The Myeloid Neoplasms Biology and Outcome Project

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital Heidelberg

About this trial

The Myeloid Neoplasms Biology and Outcome Project (MyBOP) aims to establish a registry study for patients with myeloid neoplasms. It integrates clinical data, biological samples, socio-demographic information, long-term follow-up and patient reported outcomes in a structured manner for scientific purposes.

The ultimate benefits are:

1. Improvement of evidence-based clinical management of patients with myeloid neoplasms through better understanding of the course of disease and prognostic and predictive parameters 2. Direct access to new and personalized treatment approaches through recruitment into clinical studies based on the myeloid neoplasms study platform 3. Quality assurance of participating centers by evaluating and comparing clinical outcomes and side effects of the MyBOP patients with published data.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Suspected or proven diagnosis of Myeloid Neoplasms according to the WHO Classification of Tumors of Haematopoietic and Lymphoid Tissues

Age ≥18 years

Ability to understand the nature and individual consequences of the registry

Written informed consent

Disqualifiers

None

Trial population

the patient cohort will be selected from the University Hospital Heidelberg.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

median overall survival (mOS)

Time period of survival from date of diagnosis of myeloid neoplasy

Time frame
5 years
2

overall survival (mOS)

Time period of survival from date of diagnosis of myeloid neoplasy

Time frame
10 years
3

event free survival (EFS)

Time period of event free survival from date of diagnosis of myeloid neoplasy

Time frame
5 years
4

progression free survival (PFS)

Time period of progression survival from date of diagnosis of myeloid neoplasy

Time frame
5 years

Secondary outcomes

1

Questionnaire for the health- related quality of life QLQ-C30

Standardized Quality of Life Assessment, Higher values are better

Time frame
5 years
2

Questionnaire for physical, cognitive and emotional aspects of cancer-related fatigue QLQ-FA12

Standardized Quality of Fatigue, Higher values are worse

Time frame
5 years
3

Questionnaire for anxiety and depression PHQ-4

Standardized Quality of anxiety and depression, Higher values are worse

Time frame
5 years
4

Functional Assessment of Cancer Therapy Fact-Cog

Standardized Quality of cognitive function, Higher values are better

Time frame
5 years

Other outcomes

Sponsors and contacts

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