Chronic neutrophilic leukaemia
Haematolymphoid Tumours (WHO Classification, 5th ed.)
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editContent Update To WHO 5th Edition Classification Is In Process; Content Below is Based on WHO 4th Edition ClassificationThis page was converted to the new template on 2023-12-07. The original page can be found at HAEM4:Chronic Neutrophilic Leukemia (CNL).
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Primary Author(s)*
Anamaria Munteanu, MD, Ph.D**, Harbor-UCLA Medical Center, Joseph J. Merlo Jr, MD. Ph.D**, Ashion Analytics, Fabiola Quintero-Rivera, University of California Irvine
**contributed equally
WHO Classification of Disease
| Structure | Disease |
|---|---|
| Book | Haematolymphoid Tumours (5th ed.) |
| Category | Myeloid proliferations and neoplasms |
| Family | Myeloproliferative neoplasms |
| Type | Myeloproliferative neoplasms |
| Subtype(s) | Chronic neutrophilic leukaemia |
Definition / Description of Disease
Chronic neutrophilic leukemia (CNL) is a rare heterogeneous BCR/ABL1-negative member of the WHO myeloproliferative neoplasm (MPN) category, which presents with neutrophilia lacking dysplastic features. Diagnostic criteria include sustained increased white blood cells in the peripheral blood for more than 3 months, with a predominance of band and segmented forms equal to or in excess of 25 x109/L.[1] The bone marrow is hypercellular with elevated myeloid to erythroid ratio, due to increase in neutrophilic granulocyte proliferation, with normal maturation (>80% mature forms of neutrophils and <10% neutrophil precursors) and rare (<5%) of nucleated cells represented by myeloblasts. This disease is also associated with hepatosplenomegaly, but can affect other tissues.
Diagnosis is made after exclusion of reactive neutrophilia (especially due to plasma cell neoplasms), atypical CML and of other myeloproliferative neoplasms (BCR-ABL1- positive Chronic Myeloid Leukemia, Polycythemia Vera, Essential Thrombocythemia and Primary Myelofibrosis) and and myelodysplastic syndrome/myeloproliferative neoplasms.[1][2][3] Previous use of G-CSF and leukaemogenic drugs (busulphan, melphalan) must also be excluded.
Mutations in CSF3R (colony-stimulating factor 3 receptor) are present in the majority of CNL cases and are part of diagnostic criteria. Genetic rearrangement for PDGFRA, PDGFRB, FGFR1, and PCM1-JAK2 fusion must be absent.[1]
Synonyms / Terminology
CNL
Epidemiology / Prevalence
CNL is a rare disease with the true incidence being unknown. While >200 cases were previously reported, three quarters to half of these do not meet current guidelines for a diagnosis of chronic neutrophilic leukemia[1][4] Evidence suggests that CNL is extremely rare with one report investigating chronic leukemias of myeloid origin finding less than 1/660 cases meeting criteria for establishing the diagnosis.[3][5]
Differential diagnosis of CNL includes neutrophilic leukemoid reaction associated with secretion of granulocyte stimulating factor by plasma cells in Multiple Myeloma or MGUS. Median age at presentation is 66 years old, with a nearly equal, slightly higher female to male prevalence.
Clinical Features
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| Signs and Symptoms | EXAMPLE: Asymptomatic (incidental finding on complete blood counts)
EXAMPLE: B-symptoms (weight loss, fever, night sweats) EXAMPLE: Fatigue EXAMPLE: Lymphadenopathy (uncommon) |
| Laboratory Findings | EXAMPLE: Cytopenias
EXAMPLE: Lymphocytosis (low level) |
editv4:Clinical FeaturesThe content below was from the old template. Please incorporate above.Most patients are asymptomatic, but sometimes present with fatigue. Constitutional symptoms may be present at diagnosis, including weight loss, and night sweats. Sometimes bruising, pruritus, or gout. A common clinical manifestation is hepatosplenomegaly.
Blood analysis can show elevated values for LDH, leukocyte alkaline phosphatase (LAP), serum vitamin B12, and uric acid.
Sites of Involvement
Peripheral blood and bone marrow involvement are consistently present. The spleen and liver are two of the most involved extramedullary sites with splenomegaly and/or hepatomegaly resulting from infiltrating neutrophils.[1][2][6] However, the disease can affect virtually any tissue type.
