Adding Everolimus to standard treatment for gallbladder cancer
A Randomized Controlled, Open Labeled, Two Arm, Study of Addition of Everolimus to Standard of Care in Carcinoma Gallbladder
This study is testing if adding a drug called Everolimus to regular treatment can help people with advanced gallbladder cancer live longer and feel better.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Enrollment | 56 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | All |
| Sponsor | Banaras Hindu University Academic / other |
| Drugs / interventions | Chemotherapy, Immunotherapy, Radiation |
| Locations | 1 site (Varanasi, Uttar Pradesh) |
| Trial ID | NCT05833815 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of adding Everolimus, an mTOR inhibitor, to the standard treatment regimen for patients with gallbladder cancer. The study focuses on patients with stage III inoperable or stage IV metastatic gallbladder carcinoma who have not received prior treatment. By combining Everolimus with standard chemotherapy, the trial aims to improve overall survival rates in this aggressive cancer type. The research employs a phased approach, assessing both safety and efficacy in a controlled environment.
Who should consider this trial
Good fit: Ideal candidates include individuals with stage III inoperable or stage IV metastatic gallbladder cancer who have not received prior treatment.
Not a fit: Patients with earlier-stage gallbladder cancer or those who have previously undergone treatment for metastatic disease may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve survival rates for patients with advanced gallbladder cancer.
How similar studies have performed: While there have been studies exploring mTOR inhibitors in various cancers, the specific combination with standard care for gallbladder cancer is relatively novel and untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Histological proof of cancer with stage III inoperable or Stage IV metastatic disease without any prior treatment. * Patients with histologic proof of metastatic gallbladder carcinoma who have not had previous treatment for metastatic disease or who received gemcitabine/capecitabine with or without platinum\>= 6 months ago as part of adjuvant therapy * Absolute neutrophil count (ANC) \>= 1500/uL * Platelet (PLT) \>= 100,000/uL * Total bilirubin =\< 3mg/dl for gemcitabine and any value for Capecitabine * Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =\< 2.5 x upper limit of normal (ULN) (=\< 5x ULN in patients with liver metastases) * Creatinine =\< 1.5 x Institutional ULN * Alkaline phosphatase =\< 5 x Institutional ULN * Haemoglobin (Hgb) \>= 8.0 g/dL * International normalized ratio (INR) and Partial thromboplastin time (PTT) =\< 3.0 x ULN (anticoagulation is allowed if target INR =\< 3.0 x ULN on a stable dose of warfarin or on a stable dose of low-molecular-weight \[LMW\] heparin for \> 2 weeks at time of registration) * Fasting serum glucose \< 1.5 x ULN * Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0, 1 or 2 * Ability to provide informed consent * Willingness to return for follow up * Life expectancy \>= 12 weeks * Women of childbearing potential only: Negative serum pregnancy test done =\< 7 days prior to registration. Exclusion Criteria: * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements * Clinically significant cardiac disease, especially history of myocardial infarction =\< 6 months, or congestive heart failure (New York Heart Association \[NYHA\] classification III or IV) requiring use of ongoing maintenance therapy for life-threatening ventricular arrhythmias * Patients taking strong inhibitors or inducers of CYP3A4 * Prior therapy with everolimus * Any of the following prior therapies: * Chemotherapy =\< 4 weeks prior to registration * Immunotherapy =\< 4 weeks prior to registration * Biological therapy =\< 4 weeks prior to registration * Radiation therapy =\< 4 weeks prior to registration * Radiation to \> 25% of bone marrow prior to registration * Failure to fully recover from acute, reversible effects of prior chemotherapy regardless of interval since last treatment * CNS metastases brain or leptomeningeal metastases that are not stable for at least 4 weeks prior to registration based on imaging, clinical assessment, and use of steroids * Pregnant women * Nursing women * Men or women of childbearing potential who are unwilling to employ adequate contraception * Other concurrent chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens * Immunocompromised patients (other than that related to the use of corticosteroids) including patients known to be human immunodeficiency virus (HIV) positive * Current active other malignancy, Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of everolimus (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection) * Severely impaired lung function (i.e., forced expiratory volume in one second \[FEV1\] \< 1 liter) * Received immunization with attenuated live vaccines =\< 7 days prior to study entry or during study period; close contact with those who have received attenuated live vaccines should be avoided during treatment with everolimus; examples of live vaccines include intranasal influenza, measles, mumps, rubella, oral polio, BCG, yellow fever, varicella and TY21a typhoid, SARS CoV2 vaccines * Liver disease such as cirrhosis or severe hepatic impairment (Child-Pugh class C); A detailed assessment of Hepatitis B/C medical history and risk factors will be done at screening for all patients; hepatitis B virus (HBV) deoxyribonucleic acid (DNA) and hepatitis C virus (HCV) ribonucleic acid (RNA) polymerase chain reaction (PCR) testing are required at screening for all patients with a positive medical history based on risk factors and/or confirmation of prior HBV/HCV infection.
Where this trial is running
Varanasi, Uttar Pradesh
- Banaras Hindu University — Varanasi, Uttar Pradesh, India (Recruiting)
Study contacts
- Study coordinator: Manoj Pandey
- Email: mpandey66@bhu.ac.in
- Phone: +91-542-2369332
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.