- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04777162
Tislelizumab Plus Anlotinib for Immunotherapy Resistant Gastrointestinal Cancer
Efficacy and Safety of Tislelizumab Plus Anlotinib in PD-1/PD-L1 Resistant Metastatic Gastric or Colorectal Cancer: a Single Arm Phase II Clinical Trial
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Forventet)
Fase
- Fase 2
Kontakter og plasseringer
Studiesteder
-
-
Beijing
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Beijing, Beijing, Kina, 100142
- Rekruttering
- Beijing Cancer Hospital
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- ECOG scored 0 or 1, ≥18 years old, expected OS≥3 months;
- Histology confirmed unresectable or metastatic gastric/gastroesophageal junction adenocarcinoma or colorectal cancer;
- ≥1 evaluable lesion based on RECIST 1.1;
Patients received PD-1/PD-L1 in the last treatment line, and should meet following conditions:
i) there was no severe immune-related adverse events, ii) the duration between tumor progression and screening should be 3-12 weeks, iii) the best evaluation results should be PR or CR when receiving PD-1/PD-L1 treatment but progression was confirmed in the latest evaluation, iv) patients were diagnosed with special pathology subtypes, that are sensitive to immunotherapy, such as dMMR, MSI-H tumors, or gastric cancer with PD-L1 CPS≥10, PFS≥6 months in the last treatment line;
- laboratory test should meet following standard: i) HB≥90g/l, neutrophils≥1.5*10^9/L, plt≥100*10^9, ii) ALT and AST<2.5xULN (5ULN for liver metastatic patients), TBIL≤2×ULN, Cr≤1.5×ULN, and Ccr>50μmol/L iii) APTT, INR and PT≤1.5×ULN iv) LVEF≥50%
- for female participants, Hcg should be negative and both male and female participants should have contraception measures
- participants should be informed consent, and voluntary.
Exclusion Criteria:
- received anlotinib or other TKIs previously;
- allergic to other monoclonal antibody before the treatment;
- diagnosed with other malignancy in last five years (cured skin basal carcinoma, prostate cancer or cervical caner in situ were excluded)
- concurrent with other active autoimmune disease;
- any condition that require immune suppressor, such as cortisol (>10mg/d prednisone equally), CTX;
- conditions affect oral absorption (eg: dysphagia, intestinal obstruction; chronic diarrhea);
- uncontrolled pleural effusion, hydropericardium and seroperitoneum;
- brain metastasis;
- received other anti-tumor treatment in past 3 weeks, eg: surgery, radiotherapy, target therapy, immunotherapy, and traditional Chinese therapy (target therapy less than 5 half-life period, 5-Fu less than 14 days were excluded);
- concurrent with uncontrolled other diseases, i) hypertension (>150/90mmHg) ii) unstable angina pectoris, ≥ level 2 heart failure, arrhythmia within last 6 months; iii) clinical meaningful liver disease, eg: active HBV/HCV hepatitis; iv) HIV positive; v) uncontrolled diabetes; vi) urine protein ≥++ or 24h urine protein >1g;
- injected vaccine in past 4 weeks, or administrated with antibiotics;
- investigator assumed improper conditions, such as mental disease, family or society factors.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: tislelizumab+anlotinib
patients will be administrate with dual drugs, tislelizumab plus anlotinib.
|
For included participants, tislelizumab would be administrated 200mg q3w iv.
Patients will be administrated with Anlotinib 12mg p.o. d1-d14 q3w.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
objective response rate
Tidsramme: 2 years
|
the rate of patients reached PR or CR based on RECIST 1.1
|
2 years
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
progression-free survival
Tidsramme: Up to 2 years
|
the time from recruiting to death or progression
|
Up to 2 years
|
|
overall survival
Tidsramme: Up to 2 years
|
the time from recruiting to death
|
Up to 2 years
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Forventet)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- Tislelizumab plus Anlotinib
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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