NeutropeniaPhase 3NCT05221593
Efficacy of Lithium Against Chemotherapy Induced Neutropenia in Breast Cancer Patients
A Phase 3 study testing Lithium Carbonate in people with Neutropenia, run by Al-Azhar University at 1 site in Egypt.
Trial summary
Using Lithium Carbonate to decrease incidence of neutropenia caused by using chemotherapy regimen in breast cancer patients. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Neutropenia
- What is being tested?
- Lithium Carbonate
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Aug 2020to 1 Jun 2022
- Phase
- Phase 3
- 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
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- 1. All patients presented with breast cancer documented by pathological reports stage I, II and III.
Who cannot join
- Patients receiving cardiac medication such as diuretics.
- Patients on sodium-restricted diet (to avoid lithium toxicity).
- Stage IV with expected short overall survival.
- Patients with blood or bone marrow cancer (to prevent interference).
- Patients with hepatic and renal impairment.
- Patient with untreated hypothyroidism.
- Pregnant and breast feeding patients.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Evaluation of Lithium Efficacy Against Chemotherapy Induced Neutropenia in Breast Cancer Patients
Using Lithium Carbonate to decrease incidence of neutropenia caused by using chemotherapy regimen in breast cancer patients.
Read the detailed description
Introduction:
Cytotoxic chemotherapy predictably suppresses the hematopoietic system, impairing host protective mechanisms. Neutropenia is the most serious hematologic toxicity of cancer chemotherapy, often limiting the doses of chemotherapy that can be tolerated. The degree and duration of the neutropenia determine the risk of infection. The Common Toxicity Criteria of the National Cancer Institute is the most commonly used scale for grading the severity of the cytopenias associated with cancer chemotherapy; it delineates neutropenia into 4 grades. Chemotherapy predisposes patients with cancer to infections both by suppressing the production of neutrophils and by cytotoxic effects on the cells that line the alimentary tract. Neutrophils are the first line of defence against infection as the first cellular component of the inflammatory response and a key component of innate immunity. Neutropenia blunts the inflammatory response to nascent infections, allowing bacterial multiplication and invasion. Because neutropenia reduces the signs and symptoms of infection, patients with neutropenia often may present with fever as the only sign of infection. In this setting, patients with fever and neutropenia, or febrile neutropenia (FN), must be treated aggressively, typically with intravenous antibiotics and hospitalization, because of the risk of death from rapidly spreading infection. The availability of hematopoietic growth factors and improvements in antibiotic therapy have changed greatly how clinicians approach the management of neutropenia, yet this complication remains a central concern in the delivery of cancer chemotherapy.
Lithium carbonate continues to be the most useful agent available for the prophylaxis and treatment of bipolar illness. Lithium augmentation of antidepressants is useful in the treatment of resistant unipolar depression. Its utility in other psychiatric disorders such as schizophrenia, alcoholism, or aggressive behaviour is documented only when a significant affective component exists. Hematologic changes have been associated with lithium Unexplained increases in white blood cell (WBC) counts have occurred in psychiatric patients treated with lithium. This leukocytosis occurs within 1 week of treatment and is reversible. It is unrelated to age, sex, or diagnosis. Although serum levels above 0.5 milliequivalent/L are required for the effect, there is no proportional response to dose. In 1998, Ballin et al prospectively examined eight adult patients with bipolar disorder to find whether lithium carbonate increased their peripheral blood cluster of differentiation 34 (CD34) hematopoietic stem cells (HSC). The administration of lithium salts to haematologically normal subjects is associated with increased marrow neutrophil production and enhanced release of granulocyte colony stimulating factor (G-CSF) in vitro, followed by peripheral blood neutrophilia.The unsaturated vitamin B12-binding capacity, an indirect assessment of the total-body granulocyte pool, is elevated in patients taking lithium for manic-depressive psychosis. In man, oral lithium carbonate raises urinary levels of G-CSF and augments production of G-CSF by peripheral blood mononucleated cell. Moreover, when Levitt and Quesenberry studied the effects of adding lithium to a murine bone marrow liquid culture system, lithium substantially increased the number of granulocyte-committed progenitor cells and pluripotential stem cells. Lithium therefore seems to have at least two distinct actions in haematopoiesis: It enhances the production of G-CSF, and it directly stimulates the proliferation of pluripotential stem cells. In 1978, Stein et al. first formally showed that lithium-induced granulocytosis was not merely a redistribution of granulocytes that are marginated or are in the marrow reserves, supporting the hypothesis of increased granulocyte production. Lithium also affects cytokines that involved in mobilization of neutrophils from bone marrow to blood through inhibition of Glycogen synthase kinase 3 (GSK-3) function, thereby indirectly increasing the attractive CXCL12 gradient toward a hypoxic marrow trophic niche, where HSCs can thrive. This is reflected by increased marrow trophic niche function: peripheral neutrophilia, increased platelets, and increased CD34+ counts.
