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As more new, innovative targeted cancer treatments are being developed, drug access continues to be an incredibly important aspect of Rethink’s ongoing advocacy work. We continue working with other patient groups, coalitions and cancer organizations to call for system change and more efficiencies throughout the entire process of Canadian drug approval and reimbursement process.

At the same time, we collaborate with these various bodies involved by ensuring the voice and values of breast cancer patients are considered in their decision making. This includes submitting input into drug reviews conducted by the Canadian Agency for Drugs and Technologies in Health (aka CADTH), the organization that reviews the clinical and cost-effectiveness of a drug and provides a recommendation to the public drug plans on whether or not a drug should be reimbursed for public funding.

Rethink conducts surveys and gathers the community’s direct feedback and experiences with the treatment under review. This includes in-depth patient profiles, where decision-makers can read the real stories of some in the breast cancer community and how these cancer drugs directly impact them.

Check out some of Rethink’s submissions to CADTH below. And you can learn more about the drug approval process in Canada here.

2021-2023 Submissions

TRODELVY

for HR+ HER2- metastatic breast cancer • July 28, 2023

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ENHERTU

for HER2-low metastatic breast cancer • December 22, 2022

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LYNPARZA

for high-risk early-stage breast cancer • August 26, 2022

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KEYTRUDA

for metastatic triple negative breast cancer • July 14, 2022

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VERZENIO

for early-stage breast cancer • April 14, 2022

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ENHERTU

for metastatic breast cancer • April 14, 2022

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KEYTRUDA

for Neo-adjuvant early-stage breast cancer • March 11, 2022

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TRODELVY

for metastatic triple negative breast cancer • July 21, 2021

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PIQRAY

for metastatic breast cancer • May 14, 2021

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PERJETA

for Neo-adjuvant early-stage breast cancer • May 3, 2021

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TUKYSA

for metastatic breast cancer • April 19, 2021

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