Neoadjuvant Chemoradiotherapy With Sequential Ipilimumab and Nivolumab in Rectal Cancer

Exclusion Criteria

• •Metastatic disease that is considered incurable by local therapies
• •Previous surgery of the tumor other than biopsy
• •Pregnancy, breastfeeding or expectancy to conceive
• •Disagreement of participants with reproductive potential to use contraception throughout the study period and for up to 180 days after the last dose of study therapy
• •Prior therapy with anti-CTLA-4, anti-PD-1, anti-PD-L1, anti-PD-L2 or any other agent directed against co-inhibitory T cell receptors or has previously participated in clinical studies with immunotherapy
• •Any contraindication according to the official medical information of Ipilimumab or Nivolumab
• •Live vaccine within 30 days prior to the first dose of study therapy
• •Hepatitis B or C
• •Human immunodeficiency virus (HIV)
• •Immunodeficiency
• •Allogeneic tissue or solid organ transplantation
• •Autoimmune disease that has required systemic therapy in the past 2 years with modifying agents, steroids or immunosuppressive drugs
• •Systemic steroids or any other form of immunosuppressive therapy within 7 days prior to the first dose of study treatment
• •Active non-infectious pneumonitis
• •Active infection requiring systemic therapy
• •Treatment with botanical preparations (i.e. herbal supplements or traditional Chinese medicines) intended for general health support or to treat the disease under study within 2 weeks prior to randomization/treatment
• •Participants with serious or uncontrolled medical disorders
• •Uncontrolled or significant cardiovascular disease (myocardial infarction, uncontrolled angina, any history of clinically significant arrhythmias, QTc prolongation in males \> 450 ms and \> 470 ms in females, participants with history of myocarditis)
• •Allergies and adverse drug reaction (history of allergy or hypersensitivity to study drug components, contraindications to any of the study drugs of the chemotherapy regimen)
• •White blood cells \< 2000/μL (SI: \< 2.00 × 109/L)
• •Neutrophils \< 1500/μL (SI: \< 1.50 × 109/L)
• •Platelets \< 100 × 103/μL (SI: \< 100 × 109/L) (transfusions not permitted within 72 h prior to qualifying laboratory value)
• •Hemoglobin \< 9.0 g/dl (SI: \< 90 g/L) (transfusions not permitted within 72 h prior to qualifying laboratory value)
• •Serum creatinine \> 1.5 × upper limit of normal (ULN) or calculated creatinine clearance \< 50 ml/min (using the Cockcroft-Gault formula)
• •AST/ALT: \> 3.0 × ULN
• •Total bilirubin \> 1.5 × ULN (except participants with Gilbert Syndrome who must have a total bilirubin level of \< 3.0 × ULN)
• •Troponin T (TnT) or I (TnI) \> 2 × institutional ULN. TnT or TnI levels between \> 1 to 2 × ULN will be permitted to participate in the study if a repeat assessment remains 2 × ULN and participant undergoes a cardiac evaluation. When repeat levels within 24 h are not available, a repeat test should be conducted as soon as possible.