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Randomized Phase II Trial of Chemoembolization and Sorafenib

8 stycznia 2018 zaktualizowane przez: Yale University

Randomized Phase II Trial of Chemoembolization and Sorafenib: Comparison Between Continuous and Sequential Treatment Regimens

The study will be a single-center, randomized Phase II study of conventional TACE in combination with sorafenib, given either continuously or sequentially, in patients with unresectable HCC. The primary variables will be tumor response (by MR Imaging) and plasma VEGF levels, prior to and after cTACE.

Przegląd badań

Szczegółowy opis

Transcatheter arterial chemoembolization (TACE) is the most widely performed procedure for patients with unresectable HCC. Although TACE can induce tumor necrosis, tumor recurrence and metastasis is not uncommon and likely due to stimulation of angiogenesis immediately after TACE. Plasma VEGF levels are significantly elevated following TACE procedures, usually peaking 24 to 48 hours after treatment.

Sorafenib, a multikinase inhibitor, has been shown to increase survival in patients with advanced HCC, presumably due to its predominant and strong antiangiogenic activities thereby preventing tumor growth. However, despite its targeted approach, sorafenib is not without toxicities; consequently most patients are unable to remain on full dose throughout the course of their treatment.

Because of sorafenib's antiangiogenic properties, it has been suggested that sorafenib could be used in combination with TACE to counteract the post-TACE angiogenic release and therefore prevent or minimize the risk of tumor recurrence. The possible synergy between TACE and sorafenib has been tested in numerous clinical studies. Although the safety profile has been clearly established, the efficacy of this combination therapy has yet to be demonstrated. Several combination methods have been tested, i.e., continuously where sorafenib is administered before the first TACE and then continuously throughout the planned TACE treatments, or sequentially where sorafenib is administered after the completion of TACE (usually 4 days after). Here, the investigators postulate that the sequence of the combination could have a significant impact on patient outcomes. Specifically, the investigators hypothesize that the continuous method is superior to that of the sequential protocol because the presence of sorafenib before the first TACE will preempt the peak of angiogenesis from TACE. To that end, the investigators propose to measure VEGF levels serially in order to detect differences between the two methods.

Typ studiów

Interwencyjne

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Connecticut
      • New Haven, Connecticut, Stany Zjednoczone, 06510
        • Smilow Cancer Center

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Unresectable hepatocellular carcinoma with liver-predominant disease, or patients with hepatocellular carcinoma who refuse surgery. No more than 30% of the cohort should have macrovascular invasion and/or asymptomatic extrahepatic disease. Multifocal HCC is acceptable, no diffuse HCC with greater than 70% tumor burden.
  • Patient is at least 18 years of age.
  • ECOG performance status of 0-1.
  • Child-Pugh class of A or B (up to 7).
  • Adequate end-organ function as manifested by:
  • Absolute neutrophil count of ≥ 1500/mm3 and platelets ≥ 50,000/mm3
  • Creatinine ≤ 2.0 mg/dL
  • AST, ALT < 8X ULN
  • Total bilirubin of ≤ 3 mg/dL
  • Albumin > 2.0 g/dL
  • INR < 2.0
  • Leukocyte count > 3000 cells/mm3
  • Patients who have been treated with previous hepatic surgery, radiofrequency ablation (RFA), percutaneous ethanol injection (PEI), or cryoablation are eligible if target lesion(s) have not been treated and local therapy is completed at least 6 weeks prior to entry.
  • Patients with HBV are eligible if controlled with medication. Patients with HCV must have completed treatment with sustained viral response before being eligible for study.
  • Patients with asymptomatic HIV infection are not eligible.
  • Willingness of male and female subjects, who are not surgically sterile or post-menopausal, to use reliable methods of birth control for the duration of the study and for 30 days after the last dose of study medication.
  • Patient must have signed informed consent prior to registration on study.
  • Resolution of all acute toxic effects of any prior local treatment to CTC adverse event Grade 1 or 0.
  • At least one tumor lesion can be accurately measured in at least one dimension according to RECIST (Appendix D). The lesion has not been previously treated with local therapy (such as surgery, radiation therapy, RFA, PEI, or cryoablation) unless it has shown progression in the interim.

Exclusion Criteria:

  • Patients unable to swallow oral medications.
  • Prior embolization, systemic, or radiation therapy for HCC (liver), or patients who have taken sorafenib for greater than 2 weeks. Patients randomized to the sequential arm who started taking sorafenib within 2 weeks of the planned TACE procedure will have to stop sorafenib for 2 weeks before undergoing TACE. This will prevent a possible confounding effect of sorafenib on patients randomized to the sequential arm.
  • Tumor burden in the liver exceeding 70%.
  • Complete occlusion of the main portal venous system. Partial or branch portal vein occlusion allowed if without reversal of flow.
  • Ascites refractory to diuretic therapy (minimal or trace ascites on imaging is acceptable).
  • Previous or concurrent cancer that is distinct in primary site or histology from HCC, except cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (Ta, Tis, and T1). Any cancer curatively treated more than 3 years prior to entry is permitted.
  • Patients with clinically significant gastrointestinal bleeding within 30 days prior to study entry.
  • History of bleeding within the past 4 weeks (unless deemed by PI as clinically insignificant, as for example, a brief episode of epistaxis).
  • Any contraindication to doxorubicin or mitomycin-C administration.
  • Evidence of severe or uncontrolled systemic diseases.
  • Congestive cardiac failure greater than NYHA class 2 (Appendix E), myocardial infarction within 6 months, active coronary artery disease, cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers or digoxin, unstable angina, or laboratory or clinical finding that in the view of the principal investigator makes it undesirable for the patient to participate in the study.
  • Any prior history of hypertensive crisis or hypertensive encephalopathy.
  • History of stroke or transient ischemic attack within 6 months prior to study enrollment.
  • Inadequately controlled hypertension (defined as systolic blood pressure of > 150/100 mmHg on antihypertensive medications). Patients with treated hypertension are eligible. Patients noted to be hypertensive in our clinic, but with documented normal blood pressure in the office of their referring physician, close follow-up with their referring providers, and a plan for coordination between the referring physician and our team for management of blood pressure while on therapy, are eligible.
  • Significant vascular disease (e.g. aortic aneurysm, aortic dissection, peripheral vascular disease).
  • History of organ allograft
  • Presence of grade 2 or higher hepatic encephalopathy.
  • Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an additional experimental drug.
  • Evidence of bleeding diathesis or coagulopathy or on warfarin. Note: if a patient has been on Coumadin for a period of 1 month and has been stable, they may be accepted into the protocol.
  • Presence of clinically evident central nervous system or brain metastases.
  • Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1, or anticipation of need for major surgical procedure during the course of the study.
  • Pregnant (positive pregnancy test) or lactating.
  • Inability to comply with the study and/or follow-up procedures.
  • Life expectancy of less than 12 weeks.
  • Patients with concomitant HIV infection or AIDS-related serious acute or chronic illness.
  • Substance abuse, medical, psychological, or social conditions that may interfere with the patient's participation in the study or evaluation of study results.
  • Active clinically serious infections (greater than Grade 2)
  • Patients with obvious and/or symptomatic extrahepatic disease. Findings of uncertain significance, such as lung lesions less than 10 mm in diameter or enlarged periportal lymph nodes will not exclude patients.
  • Any contraindication to an arterial procedure such as impaired clotting tests (platelet count < 50,000/mm3 or prothrombin activity < 50%).
  • Any contraindication to sorafenib administration

