Tislelizumab and Metronomic Capecitabine as Maintenance in High-risk Locoregionally-advanced Nasopharyngeal Carcinoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age21-99
SponsorNational Cancer Centre, Singapore

About this trial

Patients with "high-risk" locoregionally-advanced nasopharyngeal carcinoma (LA-NPC), defined as AJCC/UICC 8th edition TNM-stage III-IVA and high Epstein-Barr virus (EBV) DNA viral load (≥4,000 copies/mL) will require induction chemotherapy (IC) prior to chemo-radiation (CCRT) as per standard treatment. Patients who persist to manifest DETECTABLE EBV DNA following 3 cycles of IC have a higher risk of relapse, and are typically recommended for a year of low-dose oral chemotherapy after CCRT.

RIBBON-LA-01 is a single-arm, open-label, phase 2 clinical trial of maintenance tislelizumab and metronomic capecitabine (metroCap) for 52 weeks after IC and CCRT, targeting this specific group of patients who have persistent detectable EBV DNA after IC. The main objective is to evaluate the efficacy of maintenance tislelizumab and metroCap in patients with DETECTABLE EBV DNA levels after 3 cycles of IC.

Eligibility criteria

Qualifiers

Able to provide written informed consent and can understand and agree to comply with the requirements of the study and the schedule of assessments

Age ≥21 years on the day of signing the ICF

LA-NPC defined as AJCC/UICC 8th edition TNM-stage III-IVA

DETECTABLE EBV DNA levels following 3 cycles of IC, defined as >0 copies/mL

Disqualifiers

Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX 40, CD137)

Has received any prior radiotherapy (RT) or systemic anti-cancer therapy including investigational agents for NPC, except for induction chemotherapy (Cisplatin and Gemcitabine) that was completed within the last 22 days. Subjects who have started on concurrent chemo-radiotherapy (CCRT; cisplatin with radiotherapy) following completion of induction chemotherapy (Cisplatin with Gemcitabine) are allowed to enroll

Any known central nervous system metastases and/or carcinomatous meningitis

Active autoimmune diseases or history of autoimmune diseases that may relapse

Trial design

Treatments tested in this trial

  • CCRT with Maintenance Tislelizumab and Metronomic Capecitabine

Treatment groups

53 Participants
are divided into 1 treatment group

Sponsors and collaborators

National Cancer Centre, Singapore

Lead sponsor

BeOne Medicines Singapore Pte. Ltd.

Collaborator

Tan Tock Seng Hospital

Collaborator