To Study the Effects of Addition of Mebendazole to Lenvatinib in Cirrhotics With Advanced Hepatocellular Carcinoma.

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ClinicalTrials.gov Identifier: NCT04443049

Recruitment Status : Recruiting

First Posted : June 23, 2020

Last Update Posted : September 3, 2020

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Sponsor:

Information provided by (Responsible Party):

Institute of Liver and Biliary Sciences, India

Study Description

Brief Summary:

Currently the available first line palliative therapy for advanced HCC is Sorafenib and Lenvatinib of which Lenvatinib is tolerated better. Unfortunately, patients tend to progress after few months of therapy. Therefore it is imperative, to do trials by combinative therapy to the available therapy for added survival benefits and quality of life with advanced HCC. In this regard, Mebendazole appears to be a good choice for drug repurposing as it has shown very promising results either alone or in combination with other therapies in tumors of GI origin and CNS tumors. With regard to HCC Mebendazole has been found to be effective in vitro system of HCC and preclinical models. However no clinical trials have been initiated till now. The key hallmark features of HCC include activation of MAPK and angiogenesis which in turn are targeted by RTK inhibitors such as Sorafenib and Lenvatinib. In this regard Mebendazole has broad range of action by not only inhibiting angiogenesis and pro-survival pathways of MAPK, but by also inhibiting the secretion of MMPs and Tubulin polymerization which can all be beneficial in tumor regression and prevention of chemo-resistance in HCC. Mounting of a strong immune response plays an important role in identification of tumor antigen and thereby clearing of tumors. While Mebendazole can modulate the tumor, the data is scant with respect to the role of the drug. Hence repurposing Mebendazole as a combinatorial therapy appears a promising approach and forms the basis of the present work. We hypothesize that combinatorial therapy of addition of mebendazole to lenvatinib will prove more beneficial than lenvatinib alone in increasing the overall survival of patients with advanced HCC. To prove the mechanistic effects of mebendazole on HCC, we will also conduct a animal study in preclinical mice model of HCC with the help of our animal house facility. The animal study will help us to understand the additional benefits from mebendazole and lenvatinib with objective evidence of liver biopsy which is not feasible in humans.

Condition or disease	Intervention/treatment	Phase
Hepatocellular Carcinoma Liver Cirrhosis	Drug: Lenvatinib Drug: Mebendazole Other: Placebo	Not Applicable

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Detailed Description:

(A) STUDY HYPOTHESIS

Mebendazole augments response of lenvatinib by synergistic response.
Addition of anti angiogenic drugs (lenvatinib and mebendazole) to hypoxic environment generated post locoregional therapy like TACE leads to more effective control of advanced HCC resulting in improvement in overall survival.

(B) AIM: To compare the efficacy of combination of mebendazole with lenvatinib in cirrhotics with advanced Hepatocellular Carcinoma.

Primary objective:

To compare the efficacy of combination of mebendazole with lenvatinib in improving the overall survival at 15 months in cirrhotics with advanced HCC.

Secondary objective:

To compare the progression free survival with combination therapy of mebendazole and lenvatinib in advanced Hepatocellular Carcinoma (HCC).
To compare the objective response rate (ORR), disease control rate (DCR) and clinical benefit rate (CBR) with combinative therapy of mebendazole and lenvatinib in advanced HCC.
To study therapy related adverse effects of mebendazole in cirrhotics.
To develop pre-clinical HCC animal model to prove the added efficacy of combination therapy.

(D)STUDY DESIGN Type of study - Single center, prospective, open label, randomized control study Study population - cirrhosis of liver of any etiology with advanced HCC undergoing at ILBS Study duration - 22 months from the date of approval of IEC Sample size - Considering mebendazole adds 2 months more to lenvatinib which offers 13 months overall survival, power of the study as 80 %, attrition rate as 30 %, alpha error of 5%, sample size will be 85 patients in each arm ( totally 170 patients).