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Group A- continuous schedule
Subjects with HCC randomized to group A
Patients assigned to Group A will begin sorafenib on a continuous schedule starting at 400mg BID from Cycle 1 Day 1, one week prior to cTACE treatment on Cycle 1 Day 8. After week 6, cTACE will be provided on demand (as needed, up to 4 treatments total in the first 4 cycles) at week 2 in subsequent cycles, and sorafenib will continue to be administered. Patients will be allowed to undergo dose adjustments of sorafenib as long as it remains above the ¼ dose (400mg QOD).
Aktywny komparator: Group B- sequential schedule
Subjects with HCC randomized to group B
Patients assigned to Group B will undergo cTACE up to 4 treatments within the first 4 cycles as needed prior to starting sorafenib. After it is determined that no further TACE treatment is necessary (via imaging and clinical assessment on follow-up), administration of sorafenib will begin on Day 1 of the following cycle. Dosing will begin at 400mg BID and maintained continuously provided no unmanageable toxicities develop, with follow-up assessments performed on week 6 of every 1-2 cycles as needed. Patients in Group B will also be allowed to undergo dose adjustments of sorafenib as long as it remains above the ¼ dose (400mg QOD).

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Tumor Response using Response Evaluation Criteria in Solid Tumors (RECIST)
Ramy czasowe: 54 weeks

RECIST criteria for tumor response:

  • Complete response - complete disappearance of all target lesions
  • Partial response - at least 30% decrease in the sum of the longest diameter (LD) of the target lesions, taking as a reference the baseline sum LD.
  • Stable disease - all other cases.
  • Progressive disease - at least a 20% increase in the sum of the LD of the target lesions, taking as a reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.
54 weeks
Tumor Response using mREcist if applicable
Ramy czasowe: 54 weeks

mRECIST criteria for tumor response:

  • Complete response -disappearance of any intratumoral arterial enhancement in all target lesions.
  • Partial response - at least a 30% decrease in the sum of diameters of viable (enhancement in the arterial phase) target lesions, taking as reference the baseline sum of the diameters of target lesions.
  • Stable disease - Any cases that do not qualify for either partial response or progressive disease.
  • Progressive disease - An increase of at least 20% in the sum of the diameters of viable (enhancing) target lesions, taking as reference the smallest sum of the diameters of viable (enhancing) target lesions recorded since treatment started.
54 weeks
EASL criteria for tumor response
Ramy czasowe: 54 weeks
  • Complete response - Complete disappearance of all viable tumoral area and no new lesions. No new lesions may evolve during a 4 week period after initial documentation of response.
  • Partial response - Greater than 50% reduction in viable tumoral area of all measurable lesions via uptake of contrast.
  • Stable disease - All other cases.
  • Progressive disease - Greater than or equal to 25% increase in tumoral area of one or more measurable lesions or the appearance of new lesions.
54 weeks

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Laboratory Evaluations: Vascular endothelial growth factor (VEGF) Correlations
Ramy czasowe: baseline and 54 Weeks

Plasma VEGF levels will be compared between the two study arms. VEGF-A, as well as VEGF-R1 and R2 concentrations will be obtained.

VEGF concentrations will also be correlated with tumor response of target lesions as determined by imaging assessments, and with overall survival.

baseline and 54 Weeks
Overall survival (OS)
Ramy czasowe: 54 weeks
Overall survival (OS) will be measured from the initiation of therapy until the date of death. OS will be assessed for patients treated with continuous sorafenib and cTACE and compared to those treated with sequential cTACE and sorafenib.
54 weeks

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Śledczy

  • Główny śledczy: Jeff Geschwind, Professor of Radiology and Biomedical Imaging

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 czerwca 2016

Zakończenie podstawowe (Oczekiwany)

1 czerwca 2020

Ukończenie studiów (Oczekiwany)

1 czerwca 2020

Daty rejestracji na studia

Pierwszy przesłany

6 września 2016

Pierwszy przesłany, który spełnia kryteria kontroli jakości

15 września 2016

Pierwszy wysłany (Oszacować)

20 września 2016

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

10 stycznia 2018

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

8 stycznia 2018

Ostatnia weryfikacja

1 stycznia 2018

Więcej informacji

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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