgitation velocity measured by echocardiography.
Differences between groups in the difference in the indexes of left ventricular diastolic function measured by echocardiography at the end of the experiment compared to baseline.
The indexe of E/e'measured by echocardiography.
Differences between groups in the difference in the indexes of left ventricular diastolic function measured by echocardiography at the end of the experiment compared to baseline.
The indexe of left atrial volume index (LAVI)measured by echocardiography.
Differences between groups in the difference in the indexes of left ventricular diastolic function measured by echocardiography at the end of the experiment compared to baseline.
The indexe of TAPSE measured by echocardiography.
Differences between groups in the difference in the right ventricular function monitoring indicators measured by echocardiography at the end of the experiment compared to baseline.
The indexe of RV fractional area change (FAC) measured by echocardiography.
Differences between groups in the difference in the right ventricular function monitoring indicators measured by echocardiography at the end of the experiment compared to baseline.
The indexe of right ventricular free wall global longitudinal strain (RVGLS) measured by echocardiography.
Differences between groups in the difference in the right ventricular function monitoring indicators measured by echocardiography at the end of the experiment compared to baseline.

Full Information

First Posted
August 4, 2022
Last Updated
September 21, 2022
Sponsor
Qilu Hospital of Shandong University
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1. Study Identification

Unique Protocol Identification Number
NCT05504148
Brief Title
Protection of Cardiovascular Function With Crocin in BrEast Cancer Patients Undergoing Radiotherapy and Chemotherapy
Acronym
ProtECtion
Official Title
Protection of Cardiovascular Function With Crocin in BrEast Cancer Patients Undergoing Radiotherapy and Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 29, 2021 (Actual)
Primary Completion Date
June 25, 2023 (Anticipated)
Study Completion Date
September 25, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Qilu Hospital of Shandong University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The potential cardiovascular toxicity of tumor treatment and its resulting cardiovascular events have gradually become an important health risk for tumor survivors. Prevention and early identification of cardiovascular toxicity has now become one of the bottlenecks in improving the prognosis of cancer patients. Compared to conventional echocardiographic indicators, new ultrasound technology based on speckle tracking imaging (STI) has shown superiority in the diagnosis, risk stratification and prognosis evaluation of cardiovascular diseases. Crocin, one of the main active components of saffron, has been found protective effect on cardiovascular toxicity in basic studies. This is a randomized, double-blind, placebo-controlled, single-center clinical study to observe the effect of crocin on cardiovascular function caused by breast cancer treatment. One hundred and twenty breast cancer patients planning to undergo radiotherapy or chemotherapy will be included and randomly divided into a crocin group and a placebo group to observe the effect of total saffron tablets on cardiovascular function in patients with early breast cancer radiotherapy and chemotherapy. Participants will take crocin or placebo (4 tablets/time, 3 times a day) during each cycle of chemotherapy for 8 days, started on the 1st day before radiotherapy/chemotherapy. Follow-up was performed every 3 months after enrollment, and the follow-up period was 6 months. Primary study endpoints include the differences between groups in the difference in LVEF and GLS measured by echocardiography at the end of the experiment compared to baseline. Secondary study endpoint include the differences in the incidence rates of serum troponin exceeding the upper limit of normal value and NT-proBNP higher than the normal age reference value, the frequency and duration of chest tightness, chest pain and palpitation, the degree of arrhythmia and ST-T changes displayed by dynamic electrocardiogram, the other echocardiographic parameters (the E/e', global circumferential strain, global radial strain, 3D-GAS, LV torsion, LV rotation/derotation velocity, SDI, RVFWS, and indexes of left ventricular diastolic function and right ventricular function) at the end of the experiment compared to baseline between the two groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Breast cancer, Cancer therapy-related cardiac dysfunction, Crocin, Echocardiography, Speckle tracking technology

