Y-90 Alone or With Sorafenib for Pre-Transplant Hepatocellular Carcinoma
13. september 2016 oppdatert av: Laura Kulik, Northwestern University
A Single-Center Proof of Concept Pilot Study to Evaluate the Safety, Efficacy, and Tolerability of Sorafenib Combined With Therasphere in Subjects With Hepatocellular Carcinoma Awaiting Liver Transplantation.
A research study to determine the safety, efficacy, and tolerability of Therasphere® (also known as Y-90, or Y-90 Therasphere) combined with or without sorafenib (Nexavar®), in patients with hepatocellular carcinoma (HCC, or liver cancer), awaiting liver transplantation.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Because Hepatocellular carcinoma (HCC) grows by forming new blood vessels liver transplant (OLT) offers the best chance for long term survival.
However, with the growing number of patients who require OLT, prolonged wait list times often lead to drop out from the transplant list due to tumor progression.
Some patients are granted an "upgrade",within the generally accepted guidelines for transplant eligibility, in order to expedite the access of patients with early HCC to transplantation before tumor progression.
The use of therapies like radioembolization also known as Yttrium-90 ([Y-90] a procedure where very small beads coated with radiation are injected directly into the tumor through an artery in your groin) while awaiting OLT has become common at most transplant centers, including Northwestern, to help patients reach transplant.
Additionally, these treatments are being used to move patients to a status eligible for transplant.
We are studying whether a combination approach with systemic therapy and therapy applied directly to the liver, will be more successful than a single therapy .
Angiogenesis (a process involving the growth of new blood vessels from pre-existing vessels) plays an important role in the early stages of HCC.
A decrease in angiogenesis both locally within the treated tumor as well as in any existing tumor cells, not yet detected, would hopefully decrease the incidence of post transplant recurrence of HCC.
All subjects enrolled in this study will be treated with the use of Therasphere, Y-90, which is composed of nonbiodegradable glass microspheres coated with the radioactive compound Y-90 which are injected into the hepatic artery.
The concentrated radioactive microspheres within the tumor lead to "inside-out" radiation.
Half of the subjects will be treated with sorafenib (NEXAVAR®) in conjunction with Y-90.
The determination of which subjects will receive sorafenib will be made randomly, like the flip of a coin.
Sorafenib works by slowing the growth of the tumor cell , attacking the tumor from the outside.
Researchers hope to determine whether the subjects treated with sorafenib have an overall improved response to liver directed therapy with Y-90 Therasphere.
Studietype
Intervensjonell
Registrering (Faktiske)
24
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Illinois
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Chicago, Illinois, Forente stater, 60611
- Northwestern Memorial Hospital
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-
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:
- Adult > 18 years olf of either gender
- Diagnosis of HCC confirmed by biopsy, CT, or MRI
- Able to carry out activities of daily living, awake >50% of waking hours
- Meets eligibility for liver transplantation
- No prior treatment for HCC
- Ability to understand and sign the informed consent
- Child-bearing women and any men agree to use two forms of birth control (one of which should be a barrier method) during the course of therapy and for 8 weeks afterward.
Exclusion Criteria:
- Less than or = 18 years old
- Ineligible for transplant due to comorbid disease
- Renal Failure requiring dialysis of any kind
- Severe Cardiac disease
- History of a stroke
- Evidence of metastatic disease- or tumors that have spread outside the liver
- Known human immunodeficiency virus (HIV) infection
- Uncontrolled blood pressure (systolic > 160) despite medication(s)
- Major surgery within 4 weeks prior to the screening visit
- Active clinically serious infection
- Serious non-healing wound, ulcer, or bone fracture.
- History of gastrointestinal bleeding (GIB) within 6 weeks prior to the screening visit
- Prior transplant of any kind
- Must be able to swallow oral pills, tablets or capsules of any size
- Use of St. John's Wort or rifampin (rifampicin).
- Currently being treated with Interferon and/or Ribavirin therapy due to the thrombocytopenias, lymphopenias and anemias observed with use of these two medications.
- Known or suspected allergy to sorafenib or any agent given in the course of this trial.
- Any malabsorption problem
- Pregnancy or lactation. Women of childbearing potential must have a negative pregnancy test 7 days prior to beginning therapy.
- No potential living donor transplant (LDT-donor identified and worked up by the time of randomization into this study. If a living donor is later identified- the subject will be allowed to continue in the study. Sorafenib will be stopped at a minimum of 7 days prior to transplant surgery.
- Active alcohol use, drug use, or a psychiatric disease that would, in the opinion of the PI or a subinvestigator (sub-I), prevent the subject from complying with the study protocol and/or endanger the subject during their participation in the study
- Inability of the potential subject to read, understand and sign the informed consent document
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: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Aktiv komparator: A: Y-90 alone
Patients randomized to Arm A will proceed to Y-90 treatment alone in the Northwestern standard of care procedure
|
Patients undergo radioembolization with Yttrium 90 microspheres by hepatic artery infusion
Andre navn:
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Eksperimentell: B: Sorafenib + Y-90
Patients randomized to Arm B will start sorafenib at a dose of 400 mg twice daily for bilirubin ≤ 1.5 x ULN and 200 mg twice daily for bilirubin > 1.5 x ULN to ≤ 3 x ULN.
