Efficacy and Safety Doxorubicin Transdrug Study in Patients Suffering From Advanced Hepatocellular Carcinoma (ReLive)
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| ClinicalTrials.gov Identifier: NCT01655693 |
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Recruitment Status :
Completed
First Posted : August 2, 2012
Results First Posted : June 2, 2021
Last Update Posted : June 2, 2021
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Sponsor:
Valerio Therapeutics
Information provided by (Responsible Party):
Valerio Therapeutics
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Brief Summary:
The purpose of this phase III study is to determine whether Doxorubicin Transdrug (DT) is effective in the treatment of patients suffering from advanced Hepatocellular Carcinoma (HCC) after failure or intolerance to Sorafenib. Patients with HCC with or without cirrhosis and with good liver functions are eligible. Only those who can not benefit from treatment for which efficacy is demonstrated are eligible.
These patients are usually proposed either best standard of care (BSC) or participation to clinical trials. Patients eligible for the RELIVE study will receive either DT at 20 mg/m2 or DT at 30 mg/m2 or the BSC.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Carcinoma, Hepatocellular | Drug: Doxorubicin 20 mg/m2 Drug: Doxorubicin 30 mg/m2 Drug: Best Standard of Care | Phase 3 |
Doxorubicin-Transdrug™ (DT) is a nanoparticle formulation of doxorubicin.In in vitro and in vivo models, DT was shown to overcome the multidrug resistance (MDR) and to be more effective than doxorubicin on both sensitive and resistant tumour models and in particular in the X/myc bi-transgenic MDR murine model of HCC.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 397 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Multicentre, Randomised, Controlled, Open-label Study Comparing the Efficacy and Safety of Doxorubicin Transdrug™ to Best Standard of Care in Patients With Advanced Hepatocellular Carcinoma. ReLive Study. |
| Actual Study Start Date : | June 2012 |
| Actual Primary Completion Date : | May 2017 |
| Actual Study Completion Date : | May 2019 |
Resource links provided by the National Library of Medicine
| Arm | Intervention/treatment |
|---|---|
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Experimental: Doxorubicin Transdrug (DT) at 20 mg/m2
DT will be infused over 6 hours through the intravenous (IV) route at dose of 20 mg/m2 on Day 1 and will be repeated every 4 weeks until disease progression or unacceptable toxicity
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Drug: Doxorubicin 20 mg/m2
Other Name: Doxorubicin Transdrug (DT) at 20 mg/m2 |
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Experimental: Doxorubicin Transdrug (DT) at 30 mg/m2
DT will be infused over 6 hours through the IV route at dose of 30 mg/m2 on Day 1 and will be repeated every 4 weeks until disease progression or unacceptable toxicity
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Drug: Doxorubicin 30 mg/m2
Other Name: Doxorubicin Transdrug (DT) at 30 mg/m2 |
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Active Comparator: Best Standard of Care
Patients randomized in the control group will receive treatment according to the investigator's choice, until disease progression or unacceptable toxicity
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Drug: Best Standard of Care
Other Name: BSC |
Primary Outcome Measures :
- Overall Survival (OS) [ Time Frame: Time from date of randomization to the date of death from any cause with initial assessment up to 24 months and follow-up assessment up to 45 months. ]OS is defined as the time from date of randomization to the date of death from any cause.
Secondary Outcome Measures :
- Progression-free Survival (PFS) [ Time Frame: Time from date of randomization to date of first documented progression or death from any cause, which ever came first, assessed up to 20 months. ]PFS is defined as time from the date of randomisation to the date of the first documented progression or death from any cause. PFS determined by independent radiological review according to Response Evaluation Criteria In Solid Tumour (RECIST) 1.1 is determine by at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline if that is the smallest on study). In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions is considered progression.
- Objective Response Rate (ORR) [ Time Frame: Time from date of first treatment cycle to date of last cycle of treatment for the full duration of study treatment up to 24 months. ]ORR is defined as percent of patients whose best overall response is complete response (CR) or partial response (PR) during the study treatment period and based on the evaluation of independent radiological review according to RECIST 1.1 for target lesions and assessed by MRI: CR is disappearance of all targets extra nodal lesions and the regression of all nodal lesions to < 10 mm; PR is at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters; stable disease is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease (PD), taking as reference the smallest sum of diameters while on study. PD is at least a 20% increase in the sum of diameters of target lesions, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions is considered progression.
