About this trial
This prospective, multi-center, phase II randomized controlled trial will evaluate the actual benefit of adding immunotherapy with tislelizumab to the currently most effective approach against LARC, namely TNT. In this trial, we will harness several elements that may each potentially contribute to an overall high efficacy, at least in local outcomes: nCRT rather than SCRT, full length (8 cycles of mFOLFOX6) of consolidation chemotherapy, CIMT following nCRT (exploiting the upregulation of the immune response induced by the latter) and tislelizumab (with its theoretical advantage over other CPIs). In line with the changing treatment paradigms in LARC, in which high therapeutic efficacy translates into the possibility to avoid TME, the trial will have a novel primary endpoint of long-term unmaintained cCR, i.e. 3 year TME-free survival.
Eligibility criteria
Qualifiers
Subjects with histologically confirmed primary (non-recurrent) LARC (tumor 12 cm or less from the anal verge, as assessed by rigid proctoscopy), stage T3-4 N0 or TX N+ according to base-line pelvic MRI and PET-CT.
Patients who are planned for TNT and are surgical candidates as determined by the treating physician.
No prior chemotherapy, immunotherapy, radiotherapy or surgery for rectal cancer.
No prior radiotherapy to the pelvis, for any reason.
Disqualifiers
Active or background history of an autoimmune disease except for type I diabetes mellitus, hypothyroidism requiring hormone replacement only and skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment.
Medical history of vasculitis.
Prior organ transplant, including allogenic bone marrow transplantation.
Grade > 1 peripheral sensory neuropathy.
Trial design
Treatments tested in this trial
- Tislelizumab
- Total neoadjuvant therapy (TNT)
Treatment groups
Sponsors and collaborators
brenner baruch
Lead sponsor
Rabin Medical Center
Sponsor institution
Johannes Gutenberg University Mainz
Collaborator