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- Klinische proef NCT05401279
Bladder Sparing Treatment of Tislelizumab, Gemcitabine and Cisplatin for Patients With PD-L1 Positive Muscle Invasive Bladder Cancer
15 augustus 2022 bijgewerkt door: RenJi Hospital
Bladder Sparing Treatment of Tislelizumab Combined With Gemcitabine and Cisplatin for Patients With PD-L1 Positive Muscle Invasive Bladder Cancer (T2-3N0M0): a Phase II Prospective Study
This is a phase II open label single-arm prospective study aiming to investigate the efficacy of PD-1 inhibitor Tislelizumab combined with conventional gemcitabine and cisplatin as bladder sparing treatment for patients with PD-L1 positive muscle invasive bladder carcinoma (T2-3N0M0).
Studie Overzicht
Toestand
Werving
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
The study will enroll 20 patients with adequate organ function and performance status who either wish to attempt bladder preserving therapy or are ineligible for radical cystectomy.
The bladder samples must be available and assessed as positive for PD-L1 expression .
Patients will receive transurethral resection or partial cystectomy to remove all visible tumors with no residual disease left.
After the surgery, patients will receive 8 cycles of tislelizumab combined with 4-6 cycles of gemcitabine and cisplatin.
Studietype
Ingrijpend
Inschrijving (Verwacht)
20
Fase
- Fase 2
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Yunze Xu, PhD
- Telefoonnummer: +8618801967501
- E-mail: rjxuyunze@163.com
Studie Locaties
-
-
Shanghai
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Shanghai, Shanghai, China, 200127
- Werving
- Renji Hospital, School of Medicine, Shanghai Jiao Tong University
-
Contact:
- Yunze Xu, PhD
- Telefoonnummer: +8618801967501
- E-mail: rjxuyunze@163.com
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 75 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Histologically confirmed muscle-invasive urothelial cancer of the bladder within 60 days of study enrollment. Variant histology and cis are not allowed. Patients must be willing to provide a TURBT specimen during screening and prior to enrollment if adequate specimen (FFPE tissue block or 20 unstained slides) from initial TURBT documenting muscle-invasive urothelial bladder cancer is not available. The specimen must be assessed as PD-L1 positive by two pathologists using SP263 kit.
- Clinical stage T2-T3, N0, M0 urothelial bladder cancer.
- Deemed to not be a candidate for radical cystectomy by attending urologic oncologist or refuse radical cystectomy.
- Willing to receive maximal transurethral resection or partial cystectomy to remove all bladder tumors
- Be willing and able to provide written informed consent/assent for the trial.
- Have a performance status of 0 or 2 on the Eastern Cooperative Oncology Group Performance Scale.
Demonstrate adequate organ function as defined below, all screening labs should be performed within 10 days of protocol enrollment.
- Absolute neutrophil count >= 1,500 /mcL;
- Platelets >= 100,000 /mcL;
- Hemoglobin >= 9.0 g/dL;
- Serum creatinine <=1.5 x upper limit of normal (ULN) or calculated creatinine clearance >= 30 mL/min as calculated by Cockcrof-Gault formulae or by 24 hour urine collection;
- Serum total bilirubin <=1.5 x ULN or direct bilirubin <= ULN for subjects with total -bilirubin levels > 1.5 x ULN;
- Aspartate aminotransferase and alanine aminotransferase <= 1.5 x ULN;
- Albumin >= 2.5 mg/dL;
- International normalized ratio or prothrombin time (PT) <= 1.5 x ULN unless subject is receiving anticoagulant therapy as long as PT or partial prothrombin time (PTT) is within therapeutic range of intended use of anticoagulants;
- Activated Partial Thromboplastin Time (aPTT) <= 1.5 x ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants.
- Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
- Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication. Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for > 1 year.
- Male subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy.
Exclusion Criteria:
- Has received prior radiation therapy or systemic chemotherapy for urothelial bladder cancer including neoadjuvant chemotherapy. Prior intravesical chemotherapy or intravesical immunotherapy is permissible, however, no prior intravesical therapy is permitted within 4 weeks of study enrollment; adjuvant therapy is not permitted.
