test cancer 54321

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Updated on 20 February 2026
See if I qualify

Summary

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Details
Condition Medical Research
Clinical Study IdentifierNCT776451
Last Modified on20 February 2026

Eligibility

 Yes No Not Sure

Inclusion Criteria

<i>Pathologically</i> confirmed invasive <b>breast</b> cancer
Stage IIB-III invasive breast cancer (AJCC 8th edition)
Patients planned for adjuvant chemotherapy and adjuvant radiotherapy
Patients fit to receive adjuvant chemotherapy and radiotherapy
Age > 18 years

Exclusion Criteria

Hypersensitivity to taxanes
Patients receiving entire chemotherapy prior to surgery (neoadjuvant setting)
Unable or unwilling for regular follow up
Bilateral tumour needed RT to both sides
Patients planned for RT to oligometastatic sites
Unfavourable anatomical factors potentially leading to higher radiotherapy dose to heart and/or lungs (Exceeding the protocol specific mandatory dose constraints)
Pregnant patient
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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