17-Dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG) in Treating Patients With an Advanced Solid Tumor or Lymphoma

Lymphoma Clinical Trial

Official title:

A Phase I Study Of 17-Dimethylaminoethylamino-17-demethoxygeldanamycin (17DMAG) With Evaluation Of Hsp90 Client Proteins In Subjects With Solid Tumors And Lymphomas

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00088868
• Other study ID #: 040218
• Secondary ID: 04-C-0218NCI-654
• Status: Completed
• Phase: Phase 1
• First received: August 4, 2004
• Last updated: March 14, 2012
• Start date: June 2004
• Est. completion date: December 2010

Study information

• Verified date: March 2012
• Source: National Institutes of Health Clinical Center (CC)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy, such as 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG), work in different ways to stop cancer cells from dividing so they stop growing or die.

PURPOSE: This phase I trial is studying the side effects and best dose of 17-DMAG in treating patients with an advanced solid tumor or lymphoma.

Description:

OBJECTIVES:

Primary

• Determine the maximum tolerated dose of 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG) in patients with an advanced malignant solid tumor or lymphoma.

• Determine the dose-limiting toxic effects and toxicity profile of this drug in these patients.

Secondary

• Compare the effects of this drug on heat shock protein 90 (Hsp90) client proteins when assayed in peripheral blood mononuclear cells (PBMC) vs tumor tissue from patients treated with this drug.

• Correlate disturbances in key signaling pathways with administration of this drug in these patients.

• Determine the dose that alters key proteins in the majority of patients treated with this drug.

• Correlate serum proteomic patterns with target interactions or DMAG clinical effects in patients treated with this drug.

• Determine the pharmacokinetics of this drug in these patients.

OUTLINE: This is a single-center, dose-escalation study.

Patients receive 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG) IV over 1-2 hour on days 1 and 4 or days 2 and 5 weekly for 4 weeks. Treatment repeats every 4 weeks in the absence of disease progression or unacceptable toxicity.

Cohorts of 1-6 patients receive escalating doses of 17-DMAG until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of up to 6 patients experience dose-limiting toxicity. Once the MTD is determined, 10 additional patients are treated at the MTD.

PROJECTED ACCRUAL: Approximately 40 patients will be accrued for this study within 2 years.

Other known NCT identifiers

• NCT00086008

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: December 2010
• Est. primary completion date: March 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed malignant solid tumor OR lymphoma

• Metastatic or unresectable disease

• Standard curative or palliative measures are not available OR are associated with minimal survival benefit

• No known brain metastases

• Treated brain metastases allowed provided they have been stable = 6 months without steroids or anti-seizure medications

PATIENT CHARACTERISTICS:

Age

• 18 and over

Performance status

• ECOG 0-2 OR

• Karnofsky 60-100%

Life expectancy

• More than 3 months

Hematopoietic

• Absolute neutrophil count = 1,500/mm^3

• Platelet count = 100,000/mm^3

• WBC = 3,000/mm^3

• Hemoglobin > 8 g/dL

Hepatic

• AST and ALT = 2 times upper limit of normal

• Bilirubin = 1.5 times normal

• PT and PTT = 1.5 times normal (unless due to the presence of lupus anticoagulant or stable anticoagulation)

Renal

• Creatinine normal OR

• Creatinine clearance = 60 mL/min

Cardiovascular

• No symptomatic congestive heart failure

• No unstable angina pectoris

• No orthostatic hypotension > grade 2 (requiring more than brief fluid replacement or other therapy OR with physiological consequences)

• No New York Heart Association class III or IV heart failure

• LVEF = 40% by MUGA

• QTc = 450 msec (470 msec for women)

• No congenital long QT syndrome

• No myocardial infarction within the past year

• No active ischemic heart disease within the past year

• No history of uncontrolled dysrhythmias

• No history of serious ventricular arrhythmia (ventricular fibrillation or ventricular tachycardia > 3 premature ventricular contractions in a row)

• Not requiring antiarrhythmic drugs

• No poorly controlled angina

• No left bundle branch block

Pulmonary

• No uncontrolled symptomatic pulmonary disease, including any of the following:

• Dyspnea off or on exertion

• Paroxysmal nocturnal dyspnea

• Severe chronic obstructive/restrictive pulmonary disease requiring daily chronic medications and oxygen

• Must not meet the Medicare criteria for home oxygen

• No sufficiently compromised pulmonary status as measured by baseline pulmonary function tests and DLCO

Other

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for 2 months after study participation

• No known HIV positivity

• No hyponatremia indicated by sodium < 130 mmol/L

• No known immunodeficiency syndromes

• No history of allergic reaction attributed to compounds of similar chemical or biological composition to 17-dimethylaminoethylamino-17-demethoxygeldanamycin (geldanamycin or 17-AAG)

• No concurrent uncontrolled illness

• No active or ongoing uncontrolled infection

• No psychiatric illness or social situation that would preclude study compliance

PRIOR CONCURRENT THERAPY:

Biologic therapy

• More than 4 weeks since prior biologic therapy and recovered

• No concurrent prophylactic growth factors

Chemotherapy

• More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin, 8 weeks for UCN-01) and recovered

Endocrine therapy

• See Disease Characteristics

• Concurrent hormonal therapy for prostate cancer allowed provided patient has metastatic disease that has progressed despite prior hormonal therapy

Radiotherapy

• More than 4 weeks since prior radiotherapy and recovered

• No prior radiotherapy that included the heart in the field (e.g., mantle radiotherapy)

Surgery

• At least 4 weeks since prior major surgery

Other

• At least 2 weeks since prior participation in a phase 0 study

• Concurrent bisphosphonates for any cancer allowed

• Concurrent preventative doses of aspirin or non-steroidal anti-inflammatory drugs allowed

• No concurrent drugs that may prolong QTc interval

• No concurrent full anticoagulation on a regular basis

• No concurrent prophylactic antiemetics

• No other concurrent investigational agents or therapies

• No other concurrent anticancer agents or therapies

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Lymphoma
• Small Intestine Cancer
• Unspecified Adult Solid Tumor, Protocol Specific

Intervention

Drug:
• alvespimycin hydrochloride

Locations

Country	Name	City	State
United States	Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office	Bethesda	Maryland

Sponsors (2)

Lead Sponsor	Collaborator
National Institutes of Health Clinical Center (CC)	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States,