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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 everolimus

Pharmacodynamic 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

Page last updated: August 23, 2015

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