Title
Durvalumab With or Without Tremelimumab in Resectable Locally Advanced Squamous Cell Carcinoma of the Oral Cavity
Durvalumab (MEDI4736) Plus Tremelimumab in Resectable, Locally Advanced Squamous Cell Carcinoma of the Oral Cavity: a Window of Opportunity Study
Phase
Phase 1/Phase 2Lead Sponsor
Katholieke Universiteit LeuvenStudy Type
InterventionalStatus
Active, not recruitingIndication/Condition
Oral Cavity Squamous Cell CarcinomaIntervention/Treatment
Durvalumab Durvalumab + Tremelimumab [durvalumab (25207), tremelimumab (77548)]Study Participants
21This is a randomized, open-label, prospective, pilot phase I/II study with focus on translational research and on the evaluation of the biological changes that are observed in sequential tumor tissue acquisition in patients with newly diagnosed advanced (stage IV) oral cavity SCC. Patients are treated with Durvalumab (arm A) or Durvalumab + Tremelimumab (arm B) after biopsy-confirmed diagnosis of locally advanced resectable SCCHN of the oral cavity. After surgery, the standard of care treatment is radiotherapy, and, depending on risk assessment concurrent cisplatin. Patients will be treated with Durvalumab (arm A) or Durvalumab and Tremelimumab (arm B) during six additional cycles, starting from day one of the postoperative radiotherapy.
Durvalumab has shown activity in squamous cell carcinoma of the head and neck. Locally advanced resectable cancers of this type represent a challenge, as the majority of these patients still die from this disease in spite of surgery, radio- and chemotherapy.
Checkpoint inhibitors have recently proven to prolong life in recurrent/metastatic SCCHN, and several new molecules are currently tested in clinical trials in this indication, including PD-1, PD-L1, and CTLA-4 antibodies, either as single agent or in combination. These compounds might represent a valuable treatment for SCCHN patients in the adjuvant setting, given the favorable toxicity profile. Combination of Durvalumab (PD-L1 inhibition) and Tremelimumab (CTLA-4 inhibition) is currently tested in recurrent/metastatic head and neck cancer, and compared to Durvalumab as single agent, and to standard of care chemotherapy.
In this study both options, i.e. durvalumab as a single agent or Durvalumab in combination with Tremelimumab, will be tested in a randomized fashion. Randomization would be used to reduce selection bias, in a non-comparative study. Newly diagnosed patients with SCCHN of the oral cavity, will be treated with a single dose of Durvalumab with or without Tremelimumab two weeks before scheduled surgery.
When patients are first diagnosed with a resectable oral SCC, a biopsy is taken to confirm the diagnosis, and surgery is planned. This standard practice thus involves sequential tissue harvesting, both at the time of biopsy as well as the final resection specimen, making it possible to observe hallmarks of immune response when patients are treated once with Durvalumab with or without Tremelimumab after confirmation of the diagnosis on biopsy, but before surgery.
All patients will be treated with postoperative radiotherapy (66 Gy in standard fractionation). In case of positive section margins or extracapsular extension, 3 cycles of cisplatin 100 mg/msq on days 1, 22, and 43 will be added to standard fractionation radiotherapy (66 Gy). Durvalumab monotherapy (1500 mg) will be administered via IV infusion day -14 and at the start of radiation therapy, with repeat administration every 4 weeks at fixed dose for a total of 6 cycles postoperative.
All patients will be treated with postoperative radiotherapy (66 Gy in standard fractionation). In case of positive section margins or extracapsular extension, 3 cycles of cisplatin 100 mg/msq on days 1, 22, and 43 will be added to standard fractionation radiotherapy (66 Gy). Durvalumab + Tremelimumab combination therapy: Tremelimumab (75 mg) will be administered via IV infusion day -14 and at the start of radiation therapy, with repeat administration every 4 weeks at fixed dose for a total of 3 cycles postoperative, Durvalumab (1500 mg) will be administered via IV infusion day -14 and at the start of radiation therapy, with repeat administration every 4 weeks at fixed dose for a total of 6 cycles postoperative.
Inclusion Criteria: Resectable locally advanced oral cavity SCC stage IV Newly diagnosed disease Age ≥18 years at the time of screening Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at enrollment No active second malignancy during the last five years except non melanomatous skin cancer or carcinoma in situ of the cervix No prior chemotherapy, radiotherapy or targeted therapy including PD-1, PD-L1 or CTLA-4 antibodies for SCCHN, including durvalumab or tremelimumab Availability of blood samples for Translational research Negative pregnancy test Normal organ function No participation in another interventional clinical trial in the preceding 30 days prior to randomization Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial Before patient registration, written informed consent must be given according to ICH/GCP, and national/local regulations Body weight > 30 kg Exclusion Criteria: Histologically or cytologically confirmed head and neck cancer of any other primary anatomic location in the head and neck Receipt of other treatments for cancer within 30 days prior to first dose of study treatment Previous radiotherapy in the head and neck region Previous systemic therapy for SCCHN Current or prior use of immunosuppressive medication within 14 days before the first dose of their assigned IP. History of allogeneic organ transplantation Active or prior documented autoimmune or inflammatory Uncontrolled intercurrent illness Active relevant second malignancy during the last five years Mean QT interval corrected for heart rate ≥470 ms History of active primary immunodeficiency Active infection Receipt of live, attenuated vaccine within 30 days prior to the first dose of IP. Female patients of childbearing potential who are pregnant or breast- Known allergy or hypersensitivity to IP or any IP excipient Any condition that, in the opinion of the Investigator, would interfere with evaluation of the IP or interpretation of patient safety or study results Major surgical procedure (as defined by the Investigator) within 28 days prior to the first dose of IP Metastatic disease
