Multiple Myeloma(MM)NCT05439538
Serum NGAL IN Patients With Multiple Myeloma
An observational study of Multiple Myeloma(MM), run by Assiut University.
Trial summary
The aim of this study was to evaluate SERUM neutrophil gelatinase-associated lipocalin, emerging indicator of tubular damage and examine their relationship with established measures of renal function (serum creatinine, and estimated glomerular filtration rate, eGFR) among MM patients with and without renal impairment… Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Multiple Myeloma(MM)
- What is being tested?
- SERUM NGAL
- How many people
- 60 participants
- Where
- No sites listed yet
- Study dates
- 1 Oct 2022to 1 Jan 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 18 to 75 years
- All sexes
- Adult, Older adult
Study population: Patients will be recruited during admission and visits to Clinical Hematology Unit and outpatients clinic, Assiut university hospital, from October 2022 to October 2023. Sample size is 60 patients diagnosed MM with or without renal impairment
Who may be able to join
- Adult patients (>18 years) with SMM or overt multiple myeloma (MM will be confirmed based on the WHO diagnostic criteria; the presence of at least 10% plasma cells in bone marrow biopsies, presence of momoclonal protein in serum and /or urine and one of the following disorders (CRAB): hypercalcemia, renal failure, anemia, or lytic bone lesions).
Who cannot join
- ( other causes affect NAGAL level )
- Patients with other plasma cell disorders (eg. Waldenstrom macroglobulinuria, MGUS, amyloidosis )
- Recent active infection;
- History of hepatitis B, C, or HIV
- Neoplasms other than myeloma
Trial locations and contacts
No sites are listed yet.
About this study
Official title: Serum Neutrophil Gelatinase-associated Lipocalin (NGAL) as a Predictor of Renal Injury in Patients With Multiple Myeloma
The aim of this study was to evaluate SERUM neutrophil gelatinase-associated lipocalin, emerging indicator of tubular damage and examine their relationship with established measures of renal function (serum creatinine, and estimated glomerular filtration rate, eGFR) among MM patients with and without renal impairment (RI), and at various stages of MM progression.
Read the detailed description
Multiple myeloma (MM), Being one of the most common hematologic malignancies, particularly in the elderly patient, MM represents a devastating disease that occurs due to uncontrolled proliferation of a plasma cell in bone marrow , MM Presents itself with characteristic features of organ involvement: bone lesions, anemia, renal insufficiency, infections, hypercalcemia and specific malignancy biomarkers (plasma cell clonality ≥60%, involved to uninvolved serum free light chains (FLCs) ≥100 and >1 focal lesion on magnetic resonance imaging) . Additionally , Evidence of clonal plasma cell percentage of ≥10% in bone marrow or biopsy-proven plasmacytoma is necessary to define a case of MM .
MM is the second most commonly diagnosed hematological neoplasm, with an incidence rate of 5.3 per 100 000 individuals ,its incidence in Egypt 1.5 per 100 000 individuals Early mortality may not only be associated with disease progression, but also with concomitant organ involvement (i.e., renal failure) and therapy side-effects (i.e., infections) .
Production of monoclonal paraproteins, immunoglobulins (MIg) or free light chains (FLCs), is a characteristic feature of myeloma that is tied to its clinical manifestations,Although non-functional, paraproteins may be produced in excess, which alongside their physicochemical properties may precipitate the formation of lesions in vasculature and variably affect organ function. Owing to the differences between individual clones and associated MIg, kidney pathology is highly heterogeneous, with renal tubular injury associated with light chain cast nephropathy as the dominant presentation .
Renal impairment (RI) is one of the most common complications of symptomatic MM(close to one fourth of patients at the time of diagnosis). RI, defined as a serum creatinine (sCr) level > 2 mg/dL, is one of the diagnostic criteria of symptomatic MM, and it constitutes 1 of the 4 "CRAB" features (calcium level elevation, renal impairment, anemia, and bone lesions) that indicate myeloma-related organ dysfunction .. RI can carry a poor prognosis, particularly if renal function does not recover , Irreversible renal failure is less frequent, but may be present in up to 8% of patients .
