- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01679405
BIBW 2992 as add-on to Gem/Cis in Advanced Biliary Tract Cancer
Open-label, Uncontrolled, Multicenter Phase I/Ib Trial to Investigate Safety and Efficacy of BIBW 2992 and Standard Gemcitabine/Cisplatin in Chemo-naïve Patients With Advanced Biliary Tract Adenocarcinoma
Studieoversigt
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
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Mainz, Tyskland, 55131
- I. Medizinische Klinik und Poliklinik der Universitätsmedizin
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Male and female patients aged ≥ 18 years
- Signed and dated written informed consent,
Histologically confirmed adenocarcinoma of the gallbladder or intrahepatic bile ducts or extrahepatic bile ducts (metastasized) or histologically proven hepatic metastases of an earlier resected and histologically proven biliary tract cancer or a Klatskin tumour (hilar cholangiocarcinoma)
- with pain and biliary obstruction controlled
- adequate biliary drainage, no uncontrolled infection
- ECOG Performance Status of 0-1
- LFTs: bilirubin (total) ≤ 1.5 x ULN, ALT/ AST/ alkaline phosphatase ≤ 3 2.5 x ULN (≤ 5 x ULN if liver metastases are present)
- No prior systemic treatment i) previous adjuvant chemotherapy is allowed (completed ≥ 6 months if containing Gemcitabine or platinum salts); ii) previous irradiation (external radiotherapy, brachytherapy, chemoembolization) and PDT are allowed, provided that there is still at least one unidimensionally measurable target lesion in an untreated area
- Resolution of all side effects of prior surgical procedures to CTCAE grade ≤ 1 (except for the laboratory values specified below)
- At least 4 weeks from any major surgery (at first dose of study drug)
- Life expectancy of at least 12 weeks.
- Cardiac left ventricular function with resting ejection fraction (LVEF) ≥ 50%
Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to start of therapy:
- Haemoglobin > 10.0 g/dl (=6.2 mmol/l), blood transfusion is allowed
- Absolute neutrophil count (ANC) > 1,500/mm3 (=1.5x 109/L)
- Platelet count ≥ 100,000/μl (=100x 109/L)
- Total bilirubin ≤ 1.5 times the upper limit of normal
- ALT and AST ≤ 2.5 x institutional upper limit of normal (in case of liver metastases: ALT and AST ≤ 5 x institutional upper limit of normal)
- Prothrombin rate > 60% or INR < 1.5
Main exclusion criteria
- Large surgery (except diagnostic biopsy) or smaller surgical procedures, external radiotherapy, brachytherapy, or PDT within 30 days prior to start of treatment.
- Other tumor type than adenocarcinoma (e.g. leiomyosarcoma, lymphoma) or a second cancer except in patients with squamous or basal cell carcinoma of the skin or carcinoma in situ of the cervix which has been effectively treated.
- History of acute cardiac disease: congestive heart failure > NYHA class 2; active CAD (MI more than 6 months prior to study entry is allowed);
- Patients on immunosuppressant therapy or with known HIV infection
- Active clinically serious infections (> grade 2 NCI-CTC version 3.0)
- History of organ allograft
- Pregnant or breast-feeding patients.
- Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation
- Any condition that is unstable or could jeopardize the safety of the patient and their compliance in the study
- Gastrointestinal (GI) tract disease resulting in an inability to take oral medication or a requirement for IV alimentation, prior surgical procedures affecting absorption, or active peptic ulcer disease
- History of pre-existing interstitial lung disease (ILD)
- Patients with untreated or symptomatic brain metastases.
- Persistent Grade 2 or greater neurotoxicity / neuropathy from any cause
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: Dose level 1 (Part A)
30 mg BIBW 2992, Gemcitabin (1.000 mg/m² BSA i.v.)/Cisplatin (25 mg/m² BSA i.v.)
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once daily per os
Andre navne:
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Eksperimentel: Dose level -1 (Part A)
30 mg BIBW 2992, Gemcitabin (800 mg/m² BSA i.v.)/Cisplatin (20 mg/m² BSA i.v.)
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once daily per os
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Number of Adverse Events
Tidsramme: Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
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In part A the maximum tolerated dose (MTD) of BIBW 2992 administered continuously to the standard therapy of Gemcitabine / Cisplatin (Gem/Cis) (administered together on day 1 and 8 of a three-week cycle) will be evaluated in a 2 step dose escalation. Safety and toxicity will be evaluated as described and considered primary for part B of the study. |
Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Time to Progress (TTP)
Tidsramme: Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
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Median time to progress (according to RECIST 1.1 criteria) including the 95% confidence intervals were determined using Kaplan-Meier estimates.
Time from start of treatment to first documentation of objective tumour progression.
Deaths were censored at the time of death.
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Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
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Overall Survival (OS)
Tidsramme: Time from start of treatment to death due to any cause. Time to last observation will be used if a patient has not died and OS for the patient will be considered censored. Estimated time period: up to 76 weeks
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Median overall survival time including the 95% confidence interval were determined using Kaplan-Meier estimates.
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Time from start of treatment to death due to any cause. Time to last observation will be used if a patient has not died and OS for the patient will be considered censored. Estimated time period: up to 76 weeks
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Objective Response Rate
Tidsramme: Treatment period: up to eight cycles (maximum 8 months).
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Response was assessed by means of RECIST 1.1 criteria for target lesions, non-target lesions and the appearance of new lesions.
Objective response was defined as the CR, PR or SD at end of treatment
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Treatment period: up to eight cycles (maximum 8 months).
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Tumor Control Rate
Tidsramme: Treatment period: up to eight cycles (maximum 8 months).
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Tumor control rate is defined as the best tumour response (confirmed partial or complete response, stable disease) that is achieved until end of treatment according to Recist 1.1.
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Treatment period: up to eight cycles (maximum 8 months).
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Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Markus Moehler, Prof. Dr. med., University Medical Center of the Johannes Gutenberg-University Mainz
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Patologiske processer
- Neoplasmer
- Neoplastiske processer
- Neoplasma Metastase
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Antivirale midler
- Enzymhæmmere
- Antimetabolitter, Antineoplastisk
- Antimetabolitter
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Proteinkinasehæmmere
- Gemcitabin
- Cisplatin
- Afatinib
Andre undersøgelses-id-numre
- BIBW 2992
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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