Impact of abemaciclib on patients' roles and responsibilities

ISRCTN ISRCTN17281696
DOI https://doi.org/10.1186/ISRCTN17281696
IRAS number 279088
Secondary identifying numbers IRAS 279088
Submission date
16/06/2020
Registration date
16/06/2020
Last edited
28/04/2025
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Cancer
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

https://www.cancerresearchuk.org/about-cancer/find-a-clinical-trial/a-study-of-the-effect-abemaciclib-has-on-the-daily-life-of-people-who-take-it-impactor

Study website

Contact information

Dr Helena Harder
Public

SHORE-C
Brighton and Sussex Medical School
University of Sussex
Science Park Road
Falmer
Brighton
BN1 9RX
United Kingdom

ORCiD logoORCID ID 0000-0002-7296-8227
Phone +44 (0)1273 873019
Email impactor@sussex.ac.uk
Dr Helena Harder
Scientific

SHORE-C
Brighton and Sussex Medical School
University of Sussex
Science Park Road
Falmer
Brighton
BN1 9RX
United Kingdom

ORCiD logoORCID ID 0000-0002-7296-8227
Phone +44 (0)1273 873019
Email impactor@sussex.ac.uk

Study information

Study designMulti-centre observational quality of life study with nested qualitative interview study
Primary study designObservational
Secondary study designLongitudinal study
Study setting(s)Hospital
Study typeQuality of life
Participant information sheet The participant information sheet will be made available at https://shore-c.sussex.ac.uk/impactor.html
Scientific titleImpact of abemaciclib on patients' roles and responsibilities: a multi-centre observational quality of life study with nested qualitative interview study
Study acronymIMPACTOR
Study objectivesThe principal objective of the study is to investigate breast cancer patients’ experiences of abemaciclib treatment outside of a clinical trial setting. The primary aim is to chart any changes in their quality of life in the first 6 months of treatment, and the impact of this treatment on patients’ ability to perform their normal roles and responsibilities. The researchers will conduct semi-structured interviews with a subset of the participants to achieve a more in-depth, richer understanding of their experiences of treatment, both positive and negative, side effects, and ways in which their day to day activities have been affected. One of the side effects more commonly associated with abemaciclib is diarrhoea. The researchers will ask participants to record their experiences of diarrhoea, and the measures they took to manage it, using a diarrhoea diary. This will enable them to assess whether treatment-related diarrhoea is manageable and decreases over time, as current trial data suggests.
Ethics approval(s)

Approved 17/04/2020, North East Tyne and Wear South Research Ethics Committee (NHSBT Newcastle Blood Donor Centre, Holland Drive, Newcastle upon Tyne, NE2 4NQ, United Kingdom; +44 (0)207 972 2496; tyneandwearsouth.rec@hra.nhs.uk), ref: 20/NE/0101

Health condition(s) or problem(s) studiedQuality of life of women receiving abemaciclib for breast cancer
InterventionThis is a quality of life observational study. Participants will complete validated quality of life measures at baseline, 1, 3 and 6 months and a weekly diarrhoea management diary. A subset of the participants will take part in a semi-structured qualitative interview study after 3 months.
Intervention typeDrug
Pharmaceutical study type(s)
PhasePhase III/IV
Drug / device / biological / vaccine name(s)Abemaciclib
Primary outcome measure1. Quality of life assessed using the Functional Assessment of Cancer Treatment general scale (FACT-G) with diarrhoea (DS) and endocrine symptom (ES) subscale at baseline, 1, 3 and 6 months
2. Role function assessed using the Patient Roles and Responsibilities Scale (PRRS) at baseline, 1, 3 and 6 months
Secondary outcome measures1. Qualitative evidence of patients’ experience of treatment collected via a semi-structured interview at 3 months
2. Treatment-related diarrhoea measured using the Diarrhoea Management Diary (DMD) completed weekly for 6 months
3. Strategies employed to counter diarrhoea, including non-adherence to treatment, measured using the DMD completed weekly for 6 months
Overall study start date24/04/2019
Completion date08/03/2023

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
SexFemale
Target number of participants150
Total final enrolment46
Key inclusion criteria1. Patients with locally advanced or metastatic breast cancer who are prescribed either:
1.1. Abemaciclib in combination with fulvestrant (for women who have relapsed after endocrine therapy), or
1.2. Abemaciclib in combination with an aromatase inhibitor (for women who have not previously been treated)
2. Patients who are able to give fully informed consent and are able to read and speak in English
3. Patients who are 18 years old and over
Key exclusion criteria1. Patients with cancers other than breast or receiving treatments other than abemaciclib
2. Patients who are not able to provide fully informed consent or who are not able to read and speak English
3. Patients under 18 years of age
4. Patients who are currently inpatients or who are too distressed to participate
Date of first enrolment01/09/2020
Date of final enrolment31/12/2022

