The aim of this study is to investigate whether subjects with breast cancer that have certain favorable features, after performing the surgery and radiation, the chemotherapy can be safely omitted in the treatment. In addition, the investigation looks at whether the omission of chemotherapy ensures a better quality of life. Participants decide, in consultation with their treating physician, whether they choose to be treated with adjuvant chemotherapy or not.
Study Type
OBSERVATIONAL
Enrollment
490
adjuvant chemotherapy according to local/ national guidelines
no adjuvant chemotherapy
Zuyderland Medisch Centrum
Sittard-Geleen, Limburg, Netherlands
NOT_YET_RECRUITINGMedical spectrum Twente
Enschede, Overijssel, Netherlands
RECRUITINGNoordwest Ziekenhuisgroep
Alkmaar, Netherlands
NOT_YET_RECRUITINGFlevoziekenhuis
Almere Stad, Netherlands
NOT_YET_RECRUITINGMeander Medisch Centrum
Amersfoort, Netherlands
RECRUITINGAntoni van Leeuwenhoek
Amsterdam, Netherlands
RECRUITINGOnze Lieve Vrouwe Gasthuis (OLVG)
Amsterdam, Netherlands
RECRUITINGRijnstate
Arnhem, Netherlands
RECRUITINGAmphia ziekenhuis
Breda, Netherlands
RECRUITINGDeventer Ziekenhuis
Deventer, Netherlands
RECRUITING...and 18 more locations
Disease recurrence Free Interval (DRFI) - optimalisation cohort per-protocol population
Number of patients with distant recurrence or death in per-protocol population of the optimisation cohort
Time frame: up to 96 months after inclusion of the last patient
Disease recurrence Free Interval (DRFI) - optimalisation cohort intention to treat population
Number of patients with distant recurrence or death in intention to treat population of the optimisation cohort
Time frame: up to 96 months after inclusion of the last patient
Disease recurrence Free Interval (DRFI) - control cohort
Number of patients with distant recurrence or death in control cohort
Time frame: up to 96 months after inclusion of the last patient
Invasive disease-free survival (IDFS) - optimalisation cohort per-protocol population
Number of patients with breast tumor recurrence or death in the per-protocol population of the optimisation cohort
Time frame: up to 96 months after inclusion of the last patient
Invasive disease-free survival (IDFS) - optimalisation cohort intention-to-treat population
Number of patients with breast tumor recurrence or death in the the intention-to-treat population of the optimisation cohort
Time frame: up to 96 months after inclusion of the last patient
Invasive disease-free survival (IDFS) - control cohort
Number of patients with breast tumor recurrence or death in the control cohort
Time frame: up to 96 months after inclusion of the last patient
disease recurrence free survival (DRFS) - optimalisation cohort per-protocol population
time between inclusion and first distant recurrence or death from any cause in the per-protocol population of the optimisation cohort
Time frame: up to 96 months after inclusion of the last patient
disease recurrence free survival (DRFS) - optimalisation cohort the intention-to-treat population
time between inclusion and first distant recurrence or death from any cause in the intention-to-treat population of the optimisation cohort population of the optimisation cohort
Time frame: up to 96 months after inclusion of the last patient
disease recurrence free survival (DRFS) - control cohort
time between inclusion and first distant recurrence or death from any cause in the control cohort
Time frame: up to 96 months after inclusion of the last patient
Recurrence-free survival (RFS) - optimalisation cohort per-protocol population
time between inclusion and invasive ipsilateral breast tumor recurrence, local-regional invasive recurrence, distant recurrence or death from any cause in the per-protocol population of the optimisation cohort;
Time frame: up to 96 months after inclusion of the last patient
Recurrence-free survival (RFS) - optimalisation cohort the intention-to-treat population
time between inclusion and invasive ipsilateral breast tumor recurrence, local-regional invasive recurrence, distant recurrence or death from any cause in the the intention-to-treat population of the optimisation cohort;
Time frame: up to 96 months after inclusion of the last patient
Recurrence-free survival (RFS) - control cohort
time between inclusion and invasive ipsilateral breast tumor recurrence, local-regional invasive recurrence, distant recurrence or death from any cause in the control cohort;
Time frame: up to 96 months after inclusion of the last patient
Overal Survival (OS) - optimalisation cohort per-protocol population
time between inclusion and death from any cause in the per-protocol population of the optimisation cohort;
Time frame: up to 96 months after inclusion of the last patient
Overal Survival (OS) - optimalisation cohort intention-to-treat population
time between inclusion and death from any cause in the the intention-to-treat population of the optimisation cohort;
Time frame: up to 96 months after inclusion of the last patient
Overal Survival (OS) - control cohort
time between inclusion and death from any cause in the control cohort;
Time frame: up to 96 months after inclusion of the last patient
Health related Quality of Life (HRQoL) - (European Organisation on Research and Treatment of Cancer) EORTC questionnaire QLQ-C30
Difference in QoL assessed with the EORTC QLQ-C30 questionnaires between the optimisation and the control group. A higher score indicates a higher symptom burden.
Time frame: up to 2 years after inclusion
Health related Quality of Life (HRQoL) - (European Organisation on Research and Treatment of Cancer) EORTC questionnaire QLQ-BR45
Difference in QoL assessed with the EORTC QLQ-BR45 questionnaires between the optimisation and the control group. A higher score indicates a higher symptom burden.
Time frame: up to 2 years after inclusion
Fear of recurrence
Assessed with questionnaires to determine the difference in optimisation and control group
Time frame: up to 2 years after inclusion
Worries about health
Assessed with questionnaires to determine the difference in optimisation and control group. A higher score indicates a higher symptom burden.
Time frame: up to 2 years after inclusion
Cost effectiveness measured by quality-adjusted-life years (QALYs)
Measured per Quality-Adjusted Life Years (QALYs)
Time frame: up to 2 years after inclusion
Cost effectiveness measured per incremental cost-effectiveness ratio (ICER)
Measured per incremental cost-effectiveness ratio (ICER)
Time frame: up to 2 years after inclusion
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