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BIBW 2992 as add-on to Gem/Cis in Advanced Biliary Tract Cancer

26. august 2019 oppdatert av: PD Dr Markus Möhler, Johannes Gutenberg University Mainz

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

An open-label, uncontrolled, multicenter phase I/Ib trial to investigate safety and efficacy of BIBW 2992 added to the standard therapy of Gemcitabine/Cisplatin in chemo-naïve patients with advanced and/or metastatic adenocarcinoma of the biliary tract

Studieoversikt

Status

Avsluttet

Intervensjon / Behandling

Detaljert beskrivelse

The primary objective is safety and toxicity, including maximum tolerated dose, of BIBW 2992 when given as add-on therapy to Gem/Cis.

Studietype

Intervensjonell

Registrering (Faktiske)

9

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Mainz, Tyskland, 55131
        • I. Medizinische Klinik und Poliklinik der Universitätsmedizin

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Dose level 1 (Part A)
30 mg BIBW 2992, Gemcitabin (1.000 mg/m² BSA i.v.)/Cisplatin (25 mg/m² BSA i.v.)
once daily per os
Andre navn:
  • Gemcitabine and Cisplatin
Eksperimentell: Dose level -1 (Part A)
30 mg BIBW 2992, Gemcitabin (800 mg/m² BSA i.v.)/Cisplatin (20 mg/m² BSA i.v.)
once daily per os
Andre navn:
  • Gemcitabine and Cisplatin

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of Adverse Events
Tidsramme: Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.

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.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Time to Progress (TTP)
Tidsramme: Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
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.
Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
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
Median overall survival time including the 95% confidence interval were determined using Kaplan-Meier estimates.
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
Objective Response Rate
Tidsramme: Treatment period: up to eight cycles (maximum 8 months).
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
Treatment period: up to eight cycles (maximum 8 months).
Tumor Control Rate
Tidsramme: Treatment period: up to eight cycles (maximum 8 months).
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.
Treatment period: up to eight cycles (maximum 8 months).

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Markus Moehler, Prof. Dr. med., University Medical Center of the Johannes Gutenberg-University Mainz

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. august 2012

Primær fullføring (Faktiske)

1. april 2016

Studiet fullført (Faktiske)

1. april 2016

Datoer for studieregistrering

Først innsendt

17. august 2012

Først innsendt som oppfylte QC-kriteriene

31. august 2012

Først lagt ut (Anslag)

6. september 2012

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. september 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

26. august 2019

Sist bekreftet

1. august 2019

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Metastatisk sykdom

Kliniske studier på BIBW 2992

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