Safety of Continuing HER-2 Directed Therapy in Overt Left Ventricular Dysfunction: A Randomized, Controlled Trial

Who is this study for? Patients with early stage HER-2 positive breast cancer
What treatments are being studied? Trastuzumab+Pertuzumab+Trastuzumab emtansine
Status: Recruiting
Location: See all (8) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Trastuzumab is an important treatment for HER 2 positive breast cancer. But trastuzumab can cause injury to the heart, and this is one of the main reasons it cannot be administered as planned. Heart injury can often be successfully treated using cardiac medications. The objectives of SCHOLAR-2 are to evaluate whether is it safe and effective to continue trastuzumab, pertuzumab or trastuzumab-emtansine (T-DM1) in patients with early stage HER-2 positive breast cancer despite mild, minimally symptomatic or asymptomatic systolic left ventricular dysfunction as compared with a guideline-driven approach of withholding or discontinuing trastuzumab, pertuzumab or trastuzumab-emtansine (T-DM1). In SCHOLAR-2, we will compare two thresholds of withholding or discontinuing trastuzumab/pertuzumab/trastuzumab-emtansine: a threshold that is currently advocated for by existing treatment practice guidelines versus a more aggressive threshold that allows trastuzumab/pertuzumab/trastuzumab-emtansine to continue at lower levels of LVEF than currently supported by guideline documents.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Stage I-III HER-2 positive breast cancer

• Receiving adjuvant or neoadjuvant therapy with trastuzumab, pertuzumab, or trastuzumab-emtansine (T-DM1)

• Evidence of left ventricular dysfunction, as defined by at least one of:

• a) LVEF \< 54% or b) LVEF ≥54% and either i) fall in LVEF of ≥15% from prior to trastuzumab, pertuzumab, or trastuzumab-emtansine (T-DM1) exposure, or ii) New York Heart Association (NYHA) class II heart failure symptoms within the past 6 months

Locations
Other Locations
Brazil
Hospital de Clínicas de Porto Alegre
RECRUITING
Porto Alegre
Irmandade Da Santa Casa De Misericórdia De Porto Alegre
RECRUITING
Porto Alegre
Clínica de Pesquisa e Centro de Estudos em Oncologia Ginecológica e Mamária Ltda
RECRUITING
São Paulo
Hospital Alemão Oswaldo Cruz
RECRUITING
São Paulo
Canada
Juravnski Cancer Centre
RECRUITING
Hamitlon
Ottawa Hospital Research Institute
RECRUITING
Ottawa
Toronto General Hospital, University Health Network
RECRUITING
Toronto
Russian Federation
E.Meshalkin National medical research center of the Ministry of Health of the Russian Federation
SUSPENDED
Novosibirsk
Contact Information
Primary
Maha Mushtaha, BSc
maha.mushtaha@phri.ca
9052973479
Backup
Sumathy Rangarajan, MSc
sumathy.rangarajan@phri.ca
9052973479
Time Frame
Start Date: 2021-07-01
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 130
Treatments
Active_comparator: Control Group
Recommendations for continuing or holding trastuzumab, pertuzumab, or trastuzumab-emtansine (T-DM1) for the control group are guided by an adaptation of the 2008 Canadian recommendations.
Experimental: Intervention Group
The intervention group will continue to receive trastuzumab, pertuzumab, or trastuzumab-emtansine (T-DM1) in the setting of asymptomatic decline in LVEF up to an LVEF of 40% as outlined in the criteria listed in Table 3. For reasons of practicality, in the intervention group, the first dose of trastuzumab, pertuzumab, or trastuzumab-emtansine (T-DM1) after randomization can be administered up to 3 weeks late. This will allow time for the participant to be reviewed by a cardiologist and to receive ACE-I/angiotensin receptor blocker and/or beta-blocker, and for dose titration.
Related Therapeutic Areas
Sponsors
Leads: Population Health Research Institute

This content was sourced from clinicaltrials.gov

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