SAL-AML-REG-BIORecruiting

Clinical Registry for Recording Disease Progression and Collecting Biological Samples from Patients with Acute Myeloid Leukemia (AML) by the Leukemia Study Group (SAL)

Gender
Women and men
Age
18 years and older
Trial type
Observational
Line of therapy
all
Phase

What is this trial about?

Acute myeloid leukemia (AML) requires intensive and often complex treatment, with treatment approaches and chances of cure varying depending on genetic alterations and the course of the disease. The goal of the SAL study is to establish a registry of patients with AML. As comprehensive a set of medical data as possible regarding disease characteristics and progression will be collected to advance our understanding of the disease and improve treatment options. Women and men aged 18 and older who have AML are eligible to participate. Patients with a specific form of AML, known as promyelocytic leukemia (APL), may also participate in the study.

Trial flow

Requirements

Diagnosis: Acute myeloid leukaemia (AML); acute promyelocytic leukaemia (APL)

Age: 18 years and older

Line of therapy: Unabhängig von Therapielinie

Key inclusion criteria: Any stage of the disease, any type of treatment, no restrictions on therapy.

Allocation

Einarmige Studie

Treatment

Registry and Biomaterial Database Documentation of disease progression and collection of samples.

Follow-up

120 months

Detailed description

Acute leukemias are rare but rapidly progressing, aggressive forms of cancer that arise from immature white blood cells or bone marrow cells and usually spread very quickly. The malignant leukemia cells develop in the bone marrow and displace the healthy bone marrow, preventing the production of sufficient functional blood cells. In cases of this disease, patients frequently experience infections, bleeding, reduced performance, and shortness of breath. In acute myeloid leukemia (AML), the precursors of the so-called myeloid cell line of white blood cells (leukocytes) are altered.

AML is classified into different subtypes based on various genetic changes in the leukemia cells. By closely examining these changes, treatment can be better tailored to the individual patient to make the therapy as targeted and effective as possible.

The goal of this registry study is to collect various data from patients with acute myeloid leukemia (AML) in order to gain a better understanding of the disease. To this end, data on diagnosis, therapy, disease progression, and treatment success will be collected over a period of up to 10 years. In addition, tissue and blood samples will be collected from the patients. This data will help identify risk factors for the development of AML and further develop treatment approaches. Patients will be monitored throughout the course of their illness. This is a purely observational study, which means that no additional tests or treatments will be performed. Participation will not affect medical care.

Women and men aged 18 and older who have acute myeloid leukemia (AML) or acute promyelocytic leukemia (APL) are eligible to participate in the study. Patients can participate in the study at any stage of the disease.

Facts

  1. Disease: acute myeloid leukemia (AML) and promyelocytic leukemia (APL)
  2. Cancer characteristics: all stages of the disease; patients may have received prior treatment; no treatment restrictions
  3. What the study investigates: documentation of data on the incidence and age distribution of the disease, its course, and treatment outcomes; collection of samples
  4. Study objective: to gain a better understanding of AML and APL and to develop new therapies
  5. Study duration: up to 10 years
  6. Study characteristics: observational study, multicenter, no additional examinations or therapies

Trial sites

74 trial sites in Germany are listed. Find a site near you.

  • Universitätsklinikum Aachen AöR

    Pauwelsstraße 30, 52074 Aachen

    Recruiting
  • Klinikum Altenburger Land GmbH

    04600 Altenburg

    Recruiting
  • Universitätsklinikum Augsburg

    Stenglinstraße 2, 86156 Augsburg

    Recruiting
  • Klinikum Mittelbaden

    76532 Baden-Baden

    Recruiting
  • Sozialstiftung Bamberg

    96049 Bamberg

    Recruiting
  • Klinikum Bayreuth GmbH

    95445 Bayreuth

    Recruiting

This list is compiled to the best of our knowledge but without guarantee: it may be incomplete, and a site's recruitment status can change at any time.

Medical editorial team

  • Dr. med. Sebastian SommerSpecialist in internal medicine with a focus on hematology and oncology
  • PD Dr. med. Matthias FröhlichSpecialist in internal medicine, immunology and emergency medicine

This description is based on the public trial registry (NCT03188874) and was translated into plain language by our medical editorial team. Whether participation is an option for you is a decision you make together with your treating physician.