G-CSF in Patients With Anti-PD-1-axis Therapy-resistant Recurrent or Metastatic Nasopharyngeal Carcinoma

Inclusion Criteria:

1. Male or female; 18-75 years of age.
2. Subjects diagnosed with pathological confirmed non-keratinizing (WHO-II/III)metastatic NPC, or subjects with recurrent NPC that is unfit for local treatment
3. Received prior treatment with platinum agents and PD-(L)1 inhibitors.
4. Developed acquired resistant (AR) to PD-(L)1 inhibitors following the anti-PD-1/L1 orcombined with anti-target agent (VEGFR/EGFR TKI/Ab) maintenance therapy. (AR definedas disease progression after partial or complete response).
5. Patients must have at least 1 lesion that is measurable using RECIST v1.1 criteria.
6. ECOG performance status of 0 or 1.
7. Have recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to anyanti-tumor therapy 4 weeks earlier. Except for hair loss, hair color change, nailchange, fatigue, etc., which do not pose safety risks to subjects.
8. Life expectancy more than 12 weeks.
9. Patients must have adequate organ function (without blood transfusion, without growthfactor or blood components support within 14 days before enrollment) as determined by: Absolute neutrophil count (ANC) ≥1.5×109/L; Platelet count ≥ 75×109/L; Hemoglobin ≥ 9g/dL; serum total bilirubin (TBIL) ≤1.5 times the upper limit of normal (ULN); alanineaminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5×upper limit of normal (ULN), (for subjects with liver metastases, TBIL ≤3×ULN ; ALT and AST≤5×ULN);Creatinine ≤1.5×ULN or creatinine clearance rate≥50 ml/min (Cockcroft-Gault formula);serum albumin ≥28 g/L; INR, APTT≤1.5 x ULN.
10. Female subjects agree not to be pregnant or lactating from beginning of the studyscreening through at least 3 months after receiving the last dose of study treatment.Both men and women of reproductive potential must be willing and able to employ ahighly effective method of birth control/contraception to prevent pregnancy.
11. Be willing and able to provide written informed consent/assent for the trial.

Exclusion Criteria:

1. Known history of any ≥ grade 3 immune-related toxicity.
2. Known history of hypersensitivity to any components of the PEG-rhG -CSF formulation.
3. Received G-CSF concurrent with anti-PD-(L)1 antibody combined with anti-target agent (VEGFR/EGFR TKI/Ab) maintenance therapy. (Patients who received G-CSF to prevent andtreat febrile neutropenia secondary to chemotherapy are permitted)
4. Prior chemotherapy, targeted small molecule therapy, or radical therapy within 2 weeksprior to Study Day 1
5. Diagnosed and/or treated additional malignancy within 5 years of enrollment, with theexception of curatively-treated basal cell or squamous cell carcinoma of the skin,and/or curatively-resected in situ cervical and/or breast carcinoma.
6. Concurrent medical condition requiring the use of immunosuppressive medications, orimmunosuppressive doses of systemic or absorbable topical corticosteroids. Doses > 10mg/day prednisone or equivalent are prohibited within 2 weeks before study drugadministration.
7. Active central nervous system metastases and/or carcinomatous meningitis
8. Severe, uncontrolled angiocardiopathy (heart failure > class II NYHA, unstable angina,myocardial infarction within past 1 year, supraventricular or ventricular arrhythmiawhich need medical intervention, or QT interval male ≥ 450 ms, female ≥ 470 ms.).
9. History of non-infectious pneumonitis that required steroids or current pneumonitis
10. Active infection requiring systemic therapy
11. Be known to have active tuberculosis.
12. Human immunodeficiency virus (HIV) positive
13. Hepatitis B or C positive
14. Live vaccine within 30 days of planned start of study drug
15. Underlying medical condition that, in the Investigator's opinion, would increase therisks of study drug administration or obscure the interpretation of toxicitydetermination or adverse events.