Morphologic Features
Peripheral Blood: typically persistent leukocytosis >3 months with white blood cells composed predominantly of bands and segmented neutrophils exceeding or equaling 80% of white blood cells. The neutrophils have frequent Dohle bodies, sometimes vacuolation and hypersegmentation [3]. Toxic granulation may be present. Most CNL patients also have mild anemia and thrombocytopenia [4]
Bone marrow: hypercellularity with elevated myeloid to erythroid ratio (often > 10:1), due to increase in neutrophilic granulocyte proliferation, with normal maturation and minimal to absent dysplastic changes. Ingestion of neutrophils by macrophages can be seen. Erythroid lineage and megakaryocytes are normal. Less than 5% of nucleated cells are myeloblasts.[7] The development of dysplastic features may herald disease progression or transformation to acute myeloid leukemia.[1][6]
Immunophenotype
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| Finding | Marker |
|---|---|
| Positive (universal) | EXAMPLE: CD1 |
| Positive (subset) | EXAMPLE: CD2 |
| Negative (universal) | EXAMPLE: CD3 |
| Negative (subset) | EXAMPLE: CD4 |
editv4:ImmunophenotypeThe content below was from the old template. Please incorporate above.There is no specific immunophenotype.[1]
Chromosomal Rearrangements (Gene Fusions)
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| Chromosomal Rearrangement | Genes in Fusion (5’ or 3’ Segments) | Pathogenic Derivative | Prevalence | Diagnostic Significance (Yes, No or Unknown) | Prognostic Significance (Yes, No or Unknown) | Therapeutic Significance (Yes, No or Unknown) | Notes |
|---|---|---|---|---|---|---|---|
| EXAMPLE: t(9;22)(q34;q11.2) | EXAMPLE: 3'ABL1 / 5'BCR | EXAMPLE: der(22) | EXAMPLE: 20% (COSMIC)
EXAMPLE: 30% (add reference) |
Yes | No | Yes | EXAMPLE:
The t(9;22) is diagnostic of CML in the appropriate morphology and clinical context (add reference). This fusion is responsive to targeted therapy such as Imatinib (Gleevec) (add reference). |
editv4:Chromosomal Rearrangements (Gene Fusions)The content below was from the old template. Please incorporate above.CNL is by definition Philadelphia chromosome negative (BCR/ABL1-negative).[1]
Chromosomal Rearrangement Genes in Fusion (5’ or 3’ Segments) Pathogenic Derivative Prevalence t(15;19)(q13;q13.3) rare
editv4:Clinical Significance (Diagnosis, Prognosis and Therapeutic Implications).Please incorporate this section into the relevant tables found in:
- Chromosomal Rearrangements (Gene Fusions)
- Individual Region Genomic Gain/Loss/LOH
- Characteristic Chromosomal Patterns
- Gene Mutations (SNV/INDEL)
CNL can progress to myeloma or blastic transformation to acute myeloid leukemia.[4] It can also transform in other forms of MPN (PV or CMML). The presence of ASXL1 as secondary mutation confers worse prognosis.[1][8]
Thrombocytopenia also proves to be an adverse prognostic factor. Patients with CNL have a hemorrhagic tendency, leading to cerebral hemorrhage as the most significant registered cause of death.[9] Other causes of death include generalized leukemic tissue infiltration, ileus caused by a granulocytic and myelocytic infiltration of the small bowel, and pneumonia.[10]
Treatment: There is currently no standard of care or established guidelines for the management of CNL. As such, treatment may involve several therapeutic approaches.[2] Blood transfusions when necessary, hydroxyurea, allogeneic bone marrow transplantation. Clinical remission has been achieved in instances with long-term interferon α treatment.[10] Hydroxyurea is the most used therapy, but often requires a second or third line therapy.[2][5][6] Other potential pharmacologic agents include imatinib, ruxolitinib, interferon-alpha(IFN-α), hypomethylating agents, thalidomide, and cladribine. These may be used in combination.[6][2][11][12] Cases with CSF3R T618I mutation may respond to treatment with Ruxolitinib (JAK inhibitor) while cases with CSF3R truncation mutations may be sensitive to Dasatinib (SRC kinase inhibitor).[4]
The presenting features may be non-specific with organomegaly involving the liver, spleen or both, mucocutaneous bleeding, and bruising.[1] The disease has a variable prognosis with some cases rapidly evolving[6][13]; others may have an indolent course spanning decades.[14] Survival is variable, overall mean survival being between 21-30 months.