The use of novel antimyeloma agents such as proteasome inhibitors (PIs) and immunomodulatory drugs (IMiDs) as well as the improvement in supportive care has resulted in a substantial increase in patient survival. However, RI reversibility is still closely associated with MM prognosis. The persistence of severe RI is associated with significant morbidity and mortality, and remains one of the factors associated with early death, Effective anti-MM therapy and supportive care can restore renal function in several patients, Therefore, earlier recognition of disease, including its end-organ manifestations, is necessary for timely initiation and optimization of therapy but we lack biomarkers that could predict renal outcomes . Renal insufficiency is considered reversible in about 50% of cases in some reports .
Around 10% of them require haemodialysis, with a negative impact on prognosis. In addition, half of MM patients will present with at least one episode of acute kidney injury during the course of their disease. Acute kidney injury mostly reflects high tumour burden disease .
The standard assessment of renal function in patients with MM includes the measurement of sCr concentration, creatinine clearance (CrCl), blood urea nitrogen, and Estimated Glomerular Filtration Rate (eGFR), as calculated using the EPI equation. However, sCr is primarily a marker of glomerular filtration and reliant on a number of non-renal factors(comorbidity, muscle mass, medication, age), if GFR is not significantly reduced, sCr is an insensitive and late marker in the diagnosis of renal tubular injury. Novel biomarkers that will aid in predicting renal injury and chronic kidney disease development are of high interest and very early and sensitive markers .
AKI classified according to the Acute Kidney Injury Network (AKIN) classification into three stages: stage 1 Increase in serum creatinine of ≥0.3 mg/dL, stage 2 Increase in serum creatinine to 200 to 300% baseline ,stage 3 Increase in serum creatinine to >300% baseline .
One of the most promising and earliest biomarkers of kidney injury is neutrophil gelatinase-associated lipocalin (NGAL) (lipocalin 2 [LCN2]). NGAL is a lipocalin iron-carrying protein of 25 KDa expressed at low levels in several human tissues, including the kidney(16). NGAL is one of the earliest and most robust markers of acute kidney injury), reflects renal function more accurately than creatinine and correlates with both tumor burden and renal function in MM, The advantage of NGAL over conventional biomarkers of RI such as sCr and serum urea nitrogen is that the levels often increase long before any changes in sCr or urea nitrogen or urine output occur. Therefore, NGAL may also be an early, sensitive marker of RI in patients with MM .
- Conditions
- Multiple Myeloma(MM)
- Being tested
- SERUM NGAL
- Medical subject headings
- Multiple Myeloma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SERUM NGALDiagnostic test
Study the sensitivity and the specificity of serum NGAL to detect AKI in myeloma
What is being measured
The primary outcome is the main question the study is designed to answer.
serum Neutrophil Gelatinase-associated Lipocalin in patients with multiple myeloma
Role of serum Neutrophil Gelatinase-associated Lipocalin in early detection of renal impairment in patients with multiple myeloma
Measured: baseline to 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Jun 2022
- Study start1 Oct 2022 (estimated)
- Primary completion1 Oct 2024 (estimated)
- Study completion1 Jan 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (8)Papers the sponsor has linked to this study.
- Other trials for Multiple Myeloma(MM)Studies 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
- Cohort
- Time perspective
- Prospective
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assiut University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ehab A. Abdelmenam, Assiut University
- Investigators
- Essam Abdel Monem El-beih,, professor, Study director, Assiut Univ
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05439538
- Sponsor's protocol ID
- NGAL IN MM
- Status last verified
- Jun 2022
- First submitted
- 23 Jun 2022
- Last updated
- 30 Jun 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Turesson I, Bjorkholm M, Blimark CH, Kristinsson S, Velez R, Landgren O. Rapidly changing myeloma epidemiology in the general population: Increased incidence, older patients, and longer survival. Eur J Haematol. 2018 Apr 20:10.1111/ejh.13083. doi: 10.1111/ejh.13083. Online ahead of print.
PubMed 29676004Rajkumar SV, Dimopoulos MA, Palumbo A, Blade J, Merlini G, Mateos MV, Kumar S, Hillengass J, Kastritis E, Richardson P, Landgren O, Paiva B, Dispenzieri A, Weiss B, LeLeu X, Zweegman S, Lonial S, Rosinol L, Zamagni E, Jagannath S, Sezer O, Kristinsson SY, Caers J, Usmani SZ, Lahuerta JJ, Johnsen HE, Beksac M, Cavo M, Goldschmidt H, Terpos E, Kyle RA, Anderson KC, Durie BG, Miguel JF. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014 Nov;15(12):e538-48. doi: 10.1016/S1470-2045(14)70442-5. Epub 2014 Oct 26.
