- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07596121
Serplulimab Monotherapy in Elderly Patients With NSCLC and PD-L1 TPS ≥ 50%
Multicenter, Single-arm, Phase II Exploratory Study of Serplulimab Monotherapy in Elderly Patients With NSCLC and PD-L1 TPS ≥ 50%
This prospective clinical study aims to evaluate and observe the efficacy and safety of Serplulimab Monotherapy in Elderly Patients with NSCLC and PD-L1 TPS ≥ 50% using a multicenter, single-arm, phase II design.
The study is planned to be conducted in Shaanxi Province, China, with an initial target enrollment of 60 patients. The study commenced in May 2026, and recruitment is expected to conclude around May 2026, with the trial anticipated to end by May 2027.
Assuming no occurrences such as withdrawal of informed consent by subjects, intolerable adverse drug reactions, or investigator-assessed unsuitability for further participation, each participant's estimated duration of study treatment will continue until radiographically confirmed tumor progression.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Beräknad)
Fas
- Fas 2
Kontakter och platser
Studiekontakt
- Namn: Lei Pan, Dr
- Telefonnummer: 13991161903
- E-post: panlei@fmmu.edu.cn
Studieorter
-
-
Shannxi
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Xi'an, Shannxi, Kina, 710000
- Rekrytering
- Tangdu Hospital Affiliated to the Fourth Military Medical University
-
Kontakt:
- Lei Pan, Dr
- Telefonnummer: 13991161903
- E-post: panlei@fmmu.edu.cn
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Äldre vuxen
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
1.Voluntary participation and informed consent: Subjects must voluntarily join the study, sign the written informed consent form (ICF), and demonstrate good compliance.
2.Age and Gender: Aged ≥65 years at the time of signing the ICF, regardless of gender.
3.Diagnosis and Staging: Histologically or cytologically confirmed Stage IIIB (ineligible for definitive chemoradiotherapy), Stage IIIC, or Stage IV NSCLC according to the AJCC 8th edition staging system.
4.PD-L1 Expression: Tumor tissue confirmed as PD-L1 TPS≥50% by a central laboratory or a validated local laboratory, using SP263 or 22C3 assays (a formal test report must be provided).
5.Driver Gene Status: Known absence of actionable driver mutations, including but not limited to EGFR sensitive mutations, ALK fusions, and ROS1 fusions.
6.Measurable Disease: At least one measurable target lesion per RECIST v1.1 criteria (lesions must not have received prior radiotherapy).
7.Prior Treatment History: No prior systemic therapy for advanced or metastatic disease. For patients who received adjuvant or neoadjuvant chemotherapy, inclusion is permitted if disease recurrence occurred ≥6 months after the completion of the last dose.
8.Performance Status: Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-2.
9.Adequate organ and bone marrow function (no blood transfusions or hematopoietic stimulating factor therapy within 14 days prior to the first dose):
- Absolute Neutrophil Count (ANC)≥1.5 x 10^9//L
- Platelet Count (PLT)≥100 x 10^9//L
- Hemoglobin (Hb)≥90 g/L
- Serum Creatinine (Cr) ≤ 1.5 x Limit of Normal (ULN) or Creatinine Clearance ≥ 50mL/min
- Total Bilirubin (TBIL) ≤ 1.5 x ULN
- Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT)≤ 2.5 x ULN(≤ 5 x ULN for patients with liver metastases)
Exclusion Criteria:
1. Hypersensitivity: Known hypersensitivity to serplulimab or any of its excipients.
2. Prior Immunotherapy: Prior treatment with any anti-PD-1, anti-PD-L1, anti-CTLA-4, or other immune checkpoint inhibitors (ICIs).
3. Autoimmune Disease: Active autoimmune disease requiring systemic treatment (e.g., corticosteroids or immunosuppressants) within the past 2 years. Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement for adrenal or pituitary insufficiency) is permitted.
4. Lung Disease/Pneumonitis: Active interstitial lung disease (ILD) or pneumonitis, or a history of (non-infectious) pneumonitis requiring steroid treatment.
5. Infections: Active infection requiring systemic therapy. 6. CNS Metastases: Known active central nervous system (CNS) metastases and/or carcinomatous meningitis. However, patients with treated (via surgery or radiotherapy) and stable brain metastases are eligible, provided they are radiographically stable for at least 4 weeks prior to the first dose, have no evidence of new or enlarged brain lesions, and have discontinued glucocorticoids for at least 14 days.
7. Pregnancy and Breastfeeding: Pregnant or breastfeeding women. 8. Investigator Discretion: Any other condition that, in the investigator's opinion, may interfere with the evaluation of the study drug, jeopardize subject safety, or confound the interpretation of study results.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Serplulimab Monotherapy
|
The treatment follows a 21-day (3-week) cycle.
Serplulimab is administered intravenously at a fixed dose of 300 mg on Day 1 of each cycle (Q3W).
Prior to each administration, subjects shall undergo comprehensive clinical assessments-including vital signs, anthropometric measurements, physical examinations, laboratory monitoring, and ECOG performance status (PS)-to confirm safety and tolerability for continued treatment.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Progressionsfri överlevnad
Tidsram: Progressionsfri överlevnadsanalys (PFS) baserad på utredarens bedömning per RECIST 1.1, och kommer att bedömas upp till 2 år
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Progressionsfri överlevnad (PFS) avser tiden från registrering av den första kemoterapibehandlingen till datumet för sjukdomsprogression, enligt bedömning av forskare.
|
Progressionsfri överlevnadsanalys (PFS) baserad på utredarens bedömning per RECIST 1.1, och kommer att bedömas upp till 2 år
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Objektiv svarsfrekvens
Tidsram: Uppgifter som erhållits fram till progression, eller den sista utvärderbara bedömningen i frånvaro av progression, kommer att bedömas upp till 1 år.
|
Per responsutvärderingskriterier i solida tumörer version 1.1 (RECIST 1.1) Med användning av utredningsbedömningar definieras som antalet (%) av patienter med svar på fullständigt svar eller partiellt svar, kommer att bedömas upp till 1 år.
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Uppgifter som erhållits fram till progression, eller den sista utvärderbara bedömningen i frånvaro av progression, kommer att bedömas upp till 1 år.
|
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Overall Survival
Tidsram: The maximum time from receiving treatment to dying for any reason is 4 years.
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Overall survival (OS) refers to the time that researchers evaluate from recording the first chemotherapy to death (of any cause)
|
The maximum time from receiving treatment to dying for any reason is 4 years.
|
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Disease Control Rate
Tidsram: Disease Control Rate (DCR) is analysis based on investigator assessment per RECIST 1.1, and will be assessed up to 2 years.
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Disease Control Rate (DCR) is defined as the percentage of participants who achieved a Best Overall Response (BOR) of Complete Response (CR), Partial Response (PR), or Stable Disease (SD) according to Response Evaluation Criteria in Solid Tumors (RECIST)
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Disease Control Rate (DCR) is analysis based on investigator assessment per RECIST 1.1, and will be assessed up to 2 years.
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Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
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Nyckelord
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Andra studie-ID-nummer
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