Chronic myelogenous leukemia

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Chronic myelogenous leukemia
Classification and external resources
Bcrablmet.jpg
The Philadelphia chromosome as seen by metaphase FISH.
ICD-10C92.1
ICD-9205.1
ICD-O:M9875/3
DiseasesDB2659
MedlinePlus000570
eMedicinemed/371
NCIChronic myelogenous leukemia
MeSHD015464
 
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Chronic myelogenous leukemia
Classification and external resources
Bcrablmet.jpg
The Philadelphia chromosome as seen by metaphase FISH.
ICD-10C92.1
ICD-9205.1
ICD-O:M9875/3
DiseasesDB2659
MedlinePlus000570
eMedicinemed/371
NCIChronic myelogenous leukemia
MeSHD015464

Chronic myelogenous (or myeloid or myelocytic) leukemia (CML), also known as chronic granulocytic leukemia (CGL), is a cancer of the white blood cells. It is a form of leukemia characterized by the increased and unregulated growth of predominantly myeloid cells in the bone marrow and the accumulation of these cells in the blood. CML is a clonal bone marrow stem cell disorder in which a proliferation of mature granulocytes (neutrophils, eosinophils and basophils) and their precursors is found. It is a type of myeloproliferative disease associated with a characteristic chromosomal translocation called the Philadelphia chromosome. CML is now largely treated with targeted drugs called tyrosine kinase inhibitors (TKIs) which have led to dramatically improved long term survival rates since the introduction of the first such agent in 2001. These drugs have revolutionized treatment of this disease and allow most patients to have a good quality of life when compared to the former chemotherapy drugs. In Western countries it accounts for 15-20% of all adult leukemias and 14% of leukemias overall (including the paediatric population).[1]

Signs and symptoms[edit]

The way CML presents depends on the stage of the disease at diagnosis as it has been known to skip stages in some cases.[2]

Most patients (~90%) are diagnosed during the chronic stage which is most often asymptomatic. In these cases it may be diagnosed incidentally with an elevated white blood cell count on a routine laboratory test. It can also present with symptoms indicative of enlarged spleen and liver and the resulting upper quadrant pain this causes. The enlarged spleen may put pressure on the stomach causing a loss of appetite and resulting weight loss. It may also present with mild fever and night sweats due to an elevated basal level of metabolism.[2]

Some (<10%) are diagnosed during the accelerated stage which most often presents bleeding, petechiae and ecchymosis.[2] In these patients fevers are most commonly the result of opportunistic infections.[2]

Some patients are initially diagnosed in the blast phase in which the symptoms are most likely fever, bone pain and an increase in bone marrow fibrosis.[2]

Cause[edit]

In most cases no obvious cause for CML can be isolated.[3]

Risk factors[edit]

It is more common in males than in females (male to female ratio of 1.4:1) and appears more common in the elderly with a median age at diagnosis of 65 years.[3] Exposure to ionising radiation appears to be a risk factor, based on a 50 fold higher incidence of CML in Hiroshima and Nagasaki nuclear bombing survivors.[3] The rate of CML in these individuals seems to peak about 10 years after the exposure.[3]

Diagnosis[edit]

Peripheral blood (MGG stain): marked leucocytosis with granulocyte left shift
A small, hypolobated megakaryocyte (center of field) in a bone marrow aspirate, typically of chronic myelogenous leukemia.

CML is often suspected on the basis of a complete blood count, which shows increased granulocytes of all types, typically including mature myeloid cells. Basophils and eosinophils are almost universally increased; this feature may help differentiate CML from a leukemoid reaction. A bone marrow biopsy is often performed as part of the evaluation for CML, and CML is diagnosed by detecting the Philadelphia chromosome. This characteristic chromosomal abnormality can be detected by routine cytogenetics, by fluorescent in situ hybridization, or by PCR for the bcr-abl fusion gene.[4]

Controversy exists over so-called Ph-negative CML, or cases of suspected CML in which the Philadelphia chromosome cannot be detected. Many such patients in fact have complex chromosomal abnormalities that mask the (9;22) translocation, or have evidence of the translocation by FISH or RT-PCR in spite of normal routine karyotyping.[5] The small subset of patients without detectable molecular evidence of bcr-abl fusion may be better classified as having an undifferentiated myelodysplastic/myeloproliferative disorder, as their clinical course tends to be different from patients with CML.[6]

CML must be distinguished from a leukemoid reaction, which can have a similar appearance on a blood smear.[4]

Pathophysiology[edit]

CML was the first malignancy to be linked to a clear genetic abnormality, the chromosomal translocation known as the Philadelphia chromosome. This chromosomal abnormality is so named because it was first discovered and described in 1960 by two scientists from Philadelphia, Pennsylvania, USA: Peter Nowell of the University of Pennsylvania and David Hungerford of Fox Chase Cancer Center.[7]