PubMed 25439696Ludwig H, Novis Durie S, Meckl A, Hinke A, Durie B. Multiple Myeloma Incidence and Mortality Around the Globe; Interrelations Between Health Access and Quality, Economic Resources, and Patient Empowerment. Oncologist. 2020 Sep;25(9):e1406-e1413. doi: 10.1634/theoncologist.2020-0141. Epub 2020 May 7.
PubMed 32335971Mohty M, Cavo M, Fink L, Gonzalez-McQuire S, Leleu H, Mateos MV, Raab MS, Schoen P, Yong K. Understanding mortality in multiple myeloma: Findings of a European retrospective chart review. Eur J Haematol. 2019 Aug;103(2):107-115. doi: 10.1111/ejh.13264. Epub 2019 Jun 18.
PubMed 31112311Rafae A, Malik MN, Abu Zar M, Durer S, Durer C. An Overview of Light Chain Multiple Myeloma: Clinical Characteristics and Rarities, Management Strategies, and Disease Monitoring. Cureus. 2018 Aug 15;10(8):e3148. doi: 10.7759/cureus.3148.
PubMed 30345204Gonsalves WI, Milani P, Derudas D, Buadi FK. The next generation of novel therapies for the management of relapsed multiple myeloma. Future Oncol. 2017 Jan;13(1):63-75. doi: 10.2217/fon-2016-0200. Epub 2016 Aug 11.
PubMed 27513456Evison F, Sangha J, Yadav P, Aung YS, Sharif A, Pinney JA, Drayson MT, Cook M, Cockwell P. A population-based study of the impact of dialysis on mortality in multiple myeloma. Br J Haematol. 2018 Feb;180(4):588-591. doi: 10.1111/bjh.14394. Epub 2016 Oct 21. No abstract available.
PubMed 27766629Clerico A, Galli C, Fortunato A, Ronco C. Neutrophil gelatinase-associated lipocalin (NGAL) as biomarker of acute kidney injury: a review of the laboratory characteristics and clinical evidences. Clin Chem Lab Med. 2012 Feb 15;50(9):1505-17. doi: 10.1515/cclm-2011-0814.
PubMed 22962216
Study at a glance
From the registry record, last updated by the sponsor on 30 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Serum Neutrophil Gelatinase-associated Lipocalin (NGAL) as a Predictor of Renal Injury in Patients With Multiple Myeloma
- ClinicalTrials.gov ID
- NCT05439538
- Acronym / sponsor ID
- NGAL IN MM
- Conditions
- Multiple Myeloma(MM)
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Assiut UniversityUniversity, hospital or other
- Study start
- 1 Oct 2022 (estimated)
- Primary completion
- 1 Oct 2024 (estimated)
- Study completion
- 1 Jan 2025 (estimated)
- First posted
- 30 Jun 2022 (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 aim of this study was to evaluate SERUM neutrophil gelatinase-associated lipocalin, emerging indicator of tubular damage and examine their relationship with established measures of renal function (serum creatinine, and estimated glomerular filtration rate, eGFR) among MM patients with and without renal impairment (RI), and at various stages of MM progression.
Detailed description
Multiple myeloma (MM), Being one of the most common hematologic malignancies, particularly in the elderly patient, MM represents a devastating disease that occurs due to uncontrolled proliferation of a plasma cell in bone marrow , MM Presents itself with characteristic features of organ involvement: bone lesions, anemia, renal insufficiency, infections, hypercalcemia and specific malignancy biomarkers (plasma cell clonality ≥60%, involved to uninvolved serum free light chains (FLCs) ≥100 and >1 focal lesion on magnetic resonance imaging) . Additionally , Evidence of clonal plasma cell percentage of ≥10% in bone marrow or biopsy-proven plasmacytoma is necessary to define a case of MM .
MM is the second most commonly diagnosed hematological neoplasm, with an incidence rate of 5.3 per 100 000 individuals ,its incidence in Egypt 1.5 per 100 000 individuals Early mortality may not only be associated with disease progression, but also with concomitant organ involvement (i.e., renal failure) and therapy side-effects (i.e., infections) .