After 14 days of sorafenib therapy (+/- 3 days) patients will proceed to Y-90 in the Northwestern standard of care procedure
|
Patients undergo radioembolization with Yttrium 90 microspheres by hepatic artery infusion
Andre navn:
Randomized to Y-90 ± Sorafenib
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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To Evaluate sorafenib as an adjunct to Y-90 for control of HCC as a bridge/downstage to transplant
Tidsramme: Up to one year
|
Subjects randomized to receive Sorafenib take the drug for 2 weeks before treatment with Y90.
They have imaging (CT/MRI) 2 weeks after starting Sorafenib then are treated.
Post-treatment patients have blood drawn and adverse event evaluation at 2 weeks, 4 weeks, 6 weeks, and then every 6 weeks up to 1 year or time of transplant.
Repeat imaging is done at 4 weeks, and then every 3 months post-treatment.
Subjects not receiving Sorafenib are treated with Y90 and then are evaluated post-treatment the same as the subjects that receive the drug.
|
Up to one year
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
To characterize the toxicity profile of sorafenib and Y90 using NCI CTC toxicity grading scales.
Tidsramme: up to 1 year
|
Subjects randomized to receive Sorafenib take the drug for 2 weeks before treatment with Y90.
They have imaging (CT/MRI) 2 weeks after starting Sorafenib then are treated.
Post-treatment patients have blood drawn and adverse event evaluation at 2 weeks, 4 weeks, 6 weeks, and then every 6 weeks up to 1 year or time of transplant.
Repeat imaging is done at 4 weeks, and then every 3 months post-treatment.
Subjects not receiving Sorafenib are treated with Y90 and then are evaluated post-treatment the same as the subjects that receive the drug.
|
up to 1 year
|
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To identify predictive and prognostic markers of how the liver cancer will respond to treatment.
Tidsramme: up to 1 year
|
All subjects are evaluated with lab work and adverse event assessment at 2, 4, and 6 weeks post-treatment, and then every 6 weeks up to 1 year or when they receive transplant.
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up to 1 year
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Laura Kulik, MD, Northwestern University, Northwestern Memorial Hospital, Northwestern Medical Faculty Foundation
- Hovedetterforsker: Riad Salem, MD, Northwestern University, Northwestern Memorial Hospital, Northwestern Medical Faculty Foundation
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.
Generelle publikasjoner
- Kulik L, Vouche M, Koppe S, Lewandowski RJ, Mulcahy MF, Ganger D, Habib A, Karp J, Al-Saden P, Lacouture M, Cotliar J, Abecassis M, Baker T, Salem R. Prospective randomized pilot study of Y90+/-sorafenib as bridge to transplantation in hepatocellular carcinoma. J Hepatol. 2014 Aug;61(2):309-17. doi: 10.1016/j.jhep.2014.03.023. Epub 2014 Mar 27.
- Vouche M, Kulik L, Atassi R, Memon K, Hickey R, Ganger D, Miller FH, Yaghmai V, Abecassis M, Baker T, Mulcahy M, Nayar R, Lewandowski RJ, Salem R. Radiological-pathological analysis of WHO, RECIST, EASL, mRECIST and DWI: Imaging analysis from a prospective randomized trial of Y90 +/- sorafenib. Hepatology. 2013 Nov;58(5):1655-66. doi: 10.1002/hep.26487. Epub 2013 Oct 1.
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. februar 2009
Primær fullføring (Faktiske)
1. juli 2015
Studiet fullført (Faktiske)
1. september 2016
Datoer for studieregistrering
Først innsendt
16. februar 2009
Først innsendt som oppfylte QC-kriteriene
17. februar 2009
Først lagt ut (Anslag)
18. februar 2009
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
15. september 2016
Siste oppdatering sendt inn som oppfylte QC-kriteriene
13. september 2016
Sist bekreftet
1. september 2016
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i fordøyelsessystemet
- Neoplasmer etter histologisk type
- Neoplasmer
- Neoplasmer etter nettsted
- Adenokarsinom
- Neoplasmer, kjertel og epitel
- Neoplasmer i fordøyelsessystemet
- Leversykdommer
- Neoplasmer i leveren
- Karsinom
- Karsinom, hepatocellulært
- Molekylære mekanismer for farmakologisk virkning
- Enzymhemmere
- Antineoplastiske midler
- Proteinkinasehemmere
- Sorafenib
Andre studie-ID-numre
- NU08I4
- STU00005761 (Annen identifikator: Northwestern University IRB)
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. .