Additionally, lithium has anticancer activity and neuroprotective properties. One piece of experimental evidence for lithium's potential as a cancer therapy is that inhibition of GSK3 was observed to inhibit prostate cancer cell proliferation. With respect to colorectal cancer, it has been found that lithium inhibits proliferation of a colorectal cancer cell line. Phosphatase and tensin homolog (PTEN) overexpression and lithium administration were shown to cooperatively inhibit proliferation of colorectal cancer cells. Because lithium therapy is systemic rather than topical or local, it follows that lithium might inhibit metastasis. Evidence that this is the case for colon cancer comes from observation of inhibition of metastasis-inducing factors by lithium and by observation on reduced metastasis in model animals given lithium therapy. Autophagy is a key cellular process in the inhibition of cancer. Lithium has been shown to induce autophagy, due to its inhibition of inositol monophosphatase.
For these issues that mentioned above about neutropenia and lithium ability to reduce the incidence of neutropenia in patient taking chemotherapy without needing to highly costing recombinant granulocyte colony stimulating factors that Egyptian patient can't afford or using the antibiotic as a prophylactic agent that will result in resistance. we want to use lithium to attenuate neutropenia induced chemotherapy. Also because of the anti-cancer activity and neuroprotective properties of lithium that mentioned above we hypothesis that lithium will not conflict with chemotherapy treatment but will help to gain the maximum benefit of chemotherapy and minimize the side effects.
Hypothesis:
Because of the effect of lithium on WBCs and its ability to produce leukocytosis,it is hypothesized that lithium is capable of reversing the chemotherapy induced neutropenia, might be through induction of endogenous colony stimulating factor (CSF) or through alteration of the balance between cytokines that involved in neutrophils mobilization from bone marrow to the blood (CXCl12 and CXCl1).
Aim:
To investigate the efficacy of lithium carbonate in attenuating chemotherapy induced neutropenia, the effect of lithium on granulocyte colony stimulating factor and cytokines involved in neutrophils mobilization from bone marrow to blood in breast cancer patients
Patients and methodology:
This is a prospective randomized study include (50 patients) will be done in collaboration between Clinical Pharmacy Department, Faculty of Pharmacy, Al-Azhar University, Cairo and Clinical Oncology and Nuclear Medicine Department, Faculty of Medicine, Tanta University during June/2020 to June/2021 in breast cancer patients received chemotherapy which induced neutropenia.
- Conditions
- Neutropenia
- Being tested
- Lithium Carbonate
- Medical subject headings
- Neutropenia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Lithium CarbonateDrug
Also called Prianil controlled-release tablet
400 mg tablet in controlled released formula
| Study group | Role | What they receive |
|---|---|---|
| control group | No intervention | will receive chemotherapy regimen with placebo |
| study group | Experimental | will receive chemotherapy regimen with Lithium Carbonate in controlled release formula (400mg b.i.d).
In order to avoid the potential for bone marrow stimulation at the time chemotherapy was administered, the administration of lithium was started 24 hours after the administration of chemotherapy and continued for 18 days of every 21.the lithium serum level will be measured at specific times to ensure lithium serum level between 0.4-0.8 mmol\L along the treatment course. Receives: Drug: Lithium Carbonate |
What is being measured
The primary outcome is the main question the study is designed to answer.
change in white blood cells count
Measured: At baseline (on the 1st day of first cycle) before chemotherapy administration and after each cycle (on the 18th day of every cycle) for six cycles of chemotherapy. (each cycle is 21 days)
Secondary outcomes (3)
G-CSF
Measured: At baseline (on the 1st day of first cycle) before chemotherapy administration and after completion of six cycles of chemotherapy (on the 18th day of sixth cycle). (each cycle is 21 days)
CXCL12
Measured: At baseline (on the 1st day of first cycle) before chemotherapy administration and after completion of six cycles of chemotherapy (on the 18th day of sixth cycle). (each cycle is 21 days)
CXCL1
Measured: At baseline (on the 1st day of first cycle) before chemotherapy administration and after completion of six cycles of chemotherapy (on the 18th day of sixth cycle). (each cycle is 21 days)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Feb 2022
- Study start1 Aug 2020
- Primary completion1 Apr 2022
- Study completion1 Jun 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (18)Papers the sponsor has linked to this study.
