UCN-01 and Carboplatin in Treating Patients With Advanced Solid Tumors

NCT00036777 | Completed Phase 1

• 6 other identifiers: NCI-2013-00042UMGCC 0143MSGCC-0143NCI-5533CDR0000069321U01CA069854
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

Phase I trial to study the effectiveness of combining UCN-01 with carboplatin in treating patients who have advanced solid tumors. UCN-01 may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining UCN-01 with carboplatin may kill more tumor cells.

Conditions

Unspecified Adult Solid Tumor, Protocol Specific

Outcome Measures

Primary Outcomes (1)

• Maximum tolerated dose of UCN-01 when combined with carboplatin determined by dose-limiting toxicities graded according to NCI Common Toxicity Criteria (CTC)

  21 days

Secondary Outcomes (3)

• Response rate

  Up to 3 years

• Survival

  From the date of first treatment until death or last follow up, assessed up to 3 years

• Pharmacokinetics parameters of UCN-01

  Prior to and at 0.5, 1, 2, and 3 hours after the start of the infusion and at 2, 4, 8, 24, 48 hours, and 7, and 21 days after the end of the infusion

Study Arms (1)

Treatment (carboplatin, 7-hydroxystaurosporine)

EXPERIMENTAL

Patients receive carboplatin IV over 1 hour followed by UCN-01 IV over 3 hours on day 1. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of carboplatin and UCN-01 until the MTD is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Drug: carboplatin; Drug: 7-hydroxystaurosporine; Other: pharmacological study

Interventions

carboplatin DRUG

Given IV

Also known as: Carboplat, CBDCA, JM-8, Paraplat, Paraplatin

Treatment (carboplatin, 7-hydroxystaurosporine)

7-hydroxystaurosporine DRUG

Given IV

Also known as: UCN-01

Treatment (carboplatin, 7-hydroxystaurosporine)

pharmacological study OTHER

Correlative studies

Also known as: pharmacological studies

Treatment (carboplatin, 7-hydroxystaurosporine)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must have histologically confirmed malignancy that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective
• At least 4 weeks since prior chemotherapy or radiation therapy, 6 weeks if the last regimen included BCNU or mitomycin C; include site/total dose for prior radiation exposure as needed (e.g., no more than 3000 cGy to fields including substantial marrow)
• ECOG performance status =\< 2 (Karnofsky \>= 60%)
• Life expectancy of greater than 12 weeks
• Leukocytes \>= 3,000/microl
• Absolute neutrophil count \>= 1,500/microl
• Platelets \>= 100,000/microl
• Total bilirubin within normal institutional limits
• AST(SGOT)/ALT(SGPT) \>= 2.5 X institutional upper limit of normal
• Creatinine within normal institutional limits OR creatinine clearance \>= 60 mL/min/1.73 m\^2 for patients with creatinine levels above institutional normal
• Women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
• Ability to understand and the willingness to sign a written informed consent document

You may not qualify if:

• Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier
• Patients may not be receiving any other investigational agents
• Patients with known brain metastases are eligible providing the brain metastases are, in the opinion of the site investigator, asymptomatic or clinically stable after treatment with surgery and/or radiation therapy; patients should not require steroids or antiseizure medications and should have fully recovered from all therapy; at least two weeks should elapse between completion of any treatment for brain metastases (surgery, CNS irradiation) and commencement of protocol therapy
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to UCN-01 or other agents used in study
• Because of cardiopulmonary toxicity seen in patients on other studies, patients with a symptomatic cardiac disease should be excluded; patients with a history of coronary artery disease or mediastinal radiation should undergo testing of ventricular function (cardiac echocardiogram, MUGA or equivalent) and are eligible if LVEF is \>= 45%; if there is a history of prior pulmonary disease then pulmonary function tests should be performed and patients are eligible if FEV1 \>= 1 liter
• Because UCN-01 may cause hyperglycemia, patients with insulin dependent diabetes mellitus should be excluded
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements
• Pregnant women are excluded from this; breastfeeding should be discontinued if the mother is treated with UCN-01
• HIV-positive patients receiving combination anti-retroviral therapy are excluded from the study
• Patients with a history of severe allergic reactions to cisplatin or carboplatin

Sponsors & Collaborators

• National Cancer Institute (NCI): lead

Study Sites (1)

University of Maryland Greenebaum Cancer Center

Baltimore, Maryland, 21201-1595, United States

Location

MeSH Terms

Interventions

Carboplatin; 7-hydroxystaurosporine

Intervention Hierarchy (Ancestors)

Coordination Complexes; Organic Chemicals

Study Officials

• Martin Edelman

  University of Maryland Greenebaum Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: NIH
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 13, 2002
• First Posted: January 27, 2003
• Study Start: March 1, 2002
• Primary Completion: October 1, 2004
• Last Updated: July 1, 2013

Record last verified: 2013-06

Locations

US (1)