Patients with Acute LeukemiaNCT06668948
The Prognostic Role of Fibrinogen to Albumin Ratio in Acute Leukemia Patients
An observational study of Patients with Acute Leukemia, run by Assiut University.
Trial summary
The study aim to investigate whether levels of acute phase reactants at diagnosis and after 6 months of follow-up correlate with survival and response to treatment in newly diagnosed acute leukemia.Ultimately, we will evaluate the fibrinogen/albumin ratio, a simple score based on acute phase protein levels, whether it… Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Patients with Acute Leukemia
- How many people
- 90 participants
- Where
- No sites listed yet
- Study dates
- 1 Oct 2025to 1 Dec 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: 1. Newly diagnosed patients with acuteleukemia 2. Not received any treatment
Who may be able to join
- Newly diagnosed patients with acuteleukemia
- Not received any treatment
Who cannot join
- Patients with chronic inflammatory diseases (e.g., rheumatoid arthritisinflammatory bowel disease) or acute infections that may affect acute phase protein levels.
- Patients under chemotherapy or radiotherapy
Trial locations and contacts
No sites are listed yet.
Hosney Badrawy Hamed, Professor contact
About this study
The study aim to investigate whether levels of acute phase reactants at diagnosis and after 6 months of follow-up correlate with survival and response to treatment in newly diagnosed acute leukemia.Ultimately, we will evaluate the fibrinogen/albumin ratio, a simple score based on acute phase protein levels, whether it can provide relevant prognostic information in acute leukemia patients at diagnosis and after 6 months of follow-up.
Read the detailed description
Leukemia is a heterogeneous group of hematologic malignancies that arise from the dysfunctional proliferation of developing leukocytes. It is classified as either acute or chronic based on the rapidity of proliferation and as myelocytic or lymphocytic based on the cell of origin.(Chennamadhavuni et al., 2024) .
Acute myeloid leukemia (AML) is a disease of the bone marrow, a disorder of hematopoietic stem cells due to genetic alterations in blood cell precursors resulting in overproduction of neoplastic clonal myeloid stem cells.(Grimwade D HB, Ivey A. Molecular landscape of acute myeloid leukemia in younger adults and its clinical relevance. Blood. 2016;127).It is the most common acute leukemia in adults and it is the most aggressive cancer with a variable prognosis depending upon the molecular subtypes.(Arber et al., 2016) Acute lymphoblastic leukemia (ALL) is the most common leukemia in the pediatric population, accounting for up to 80% of cases in this group vs. 20% of cases in adults. (Arber et al., 2016). It is a malignancy of B or T lymphoblasts characterized by uncontrolled proliferation of abnormal, immature lymphocytes and their progenitors.(Puckett and Chan, 2024).
Clinical presentation can be nonspecific and span a spectrum of symptoms and signs. The majority of patients present with fever, pallor, and bruising as early signs of marrow suppression or hematologic abnormalities, whereas over 60% can demonstrate organomegaly (spleen and liver). A significant number will have a history of recurrent infections, fatigue, lymphadenopathy, and skin rashes (Clarke RT, Van den Bruel A, Bankhead. 2016)
The complicated interplay between inflammation and cancer development was first proposed in the nineteenth century(Coussens and Werb 2002).Also chronic inflammation promotes carcinogenesis, chemoresistance as well as regional or distal metastasis(Zitvogel, Pietrocola et al. 2017).Furthermore, Malnutrition damages the anatomic barriers, immunity and other defense mechanisms(Ataseven, du Bois et al. 2015).
As a result, the involvement of acute phase proteins has been studied not just during inflammatory illnesses, but also in cancers. Fibrinogen is an acute phase reactant produced by hepatocytes in response to tissue damage or infection via interleukin (IL) (namely IL-6 and IL-1) and tumor necrosis factor-alpha signaling pathways(Gabay and Kushner 1999).
These mediators are upregulated during inflammatory processes, while "negative" acute phase reactants, like transferrin and serum albumin, are downregulated because of decreased synthesis or increased breakdown(Pepys and Hirschfield 2003).
Fibrinogen is a crucial component of the coagulation cascade because it promotes platelet aggregation and acts as a substrate for the production of clots when thrombin converts it to fibrin(Weisel, Phillips Jr et al. 1983).
Plasma fibrinogen levels have been linked to tumor growth and prognosis in several malignancies, including colorectal, endometrial, hepatocellular, and pancreatic (Gan, Yi et al. 2018). The liver produces albumin, which is considered a negative acute phase protein(Spinella, Sawhney et al. 2016).