- Other trials for NeutropeniaStudies of the same condition, open and under way.
- More trials run by Al-Azhar 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
- Interventional
- Phase
- Phase 3
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 50 participants (actual)
Sponsor and investigators
- Lead sponsor
- Al-Azhar University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ahmed osama elbastawesy hassan elkasar, Al-Azhar University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05221593
- Sponsor's protocol ID
- lithium and breast cancer
- Status last verified
- Oct 2022
- First submitted
- 25 Dec 2021
- Last updated
- 21 Oct 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Bodey GP, Buckley M, Sathe YS, Freireich EJ. Quantitative relationships between circulating leukocytes and infection in patients with acute leukemia. Ann Intern Med. 1966 Feb;64(2):328-40. doi: 10.7326/0003-4819-64-2-328. No abstract available.
PubMed 5216294el-Mallakh RS. Lithium. Conn Med. 1990 Mar;54(3):115-26.
PubMed 2182284Slater V, Milanes F, Talcott V, Okafor KC. Influence of age on lithium therapy. South Med J. 1984 Feb;77(2):153-4, 158. doi: 10.1097/00007611-198402000-00003.
PubMed 6701582Yassa R. Leukocytosis during long-term lithium treatment. N Y State J Med. 1981 Sep;81(10):1479-80. No abstract available.
PubMed 6792575Ballin A, Lehman D, Sirota P, Litvinjuk U, Meytes D. Increased number of peripheral blood CD34+ cells in lithium-treated patients. Br J Haematol. 1998 Jan;100(1):219-21. doi: 10.1046/j.1365-2141.1998.00537.x.
PubMed 9450814RADOMSKI JL, FUYAT HN, NELSON AA, SMITH PK. The toxic effects, excretion and distribution of lithium chloride. J Pharmacol Exp Ther. 1950 Dec;100(4:1):429-44. No abstract available.
PubMed 14804282Petrini M, Vaglini F, Carulli G, Azzara A, Ambrogi F, Bertelli A. Effects of lithium and rubidium on the differentiation of mononuclear cells. Int J Tissue React. 1986;8(5):391-2.
PubMed 3781770Tisman G, Herbert V, Rosenblatt S. Evidence that lithium induces human granulocyte proliferation: elevated serum vitamin B 12 binding capacity in vivo and granulocyte colony proliferation in vitro. Br J Haematol. 1973 Jun;24(6):767-71. doi: 10.1111/j.1365-2141.1973.tb01704.x. No abstract available.
PubMed 4716059Harker WG, Rothstein G, Clarkson D, Athens JW, Macfarlane JL. Enhancement of colony-stimulating activity production by lithium. Blood. 1977 Feb;49(2):263-7.
PubMed 299818Levitt LJ, Quesenberry PJ. The effect of lithium on murine hematopoiesis in a liquid culture system. N Engl J Med. 1980 Mar 27;302(13):713-9. doi: 10.1056/NEJM198003273021303.
PubMed 6965517Stein RS, Hanson G, Koethe S, Hansen R. Lithium-induced granulocytosis. Ann Intern Med. 1978 Jun;88(6):809-10. doi: 10.7326/0003-4819-88-6-809_2. No abstract available.
PubMed 666142Kast RE. How lithium treatment generates neutrophilia by enhancing phosphorylation of GSK-3, increasing HIF-1 levels and how this path is important during engraftment. Bone Marrow Transplant. 2008 Jan;41(1):23-6. doi: 10.1038/sj.bmt.1705872. Epub 2007 Oct 1.
PubMed 17906701Li H, Huang K, Liu X, Liu J, Lu X, Tao K, Wang G, Wang J. Lithium chloride suppresses colorectal cancer cell survival and proliferation through ROS/GSK-3beta/NF-kappaB signaling pathway. Oxid Med Cell Longev. 2014;2014:241864. doi: 10.1155/2014/241864. Epub 2014 Jun 5.
