Alvocidib in Treating Patients With Locally Advanced or Metastatic Solid Tumors

National Cancer Institute (NCI)

Status and phase: Terminated; Phase 1

Conditions: Unspecified Adult Solid Tumor, Protocol Specific

Treatments: Other: pharmacological study; Other: laboratory biomarker analysis; Drug: alvocidib

Study type: Interventional

Funder types: NIH

Identifiers

NCT00112684

NCI-2009-00135 (Registry Identifier)

OSU-2005C0009

NCI-7204

U01CA076576 (U.S. NIH Grant/Contract)

OSU-04111

7204 (Other Identifier)

CDR0000429582

P30CA016058 (U.S. NIH Grant/Contract)

OSU 04111 (Other Identifier)

Details and patient eligibility

About

This phase I trial is studying the side effects and best dose of alvocidib in treating patients with locally advanced or metastatic solid tumors. Drugs used in chemotherapy, such as alvocidib, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Alvocidib may also stimulate the immune system in different ways and stop tumor cells from growing. It may also stop the growth of solid tumors by blocking blood flow to the tumor.

Full description

PRIMARY OBJECTIVES:

I. Determine the toxicity profile and dose-limiting toxicity of flavopiridol (alvocidib) in patients with locally advanced or metastatic solid tumors.

II. Determine the maximum tolerated dose of this drug in these patients.

SECONDARY OBJECTIVES:

I. Determine the pharmacokinetics and pharmacodynamics of this drug in these patients.

II. Determine the immunomodulatory effects of this drug in these patients. III. Determine pharmacogenomics of this drug, using peripheral blood mononuclear cells, in patients who experience clinical response.

OUTLINE: This is a pilot, dose-escalation study.

Patients receive alvocidib intravenously (IV) over 4½ hours once weekly in weeks 1-4. Treatment repeats every 6 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity. Patients achieving stable disease after 4 courses of therapy discontinue study treatment. Patients who achieve complete remission (CR) receive 1 additional course of therapy beyond documentation of CR. Cohorts of 3-6 patients receive escalating doses of alvocidib until the maximum tolerated dose (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. A total of 10 patients are treated at the MTD.

After completion of study treatment, patients are followed within 4 weeks.

Enrollment: 25 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically or cytologically confirmed solid tumor

  • Locally advanced or metastatic disease for which curative treatment does not exist or is no longer effective

• Measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral CT scan

  • No previously irradiated* measurable lesion unless lesion demonstrates progressive disease OR there are other measurable lesions outside the irradiated* field

  • The following are not considered measurable disease:

    • Bone lesions
    • Leptomeningeal disease
    • Ascites
    • Pleural or pericardial effusion
    • Lymphangitis cutis/pulmonis
    • Abdominal masses that are not confirmed and followed by imaging techniques
    • Cystic lesions

• No uncontrolled brain metastases

• Performance status - ECOG 0-1

• At least 6 months

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

• Platelet count ≥ 100,000/mm^3

• AST and ALT ≤ 2.5 times upper limit of normal (ULN)

• Bilirubin ≤ 1.5 times ULN

• Creatinine ≤ 1.5 times ULN

• No symptomatic congestive heart failure

• No unstable angina pectoris

• No uncontrolled cardiac arrhythmia

• No uncontrolled hypertension

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No history of allergic reaction attributed to compounds of similar chemical or biological composition to flavopiridol

• No ongoing or active infection

• No uncontrolled illness

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

• More than 12 weeks since prior hepatic arterial chemoembolization

• More than 4 weeks since prior systemic chemotherapy

• No prior flavopiridol

• See Disease Characteristics

• More than 12 weeks since prior radioactive metaiodobenzylguanidine (MIBG)

• More than 4 weeks since prior external beam radiotherapy

• Recovered from all prior tumor-specific therapy

• More than 4 weeks since prior investigational tumor-specific therapy

• Concurrent octreotide for control of carcinoid syndrome allowed

• No concurrent combination anti-retroviral therapy for HIV-positive patients

• No other concurrent tumor-specific therapy

• No other concurrent investigational therapy

• No other concurrent anticancer therapy

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 1 patient group

Treatment (chemotherapy, biological therapy)

Experimental group

Description:

Patients receive alvocidib IV over 4½ hours once weekly in weeks 1-4. Treatment repeats every 6 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Treatment:

Drug: alvocidib

Other: laboratory biomarker analysis

Other: pharmacological study