Vorinostat and Gemcitabine in Treating Patients With Metastatic or Unresectable Solid Tumors

Completed · Phase 1

Conditions studied: Unspecified Adult Solid Tumor, Protocol Specific

In brief

This phase I trial is studying the side effects and best dose of vorinostat and gemcitabine in treating patients with metastatic or unresectable solid tumors. Drugs used in chemotherapy, such as vorinostat and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Vorinostat may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

Key facts

Study ID

NCT00243100

Run by

National Cancer Institute (NCI)

People needed

21

Starts

2005-11-01

Last updated by the study team

2013-12-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ECOG 0-2 OR Karnofsky 60-100%
• AST and ALT =< 2.5 times ULN
• Bilirubin =< 1.5 times upper limit of normal (ULN)
• Platelet count >= 100,000/mm3
• Absolute neutrophil count >= 1,500/mm3
• Creatinine normal OR creatinine clearance ≥ 60 mL/min
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• Any number and type of prior chemotherapies are allowed including prior use of gemcitabine chemotherapy. A washout phase of at least 2 weeks since use of prior chemotherapy or radiation therapy, 6 weeks if the last regimen included nitrosoureas or mitomycin C, is required.
• Patients must have histologically confirmed epithelial malignancy that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective.
• Ability to understand and the willingness to sign a written informed consent document.
• Patients must have at least one measurable lesion as per the RECIST Criteria that can be accurately measured in at least one dimension, with minimum lesion size equal to or more than twice the slice thickness of the imaging study used.

You may not qualify if…

• No symptomatic congestive heart failure
• No cardiac arrhythmia
• No ongoing or active infection
• No psychiatric illness or social situation that would preclude study compliance
• No history of allergy, significant side effects, or poor tolerance to gemcitabine
• No history of allergic reaction attributed to compounds of similar chemical or biological composition to vorinostat (SAHA)
• At least 2 weeks since prior radiotherapy
• Recovered from prior therapy
• No concurrent combination antiretroviral therapy for HIV-positive patients
• No other uncontrolled illness
• More than 2 weeks since prior valproic acid
• No other concurrent investigational drugs
• No other concurrent anticancer therapy
• Patients with known brain metastases are excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.

Where it is running

• M D Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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