Production of monoclonal paraproteins, immunoglobulins (MIg) or free light chains (FLCs), is a characteristic feature of myeloma that is tied to its clinical manifestations,Although non-functional, paraproteins may be produced in excess, which alongside their physicochemical properties may precipitate the formation of lesions in vasculature and variably affect organ function. Owing to the differences between individual clones and associated MIg, kidney pathology is highly heterogeneous, with renal tubular injury associated with light chain cast nephropathy as the dominant presentation .
Renal impairment (RI) is one of the most common complications of symptomatic MM(close to one fourth of patients at the time of diagnosis). RI, defined as a serum creatinine (sCr) level > 2 mg/dL, is one of the diagnostic criteria of symptomatic MM, and it constitutes 1 of the 4 "CRAB" features (calcium level elevation, renal impairment, anemia, and bone lesions) that indicate myeloma-related organ dysfunction .. RI can carry a poor prognosis, particularly if renal function does not recover , Irreversible renal failure is less frequent, but may be present in up to 8% of patients .
The use of novel antimyeloma agents such as proteasome inhibitors (PIs) and immunomodulatory drugs (IMiDs) as well as the improvement in supportive care has resulted in a substantial increase in patient survival. However, RI reversibility is still closely associated with MM prognosis. The persistence of severe RI is associated with significant morbidity and mortality, and remains one of the factors associated with early death, Effective anti-MM therapy and supportive care can restore renal function in several patients, Therefore, earlier recognition of disease, including its end-organ manifestations, is necessary for timely initiation and optimization of therapy but we lack biomarkers that could predict renal outcomes . Renal insufficiency is considered reversible in about 50% of cases in some reports .
Around 10% of them require haemodialysis, with a negative impact on prognosis. In addition, half of MM patients will present with at least one episode of acute kidney injury during the course of their disease. Acute kidney injury mostly reflects high tumour burden disease .
The standard assessment of renal function in patients with MM includes the measurement of sCr concentration, creatinine clearance (CrCl), blood urea nitrogen, and Estimated Glomerular Filtration Rate (eGFR), as calculated using the EPI equation. However, sCr is primarily a marker of glomerular filtration and reliant on a number of non-renal factors(comorbidity, muscle mass, medication, age), if GFR is not significantly reduced, sCr is an insensitive and late marker in the diagnosis of renal tubular injury. Novel biomarkers that will aid in predicting renal injury and chronic kidney disease development are of high interest and very early and sensitive markers .
AKI classified according to the Acute Kidney Injury Network (AKIN) classification into three stages: stage 1 Increase in serum creatinine of ≥0.3 mg/dL, stage 2 Increase in serum creatinine to 200 to 300% baseline ,stage 3 Increase in serum creatinine to >300% baseline .
One of the most promising and earliest biomarkers of kidney injury is neutrophil gelatinase-associated lipocalin (NGAL) (lipocalin 2 [LCN2]). NGAL is a lipocalin iron-carrying protein of 25 KDa expressed at low levels in several human tissues, including the kidney(16). NGAL is one of the earliest and most robust markers of acute kidney injury), reflects renal function more accurately than creatinine and correlates with both tumor burden and renal function in MM, The advantage of NGAL over conventional biomarkers of RI such as sCr and serum urea nitrogen is that the levels often increase long before any changes in sCr or urea nitrogen or urine output occur. Therefore, NGAL may also be an early, sensitive marker of RI in patients with MM .
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Patients will be recruited during admission and visits to Clinical Hematology Unit and outpatients clinic, Assiut university hospital, from October 2022 to October 2023. Sample size is 60 patients diagnosed MM with or without renal impairment
Key inclusion criteria (1 listed)
- Adult patients (>18 years) with SMM or overt multiple myeloma (MM will be confirmed based on the WHO diagnostic criteria; the presence of at least 10% plasma cells in bone marrow biopsies, presence of momoclonal protein in serum and /or urine and one of the following disorders (CRAB): hypercalcemia, renal failure, anemia, or lytic bone lesions).
