Clinical trial · Interventional
A Real-world Study of the Efficacy and Safety of PD-1 Inhibitors Combined With Chemoradiotherapy in Lung Metastatic Nasopharyngeal Carcinoma
NCT07062484CI-TRIAL-00092086not yet recruitingN/AClinicalTrials.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)
This study is a retrospective real-world study. In this study, we plan to collect the clinical data of lung metastatic nasopharyngeal carcinoma patients who received PD-1 inhibitors and chemotherapy combined with or without radiotherapy.
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 |
|---|---|---|---|
| Lung Metastatic Nasopharyngeal Carcinoma | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Control: gemcitabine, cisplatin, tirelizumab | Drug | — | UNRESOLVED |
| Experimental: gemcitabine, cisplatin, tirelizumab and radiotherapy | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Control Group
- interventionNames
- Drug: Control: gemcitabine, cisplatin, tirelizumab
- type
- EXPERIMENTAL
- label
- Experimental group
- interventionNames
- Drug: Experimental: gemcitabine, cisplatin, tirelizumab and radiotherapy
Primary outcomes (1)
- measure
- Objective response rate
- timeFrame
- 3 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. age of at least 18 years; 2. Karnofsky Performance Status (KPS) ≥60; 3. histologically confirmed nasopharyngeal squamous carcinoma; 4. metastatic disease after primary standard treatment (patients who had metastatic diseases over six months after treatment); 5. at least 1 measurable metastatic lesions in lung or mediastinal or pleura (imaging for distant metastases with FDG-PET/CT or chest/abdomen CT with contrast); 6. adequate renal , liver and bone marrow function. Exclusion Criteria: 1. previous treatment with an immune checkpoint inhibitor; 2. recurrent disease; 3. previous systemic chemotherapy for metastatic disease; 4. symptomatic central nervous system metastases; 5. a history of non-infectious pneumonitis that required glucocorticoids, or active autoimmune disease; 6. severe organ dysfunction or not suitable for chemoradiotherapy; 7. individuals that had serious kidney, heart, blood, nervous system, or liver diseases or psychiatric disorders; 8. individuals that had taken part in any other clinical trials testing other drugs within 3 months of the present study; 9. other patients whom researchers deemed unsuitable to participate in the study.
References
Publications (0)
Data not yet available
No reference posted for this study.