(F) Methodology: Cirrhotics with advanced HCC proven by imaging and or biopsy or cytology, fulfilling the eligibility criteria will be enrolled in the study. They may undergo 1 or 2 sessions of locoregional therapy (TACE/ SBRT/RFA) if feasible. All patients will undergo complete physical examination, CBC, LFT, KFT, INR, AFP, PIVKAII, CEMRI/ CECT upper abdomen (Triple phase ), UGI endoscopy at baseline before randomization.

Randomization:

Those patients who are not feasible for locoregional therapy will be randomized at baseline. Those patients undergoing locoregional therapy will be randomized after 1 month of last locoregional therapy (patient may undergo maximum of two sessions of locoregional therapy before randomization). The response will be determined by m RECIST criteria before randomization. Those patients requiring further sessions of locoregional therapy beyond two sessions will not be randomized into study.

Patient will be then randomized to one of the two groups Arm I :Lenvatinib +Placebo( Lenvatinib will be given once a day(OD) orally at dose of 8 mg if body weight is < 60 kg and 12 mg if body weight is > 60 kg ) with placebo (Tab Mecovit) orally twice a day (BD) daily Arm II : Lenvatinib and mebendazole ( Lenvatinib will be given orally once a day (OD) at dose of 8 mg if body weight is < 60 kg and 12 mg if body weight is > 60 kg) and mebendazole will be given at dose of 100 mg orally twice a day (BD) daily

Follow-up Patients will be followed up with clinical events, CBC, LFT, KFT, INR, AFP, PIVKAII, CEMRI/ CECT upper abdomen (Triple phase ) at the end of 1 month, 3 months, 6 months, 9 months, 12 months and 15 months.

INVESTIGATIONS AND FOLLOW UP At Baseline (before therapy) and during follow up

Hematology- repeated at the end of 1, 3, 6, 9, 12, 15 months.

- CBC
Biochemistry - repeated at the end of 1, 3, 6, 9, 12, 15 months.
- Serum Electrolytes, Kidney function test
- Liver function test, INR
CTP and MELD scores
AFP, PIVKA II - repeated at the end of 1, 3, 6, 9, 12, 15 months.
UGIE at baseline
CEMRI / CECT upper abdomen - Triple phase - repeated at the end of 1, 3, 6, 9, 12, 15 months.
PET CT - if systemic spread suspected or else at the end of 6 and 15 months
Liver Biopsy/FNAC will be done in cases where its clinically indicated.

The pre-clinical model will be developed in mice, for which separate application will be submitted to the animal ethics committee of the institute.

Timeline of follow up

At the end of first month
Then every 3 months until 15 months after starting therapy

STATISTICAL ANALYSIS

Data will be reported as mean + SD
Categorical variables will be compared using the chi-square test or Fisher exact test
Normal continuous variables will be compared using the Student t test
Non normal continuous variables will be compared using the Mann-Whitney rank-sum test (unpaired data) or the Wilcoxon test (paired data).
Comparison between groups on quantitative variables will be analyzed by ANOVA
The actuarial probability of survival will be calculated by the Kaplan-Meier method and compared using the log-rank test
A Cox regression analysis will be performed to identify independent prognostic factors for survival.

Intervention: This Randomized Controlled trial will be conducted at Institute of Liver & Biliary SciencesLBS New Delhi between June 2020 and March 2022

Salvage therapy

TACE or TARE if progressive disease
Nivolilumab if the patient had a progressive disease at 6 months of therapy

Study Design

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Study Type :	Interventional (Clinical Trial)
Estimated Enrollment :	170 participants
Allocation:	Randomized
Intervention Model:	Parallel Assignment
Masking:	None (Open Label)
Primary Purpose:	Treatment
Official Title:	To Study the Effects of Addition of Mebendazole to Lenvatinib in Cirrhotics With Advanced Hepatocellular Carcinoma.
Actual Study Start Date :	July 10, 2020
Estimated Primary Completion Date :	June 19, 2022
Estimated Study Completion Date :	June 19, 2022