Diagram showing the translocation found in the Philadelphia chromosome

In this translocation, parts of two chromosomes (the 9th and 22nd) switch places. As a result, part of the BCR ("breakpoint cluster region") gene from chromosome 22 is fused with the ABL gene on chromosome 9. This abnormal "fusion" gene generates a protein of p210 or sometimes p185 weight (p210 is short for 210 kDa protein, a shorthand used for characterizing proteins based solely on size). Because abl carries a domain that can add phosphate groups to tyrosine residues (a tyrosine kinase), the bcr-abl fusion gene product is also a tyrosine kinase.[8][9]

Diagram showing the cells CML can develop from

The fused BCR-ABL protein interacts with the interleukin 3beta(c) receptor subunit. The BCR-ABL transcript is continuously active and does not require activation by other cellular messaging proteins. In turn, BCR-ABL activates a cascade of proteins that control the cell cycle, speeding up cell division. Moreover, the BCR-ABL protein inhibits DNA repair, causing genomic instability and making the cell more susceptible to developing further genetic abnormalities. The action of the BCR-ABL protein is the pathophysiologic cause of chronic myelogenous leukemia. With improved understanding of the nature of the BCR-ABL protein and its action as a tyrosine kinase, targeted therapies (the first of which was imatinib mesylate) that specifically inhibit the activity of the BCR-ABL protein have been developed. These tyrosine kinase inhibitors can induce complete remissions in CML, confirming the central importance of bcr-abl as the cause of CML.[9]

Classification[edit]

CML is often divided into three phases based on clinical characteristics and laboratory findings. In the absence of intervention, CML typically begins in the chronic phase, and over the course of several years progresses to an accelerated phase and ultimately to a blast crisis. Blast crisis is the terminal phase of CML and clinically behaves like an acute leukemia. Drug treatment will usually stop this progression if started early. One of the drivers of the progression from chronic phase through acceleration and blast crisis is the acquisition of new chromosomal abnormalities (in addition to the Philadelphia chromosome).[8] Some patients may already be in the accelerated phase or blast crisis by the time they are diagnosed.[4]

Chronic phase[edit]

Approximately 85% of patients with CML are in the chronic phase at the time of diagnosis. During this phase, patients are usually asymptomatic or have only mild symptoms of fatigue, left side pain, joint and/or hip pain, or abdominal fullness. The duration of chronic phase is variable and depends on how early the disease was diagnosed as well as the therapies used. In the absence of treatment, the disease progresses to an accelerated phase.[4]

Accelerated phase[edit]

Criteria for diagnosing transition into the accelerated phase are somewhat variable; the most widely used criteria are those put forward by investigators at M.D. Anderson Cancer Center,[10] by Sokal et al.,[11] and the World Health Organization.[6][12] The WHO criteria are perhaps most widely used, and define the accelerated phase by any of the following:

The patient is considered to be in the accelerated phase if any of the above are present. The accelerated phase is significant because it signals that the disease is progressing and transformation to blast crisis is imminent. Drug treatment often becomes less effective in the advanced stages.[6]

Blast crisis[edit]

Blast crisis is the final phase in the evolution of CML, and behaves like an acute leukemia, with rapid progression and short survival.[4] Blast crisis is diagnosed if any of the following are present in a patient with CML:[13]

Treatment[edit]

The only curative treatment for CML is a bone marrow transplant or an allogenic stem cell transplant.[14] Other than this there are four major mainstays of treatment in CML: treatment with tyrosine kinase inhibitors, myelosuppressive or leukopheresis therapy (to counteract the leucocytosis during early treatment), splenectomy and interferon alfa-2b treatment.[14]

Chronic phase[edit]

In the past, antimetabolites (e.g., cytarabine, hydroxyurea), alkylating agents, interferon alfa 2b, and steroids were used as treatments of CML in the chronic phase, but since the 2000s have been replaced by Bcr-Abl tyrosine-kinase inhibitors[15] drugs that specifically target BCR-ABL, the constitutively activated tyrosine kinase fusion protein caused by the Philadelphia chromosome translocation. Despite the move to replacing cytotoxic antineoplastics (standard anticancer drugs) with tyrosine kinase inhibitors sometimes hydroxyurea is still used to counteract the high WBCs encountered during treatment with tyrosine kinase inhibitors like imatinib; in these situations it may be the preferred myelosuppressive agent due to its relative lack of leukemogenic effects and hence the relative lack of potential for secondary haematologic malignancies to result from treatment.[16] IRIS, an international study that compared interferon/cytarabine combination and the first of these new drugs imatinib, with long-term follow up, demonstrated the clear superiority of tyrosine-kinase-targeted inhibition over existing treatments.[17]

Imatinib[edit]

The first of this new class of drugs was imatinib mesylate (marketed as Gleevec or Glivec), approved by the U.S. Food and Drug Administration (FDA) in 2001. Imatinib was found to inhibit the progression of CML in a the majority of patients (65–75%) sufficiently to achieve regrowth of their normal bone marrow stem cell population (a cytogenetic response) with stable proportions of maturing white blood cells. Because some leukemic cells (as evaluated by RT-PCR) persist in nearly all patients, the treatment has to be continued indefinitely. Since the advent of imatinib, CML has become the first cancer in which a standard medical treatment may give to the patient a normal life expectancy.[18]

