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RecruitingLast updated:15 August 2023

DISCERN: This study aims to comprehensively assess the molecular profile of the tumour ecosystem of cutaneous squamous cell carcinoma patients who receive immunotherapy in the neoadjuvant curative setting in order to identify molecular mechanisms facilitating treatment response and resistance and to identify molecular markers for disease monitoringComprehensive and Deep Profiling in Cutaneous Squamous Cell Carcinomas to Unravel Treatment Efficacy in Immunotherapy Treated Patients

Clinical summary

Summary

Eligible participants will receive immunotherapy (cemiplimab) at a dose of 250mg intravenously every 3 weeks for up to 12 weeks. This study has primarily a translational research objective with the clinical component conducted as a prospective, single arm open label study.

Treatment Type

Radiotherapy,Systemic therapy (chemotherapy, hormone therapy or immunotherapy)

Age

People18+

Phase

II

Trial Acronym

DISCERN

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Trial Identifiers

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Commercial Sponsor

Peter MacCallum Cancer Centre

Scientific Title

Comprehensive and Deep Profiling in Cutaneous Squamous Cell Carcinomas to Unravel Treatment Efficacy in Immunotherapy Treated Patients

Eligibility

Inclusion

  • You have certain types of non-cancer medical conditions.
  • You have been diagnosed with a prior or secondary type of cancer.
  • You have had certain treatments, surgical procedures or drugs.

Exclusion

  • Your cancer has not spread to other parts of the body.
Message

Clinical trials have complex eligibility criteria.

Ask your doctor if this trial could be right for you.

Participating hospitals

Recruiting hospitals

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