PubMed 25002914de Araujo WM, Robbs BK, Bastos LG, de Souza WF, Vidal FC, Viola JP, Morgado-Diaz JA. PTEN Overexpression Cooperates With Lithium to Reduce the Malignancy and to Increase Cell Death by Apoptosis via PI3K/Akt Suppression in Colorectal Cancer Cells. J Cell Biochem. 2016 Feb;117(2):458-69. doi: 10.1002/jcb.25294.
PubMed 26224641Maeng YS, Lee R, Lee B, Choi SI, Kim EK. Lithium inhibits tumor lymphangiogenesis and metastasis through the inhibition of TGFBIp expression in cancer cells. Sci Rep. 2016 Feb 9;6:20739. doi: 10.1038/srep20739.
PubMed 26857144
Study at a glance
From the registry record, last updated by the sponsor on 21 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Lithium Efficacy Against Chemotherapy Induced Neutropenia in Breast Cancer Patients
- ClinicalTrials.gov ID
- NCT05221593
- Acronym / sponsor ID
- lithium and breast cancer
- Conditions
- Neutropenia
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 50 participants (actual)
- Lead sponsor
- Al-Azhar UniversityUniversity, hospital or other
- Study start
- 1 Aug 2020 (actual)
- Primary completion
- 1 Apr 2022 (actual)
- Study completion
- 1 Jun 2022 (actual)
- First posted
- 3 Feb 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.
Using Lithium Carbonate to decrease incidence of neutropenia caused by using chemotherapy regimen in breast cancer patients.
Detailed description
Introduction:
Cytotoxic chemotherapy predictably suppresses the hematopoietic system, impairing host protective mechanisms. Neutropenia is the most serious hematologic toxicity of cancer chemotherapy, often limiting the doses of chemotherapy that can be tolerated. The degree and duration of the neutropenia determine the risk of infection. The Common Toxicity Criteria of the National Cancer Institute is the most commonly used scale for grading the severity of the cytopenias associated with cancer chemotherapy; it delineates neutropenia into 4 grades. Chemotherapy predisposes patients with cancer to infections both by suppressing the production of neutrophils and by cytotoxic effects on the cells that line the alimentary tract. Neutrophils are the first line of defence against infection as the first cellular component of the inflammatory response and a key component of innate immunity. Neutropenia blunts the inflammatory response to nascent infections, allowing bacterial multiplication and invasion. Because neutropenia reduces the signs and symptoms of infection, patients with neutropenia often may present with fever as the only sign of infection. In this setting, patients with fever and neutropenia, or febrile neutropenia (FN), must be treated aggressively, typically with intravenous antibiotics and hospitalization, because of the risk of death from rapidly spreading infection. The availability of hematopoietic growth factors and improvements in antibiotic therapy have changed greatly how clinicians approach the management of neutropenia, yet this complication remains a central concern in the delivery of cancer chemotherapy.
Lithium carbonate continues to be the most useful agent available for the prophylaxis and treatment of bipolar illness. Lithium augmentation of antidepressants is useful in the treatment of resistant unipolar depression. Its utility in other psychiatric disorders such as schizophrenia, alcoholism, or aggressive behaviour is documented only when a significant affective component exists. Hematologic changes have been associated with lithium Unexplained increases in white blood cell (WBC) counts have occurred in psychiatric patients treated with lithium. This leukocytosis occurs within 1 week of treatment and is reversible. It is unrelated to age, sex, or diagnosis. Although serum levels above 0.5 milliequivalent/L are required for the effect, there is no proportional response to dose. In 1998, Ballin et al prospectively examined eight adult patients with bipolar disorder to find whether lithium carbonate increased their peripheral blood cluster of differentiation 34 (CD34) hematopoietic stem cells (HSC). The administration of lithium salts to haematologically normal subjects is associated with increased marrow neutrophil production and enhanced release of granulocyte colony stimulating factor (G-CSF) in vitro, followed by peripheral blood neutrophilia.The unsaturated vitamin B12-binding capacity, an indirect assessment of the total-body granulocyte pool, is elevated in patients taking lithium for manic-depressive psychosis. In man, oral lithium carbonate raises urinary levels of G-CSF and augments production of G-CSF by peripheral blood mononucleated cell. Moreover, when Levitt and Quesenberry studied the effects of adding lithium to a murine bone marrow liquid culture system, lithium substantially increased the number of granulocyte-committed progenitor cells and pluripotential stem cells. Lithium therefore seems to have at least two distinct actions in haematopoiesis: It enhances the production of G-CSF, and it directly stimulates the proliferation of pluripotential stem cells. In 1978, Stein et al. first formally showed that lithium-induced granulocytosis was not merely a redistribution of granulocytes that are marginated or are in the marrow reserves, supporting the hypothesis of increased granulocyte production. Lithium also affects cytokines that involved in mobilization of neutrophils from bone marrow to blood through inhibition of Glycogen synthase kinase 3 (GSK-3) function, thereby indirectly increasing the attractive CXCL12 gradient toward a hypoxic marrow trophic niche, where HSCs can thrive. This is reflected by increased marrow trophic niche function: peripheral neutrophilia, increased platelets, and increased CD34+ counts.
Additionally, lithium has anticancer activity and neuroprotective properties. One piece of experimental evidence for lithium's potential as a cancer therapy is that inhibition of GSK3 was observed to inhibit prostate cancer cell proliferation. With respect to colorectal cancer, it has been found that lithium inhibits proliferation of a colorectal cancer cell line. Phosphatase and tensin homolog (PTEN) overexpression and lithium administration were shown to cooperatively inhibit proliferation of colorectal cancer cells. Because lithium therapy is systemic rather than topical or local, it follows that lithium might inhibit metastasis. Evidence that this is the case for colon cancer comes from observation of inhibition of metastasis-inducing factors by lithium and by observation on reduced metastasis in model animals given lithium therapy. Autophagy is a key cellular process in the inhibition of cancer. Lithium has been shown to induce autophagy, due to its inhibition of inositol monophosphatase.
For these issues that mentioned above about neutropenia and lithium ability to reduce the incidence of neutropenia in patient taking chemotherapy without needing to highly costing recombinant granulocyte colony stimulating factors that Egyptian patient can't afford or using the antibiotic as a prophylactic agent that will result in resistance. we want to use lithium to attenuate neutropenia induced chemotherapy. Also because of the anti-cancer activity and neuroprotective properties of lithium that mentioned above we hypothesis that lithium will not conflict with chemotherapy treatment but will help to gain the maximum benefit of chemotherapy and minimize the side effects.
Hypothesis:
Because of the effect of lithium on WBCs and its ability to produce leukocytosis,it is hypothesized that lithium is capable of reversing the chemotherapy induced neutropenia, might be through induction of endogenous colony stimulating factor (CSF) or through alteration of the balance between cytokines that involved in neutrophils mobilization from bone marrow to the blood (CXCl12 and CXCl1).
Aim:
To investigate the efficacy of lithium carbonate in attenuating chemotherapy induced neutropenia, the effect of lithium on granulocyte colony stimulating factor and cytokines involved in neutrophils mobilization from bone marrow to blood in breast cancer patients
Patients and methodology:
This is a prospective randomized study include (50 patients) will be done in collaboration between Clinical Pharmacy Department, Faculty of Pharmacy, Al-Azhar University, Cairo and Clinical Oncology and Nuclear Medicine Department, Faculty of Medicine, Tanta University during June/2020 to June/2021 in breast cancer patients received chemotherapy which induced neutropenia.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| control group | No intervention | –will receive chemotherapy regimen with placebo |
| study group | Experimental | Drug: Lithium Carbonatewill receive chemotherapy regimen with Lithium Carbonate in controlled release formula (400mg b.i.d). In order to avoid the potential for bone marrow stimulation at the time chemotherapy was administered, the administration of lithium was started 24 hours after the administration of chemotherapy and continued for 18 days of every 21.the lithium serum level will be measured at specific times to ensure lithium serum level between 0.4-0.8 mmol\L along the treatment course. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- 1. All patients presented with breast cancer documented by pathological reports stage I, II and III.
Key exclusion criteria (7 listed)
- Patients receiving cardiac medication such as diuretics.
- Patients on sodium-restricted diet (to avoid lithium toxicity).
- Stage IV with expected short overall survival.
- Patients with blood or bone marrow cancer (to prevent interference).
- Patients with hepatic and renal impairment.
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 |
|---|---|---|
| Lithium CarbonateAlso: Prianil controlled-release tablet400 mg tablet in controlled released formula | Drug | study group |
Primary outcome
change in white blood cells count
Time frame: At baseline (on the 1st day of first cycle) before chemotherapy administration and after each cycle (on the 18th day of every cycle) for six cycles of chemotherapy. (each cycle is 21 days)
3 secondary outcomes
G-CSF
Time frame: At baseline (on the 1st day of first cycle) before chemotherapy administration and after completion of six cycles of chemotherapy (on the 18th day of sixth cycle). (each cycle is 21 days)
CXCL12
Time frame: At baseline (on the 1st day of first cycle) before chemotherapy administration and after completion of six cycles of chemotherapy (on the 18th day of sixth cycle). (each cycle is 21 days)
CXCL1
Time frame: At baseline (on the 1st day of first cycle) before chemotherapy administration and after completion of six cycles of chemotherapy (on the 18th day of sixth cycle). (each cycle is 21 days)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Oct 2022.
- Background: PubMed 5216294Bodey GP, Buckley M, Sathe YS, Freireich EJ. Quantitative relationships between circulating leukocytes and infection in patients with acute leukemia. Ann Intern Med. 1966 Feb;64(2):328-40. doi: 10.7326/0003-4819-64-2-328. No abstract available.
- Background: PubMed 2182284el-Mallakh RS. Lithium. Conn Med. 1990 Mar;54(3):115-26.
- Background: PubMed 6701582Slater V, Milanes F, Talcott V, Okafor KC. Influence of age on lithium therapy. South Med J. 1984 Feb;77(2):153-4, 158. doi: 10.1097/00007611-198402000-00003.
- Background: PubMed 6792575Yassa R. Leukocytosis during long-term lithium treatment. N Y State J Med. 1981 Sep;81(10):1479-80. No abstract available.
- Background: PubMed 9450814Ballin A, Lehman D, Sirota P, Litvinjuk U, Meytes D. Increased number of peripheral blood CD34+ cells in lithium-treated patients. Br J Haematol. 1998 Jan;100(1):219-21. doi: 10.1046/j.1365-2141.1998.00537.x.
- Background: PubMed 14804282RADOMSKI JL, FUYAT HN, NELSON AA, SMITH PK. The toxic effects, excretion and distribution of lithium chloride. J Pharmacol Exp Ther. 1950 Dec;100(4:1):429-44. No abstract available.
- Background: PubMed 3781770Petrini M, Vaglini F, Carulli G, Azzara A, Ambrogi F, Bertelli A. Effects of lithium and rubidium on the differentiation of mononuclear cells. Int J Tissue React. 1986;8(5):391-2.
- Background: PubMed 4716059Tisman G, Herbert V, Rosenblatt S. Evidence that lithium induces human granulocyte proliferation: elevated serum vitamin B 12 binding capacity in vivo and granulocyte colony proliferation in vitro. Br J Haematol. 1973 Jun;24(6):767-71. doi: 10.1111/j.1365-2141.1973.tb01704.x. No abstract available.
- Background: PubMed 299818Harker WG, Rothstein G, Clarkson D, Athens JW, Macfarlane JL. Enhancement of colony-stimulating activity production by lithium. Blood. 1977 Feb;49(2):263-7.
- Background: PubMed 6965517Levitt LJ, Quesenberry PJ. The effect of lithium on murine hematopoiesis in a liquid culture system. N Engl J Med. 1980 Mar 27;302(13):713-9. doi: 10.1056/NEJM198003273021303.
- Background: PubMed 666142Stein RS, Hanson G, Koethe S, Hansen R. Lithium-induced granulocytosis. Ann Intern Med. 1978 Jun;88(6):809-10. doi: 10.7326/0003-4819-88-6-809_2. No abstract available.
- Background: PubMed 17906701Kast RE. How lithium treatment generates neutrophilia by enhancing phosphorylation of GSK-3, increasing HIF-1 levels and how this path is important during engraftment. Bone Marrow Transplant. 2008 Jan;41(1):23-6. doi: 10.1038/sj.bmt.1705872. Epub 2007 Oct 1.
- Individual participant dataSharing planned: Undecided
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Lithium Carbonate in people with Neutropenia, run by Al-Azhar University at 1 site in Egypt.
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 7 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: finished, as of the sponsor's last update on 21 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
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.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
change in white blood cells count (time frame: At baseline (on the 1st day of first cycle) before chemotherapy administration and after each cycle (on the 18th day of every cycle) for six cycles of chemotherapy. (each cycle is 21 days)). 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 NCT05221593, which also lists 18 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 21 Oct 2022.