Targeted Therapy in Treating Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia or Acute Myelogenous Leukemia

NCT01620216 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2021-11-04

Study results available
· View outcomes & findings →

Summary

This phase II trial studies how well targeted therapy works in treating patients with acute lymphoblastic leukemia or acute myelogenous leukemia that has come back after a period of improvement or does not respond to treatment. Testing patients' blood or bone marrow to find out if their type of cancer may be sensitive to a specific drug may help doctors choose more effective treatments. Dasatinib, sunitinib malate, sorafenib tosylate, ponatinib hydrochloride, pacritinib, ruxolitinib, and idelalisib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving targeted therapy based on cancer type may be an effective treatment for acute lymphoblastic leukemia or acute myelogenous leukemia.

Conditions

  • Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome
  • Chronic Myelomonocytic Leukemia
  • Recurrent Acute Lymphoblastic Leukemia
  • Recurrent Acute Myeloid Leukemia
  • Refractory Acute Lymphoblastic Leukemia
  • Refractory Acute Myeloid Leukemia

Interventions

OTHER

Antitumor Drug Screening Assay

Undergo pre clinical kinase inhibitor activity screening

DRUG

Dasatinib

Given PO

DRUG

Idelalisib

Given PO

OTHER

Laboratory Biomarker Analysis

Correlative studies

DRUG

Pacritinib

Given PO

OTHER

Pharmacological Study

Correlative studies

DRUG

Ponatinib

Given PO

DRUG

Ponatinib Hydrochloride

Given PO

DRUG

Ruxolitinib

Given PO

DRUG

Sorafenib

Given PO

DRUG

Sorafenib Tosylate

Given PO

DRUG

Sunitinib

Given PO

DRUG

Sunitinib Malate

Given PO

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Oregon Health and Science University

    collaborator OTHER
  • OHSU Knight Cancer Institute

    lead OTHER

Principal Investigators

  • Marc Loriaux · OHSU Knight Cancer Institute

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-11
Primary Completion
2017-04-25
Completion
2017-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01620216 on ClinicalTrials.gov