Other Outcome Measures:
- Number of Participants Experiencing Treatment Emergent Adverse Events (TEAEs) Considered Related to Treatment Categorized by Severity, Withdrawal From Study, or Death [ Time Frame: Time from date of initial treatment to date of death, disease progression, or participant withdrawal from the study. ]The number of participants experiencing TEAEs considered related to treatment and categorized by severity of all related TEAEs according to National Cancer Institute/Common Toxicity Criteria (NCI-CTCAE) v4.0 and resulting in patient withdrawal from study or death.
- Number of Participants With Cardiovascular and Respiratory Events Related to Study Drug [ Time Frame: Time from date of initial treatment to date of death, disease progression, or patient withdrawal from the study. ]The number of participants with cardiovascular and respiratory adverse events (AEs) were assessed according to National Cancer Institute (NCI)-Common Terminology Criteria for Adverse Events (CTCAE) criteria version 4.0, using the Medical Dictionary for Regulatory Activities (MedDRA). The AE numbers reported are those considered related to treatment. Related AEs are those that are judged unlikely, possibly, probably or definitely related to the study or study drug by the investigator.
- Number of Participants Experiencing a Reduction of Oxygen Saturation (SaO2) During and After Doxorubicin Transdrug (DT) Infusion [ Time Frame: Time from start of infusion to resolution of reduction in oxygen saturation. ]Number of participants experiencing an SaO2 reduction defined as a decrease =< 90% during or after DT infusion until resolution to =>93%. Participants had continuous monitoring of SaO2 saturation with pulse oximeter during 6 hour infusion and up to 24 hour after infusion start. SaO2 measures the amount of oxygen (in percent) bound to hemoglobin in red blood cells. SaO2 saturation was only monitored and reported in the DT infusion group. Reduction in SaO2 could result in modify DT dosing regimen. Decreases in SaO2 are a known and expected occurrence with DT infusions, and close monitoring of SaO2 was specified by the protocol to protect patients from potential respiratory distress during infusions.
- Number of Participants With Clinically Significant Abnormal Change in Respiratory Function [ Time Frame: Time from baseline assessment to time of death, disease progression, or withdrawal of patient from the study. ]Number of participants with any clinically significant abnormal change in respiratory function test over the study to include carbon monoxide diffusing capacity to measure lung function, forced expiratory volume in 1 second to measure ability to expel air from your lungs, total lung capacity to measure total amount of air in the lungs after taking the deepest breath possible, and vital capacity to measure the greatest volume of air that can be expelled from the lungs after taking the deepest breath possible. Clinically significant abnormal changes in respiratory function was determined by the investigator.
- Number of Participants Experiencing Clinically Significant Abnormal Electrocardiogram (ECG) Changes From Baseline [ Time Frame: Time from baseline assessment to time of death, disease progression, or withdrawal of patient from the study. ]Number of participants experiencing clinically significant abnormal ECG changes from baseline over the course of the study. ECG were completed every month before each infusion. ECG will detect changes in heart rhythm. Clinically significant abnormal changes in ECG were determined by the investigator.
- Number of Participants Experiencing Clinically Significant Changes in Left Ventricular Ejection Fraction (LVEF) and the Severity of the Event [ Time Frame: Time from baseline assessment to time of death, disease progression, or withdrawal of patient from the study. ]Number of participants that experienced a change from baseline in LVEF with severity of LVEF noted as follows: Normal: 100 - 50%, 0 - 9% drop from baseline resting ejection fraction (EF), Grade 2 = 50 - 40%, 10 - 19% drop from baseline resting EF; Grade 3 = 39 - 20%, >20% drop from baseline; Grade 4 = <20%. LVEF was monitored every other month. LVEF measures how much blood the left ventricle of the heart pumps out with each contraction and is used to assess the severity of left ventricle dysfunction in the heart. Clinical significance changes were determined by the investigator.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Male or non-pregnant, non-breast feeding female;
- Aged ≥ 18 years;
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Patient with:
- advanced HCC (BCLC-C according to BCLC staging classification) having progressed under Sorafenib therapy or intolerant to Sorafenib, or;
- intermediate HCC (BCLC-B) non eligible or non responders to transarterial chemoembolization (TACE), and having progressed under or intolerant to Sorafenib therapy
- Patients with porta hepatis lymph nodes, extrahepatic metastases, or portal/suprahepatic vein thrombosis without extension in inferior/superior vena cava, are eligible;
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HCC diagnosed according to the American Association for Study of Liver Diseases (AASLD) and/or European Association for the Study of the Liver (EASL) criteria:
- Radiological Criteria applicable in cirrhotic liver:
- Nodule ≥ 10 mm: one imaging technique among MRI and CT-scan showing typical appearances for HCC defined as arterial enhancement and rapid washout in portal venous or delayed phase;
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If appearance not typical for HCC on initial imaging: second contrast enhanced study (CT or MRI) showing typical appearances for HCC defined as arterial enhancement and rapid wash-out in portal venous or delayed phase;
- And/Or cyto-histology criteria (e.g. in case of atypical lesions for HCC at imaging, absence of cirrhosis);
- Without cirrhosis or with a non decompensated cirrhosis (Child-Pugh score from A5 to B7 included);
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1;
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Laboratory tests as follows:
- Platelets ≥ 50,000 /mm3
- Neutrophil count ≥ 1000/mm3
- Hemoglobin ≥ 10g/dL
- Serum transaminases < 5 upper limit normal (ULN) (NCI/common toxicity criteria (CTC) grades 0, 1, or 2)
- Alkaline phosphatases < 5 ULN (NCI/CTC grades 0, 1, or 2)
- Serum bilirubin < 35 micromolar (µM)/L (or 2.0 mg/dL);
- Signed and dated written informed consent form.
