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Clinical Trials/NCT02551718
NCT02551718
Completed
N/A

Individualized Treatment for Relapsed/Refractory Acute Leukemia Based on Chemosensitivity and Genomics/Gene Expression Data

University of Washington1 site in 1 country34 target enrollmentSeptember 11, 2015

Overview

Phase
N/A
Intervention
Chemosensitivity Assay
Conditions
Recurrent Acute Leukemia of Ambiguous Lineage
Sponsor
University of Washington
Enrollment
34
Locations
1
Primary Endpoint
Percentage of Patients we Are Able to Test and Initiate Treatment Within a 21 Day Period
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This pilot clinical trial studies the feasibility of choosing treatment based on a high throughput ex vivo drug sensitivity assay in combination with mutation analysis for patients with acute leukemia that has returned after a period of improvement (relapsed) or does not respond to treatment (refractory). A high throughput screening assay tests many different drugs individually or in combination that kill leukemia cells in tiny chambers at the same time. High throughput drug sensitivity assay and mutation analysis may help guide the choice most effective for an individual's acute leukemia.

Detailed Description

PRIMARY OBJECTIVES: I. To test patient cells in a high throughput assay against individual drugs and drug combinations within 21 days to enable optimal choice of drug combinations for therapy. II. To test gene expression that reveals activation of druggable pathways or mutations in genes that confer susceptibility to specific agents may also be considered in choice of treatment. SECONDARY OBJECTIVE: I. To evaluate the response to the chosen therapy. OUTLINE: Leukemia cells obtained from blood or bone marrow are analyzed for sensitivity to both individual drugs and drug combinations via high throughput chemotherapy sensitivity assay and next generation sequencing assays. Doctors will then recommend chemotherapy regimens based on the results. After completion of the chemotherapy regimen, patients are followed up at 2-4 weeks for response, and then every 3 months for 2 years for duration of response and survival.

Registry
clinicaltrials.gov
Start Date
September 11, 2015
End Date
May 13, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mary-Beth Percival

Assistant Professor, Division of Hematology

University of Washington

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of acute leukemia by World Health Organization (WHO) criteria (e.g.-acute myeloid leukemia, acute lymphoblastic leukemia, acute leukemia of ambiguous origin)
  • Relapsed after or refractory to prior treatment with at least two regimens or lines of treatment
  • Prior failure of at least one regimen or line of treatment, with poor cytogenetic or other risk factors, and ineligible for other clinical trials
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 - 3
  • Expectation that we can obtain about 10 million blasts from blood and/or marrow (e.g., circulating blast count of 5,000 or greater or cellular marrow with greater than or equal to 20% blasts)
  • Bilirubin =\< 1.5 x upper limit of normal (ULN) unless elevation is thought to be due to Gilbert's syndrome, hemolysis, or hepatic infiltration by the hematologic malignancy
  • Serum glutamic oxaloacetic transaminase (SGOT) (aspartate aminotransferase \[AST\]) and serum glutamate pyruvate transaminase (SPGT) (alanine aminotransferase \[ALT\]) =\< 2.5 x ULN, unless elevation is thought to be due to hepatic infiltration by the hematologic malignancy
  • Alkaline phosphatase =\< 2.5 x ULN, unless elevation is thought to be due to hepatic infiltration by the hematologic malignancy
  • Serum creatinine =\< 2.0 mg/dL
  • Informed consent

Exclusion Criteria

  • No other active cancer that requires systemic chemotherapy or radiation
  • Active systemic fungal, bacterial, viral or other infection, unless disease is under treatment with antimicrobials and considered controlled in the opinion of the investigator
  • Significant organ compromise that will increase risk of toxicity or mortality
  • Pregnancy or lactation

Arms & Interventions

Treatment (chemosensitivity testing, chemotherapy)

Leukemia cells purified from blood or bone marrow samples are analyzed for sensitivity to individual drugs and drug combination and by next generation sequencing.

Intervention: Chemosensitivity Assay

Treatment (chemosensitivity testing, chemotherapy)

Leukemia cells purified from blood or bone marrow samples are analyzed for sensitivity to individual drugs and drug combination and by next generation sequencing.

Intervention: Cytology Specimen Collection Procedure

Treatment (chemosensitivity testing, chemotherapy)

Leukemia cells purified from blood or bone marrow samples are analyzed for sensitivity to individual drugs and drug combination and by next generation sequencing.

Intervention: Gene Expression Analysis

Treatment (chemosensitivity testing, chemotherapy)

Leukemia cells purified from blood or bone marrow samples are analyzed for sensitivity to individual drugs and drug combination and by next generation sequencing.

Intervention: Genetic Variation Analysis

Treatment (chemosensitivity testing, chemotherapy)

Leukemia cells purified from blood or bone marrow samples are analyzed for sensitivity to individual drugs and drug combination and by next generation sequencing.

Intervention: In Vitro Sensitivity-Directed Chemotherapy

Outcomes

Primary Outcomes

Percentage of Patients we Are Able to Test and Initiate Treatment Within a 21 Day Period

Time Frame: Up to 21 days

The study will be considered successful (feasibility demonstrated) if it is possible to choose and initiate a combination drug regimen within 21 days in 9 out of 15 patients. With that outcome, there would be 90% confidence that the true feasibility rate is at least 40%.

Secondary Outcomes

  • Rate of Complete Remission(Up to 2 years)
  • Survival(Up to 2 years)

Study Sites (1)

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