Locations

Countries of recruitment

  • England
  • Scotland
  • United Kingdom

Study participating centres

Brighton and Sussex University Hospitals NHS Trust
Royal Sussex County Hospital
Eastern Road
Brighton
BN2 5BE
United Kingdom
The Clatterbridge Cancer Centre NHS Foundation Trust
Clatterbridge Road
Bebington
Wirral
CH63 4JY
United Kingdom
The Royal Marsden NHS Foundation Trust
Fulham Road
London
SW3 6JJ
United Kingdom
The Christie NHS Foundation Trust
Wilmslow Road
Manchester
M20 4BX
United Kingdom
Airedale General Hospital
Airdale NHS Foundation Trust
Skipton Road
Steeton
Keighley
BD20 6TD
United Kingdom
Kent and Canterbury Hospital
East Kent Hospitals University NHS Foundation Trust
Ethelbert Road
Canterbury
CT1 3NG
United Kingdom
The Royal Bournemouth Hospital
Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust
Castle Lane East
Bournemouth
BH7 7DW
United Kingdom
Royal Surrey NHS Foundation Trust
Egerton Road
Guildford
GU2 7XX
United Kingdom
Lothian Health Board
Waverley Gate
2-4 Waterloo Place
Edinburgh
EH1 3EG
United Kingdom
Yeovil District Hospital NHS Foundation Trust
Higher Kingston
Yeovil
BA21 4AT
United Kingdom

Sponsor information

University of Sussex
University/education

Research and Enterprise Services
Falmer
Brighton
BN1 9QF
England
United Kingdom

Phone +44 (0)1273 872748
Email researchsponsorship@sussex.ac.uk
Website http://www.sussex.ac.uk/
ROR logo "ROR" https://ror.org/00ayhx656

Funders

Funder type

Industry

Eli Lilly and Company
Government organisation / For-profit companies (industry)
Alternative name(s)
Lilly, Eli Lilly & Company, Eli Lilly & Co., Eli Lilly And Co
Location
United States of America

Results and Publications

Intention to publish date26/04/2025
Individual participant data (IPD) Intention to shareYes
IPD sharing plan summaryAvailable on request
Publication and dissemination planCurrent publication and dissemination plan as of 28/04/2025:
The researchers published the findings from this research in a high-impact peer-reviewed journal (Supportive Care of Cancer, April 2025; please see https://doi.org/10.1007/s00520-025-09440-7 and https://doi.org/10.1007/s00520-025-09444-3). A plain language summary of the findings will be sent to all study participants and published on the study website: https://shore-c.sussex.ac.uk/impactor.html. Additional documents are not currently available.

Previous publication and dissemination plan:
The researchers plan to publish the findings from this research in a high-impact peer-reviewed journal. A plain language summary of the findings will be sent to all study participants and published on the study website: https://shore-c.sussex.ac.uk/impactor.html. Additional documents are not currently available.
IPD sharing planThe anonymised datasets generated during and/or analysed during the current study will be available upon (reasonable) request after publication of the findings from Sussex Health Outcomes Research and Education in Cancer (adminshore-c@sussex.ac.uk).

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
HRA research summary 26/07/2023 No No
Other publications Qualitative analysis 26/04/2025 28/04/2025 Yes No
Results article 26/04/2025 28/04/2025 Yes No

Editorial Notes

28/04/2025: Publication references and IPD sharing plan added, publication and dissemination plan updated.
20/08/2024: The intention to publish date was changed from 31/08/2024 to 01/01/2025. Total final enrolment added.
08/03/2024: The following changes were made:
1. The overall study end date was changed from 30/06/2023 to 08/03/2023.
2. The intention to publish date was changed from 30/06/2024 to 31/08/2024.
15/12/2022: The contact confirmed the record is up to date.
20/06/2022: The following changes were made to the trial record:
1. The recruitment end date was changed from 30/06/2022 to 31/12/2022.
2. The overall end date was changed from 15/12/2022 to 30/06/2023.
3. The intention to publish date was changed from 01/08/2023 to 30/06/2024.
24/11/2021: The following changes have been made:
1. The recruitment end date has been changed from 30/06/2021 to 30/06/2022.
2. The overall trial end date has been changed from 31/03/2022 to 15/12/2022.
3. The intention to publish date has been changed from 31/12/2022 to 01/08/2023.
21/09/2021: The overall end date was changed from 31/12/2021 to 31/03/2022.
09/12/2020: The following changes were made to the trial record:
1. The trial participating centres Airedale General Hospital, Kent and Canterbury Hospital, The Royal Bournemouth Hospital, Royal Surrey NHS Foundation Trust, Lothian Health Board, Yeovil District Hospital NHS Foundation Trust were added.
2. The link in the plain English summary was corrected.
07/12/2020: The public and scientific contact has been changed.
21/10/2020: Cancer Research UK lay summary link added to plain English summary field.
16/06/2020: Trial's existence confirmed by Health Research Authority and Health and Care Research Wales (HCRW).