Key exclusion criteria (5 listed)
- ( other causes affect NAGAL level )
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SERUM NGALStudy the sensitivity and the specificity of serum NGAL to detect AKI in myeloma | Diagnostic test | – |
Primary outcome
serum Neutrophil Gelatinase-associated Lipocalin in patients with multiple myeloma
Time frame: baseline to 3 months
Role of serum Neutrophil Gelatinase-associated Lipocalin in early detection of renal impairment in patients with multiple myeloma
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jun 2022.
- Background: PubMed 29676004Turesson I, Bjorkholm M, Blimark CH, Kristinsson S, Velez R, Landgren O. Rapidly changing myeloma epidemiology in the general population: Increased incidence, older patients, and longer survival. Eur J Haematol. 2018 Apr 20:10.1111/ejh.13083. doi: 10.1111/ejh.13083. Online ahead of print.
- Background: PubMed 25439696Rajkumar SV, Dimopoulos MA, Palumbo A, Blade J, Merlini G, Mateos MV, Kumar S, Hillengass J, Kastritis E, Richardson P, Landgren O, Paiva B, Dispenzieri A, Weiss B, LeLeu X, Zweegman S, Lonial S, Rosinol L, Zamagni E, Jagannath S, Sezer O, Kristinsson SY, Caers J, Usmani SZ, Lahuerta JJ, Johnsen HE, Beksac M, Cavo M, Goldschmidt H, Terpos E, Kyle RA, Anderson KC, Durie BG, Miguel JF. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014 Nov;15(12):e538-48. doi: 10.1016/S1470-2045(14)70442-5. Epub 2014 Oct 26.
- Background: PubMed 32335971Ludwig H, Novis Durie S, Meckl A, Hinke A, Durie B. Multiple Myeloma Incidence and Mortality Around the Globe; Interrelations Between Health Access and Quality, Economic Resources, and Patient Empowerment. Oncologist. 2020 Sep;25(9):e1406-e1413. doi: 10.1634/theoncologist.2020-0141. Epub 2020 May 7.
- Background: PubMed 31112311Mohty M, Cavo M, Fink L, Gonzalez-McQuire S, Leleu H, Mateos MV, Raab MS, Schoen P, Yong K. Understanding mortality in multiple myeloma: Findings of a European retrospective chart review. Eur J Haematol. 2019 Aug;103(2):107-115. doi: 10.1111/ejh.13264. Epub 2019 Jun 18.
- Background: PubMed 30345204Rafae A, Malik MN, Abu Zar M, Durer S, Durer C. An Overview of Light Chain Multiple Myeloma: Clinical Characteristics and Rarities, Management Strategies, and Disease Monitoring. Cureus. 2018 Aug 15;10(8):e3148. doi: 10.7759/cureus.3148.
- Background: PubMed 27513456Gonsalves WI, Milani P, Derudas D, Buadi FK. The next generation of novel therapies for the management of relapsed multiple myeloma. Future Oncol. 2017 Jan;13(1):63-75. doi: 10.2217/fon-2016-0200. Epub 2016 Aug 11.
- Background: PubMed 27766629Evison F, Sangha J, Yadav P, Aung YS, Sharif A, Pinney JA, Drayson MT, Cook M, Cockwell P. A population-based study of the impact of dialysis on mortality in multiple myeloma. Br J Haematol. 2018 Feb;180(4):588-591. doi: 10.1111/bjh.14394. Epub 2016 Oct 21. No abstract available.
- Background: PubMed 22962216Clerico A, Galli C, Fortunato A, Ronco C. Neutrophil gelatinase-associated lipocalin (NGAL) as biomarker of acute kidney injury: a review of the laboratory characteristics and clinical evidences. Clin Chem Lab Med. 2012 Feb 15;50(9):1505-17. doi: 10.1515/cclm-2011-0814.
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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.
Essam Abdel Monem El-beih,, professor study director
Assiut Univ
Questions about this trial
What is this clinical trial studying?
An observational study of Multiple Myeloma(MM), 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 1 inclusion and 5 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 30 Jun 2022. 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 Ehab ahmed Abdel moniem, assistant lecturer (201097796359, ehabahmed200@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
serum Neutrophil Gelatinase-associated Lipocalin in patients with multiple myeloma (time frame: baseline to 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05439538, which also lists 8 linked publications.
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 30 Jun 2022.