| Eligibility |
Inclusion Criteria:
1. All subjects voluntarily participated in the study and signed informed consent;
2. Male or female aged =18 years ;
3. Expected survival time =3 months;
4. ECOG 0-1;
5. Patients with extensive-stage small-cell Lung cancer confirmed by histopathology
and/or cytology (according to Veterans Administration Lung Study Group (VALG)
staging); 5-1)Cohort_1 patients who have not received any previous systemic anti-tumor
therapy for extensive-stage small cell lung cancer, and included all patients with =5
extrapulmonary metastases.
5-2)Cohort_2 patients with previous failure or intolerance to standard therapy for
extensive-stage small cell lung cancer and received at most one systemic treatment:
a) Those who have previously failed first-line platinum-based chemotherapy combined
with immune checkpoint inhibitors, and have received at most one systemic treatment,
as follows:
- Receiving less than 2 lines of systemic therapy in the advanced stage of the
disease;
?Immune checkpoint inhibitors include atezolizumab, durvalumab, slulimumab,
adebelimab, etc.;
?Disease progression confirmed by imaging during or after the latest treatment b)
Those who have only received first-line platinum-containing drug treatment in the
past and failed, and have not received immune checkpoint inhibitor treatment, as
follows:
- Receiving less than 2 lines of systemic therapy in the advanced stage of the
disease; ? The first-line treatment must be platinum-containing chemotherapy; ?
Disease progression confirmed by imaging during or after the latest treatment
6. Consent to provide archival tumor tissue specimens (10 unstained sections (anti-slip)
surgical specimens (thickness 4-5µm)) or fresh tissue samples from primary or
metastatic lesions within 3 years. If participants cannot provide tumor tissue
samples, they can be enrolled if they meet other inclusion and exclusion criteria,
after the evaluation of the investigator;
7. Must have at least one measurable lesion according to RECIST v1.1 definition; Lesions
that had been previously treated with radiation could be included in a measurable
lesion only if there was definite disease progression after radiation therapy.
8. Organ function level must meet the following criteria: 8-1) Blood routine: hemoglobin
(HGB) = 90g/L; Absolute neutrophil count (NEUT) = 1.5×10 9 /L; Platelet count (PLT) =
100×10 9 /L; 8-2) Renal function: creatinine (Cr) =1.5 ULN, or creatinine clearance
(Ccr) =50 mL/min (according to Cockcroft and Gault formula).
8-3) Liver function: total bilirubin (TBIL=1.5 ULN), alanine aminotransferase (ALT)
and aspartate aminotransferase (AST) were all =2.5 ULN, and AST and ALT were both =5.0
ULN when liver metastasis was present; 8-4) coagulation function: international
normalized ratio (INR) =1.5 and activated partial thromboplastin time (APTT) =1.5ULN;
8-5) no severe cardiac dysfunction with left ventricular ejection fraction =50%; 8-6)
proteinuria =2+ or =1000mg/24h; 8-7) Toxicity of previous antineoplastic therapy has
returned to = grade 1 as defined by NCI-CTCAE v5.0 (except for asymptomatic laboratory
abnormalities such as ALP elevation, hyperuricemia, and hyperglycemia, as judged by
the investigator, and toxicity without safety risk, such as alopecia, grade 2
peripheral neurotoxicity, or decreased hemoglobin =90g/L, as judged by the
investigator); 8-8) For premenopausal women with childbearing potential, a pregnancy
test must be performed within 7 days before the start of treatment, the serum or urine
pregnancy test must be negative, and the patient must not be lactating; All enrolled
patients should take adequate barrier contraception during the whole treatment cycle
and for 6 months after the end of treatment.
9. Women of reproductive age should agree to use effective contraception during the study
period and for six months after the study ends; Have a negative serum or urine
pregnancy test within 7 days prior to study enrollment and must be non-lactating; Men
should agree to use contraception during the study period and for six months after the
study period ends;
10. Patients will be able to communicate well with the investigator, understand and comply
with the requirements of the study.
Exclusion Criteria:
1. Histologically or cytologically confirmed NSCLC;
2. Previous medications:For Cohort_1: Exclude those who have received systemic anti-tumor
therapy or with >5 extrapulmonary metastases; For Cohort_2: Those who have received
more than one systemic treatment regimen
3. Participated in other domestic unapproved or unmarketed drug clinical trials and
accepted the corresponding experimental drug treatment within 4 weeks before
enrollment;
4. Imaging during the screening period shows that the tumor surrounds important blood
vessels or has obvious necrosis or cavities, and the researcher determines that
entering the study will cause a risk of bleeding(Only for Cohort_2).
5. Received any surgery or invasive treatment or operation within 4 weeks before
enrollment (excluding intravenous catheterization, puncture drainage, puncture biopsy,
etc.)
6. The patient currently has central nervous system (CNS) metastases or active brain or
meningeal metastases. Treated subjects with BMS were required to meet the following
criteria: asymptomatic; No radiographically demonstrated progression =4 weeks after
completion of treatment; Completion of treatment =14 days before the first dose of the
study drug; Systemic corticosteroid therapy (> 10mg/ day prednisone or equivalent) is
not required for =14 days prior to the first dose of the study drug
7. Known allogeneic organ transplantation (except corneal transplantation) or allogeneic
hematopoietic stem cell transplantation;
8. Any other medical condition, clinically significant metabolic abnormality, physical
abnormality, or laboratory abnormality that, in the investigator's judgment,
reasonably suspects the patient to have a medical condition or condition that is not
suitable for the use of the study drug (such as having seizures that require
treatment), or that would affect the interpretation of the study results, or put the
patient at high risk;
9. Have received or plan to receive live attenuated vaccine within 4 weeks prior to
initial administration;
10. Currently receiving anti-HBV treatment;
11. Received approved or under development systematic anti-tumor therapy within 28 days
before enrollment;
12. Those who are known to be allergic to the active ingredient or excipients of the drug
in this study;
13. Women who are pregnant (positive pregnancy test before medication) or breastfeeding.
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