Resource links provided by the National Library of Medicine

MedlinePlus Genetics related topics: North American Indian childhood cirrhosis

Drug Information available for: Mebendazole Lenvatinib

U.S. FDA Resources

Arms and Interventions

Arm	Intervention/treatment
Active Comparator: Lenvatinib +Placebo Lenvatinib will be given once a day(OD) orally at dose of 8 mg if body weight is < 60 kg and 12 mg if body weight is > 60 kg ) with placebo (Tab Mecovit) orally twice a day (BD) daily	Drug: Lenvatinib Lenvatinib will be given once a day(OD) orally at dose of 8 mg if body weight is < 60 kg and 12 mg if body weight is > 60 kg Other: Placebo Placebo (Tab Mecovit) orally twice a day (BD) daily
Experimental: Lenvatinib and mebendazole Lenvatinib will be given orally once a day (OD) at dose of 8 mg if body weight is < 60 kg and 12 mg if body weight is > 60 kg) and mebendazole will be given at dose of 100 mg orally twice a day (BD) daily	Drug: Lenvatinib Lenvatinib will be given once a day(OD) orally at dose of 8 mg if body weight is < 60 kg and 12 mg if body weight is > 60 kg Drug: Mebendazole mebendazole will be given at dose of 100 mg orally twice a day (BD) daily

Outcome Measures

Primary Outcome Measures :

Overall survival in both groups [ Time Frame: 15 months ]
Death [ Time Frame: 2 year ]
Progressive disease requiring change of therapy in both groups [ Time Frame: 2 year ]

Secondary Outcome Measures :

Progressive disease requiring quitting therapy in both groups [ Time Frame: 2 year ]
Therapy related adverse effects in both groups [ Time Frame: 2 year ]
Worsening of performance status in both groups [ Time Frame: 2 year ]
Worsening of performance will be measured by Eastern Cooperative Oncology Group (ECOG) Criteria.
Decompensation of underlying cirrhosis in both groups [ Time Frame: 2 year ]
Barcelona-Clinic Liver Cancer (BCLC) staging classification will be used.

Eligibility Criteria

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Ages Eligible for Study:	18 Years to 70 Years (Adult, Older Adult)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Cirrhosis of Liver with HCC on imaging and/or biopsy or cytology
Child Pugh A, Child Pugh B < 8
Advanced HCC - as defined by BCLC - C
ECOG Performance Status 1-2
Adequately controlled blood pressure (BP) with up to 3 antihypertensive agents, defined as BP ≤150/90 millimeters of mercury (mmHg) at screening and no change in antihypertensive therapy within 1 week prior to commencement of intervention.
Valid Consent
Age 18-70 years

Exclusion Criteria:

Decompensated Cirrhosis
Child Pugh C, Child Pugh B > 7
HCC patients with a curative therapy (RFA/MWA or LT)
Prior systemic therapies (or) immunotherapy for HCC
ECOG Performance Status 3-4
Post Liver transplant HCC recurrence
Pregnancy

Contacts and Locations

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): NCT04443049

Contacts

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Contact: Dr Navin Kumar, MD	01146300000	navinktanvi10@gmail.com

Locations

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India
Institute of Liver & Biliary Sciences	Recruiting
New Delhi, Delhi, India, 110070
Contact: Dr Naveen Kumar, MD 01146300000 navinktanvi10@gmail.com

Sponsors and Collaborators

Institute of Liver and Biliary Sciences, India

More Information

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Responsible Party:	Institute of Liver and Biliary Sciences, India
ClinicalTrials.gov Identifier:	NCT04443049
Other Study ID Numbers:	ILBS-Cirrhosis-32
First Posted:	June 23, 2020 Key Record Dates
Last Update Posted:	September 3, 2020
Last Verified:	September 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD:	Undecided

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Studies a U.S. FDA-regulated Drug Product:	No
Studies a U.S. FDA-regulated Device Product:	No

Additional relevant MeSH terms:

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Carcinoma Carcinoma, Hepatocellular Liver Cirrhosis Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Adenocarcinoma Liver Neoplasms Digestive System Neoplasms Neoplasms by Site Digestive System Diseases Liver Diseases Mebendazole Piperazine	Piperazine citrate Lenvatinib DMP 777 Antineoplastic Agents Protein Kinase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Antinematodal Agents Anthelmintics Antiparasitic Agents Anti-Infective Agents Tubulin Modulators Antimitotic Agents Mitosis Modulators

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