Plasma albumin regulates plasma osmotic pressure, antioxidant levels, capillary permeability, and immunological function(Arabi, Asiri et al. 2020).
An increasing number of studies have found a link between plasma albumin levels, inflammation, and cancer(Dupré and Malik 2018).
Hypoproteinemia is highly related with poor quality of life in cancer patients and poor prognosis in individuals with a variety of malignancies (Murakawa, Yamamoto et al. 2020).
High fibrinogen and low albumin levels are connected with a bad prognosis in cancer patients(Sohda, Sakai et al. 2022).
The fibrinogen-to-albumin ratio (FAR), a new independent predictor that is both simple and effective, has a higher predictive value than either low serum albumin or high fibrinogen. FAR has been identified as a possible predictor of unfavorable outcomes in a number of cancers(Tan, Zhang et al. 2017).
It was found that high fibrinogen levels were related with poor survival innewly diagnosed leukemia patients (Berger, Heini et al. 2017).
The fibrinogen/albumin ratio (FAR) has emerged as a valuable biomarker reflecting both inflammatory and nutritional status, both of which are critical factors in cancer prognosis. In all types of acute leukemia, the interplay between systemic inflammation and compromised nutritional health is particularly pronounced due to the nature of the disease and the intensity of treatments. Elevated fibrinogen, a key acute phase reactant, is associated with tumor progression, increased coagulation, and worse survival outcomes in malignancies, including leukemia. Meanwhile, albumin serves as a negative acute phase protein, with low levels indicating poor nutritional status and higher inflammatory burdens. The combination of these two markers in the form of the FAR provides a more comprehensive measure of a patient's health than either marker alone(Zhang and Xiao 2019).
FAR consists of fibrinogen and albumin, both of which are commonly used laboratory tests that are easy and inexpensive to obtain. In the future, if FAR can be used in clinical treatment, it will improve the efficiency of diagnosis and reduce the cost of treatment for cancer patients.(Li et al., 2022).
- Conditions
- Patients with Acute Leukemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| patients with acute leukemia | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
The prognostic role of fibrinogen to albumin ratio in acute leukemia patients
Measured: 2025
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Nov 2024
- Study start1 Oct 2025 (estimated)
- Primary completion1 Nov 2025 (estimated)
- Study completion1 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Patients with Acute LeukemiaStudies of the same condition, open and under way.
- More trials run by Assiut UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 90 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assiut University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Asmaa Abdelraouf Aboeladab Elnaggar, Assiut University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06668948
- Sponsor's protocol ID
- fibrinogen to albumin ratio
- Status last verified
- Oct 2024
- First submitted
- 30 Oct 2024
- Last updated
- 1 Nov 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Nov 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Prognostic Role of Fibrinogen to Albumin Ratio in Acute Leukemia Patients
- ClinicalTrials.gov ID
- NCT06668948
- Acronym / sponsor ID
- fibrinogen to albumin ratio
- Conditions
- Patients with Acute Leukemia
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 90 participants (estimated)
- Lead sponsor
- Assiut UniversityUniversity, hospital or other
- Study start
- 1 Oct 2025 (estimated)
- Primary completion
- 1 Nov 2025 (estimated)
- Study completion
- 1 Dec 2025 (estimated)
- First posted
- 1 Nov 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The study aim to investigate whether levels of acute phase reactants at diagnosis and after 6 months of follow-up correlate with survival and response to treatment in newly diagnosed acute leukemia.Ultimately, we will evaluate the fibrinogen/albumin ratio, a simple score based on acute phase protein levels, whether it can provide relevant prognostic information in acute leukemia patients at diagnosis and after 6 months of follow-up.
Detailed description
Leukemia is a heterogeneous group of hematologic malignancies that arise from the dysfunctional proliferation of developing leukocytes. It is classified as either acute or chronic based on the rapidity of proliferation and as myelocytic or lymphocytic based on the cell of origin.(Chennamadhavuni et al., 2024) .
Acute myeloid leukemia (AML) is a disease of the bone marrow, a disorder of hematopoietic stem cells due to genetic alterations in blood cell precursors resulting in overproduction of neoplastic clonal myeloid stem cells.(Grimwade D HB, Ivey A. Molecular landscape of acute myeloid leukemia in younger adults and its clinical relevance. Blood. 2016;127).It is the most common acute leukemia in adults and it is the most aggressive cancer with a variable prognosis depending upon the molecular subtypes.(Arber et al., 2016) Acute lymphoblastic leukemia (ALL) is the most common leukemia in the pediatric population, accounting for up to 80% of cases in this group vs. 20% of cases in adults. (Arber et al., 2016). It is a malignancy of B or T lymphoblasts characterized by uncontrolled proliferation of abnormal, immature lymphocytes and their progenitors.(Puckett and Chan, 2024).
