Cisplatin and Everolimus in Treating Patients With Advanced Solid Tumors
Information source: Memorial Sloan Kettering Cancer Center
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Unspecified Adult Solid Tumor, Protocol Specific
Intervention: cisplatin (Drug); everolimus (Drug); gene expression analysis (Genetic); immunohistochemistry staining method (Other); laboratory biomarker analysis (Other); pharmacological study (Other); biopsy (Procedure)
Phase: Phase 1
Status: Completed
Sponsored by: Memorial Sloan Kettering Cancer Center Official(s) and/or principal investigator(s): Matthew G. Fury, MD, PhD, Principal Investigator, Affiliation: Memorial Sloan Kettering Cancer Center David G. Pfister, MD, Principal Investigator, Affiliation: Memorial Sloan Kettering Cancer Center
Summary
RATIONALE: Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the
growth of tumor cells, either by killing the cells or by stopping them from dividing.
Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for
cell growth. Everolimus may also help cisplatin work better by making tumor cells more
sensitive to the drug. Giving cisplatin together with everolimus may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of everolimus when
given together with cisplatin in treating patients with advanced solid tumors or recurrent
or metastatic solid tumors.
Clinical Details
Official title: A Phase I Study of Weekly Low-Dose Cisplatin Plus Escalating Doses of Oral RAD001(Everolimus) for Patients With Advanced Solid Tumors
Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Recommended phase II dose of everolimus
Secondary outcome: Pharmacokinetic profile of cisplatin and everolimusPharmacodynamic profile of cisplatin and everolimus
Detailed description:
OBJECTIVES:
Primary
- Determine the recommended phase II dose of everolimus when administered with low-dose
cisplatin in patients with advanced solid tumors.
Secondary
- Determine the safety and tolerability of this regimen in these patients.
- Describe the pharmacokinetics of this regimen in patients with advanced solid tumors.
- Assess the effects of this regimen on p53 and p21 immunohistochemistry assays of pre-
and post-treatment tumor biopsies from patients with recurrent or metastatic solid
tumors.
OUTLINE: This is a dose-escalation study of everolimus (part A) followed by a biological
marker study (part B).
- Part A (closed to accrual as of 1/2009): Patients receive cisplatin* IV over 30 minutes
on days 1, 8, and 15 and oral everolimus* once daily on days 1-21. Treatment repeats
every 28 days for up to 1 year in the absence of disease progression or unacceptable
toxicity.
Cohorts of 3-6 patients receive escalating doses of everolimus until the maximum tolerated
dose (MTD) is determined. The MTD is defined as the dose proceeding that at which 2 of 6
patients experience dose-limiting toxicity (DLT) during course 1. The recommended phase II
dose is defined as the dose at which 1 of 6 patients experience DLT during course 1.
Blood is drawn periodically on days 1 and 8 of course 1 for pharmacokinetic studies.
- NOTE: *Patients who have completed 5 courses of treatment and maintain stable disease
or better may continue treatment with everolimus alone or in combination with cisplatin
- Part B: Patients undergo biopsy of the primary tumor, metastatic deposit, or involved
lymph node. No more than 14 days later, patients receive everolimus at the recommended
phase II dose and cisplatin as in part A.
Patients undergo another tumor biopsy on day 15 of course 1, before receiving chemotherapy.
The pre- and post-therapy tissue is examined by immunochemistry and analyzed for p53 and p21
expression.
PROJECTED ACCRUAL: A total of 30 people will be accrued for this study.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
DISEASE CHARACTERISTICS:
- Histologically confirmed diagnosis of 1 of the following:
- Advanced solid tumor (part A)
- Confirmation by core biopsy or fine-needle aspiration allowed
- Solid tumor (part B)
- Recurrent or metastatic disease
- Easily accessible for biopsy
- Measurable disease
- No uncontrolled brain or leptomeningeal metastases
- No requirement for glucocorticoids
PATIENT CHARACTERISTICS:
- Karnofsky performance status 70-100%
- Absolute neutrophil count ≥ 1,500/mm³
- Platelet count ≥ 100,000/mm³
- Hemoglobin > 10 g/dL
- Bilirubin ≤ 1. 5 times upper limit of normal (ULN)
- AST and ALT ≤ 2. 5 times ULN (< 5 times ULN if liver metastases are present)
- Creatinine normal OR creatinine clearance ≥ 55 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for at least 3 months
after completion of study therapy
- No HIV positivity
- No peripheral neuropathy ≥ grade 2
- No hypertriglyceridemia ≥ grade 2
- No impaired gastrointestinal function or gastrointestinal disease that may alter the
absorption of everolimus, including any of the following:
- Ulcerative disease
- Uncontrolled nausea
- Vomiting
- Diarrhea
- Malabsorption syndrome
- Small bowel resection
- No other concurrent severe and/or uncontrolled medical disease that would compromise
study participation, including any of the following:
- Uncontrolled diabetes
- Unstable angina
- New York Heart Association class III or IV congestive heart failure
PRIOR CONCURRENT THERAPY:
- No more than 3 prior cytotoxic chemotherapy regimens for recurrent or metastatic
disease
- At least 4 weeks since prior major surgery and recovered
- At least 4 weeks since prior radiation therapy and recovered
- At least 4 weeks since prior systemic anticancer therapy and recovered
- At least 4 weeks since prior and no other concurrent investigational drugs
- No prior everolimus or other agents specifically targeting mTOR
- No prior radiation therapy to > 25% of the bone marrow
- No prior radiation therapy to the whole pelvis and/or brain
- No concurrent chronic steroid treatment (> 5 mg/day of prednisone)
- Concurrent low-dose steroid replacement regimens (≤ 5 mg/day of prednisone)
allowed
- No concurrent immunosuppressive agents
- No other concurrent anticancer agents
- No concurrent agents known to be strong inhibitors or inducers of isoenzyme CYP3A
Locations and Contacts
Memorial Sloan-Kettering Cancer Center, New York, New York 10065, United States
Additional Information
Clinical trial summary from the National Cancer Institute's PDQ® database
Starting date: November 2006
Last updated: May 22, 2015
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