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Drug-screening in AML at Relapse for Targeted Treatment

Not Applicable
Completed
Conditions
AML
Interventions
Diagnostic Test: Image-based ex-vivo drug screening platform (pharmacoscopy)
Registration Number
NCT05732688
Lead Sponsor
Insel Gruppe AG, University Hospital Bern
Brief Summary

This is a non-randomised clinical study investigating subsequent patients with specific AML treatment started between January 1, 2022 until December 31, 2022.

Patients with relapsing disease are planned to be analyzed in this study

Detailed Description

The standard treatment for young fit patients with acute myeloid leukemia (AML) is intensive chemotherapy followed by consolidation treatment with curative intent. Usually, two cycles of intensive chemotherapy are given, with subsequent consolidation treatment depending on the genetic risk-assessment of the patients as well as on the response to the induction treatment.

For elderly or unfit patients, such an intensive approach is not feasible, and palliative treatment must be considered. The standard first-line-treatment for such patients since more than a decade comprises repetitive cycles of a hypomethylating agent (either Azacitidine or Decitabine). The median progression free survival following these approaches in this population is between 4 and 8 months, with an overall-survival of up to 12 months. More recently, the addition of the Bcl-2 inhibitor Venetoclax to hypomethylating agents has led to a modest improvement both of progression-free and overall survival. However, overall survival in such patients usually does not exceed 14-16 months.

The laboratory of Prof. Berend Snijder, Institute of Molecular Systems Biology, at the ETH (Eidgenössische Technische Hochschule) Zurich has developed an image-based ex-vivo drug screening platform for patients with aggressive haematological malignancies, also called pharmacoscopy. Using such a technique, leukemic cells from a patient at relapse can be rapidly screened for sensitivity to single compounds. A drug score is calculated for each compound.

Starting in Q2/2021, the investigator at the Department of Medical Oncology, University Hospital Inselspital in Bern, collected experiences using such an approach. Having received information from the laboratory on top sensitivity of leukemic cells of a given patient to a specific drug, a process is initiated to try to obtain access to such off-label drugs.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Included are patients with AML at relapse treated at the Department of Medical Oncology at the University Hospital Inselspital in Bern.
  • Patients are not planned to undergo intensive reinduction treatment with subsequent allogeneic hematopoietic transplantation in a curative intent.
  • Patients have exhausted all standard therapeutic options and they must have no available licensed standard treatment for relapsed AML.
  • Written informed consent
Exclusion Criteria
  • Patients able to undergo intensive reinduction treatment with subsequent allogeneic hematopoietic transplantation in a curative intent
  • Patients have available standard therapeutic options

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
PharmacoscopyImage-based ex-vivo drug screening platform (pharmacoscopy)Leukemic cells from a patient at relapse can be screened for sensitivity to single compounds
Primary Outcome Measures
NameTimeMethod
Treatment with identified effective drug12 months

Percentage of patients with relapsing AML in which drug screening identifies a promising effective drug and in which such a treatment effectively is started

Secondary Outcome Measures
NameTimeMethod
Duration of response12 months

Duration of response of patients effectively treated with a drug identified by drug screening

Response rate of patients depending on the RBF (relative blast fraction) value12 months

Number of patients responding to their chosen therapy regimen in correlation to the RBF (relative blast fraction) value

Overall survival of patients depending on the RBF (relative blast fraction) value12 months

Overall survival of patients responding to their chosen therapy regimen in correlation to the RBF (relative blast fraction) value

Identification of effective drug12 months

Percentage of patients in which a promising drug can be identified using drug screening

Overall survival12 months

Overall survival of patients effectively being treated with a drug identified by drug screening.

Duration of response of patients depending on the RBF (relative blast fraction) value12 months

Duration of response in patients responding to their chosen therapy regimen in correlation to the RBF (relative blast fraction) value

Trial Locations

Locations (1)

Departement of Medical Oncology, University Hospital Berne

🇨🇭

Berne, Switzerland

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