Clinical presentation can be nonspecific and span a spectrum of symptoms and signs. The majority of patients present with fever, pallor, and bruising as early signs of marrow suppression or hematologic abnormalities, whereas over 60% can demonstrate organomegaly (spleen and liver). A significant number will have a history of recurrent infections, fatigue, lymphadenopathy, and skin rashes (Clarke RT, Van den Bruel A, Bankhead. 2016)
The complicated interplay between inflammation and cancer development was first proposed in the nineteenth century(Coussens and Werb 2002).Also chronic inflammation promotes carcinogenesis, chemoresistance as well as regional or distal metastasis(Zitvogel, Pietrocola et al. 2017).Furthermore, Malnutrition damages the anatomic barriers, immunity and other defense mechanisms(Ataseven, du Bois et al. 2015).
As a result, the involvement of acute phase proteins has been studied not just during inflammatory illnesses, but also in cancers. Fibrinogen is an acute phase reactant produced by hepatocytes in response to tissue damage or infection via interleukin (IL) (namely IL-6 and IL-1) and tumor necrosis factor-alpha signaling pathways(Gabay and Kushner 1999).
These mediators are upregulated during inflammatory processes, while "negative" acute phase reactants, like transferrin and serum albumin, are downregulated because of decreased synthesis or increased breakdown(Pepys and Hirschfield 2003).
Fibrinogen is a crucial component of the coagulation cascade because it promotes platelet aggregation and acts as a substrate for the production of clots when thrombin converts it to fibrin(Weisel, Phillips Jr et al. 1983).
Plasma fibrinogen levels have been linked to tumor growth and prognosis in several malignancies, including colorectal, endometrial, hepatocellular, and pancreatic (Gan, Yi et al. 2018). The liver produces albumin, which is considered a negative acute phase protein(Spinella, Sawhney et al. 2016).
Plasma albumin regulates plasma osmotic pressure, antioxidant levels, capillary permeability, and immunological function(Arabi, Asiri et al. 2020).
An increasing number of studies have found a link between plasma albumin levels, inflammation, and cancer(Dupré and Malik 2018).
Hypoproteinemia is highly related with poor quality of life in cancer patients and poor prognosis in individuals with a variety of malignancies (Murakawa, Yamamoto et al. 2020).
High fibrinogen and low albumin levels are connected with a bad prognosis in cancer patients(Sohda, Sakai et al. 2022).
The fibrinogen-to-albumin ratio (FAR), a new independent predictor that is both simple and effective, has a higher predictive value than either low serum albumin or high fibrinogen. FAR has been identified as a possible predictor of unfavorable outcomes in a number of cancers(Tan, Zhang et al. 2017).
It was found that high fibrinogen levels were related with poor survival innewly diagnosed leukemia patients (Berger, Heini et al. 2017).
The fibrinogen/albumin ratio (FAR) has emerged as a valuable biomarker reflecting both inflammatory and nutritional status, both of which are critical factors in cancer prognosis. In all types of acute leukemia, the interplay between systemic inflammation and compromised nutritional health is particularly pronounced due to the nature of the disease and the intensity of treatments. Elevated fibrinogen, a key acute phase reactant, is associated with tumor progression, increased coagulation, and worse survival outcomes in malignancies, including leukemia. Meanwhile, albumin serves as a negative acute phase protein, with low levels indicating poor nutritional status and higher inflammatory burdens. The combination of these two markers in the form of the FAR provides a more comprehensive measure of a patient's health than either marker alone(Zhang and Xiao 2019).
FAR consists of fibrinogen and albumin, both of which are commonly used laboratory tests that are easy and inexpensive to obtain. In the future, if FAR can be used in clinical treatment, it will improve the efficiency of diagnosis and reduce the cost of treatment for cancer patients.(Li et al., 2022).
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| patients with acute leukemia | – | – |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- 1. Newly diagnosed patients with acuteleukemia 2. Not received any treatment
Key inclusion criteria (2 listed)
Key exclusion criteria (2 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
The prognostic role of fibrinogen to albumin ratio in acute leukemia patients
Time frame: 2025
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Nov 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Hosney Badrawy Hamed, Professor contact
Questions about this trial
What is this clinical trial studying?
An observational study of Patients with Acute Leukemia, run by Assiut University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 1 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact asmaa abdelraouf Abeladab, Resident doctor (0152340834, asmaaabdelraouf85@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The prognostic role of fibrinogen to albumin ratio in acute leukemia patients (time frame: 2025). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Nov 2024.