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Exercise Interventions for Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy (BENEFIT)

Primary Purpose

Breast Cancer

Status
Active
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Resistance exercise
Aerobic exercise
Usual care during neoadjuvant chemotherapy/Exercise after surgery
Sponsored by
German Cancer Research Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring exercise, resistance training, aerobic training, breast cancer, neoadjuvant chemotherapy, fatigue, quality of life, tumor response

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women ≥ 18 years of Age
  • Unilateral or bilateral primary carcinoma of the breast, confirmed histologically by core biopsy
  • Scheduled for neoadjuvant CTx (but not yet started)
  • Confirmed hormone receptor and Her2 status
  • Sufficient German language skills
  • Willing to train at the exercise facilities twice per week

Exclusion Criteria:

  • Any physical or mental conditions that would hamper the adherence to the training programs or the completion of the study procedures
  • Engaging in systematic intense exercise training (at least 1h twice per week)

Sites / Locations

  • National Center for Tumor Diseases (NCT)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Other

Arm Label

Resistance exercise

Aerobic exercise

Waitlist control

Arm Description

Outcomes

Primary Outcome Measures

Tumor size
percentage of change from the maximal diameter of the lesion assessed before neoadjuvant chemotherapy (by mammography or sonography) to the maximal diameter of the tumor assessed after neoadjuvant chemotherapy at breast surgery

Secondary Outcome Measures

CPS-EG score
The Clinical-Pathologic Stage (CPS-EG) score combines clinical tumor stage prior to neoadjuvant therapy (CS), pathological tumor stage after neoadjuvant treatment (PS), estrogen receptor status (E) and grading (G). It has been shown to be a valid prognostic factor to discriminate among patient subgroups with respect to survival after neoadjuvant CTx.
pCR
The Pathological Complete Response (pCR) is defined as ypT0/is ypN0 and has been consistently demonstrated to be a good prognostic factor for long-term benefit from neoadjuvant CTx.
Fatigue Assessment Questionnaire (FAQ)
Validated 20-item multidimensional self-assessment questionnaire to assess the physical, affective, and cognitive dimension of cancer-related fatigue
EORTC QLQ-C30 / BR23
Validated 30-item self-assessment questionnaire to assess quality of life aspects.
Patient Health Questionnaire for Depression and Anxiety (PHQ-4)
A validated 4-item screener for depression and anxiety.
Pittsburgh Sleep Quality Index (PSQI)
Validated questionnaire to assess sleep quality and sleep problems.
Spiroergometry (VO2max)
Isometric and isokinetic muscle strength measured by ISOMED 2000
Body mass index
Self-developed physical activity questionnaire including type, duration, frequency and intensity of sports, cycling,and walking
Cognitive function - HVLT-R
Hopkins Verbal Learning Test - Revised (HVLT-R)
Cognitive function - TMT
Trail Making Test
Cognitive function - COWA
Controlled Oral Word Association
Sleep quality
Measured with ActiGraph (accelerometry)
Sleep efficiency
Measured with ActiGraph (accelerometry)

Full Information

First Posted
May 6, 2016
Last Updated
February 22, 2023
Sponsor
German Cancer Research Center
Collaborators
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT02999074
Brief Title
Exercise Interventions for Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy
Acronym
BENEFIT
Official Title
A Randomized 3-arm Exercise Intervention Trial for Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2016 (undefined)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
July 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
German Cancer Research Center
Collaborators
University Hospital Heidelberg

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The BENEFIT-Study is a randomized controlled 3-arm intervention trial investigating the currently discussed hypothesis that exercise concomitant to chemotherapy (CTx) may have a beneficial effect on cancer prognosis by boosting the anti-tumoral effect of the cytostatics or by enhancing therapy compliance. This hypothesis is based on pre-clinical and exploratory clinical trials. Breast cancer patients scheduled for neoadjuvant CTx will be randomized to either a resistance training or an aerobic training concomitant to the neoadjuvant CTx, or a waiting list control group that will get no exercise intervention during neoadjuvant CTx (i.e. usual care) but will exercise after breast surgery. The primary study endpoint is the tumor size. Further, the effects of resistance and aerobic exercise on the clinical-pathologic stage (CPS-EG) score, the pathological complete response (pCR), tolerability and compliance to CTx, physical fitness, patient reported outcomes such as fatigue, sleep problems, quality of life, depressive symptoms, anxiety and pain, as well as cognitive function, and selected biomarkers will be investigated. A confirmation of the study hypothesis would be a strong argument for patients to engage in exercise as early as during neoadjuvant CTx. The trial will also provide evidence-based guidance for patients regarding type and timing of training.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
exercise, resistance training, aerobic training, breast cancer, neoadjuvant chemotherapy, fatigue, quality of life, tumor response

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
183 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Resistance exercise
Arm Type
Active Comparator
Arm Title
Aerobic exercise
Arm Type
Active Comparator
Arm Title
Waitlist control
Arm Type
Other
Intervention Type
Other
Intervention Name(s)
Resistance exercise
Intervention Description
The training will take place twice weekly over the course of neoadjuvant CTx at the NCT Heidelberg or in regional qualified centers under supervision and guidance of experienced exercise therapists. The progressive resistance exercise comprises 8 machine-based exercises, each performed in 3 sets, 12 repetitions at 60-80% of one repetition maximum (1-RM).
Intervention Type
Other
Intervention Name(s)
Aerobic exercise
Intervention Description
The training will take place twice weekly over the course of neoadjuvant CTx at the NCT Heidelberg or in regional qualified centers under supervision and guidance of experienced exercise therapists. The aerobic exercise will be performed on a cycle ergometer (or alternatively at a treadmill, elliptical, rowing ergometer, or combination) progressing from 60% to 70% VO2max with increasing duration. During weeks 7-18 the goal is to perform an extensive interval training.
Intervention Type
Other
Intervention Name(s)
Usual care during neoadjuvant chemotherapy/Exercise after surgery
Intervention Description
The control group receives no exercise intervention during neoadjuvant CTx, which reflects the usual care condition. To investigate effects of different exercise timing, and to provide those patients also a potential health benefit and reduce drop-out and contamination, the control group will receive 18 weeks resistance or aerobic exercise (according to their personal preferences) after breast cancer surgery.
Primary Outcome Measure Information:
Title
Tumor size
Description
percentage of change from the maximal diameter of the lesion assessed before neoadjuvant chemotherapy (by mammography or sonography) to the maximal diameter of the tumor assessed after neoadjuvant chemotherapy at breast surgery
Time Frame
change from baseline (before start of neoadjuvant chemotherapy) to breast surgery
Secondary Outcome Measure Information:
Title
CPS-EG score
Description
The Clinical-Pathologic Stage (CPS-EG) score combines clinical tumor stage prior to neoadjuvant therapy (CS), pathological tumor stage after neoadjuvant treatment (PS), estrogen receptor status (E) and grading (G). It has been shown to be a valid prognostic factor to discriminate among patient subgroups with respect to survival after neoadjuvant CTx.
Time Frame
at breast surgery
Title
pCR
Description
The Pathological Complete Response (pCR) is defined as ypT0/is ypN0 and has been consistently demonstrated to be a good prognostic factor for long-term benefit from neoadjuvant CTx.
Time Frame
at breast surgery
Title
Fatigue Assessment Questionnaire (FAQ)
Description
Validated 20-item multidimensional self-assessment questionnaire to assess the physical, affective, and cognitive dimension of cancer-related fatigue
Time Frame
at baseline, week 9, post-chemotherapy (before breast surgery); months 6 and 12 after breast surgery
Title
EORTC QLQ-C30 / BR23
Description
Validated 30-item self-assessment questionnaire to assess quality of life aspects.
Time Frame
at baseline, week 9, post-chemotherapy (before breast surgery); months 6 and 12 after breast surgery
Title
Patient Health Questionnaire for Depression and Anxiety (PHQ-4)
Description
A validated 4-item screener for depression and anxiety.
Time Frame
at baseline, week 9, post-chemotherapy (before breast surgery); months 6 and 12 after breast surgery
Title
Pittsburgh Sleep Quality Index (PSQI)
Description
Validated questionnaire to assess sleep quality and sleep problems.
Time Frame
at baseline, week 9, post-chemotherapy (before breast surgery); months 6 and 12 after breast surgery
Title
Spiroergometry (VO2max)
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Isometric and isokinetic muscle strength measured by ISOMED 2000
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Body mass index
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Self-developed physical activity questionnaire including type, duration, frequency and intensity of sports, cycling,and walking
Time Frame
Follow-up (6 months and 12 months after breast surgery)
Title
Cognitive function - HVLT-R
Description
Hopkins Verbal Learning Test - Revised (HVLT-R)
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Cognitive function - TMT
Description
Trail Making Test
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Cognitive function - COWA
Description
Controlled Oral Word Association
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Sleep quality
Description
Measured with ActiGraph (accelerometry)
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery
Title
Sleep efficiency
Description
Measured with ActiGraph (accelerometry)
Time Frame
at baseline, post-chemotherapy (before breast surgery); month 6 after breast surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women ≥ 18 years of Age Unilateral or bilateral primary carcinoma of the breast, confirmed histologically by core biopsy Scheduled for neoadjuvant CTx (but not yet started) Confirmed hormone receptor and Her2 status Sufficient German language skills Willing to train at the exercise facilities twice per week Exclusion Criteria: Any physical or mental conditions that would hamper the adherence to the training programs or the completion of the study procedures Engaging in systematic intense exercise training (at least 1h twice per week)
Facility Information:
Facility Name
National Center for Tumor Diseases (NCT)
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32556623
Citation
Kreutz C, Muller J, Schmidt ME, Steindorf K. Comparison of subjectively and objectively assessed sleep problems in breast cancer patients starting neoadjuvant chemotherapy. Support Care Cancer. 2021 Feb;29(2):1015-1023. doi: 10.1007/s00520-020-05580-0. Epub 2020 Jun 19.
Results Reference
derived

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Exercise Interventions for Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy

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