- Has received prior pelvic radiation therapy.
- Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment.
- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment.
- Has a known history of active TB (Bacillus Tuberculosis).
- Hypersensitivity to tislelizumab or any of its excipients.
- Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to agents administered more than 4 weeks earlier.
- If subject received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy.
- Any prior history of invasive malignancy within the past 5 years except non-melanoma skin cancer, carcinoma in-situ, localized prostate cancer without biochemical recurrence following definitive treatment.
- Has other active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
- History of Guillain-Barre Syndrome or Stevens-Johnson Syndrome
- Has known history of, or any evidence of active, non-infectious pneumonitis.
- Has an active infection requiring systemic therapy.
- Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
- Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment.
- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.
- Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
- Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA [qualitative] is detected).
- Has received a live vaccine within 30 days of planned start of study therapy. Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Gemcitabine, Cisplatin and Tislelizumab
Patients will receive transurethral resection or partial cystectomy to remove all visible tumors with no residual disease left.
2-4 weeks after the surgery, patients will receive 8 cycles of tislelizumab combined with 4-6 cycles of gemcitabine and cisplatin.
|
Tislelizumab 200mg will be administered on Day 1 of each 21 day cycle for 8 21-day cycles.
Gemcitabine 1000mg/m^2 will be administered on Days 1 and 8 for four to six 21-day cycles.
Cisplatin 70mg^m2 will be administered on Day 1 for four to six 21-day cycles.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Ziektevrije overlevingskans na twee jaar bij intacte blaas
Tijdsspanne: 2 jaar
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Blaas-intacte ziektevrije overleving wordt gedefinieerd als de tijd vanaf het begin van de protocoltherapie tot de ontwikkeling van spierinvasief blaaskanker-recidief, regionaal bekken-recidief, metastasen op afstand, aan blaaskanker gerelateerd overlijden of cystectomie.
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2 jaar
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Adverse Events
Tijdsspanne: 2 years
|
The adverse events are evaluated per Common Terminology Criteria for Adverse Events (CTCAE) 5.
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2 years
|
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Overall survival
Tijdsspanne: up to 5 years
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Defined as time to death from beginning of protocol therapy
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up to 5 years
|
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Metastasevrije overleving
Tijdsspanne: tot 5 jaar
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Gedefinieerd als de tijd tot de ontwikkeling van radiografische metastasen op afstand vanaf het begin van de protocoltherapie.
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tot 5 jaar
|
|
Disease-free survival
Tijdsspanne: up to 5 years
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Defined as time to recurrence, metastasis or death from beginning of protocol therapy.
|
up to 5 years
|
|
Disease specific survival
Tijdsspanne: up to 5 years
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Defined as time to death because of bladder cancer from beginning of protocol therapy
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up to 5 years
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Wei Xue, PhD, Renji Hospital, School of Medicine, Shanghai Jiao Tong University
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 juni 2022
Primaire voltooiing (Verwacht)
1 april 2024
Studie voltooiing (Verwacht)
1 mei 2025
Studieregistratiedata
Eerst ingediend
29 mei 2022
Eerst ingediend dat voldeed aan de QC-criteria
29 mei 2022
Eerst geplaatst (Werkelijk)
2 juni 2022
Updates van studierecords
Laatste update geplaatst (Werkelijk)
18 augustus 2022
Laatste update ingediend die voldeed aan QC-criteria
15 augustus 2022
Laatst geverifieerd
1 augustus 2022
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata
- Urologische neoplasmata
- Urogenitale neoplasmata
- Neoplasmata per site
- Urologische ziekten
- Ziekten van de urineblaas
- Neoplasmata van de urineblaas
- Fysiologische effecten van medicijnen
- Moleculaire mechanismen van farmacologische werking
- Anti-infectieuze middelen
- Antivirale middelen
- Enzymremmers
- Antimetabolieten, antineoplastische
- Antimetabolieten
- Antineoplastische middelen
- Immunosuppressieve middelen
- Immunologische factoren
- Gemcitabine
Andere studie-ID-nummers
- TICIG
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Nee
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
product vervaardigd in en geëxporteerd uit de V.S.
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .