| Eligibility |
Inclusion Criteria:
1. The histopathological diagnosis was recurrent or distant metastatic nasopharyngeal
carcinoma;
2. Have received two or more lines of treatment, including at least one immunocheckpoint
inhibitor related therapy containing PD-1/L1, and have achieved clinical benefit;
3. Aged between 18 and 65 at the date of signing the informed consent;
4. ECOG score 0-1;
5. At least =1 measurable lesion according to Recist v1.1, or =1 measurable lesion with
definite progression after local treatment (based on Recist v1.1 criteria);At the same
time, there were more than 1 radiotherapy foci and lesions with radiographic
evaluation of distant effect.
6. Life expectancy =12 weeks;
7. Major organ functions within 28 days prior to treatment meet the following criteria:
A. Routine blood test criteria (without blood transfusion within 14 days) : hemoglobin (Hb)
=80g/L;Neutrophils absolute value (ANC) =1.5×109/L;Platelet (PLT) =80×109/L; B. Biochemical
tests should meet the following criteria: total bilirubin (TBIL) =1.5 times the upper limit
of normal (ULN);Alanine aminotransferase (ALT) and aspartate aminotransferase (AST)
=2.5×ULN, if accompanied by liver metastasis, ALT and AST=5×ULN;Serum creatinine (CR)
=1.5×ULN or creatinine clearance rate (CCR)=60ml/min; C. Coagulograms should meet the
following criteria: International Standardized Ratio (INR) or Prothrombin Time (PT) =
1.5ULN;Activated partial thromboplastin time (APTT) =1.5 ULN (if the patient is receiving
anticoagulant therapy, as long as PT and APTT are within the expected treatment range); D.
centrifuge markers and urinary natriuretic peptide (BNP) =ULN; E. Thyroid function: T3 and
T4 levels were normal after medication; 8. Women of reproductive age should agree to use
contraceptives (such as intrauterine devices, contraceptives or condoms) during the study
period and for 120 days after the end of the study;Negative serum or urinary pregnancy test
within 7 days prior to study enrollment; 9. With my consent and signed the informed
consent.
Exclusion Criteria:
1. Previous use of immunocheckpoint inhibitors combined with radiotherapy after
recurrence and metastasis;
2. A history of other malignant tumors within the previous 5 years or at the same time,
except cured basal cell carcinoma of the skin, carcinoma in situ of the cervix and
papillary carcinoma of the thyroid;
3. known allergic reactions to active ingredients of PD-1 monoclonal antibody or any
excipients;
4. Symptomatic central nervous system metastasis;
5. Those who had received potent CYP3A4 inhibitor treatment within one week before
enrollment, or inducer CYP3A4 treatment within two weeks before enrollment;
6. The New York Heart Association's cardiac function classification is Grade III-IV
congestive heart failure;
7. An ischemic cardiovascular event occurred within 1 year prior to treatment;
8. QT interval of ECG >500 ms;
9. Have received systemic immunosuppressive therapy;
10. Participate in clinical trials of other interventional drugs within 4 weeks before the
first administration;
11. Subjects who require systematic treatment with corticosteroids (greater than 10mg
equivalent daily dose of prednisone) or other immunosuppressant within 2 weeks prior
to the first use of the study drug;
12. Have received an anti-tumor vaccine or a live vaccine within 4 weeks before the first
administration of the investigational drug;
13. Major surgery or severe trauma within 4 weeks before the first use of the study drug;
14. Severe infections (CTCAE > grade 2) occurred within 4 weeks before the first use of
the study drug, such as severe pneumonia, bacteremia, infection complications, etc.,
requiring hospitalization;Baseline chest imaging examination suggests active pulmonary
inflammation, signs and symptoms of infection within 2 weeks prior to the first use of
the study drug, or the need for oral or intravenous antibiotic treatment (excluding
prophylactic use of antibiotics);
15. Have a history of active autoimmune diseases or autoimmune diseases (such as
interstitial pneumonia, colitis, hepatitis, pituitaritis, vasculitis, nephritis,
hyperthyroidism, hypothyroidism, including but not limited to these diseases and
syndromes);Autoimmune-mediated hypothyroidism treated with a steady dose of
thyroid-replacement hormone and with a steady dose of insulin in type 1 diabetes were
included;This does not include patients with vitiligo or cured childhood
asthma/allergies who do not need any intervention as adults;
16. Have a history of immunodeficiency, including HIV positive or other acquired or
congenital immunodeficiency diseases, or have a history of organ transplantation or
bone marrow transplantation;
17. History of non-infectious pneumonia
18. Patients with active tuberculosis infection found by medical history or CT
examination, or patients with active tuberculosis infection found within 1 year before
enrollment, or patients with active tuberculosis infection found before 1 year but
without formal treatment;
19. Subsubjects had active hepatitis (HBV DNA=2000IU/ mL or 10000 copies/ mL) and
hepatitis C (HCV antibody positive and HCV-RNA above the detection limit of the assay
method);
20. A history of known abuse of psychotropic substances, alcoholism and drug abuse;
21. Being pregnant or lactating;
22. There is any history, disease, treatment, or abnormal laboratory result that may
interfere with the results of the study and prevent subjects from participating fully
in the study, or the investigator deems that participation is not in the best interest
of the subjects.
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