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Inclusion criteria: Age 25-80 years old, female; Patients diagnosed with breast cancer by histopathology; Patients who plan to receive adjuvant radiotherapy/chemotherapy or combined adjuvant trastuzumab or pertuzumab targeted therapy; Patients who completed at least 6 cycles of treatment after enrollment; Exclusion criteria: pregnant or breastfeeding women; Patients with poor echocardiographic image quality; Persistent atrial fibrillation and severe arrhythmia affect the collection and analysis of ultrasound data; Patients who are participating in other clinical studies. Eligible patients were randomly divided into 1:1 group and divided into crocin group and placebo control group. Both groups of subjects received crocin or placebo on the basis of standard anti-tumor treatment.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Crocin group
Arm Type
Experimental
Arm Description
The chemotherapy/radiotherapy protocols are made by oncologists adopted for patients depending on specific conditions , take saffron total glucosides tablets(provided by Reyoung Pharmaceutical Co., Ltd.) for 8 days during each chemotherapy (started on the 1st day before chemotherapy), 4 tablets/time, 3 times a day.
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
Undergoing chemotherapy/radiotherapy protocols as planned, take placebo piece during(the same appearance of crocin tablets, production unit:Reyoung Pharmaceutical Co., Ltd.) for 8 days during each chemotherapy (started on the 1st day before chemotherapy), 4 tablets/time, 3 times a day
Intervention Type
Drug
Intervention Name(s)
crocin
Intervention Description
Take saffron total glucosides tablets for 8 days during each chemotherapy (started on the 1st day before radiotherapy/chemotherapy), 4 tablets/time, 3 times a day.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Take placebo piece during for 8 days during each chemotherapy (started on the 1st day before radiotherapy/chemotherapy), 4 tablets/time, 3 times a day
Primary Outcome Measure Information:
Title
The change of LVEF measured by echocardiography
Description
The differences between the two groups in the difference of LVEF measured by Echocardiography at the end of the experiment compared to that at the baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The change of GLS measured by echocardiography
Description
The differences between the two groups in the difference of GLS measured by Echocardiography at the end of the experiment compared to that at the baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Secondary Outcome Measure Information:
Title
The incidences of the increase of serum troponin and/or NT-proBNP
Description
Differences in the incidence rates of serum troponin exceeding the upper limit of normal value and NT-proBNP higher than the normal age reference value between the two groups during follow-up.
Time Frame
During 6 months of following up
Title
The incidences of chest tightness, chest pain and palpitation
Description
The differences in the incidence of chest tightness, chest pain and palpitation between the two groups
Time Frame
During 6 months of following up
Title
The incidences of arrhythmia and ST-T changes
Description
Differences between the two groups in the incidences of arrhythmia and ST-T changes displayed by dynamic electrocardiogram.
Time Frame
During 6 months of following up
Title
The differences of global circumferential strain, global radial strain, global area strain measured by echocardiography.
Description
Differences between groups in the difference in global circumferential strain, global radial strain, global area strain measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The indexes of E, e', a', tricuspid regurgitation velocity measured by echocardiography.
Description
Differences between groups in the difference in the indexes of left ventricular diastolic function measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The indexe of E/e'measured by echocardiography.
Description
Differences between groups in the difference in the indexes of left ventricular diastolic function measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The indexe of left atrial volume index (LAVI)measured by echocardiography.
Description
Differences between groups in the difference in the indexes of left ventricular diastolic function measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The indexe of TAPSE measured by echocardiography.
Description
Differences between groups in the difference in the right ventricular function monitoring indicators measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The indexe of RV fractional area change (FAC) measured by echocardiography.
Description
Differences between groups in the difference in the right ventricular function monitoring indicators measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline
Title
The indexe of right ventricular free wall global longitudinal strain (RVGLS) measured by echocardiography.
Description
Differences between groups in the difference in the right ventricular function monitoring indicators measured by echocardiography at the end of the experiment compared to baseline.
Time Frame
At the end of 6-month follow-up compared to the baseline

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Age 25-80 years old, female; Patients diagnosed with breast cancer by histopathology; Patients who plan to receive adjuvant radiotherapy/chemotherapy or combined adjuvant trastuzumab or pertuzumab targeted therapy; Patients who completed at least 6 cycles of treatment after enrollment; Exclusion criteria: pregnant or breastfeeding women; Patients with poor echocardiographic image quality; Persistent atrial fibrillation and severe arrhythmia affect the collection and analysis of ultrasound data; Patients who are participating in other clinical studies.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mei Zhang, PhD
Phone
+86-18560086629
Email
daixh@vip.sina.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaoling Liu, PhD
Phone
+86-18560086718
Email
xiaolingliusdu@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mei Zhang, PhD
Organizational Affiliation
Qilu Hospital of Shandong University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Qilu Hospital of Shandong University
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250012
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lijuan Bu, PhD
Phone
+86-18560088816
Email
qlyykyc@163.ocm

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We plan to share the study protocol,statistical Analysis Plan (SAP)and Informed Consent Form (ICF)of this research.
IPD Sharing Time Frame
The sharing time period is 6 months to 1 year after the data is released.
IPD Sharing Access Criteria
Share IPD under the conditions of protecting the privacy of patients and ensuring the safety of all diseases. It is necessary to contact the researcher and open the sharing authority after the researcher's consent.
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Protection of Cardiovascular Function With Crocin in BrEast Cancer Patients Undergoing Radiotherapy and Chemotherapy

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