Individual Region Genomic Gain / Loss / LOH
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| Chr # | Gain / Loss / Amp / LOH | Minimal Region Genomic Coordinates [Genome Build] | Minimal Region Cytoband | Diagnostic Significance (Yes, No or Unknown) | Prognostic Significance (Yes, No or Unknown) | Therapeutic Significance (Yes, No or Unknown) | Notes |
|---|---|---|---|---|---|---|---|
| EXAMPLE:
7 |
EXAMPLE: Loss | EXAMPLE:
chr7:1- 159,335,973 [hg38] |
EXAMPLE:
chr7 |
Yes | Yes | No | EXAMPLE:
Presence of monosomy 7 (or 7q deletion) is sufficient for a diagnosis of AML with MDS-related changes when there is ≥20% blasts and no prior therapy (add reference). Monosomy 7/7q deletion is associated with a poor prognosis in AML (add reference). |
| EXAMPLE:
8 |
EXAMPLE: Gain | EXAMPLE:
chr8:1-145,138,636 [hg38] |
EXAMPLE:
chr8 |
No | No | No | EXAMPLE:
Common recurrent secondary finding for t(8;21) (add reference). |
Characteristic Chromosomal Patterns
Put your text here (EXAMPLE PATTERNS: hyperdiploid; gain of odd number chromosomes including typically chromosome 1, 3, 5, 7, 11, and 17; co-deletion of 1p and 19q; complex karyotypes without characteristic genetic findings; chromothripsis. Do not delete table.)
| Chromosomal Pattern | Diagnostic Significance (Yes, No or Unknown) | Prognostic Significance (Yes, No or Unknown) | Therapeutic Significance (Yes, No or Unknown) | Notes |
|---|---|---|---|---|
| EXAMPLE:
Co-deletion of 1p and 18q |
Yes | No | No | EXAMPLE:
See chromosomal rearrangements table as this pattern is due to an unbalanced derivative translocation associated with oligodendroglioma (add reference). |
editv4:Characteristic Chromosomal Aberrations / PatternsThe content below was from the old template. Please incorporate above.Karyotypic abnormalities occur in ~10% of cases while 90% of CNL cases demonstrate a normal karyotype.[1][4] There are no diagnostic gains, chromosome losses or losses of heterozygosity (LOH) associated with CNL.
Non-specific gains of 8 (most frequent), 9, and 21.
Losses have been reported including del(7q), del(20q) (most frequent), del(11q) or 12p.
Sometimes a complex karyotype is present.
Gene Mutations (SNV / INDEL)
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| Gene; Genetic Alteration | Presumed Mechanism (Tumor Suppressor Gene [TSG] / Oncogene / Other) | Prevalence (COSMIC / TCGA / Other) | Concomitant Mutations | Mutually Exclusive Mutations | Diagnostic Significance (Yes, No or Unknown) | Prognostic Significance (Yes, No or Unknown) | Therapeutic Significance (Yes, No or Unknown) | Notes |
|---|---|---|---|---|---|---|---|---|
| EXAMPLE: TP53; Variable LOF mutations
EXAMPLE: EGFR; Exon 20 mutations EXAMPLE: BRAF; Activating mutations |
EXAMPLE: TSG | EXAMPLE: 20% (COSMIC)
EXAMPLE: 30% (add Reference) |
EXAMPLE: IDH1 R123H | EXAMPLE: EGFR amplification | EXAMPLE: Excludes hairy cell leukemia (HCL) (add reference).
|
Note: A more extensive list of mutations can be found in cBioportal (https://www.cbioportal.org/), COSMIC (https://cancer.sanger.ac.uk/cosmic), ICGC (https://dcc.icgc.org/) and/or other databases. When applicable, gene-specific pages within the CCGA site directly link to pertinent external content.
editv4:Gene Mutations (SNV/INDEL)The content below was from the old template. Please incorporate above.CNL has been strongly associated with mutations in CSF3R.[2][15] Two types of CSF3R mutations have been described. The first is a missense mutation involving the juxta-membrane region (e.g. T618I, the most common CSF3R mutation in CNL). The other results in a nonsense or frameshift mutation leading to a truncated protein and subsequent loss of the C-terminus tail region (e.g. CSF3R D771fs, S783 fs, Y752X, and W791Z).[2][15] CNL can also be associated with several genes involved in mRNA splicing, epigenetic modifications, and signaling proteins. Notably, mutations in SETBP1 and ASXL1 have been described as frequent co-occurrences in association with mutated CSF3R.[15][8] Less frequently, concurrent JAK2 mutations have also been identified with mutated CSF3R.[1][2][15][8]
Gene Mutation Oncogene/Tumor Suppressor/Other Presumed Mechanism (LOF/GOF/Other; Driver/Passenger) Prevalence (COSMIC/TCGA/Other) CSF3R T618I, T615A, truncation[15]
JAK2 V617F Other Mutations
SETBP1, ASXL1, TET2, SRSF2, U2AF1, CALR
Type Gene/Region/Other Concomitant Mutations CSF3R and SETBP1, CSF3R AND ASXL1 Mutually Exclusive JAK2 V617F and CSF3R T618I
Epigenomic Alterations
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Genes and Main Pathways Involved
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| Gene; Genetic Alteration | Pathway | Pathophysiologic Outcome |
|---|---|---|
| EXAMPLE: BRAF and MAP2K1; Activating mutations | EXAMPLE: MAPK signaling | EXAMPLE: Increased cell growth and proliferation |
| EXAMPLE: CDKN2A; Inactivating mutations | EXAMPLE: Cell cycle regulation | EXAMPLE: Unregulated cell division |
| EXAMPLE: KMT2C and ARID1A; Inactivating mutations | EXAMPLE: Histone modification, chromatin remodeling | EXAMPLE: Abnormal gene expression program |
editv4:Genes and Main Pathways InvolvedThe content below was from the old template. Please incorporate above.Colony-stimulating factor 3 receptor (CSF3R) is a gene located on chromosome 1p34.3 encoding the cytokine receptor for granulocyte colony-stimulating factor (G-CSF) or otherwise known as colony-stimulating factor 3 (CSF 3). Its binding activates the Janus kinase (JAK)/signal transducer and activator of transcription (STAT), Ras/Raf/MAP kinases, and PI3K/Akt pathways; CSF3R has been shown to signal through the JAK–STAT pathway, the nonreceptor tyrosine kinase SYK, and the SRC family kinase LYN.[16][17] In bone marrow it stimulates granulopoesis by inducing proliferation and differentiation of precursor cells into mature granulocytes.[4]
Genetic Diagnostic Testing Methods
Gene sequencing, karyotype, peripheral blood smear, flow cytometry, bone marrow biopsy, FISH, NGS.[1]
Familial Forms
No familial forms have been described.
Additional Information
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Links
SEER Hematopoietic and Lymphoid Neoplasm Database; Chronic Neutrophilic Leukemia
References
(use the "Cite" icon at the top of the page) (Instructions: Add each reference into the text above by clicking on where you want to insert the reference, selecting the “Cite” icon at the top of the page, and using the “Automatic” tab option to search such as by PMID to select the reference to insert. The reference list in this section will be automatically generated and sorted. If a PMID is not available, such as for a book, please use the “Cite” icon, select “Manual” and then “Basic Form”, and include the entire reference.)
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 Bain BJ, et al., (2017). Chronic Neutrophilic Leukaemia, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, Revised 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Arber DA, Hasserjian RP, Le Beau MM, Orazi A, and Siebert R, Editors. IARC Press: Lyon, France, p37-38.
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Szuber, Natasha; et al. (02 2020). "Chronic neutrophilic leukemia: 2020 update on diagnosis, molecular genetics, prognosis, and management". American Journal of Hematology. 95 (2): 212–224. doi:10.1002/ajh.25688. ISSN 1096-8652. PMID 31769070. Check date values in:
|date=(help) - ↑ 3.0 3.1 3.2 Bj, Bain; et al. (2015). "Chronic neutrophilic leukaemia and plasma cell-related neutrophilic leukaemoid reactions". PMID 26218186.
- ↑ 4.0 4.1 4.2 4.3 4.4 4.5 N, Szuber; et al. (2018). "Chronic neutrophilic leukemia: new science and new diagnostic criteria". doi:10.1038/s41408-018-0049-8. PMC 5811432. PMID 29440636.CS1 maint: PMC format (link)
- ↑ 5.0 5.1 Elliott, M. A.; et al. (2005-02). "WHO-defined chronic neutrophilic leukemia: a long-term analysis of 12 cases and a critical review of the literature". Leukemia. 19 (2): 313–317. doi:10.1038/sj.leu.2403562. ISSN 0887-6924. PMID 15549147. Check date values in:
|date=(help) - ↑ 6.0 6.1 6.2 6.3 6.4 Silva, Patrícia Rocha; et al. (2015-06). "Diagnosis, complications and management of chronic neutrophilic leukaemia: A case report". Oncology Letters. 9 (6): 2657–2660. doi:10.3892/ol.2015.3148. ISSN 1792-1074. PMC 4473643. PMID 26137123. Check date values in:
|date=(help) - ↑ Chronic Neutrophilic Leukemia in Bone Marrow Pathology. Kathryn Foucar, Kaaren Reichard, David Czuchlewski, ASCP Press, 2020, p284-288.
- ↑ 8.0 8.1 8.2 Ma, Elliott; et al. (2015). "ASXL1 mutations are frequent and prognostically detrimental in CSF3R-mutated chronic neutrophilic leukemia". PMID 25850813.
- ↑ T, Mitsumori; et al. (2016). "A CSF3R T618I Mutation in a Patient with Chronic Neutrophilic Leukemia and Severe Bleeding Complications". PMID 26875968.
- ↑ 10.0 10.1 J, Böhm; et al. (2002). "Chronic neutrophilic leukaemia: 14 new cases of an uncommon myeloproliferative disease". doi:10.1136/jcp.55.11.862. PMC 1769801. PMID 12401827.CS1 maint: PMC format (link)
- ↑ Dao, Kim-Hien T.; et al. (2020-04-01). "Efficacy of Ruxolitinib in Patients With Chronic Neutrophilic Leukemia and Atypical Chronic Myeloid Leukemia". Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology. 38 (10): 1006–1018. doi:10.1200/JCO.19.00895. ISSN 1527-7755. PMC 7106977 Check
|pmc=value (help). PMID 31880950. - ↑ Gunawan, Arief S.; et al. (06 2017). "Ruxolitinib, a potent JAK1/JAK2 inhibitor, induces temporary reductions in the allelic burden of concurrent CSF3R mutations in chronic neutrophilic leukemia". Haematologica. 102 (6): e238–e240. doi:10.3324/haematol.2017.163790. ISSN 1592-8721. PMC 5451352. PMID 28302714. Check date values in:
|date=(help) - ↑ Zittoun, R.; et al. (1994-02). "Chronic neutrophilic leukemia. A study of four cases". Annals of Hematology. 68 (2): 55–60. doi:10.1007/BF01715131. ISSN 0939-5555. PMID 8148416. Check date values in:
|date=(help) - ↑ Uppal, Guldeep; et al. (2015-09). "Chronic neutrophilic leukaemia". Journal of Clinical Pathology. 68 (9): 680–684. doi:10.1136/jclinpath-2015-203060. ISSN 1472-4146. PMID 26082513. Check date values in:
|date=(help) - ↑ 15.0 15.1 15.2 15.3 15.4 Je, Maxson; et al. (2013). "Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML". doi:10.1056/NEJMoa1214514. PMC 3730275. PMID 23656643.CS1 maint: PMC format (link)
- ↑ Corey, S. J.; et al. (1998-02-06). "Requirement of Src kinase Lyn for induction of DNA synthesis by granulocyte colony-stimulating factor". The Journal of Biological Chemistry. 273 (6): 3230–3235. doi:10.1074/jbc.273.6.3230. ISSN 0021-9258. PMID 9452436.
- ↑ Corey, S. J.; et al. (1994-05-24). "Granulocyte colony-stimulating factor receptor signaling involves the formation of a three-component complex with Lyn and Syk protein-tyrosine kinases". Proceedings of the National Academy of Sciences of the United States of America. 91 (11): 4683–4687. doi:10.1073/pnas.91.11.4683. ISSN 0027-8424. PMC 43852. PMID 8197119.CS1 maint: PMC format (link)
Notes
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