Exclusion Criteria:
- Cirrhosis with a Child-Pugh score B8-C15;
- Untreated chronic hepatitis B;
- Patients eligible for curative treatments (transplantation, surgical resection, percutaneous treatment);
- Patients eligible for palliative treatments with demonstrated efficacy: TACE, Sorafenib; Patients who failed to Sorafenib treatment or intolerant to sorafenib are eligible and can be included if Sorafenib has been stopped at least 2 weeks before randomization;
- Prior history of malignancy with the exception of adequately treated basal cell carcinoma or in situ cervical cancer in complete remission since five years at least;
- HCC developed on transplanted liver;
- HIV infection;
- Risk of variceal bleeding;
- Oxygen saturation (SaO2) < 95%;
- Presence of a significant acute or chronic respiratory disease defined as NCI/CTCAE > grade 2;
- Presence of recent (< 6 months) or current cardiac failure (class III or IV New York Heart Association (NYHA) classification), recent (< 6 months) acute coronary syndrome, clinically significant ECG abnormalities or recent (less than 6 months) acute vascular diseases (stroke, myocardial infarction (MI)…);
- Prior cumulative dose of 300 mg/m² of doxorubicin or equivalent;
- Patients currently treated with immunosuppressive agents that cannot be stopped;
- Patients whose medical or surgical conditions are unstable and may not allow the study completion or compliance, and specially patients with uncontrolled diabetes;
- Uncontrolled systemic infection;
- Patients with a life expectancy of less than 2 months;
- Patients who have received an experimental drug in another clinical trial in the last 30 days prior to randomization in the present clinical trial;
- Women of child-bearing age who are unwilling or unable to use an effective contraception method during the study treatment period and for 6 months after the last administration of study drug, and their male partner(s) refusing to use a condom (if applicable);
- Men who are unwilling or unable to use a condom during the study treatment period and for 6 months after the last administration of study drug, and their female partner(s) refusing to use one of the appropriate effective contraception methods (if applicable);
- Patients unwilling or unable to comply with protocol requirements and scheduled visits.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01655693
Locations
Show 70 study locations
Sponsors and Collaborators
Valerio Therapeutics
Investigators
| Principal Investigator: | Philippe Merle, MD | Croix-Rousse Hospital - Lyon-France |
Study Documents (Full-Text)
Documents provided by Valerio Therapeutics:
Documents provided by Valerio Therapeutics:
Study Protocol and Statistical Analysis Plan [PDF] July 27, 2017
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Valerio Therapeutics |
| ClinicalTrials.gov Identifier: | NCT01655693 |
| Other Study ID Numbers: |
BA2011/03/04 2011-002843-92 ( EudraCT Number ) |
| First Posted: | August 2, 2012 Key Record Dates |
| Results First Posted: | June 2, 2021 |
| Last Update Posted: | June 2, 2021 |
| Last Verified: | May 2021 |
Keywords provided by Valerio Therapeutics:
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Intermediate/advanced hepatocellular carcinoma After failure or intolerance to Sorafenib. |
Additional relevant MeSH terms:
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Carcinoma Carcinoma, Hepatocellular Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Adenocarcinoma Liver Neoplasms Digestive System Neoplasms Neoplasms by Site Digestive System Diseases |
Liver Diseases Doxorubicin Liposomal doxorubicin Antibiotics, Antineoplastic Antineoplastic Agents Topoisomerase II Inhibitors Topoisomerase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |