Clinical trial · Interventional
Capecitabine Plus Toripalimab Maintenance Therapy in Metastatic Nasopharyngeal Carcinoma After First-line Treatment
Capecitabine Plus Toripalimab Maintenance Therapy in Metastatic Nasopharyngeal Carcinoma After First-line Gemcitabine/Cisplatin Plus Toripalimab Treatment: a Single Arm, Open Label, Multicenter, Phase II Clinical Study
NCT05484375CI-TRIAL-00060027not yet recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
to evaluate the efficacy and safety of toripalimab and capecitabine maintenance therapy in patients with metastatic nasopharyngeal carcinoma (NPC) after first-line gemcitabine/cisplatin combined with toripalimab.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Metastatic Nasopharyngeal Carcinoma | Nasopharyngeal Carcinoma | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Capecitabine plus toripalimab | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Capecitabine plus toripalimab maintenance therapy
- description
- capecitabine and toripalimab were used as maintenance therapy every 3 weeks until toxicity was unacceptable, disease progression, consent withdrawal, or withdrawal was determined by the investigator, or a maximum of 2 years of treatment had been reached.
- interventionNames
- Drug: Capecitabine plus toripalimab
Primary outcomes (1)
- measure
- progression-free survival(PFS)
- timeFrame
- up to 24 month
- description
- The time is defined from the enrolment to progression or death from any cause
Secondary outcomes (5)
- measure
- overall survival(OS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histology confirmed metastatic nasopharyngeal carcinoma following radical treatment(Stage IVb, AJCC/UICC 8th,any T,any N,M1) 2. Patients receiving gemcitabine/cisplatin in combination with terriprizumab received complete response (CR) or partial response (PR) after 4-6 cycles of imaging studies 3. Age ≥18 years and ≤65 years 4. WBC≥4×10\^9/L, platelet ≥ 100×10\^9/L, hemoglobin ≥ 90g/L and Albumin≥28 g/L 5. With normal liver function test (TBIL#ALT#AST ≤ 2.5×uln) (patients with liver metastasis≤5×uln) 6. With normal renal function test (creatinine ≤ 1.5×uln or CCR ≥ 60ml/min) 7. ECOG score is 0-1 8. At least one measurable lesion according to RECIST v 1.1 (prior to gemcitabine/cisplatin plus toripalimab) 9. Life expectancy is at least 12 weeks 10. Patients sign informed consent forms Exclusion Criteria: 1. History of severe anaphylaxis to any component of capecitabine or toripalimab 2. Active or untreated central nervous system metastases 3. Patient with necrotic lesions and judged by the investigator to be at risk of excessive bleeding 4. Patients with poorly controlled pleural effusion, pericardial effusion, or ascites requiring frequent drainage. Patients with indwelled catheters are allowed to participate. 5. Patients with poorly controlled or symptomatic hypercalcemia 6. Pregnancy or lactation 7. Malignancies other than nasopharyngeal carcinoma, with negligible risk of metastasis or death and radical outcome expected after treatment, within the 5 years prior to enrollment. 8. Patients who have previously received allogeneic bone marrow transplants or solid organ transplants. 9. History of autoimmune diseases 10. Received systemic immunostimulant therapy (except toripalimab in palliative chemotherapy, including but not limited to interferon or IL-2) within 4 weeks prior to enrollment or during 5 half-lives of the drug. 11. Receive any active vaccine within 4 weeks prior to enrollment 12. Basic medical conditions that the investigator identified as likely to affect significantly drug administration and protocol adherence of the study 13. Active pneumonia 14. Active infections, including tuberculosis, hepatitis B, hepatitis C or HIV. 15. Presence of severe neurological or psychiatric disorders, including dementia and seizures. 16. Peripheral nerves which was graded as≥ 2 according to NCI-CTCAE 17. Major cardiovascular diseases
References
Publications (0)
Data not yet available
No reference posted for this study.