Dasatinib and nilotinib[edit]

To overcome imatinib resistance and to increase responsiveness to TK inhibitors, two novel agents were later developed. The first, dasatinib, blocks several further oncogenic proteins, in addition to more potent inhibition of the BCR-ABL protein, and was initially approved in 2007 by the US FDA to treat CML in patients who were either resistant to or intolerant of imatinib. A second new TK inhibitor, nilotinib, was also approved by the FDA for the same indication. In 2010, nilotinib and dasatinib were also approved for first-line therapy, making three drugs in this class available for treatment of newly diagnosed CML.

Treatment-resistant CML[edit]

Whilst capable of producing significantly improved responses compared with the action of imatinib, neither dasatinib nor nilotinib could overcome drug resistance caused by one particular mutation found to occur in the structure of BCR-ABL known as the T315I mutation. Two approaches were developed to the treatment of CML as a result.

In 2007, Chemgenex released results of an open-label Phase 2/3 study (CGX-635-CML-202) that investigated the use of a non BCR-ABL targeted agent omacetaxine, administered subcutaneously (under the skin) in patients who had failed with imatinib and exhibited T315I kinase domain mutation.[19][20] This is a study which is ongoing through 2014.[21] In September 2012,the FDA approved omacetaxine for the treatment of CML in the case of resistance to other chemotherapeutic agents.[22][23]

Independently, ARIAD pharmaceuticals, adapting the chemical structures from first and second-generation TK inhibitors, arrived at a new pan-BCR-ABL inhibitor which showed (for the first time) efficacy against T315I, as well as all other known mutations of the oncoprotein. The drug, Ponatinib, gained FDA approval in December 2012 for treatment of patients with resistant or intolerant CML. Just as with second generation TK inhibitors, early approval is being sought to extend the use of Ponatinib to newly diagnosed CML also.[citation needed]

Due to the high median age of patients with CML it is relatively rare for CML to be seen in pregnant women, despite this, however, chronic myelogenous leukemia can be treated with relative safety at any time during pregnancy with Interferon-alpha hormones.[24]

Vaccination[edit]

In 2005, encouraging but mixed results of vaccination were reported with the BCR/abl p210 fusion protein in patients with stable disease, with GM-CSF as an adjuvant.[25]

Prognosis[edit]

Before the advent of tyrosine kinase inhibitors, the median survival time for CML patients had been about 3–5 years from the time of diagnosis.[1]

With the use of tyrosine kinase inhibitors, survival rates have improved dramatically. Regarding therapy with a tyrosine kinase inhibitor, a follow-up on patients using imatinib published in the New England Journal of Medicine in 2006 showed an overall survival rate of 89% after five years.[26]

In 2011, an independent study performed in 832 CML patients worldwide reported that the group of patients who achieve a stable cytogenetic response with imatinib shows an overall survival rate of 95.2% after 8 years, which is similar to the rate in the general population. Less than 1% of patients died because of leukemia progression.[18]

References[edit]

  1. ^ a b Besa, EC; Buehler, B; Markman, M; Sacher, RA (27 December 2013). "Chronic Myelogenous Leukemia". In Krishnan, K. Medscape Reference. WebMD. Retrieved 3 January 2014. 
  2. ^ a b c d e Besa, EC; Buehler, B; Markman, M; Sacher, RA (27 December 2013). "Chronic Myelogenous Leukemia Clinical Presentation". In Krishnan, K. Medscape Reference. WebMD. Retrieved 3 January 2014. 
  3. ^ a b c d Provan, D; Gribben, JG (2010). "Chapter 7 Chronic myelogenous leukemia". Molecular Hematology (3rd ed.). Singapore: Wiley-Blackwell. p. 76. ISBN 9781444318548. 
  4. ^ a b c d e Tefferi A (2006). "Classification, diagnosis and management of myeloproliferative disorders in the JAK2V617F era". Hematology Am Soc Hematol Educ Program 2006: 240–5. doi:10.1182/asheducation-2006.1.240. PMID 17124067. 
  5. ^ Savage DG; Szydlo RM; Goldman JM (1997). "Clinical features at diagnosis in 430 patients with chronic myeloid leukemia seen at a referral centre over a 16-year period". Br J Haematol 96 (1): 111–6. doi:10.1046/j.1365-2141.1997.d01-1982.x. PMID 9012696. 
  6. ^ a b c Tefferi A, Thiele J, Orazi A, Kvasnicka HM, Barbui T, Hanson CA, Barosi G, Verstovsek S, Birgegard G, Mesa R, Reilly JT, Gisslinger H, Vannucchi AM, Cervantes F, Finazzi G, Hoffman R, Gilliland DG, Bloomfield CD, Vardiman JW (2007). "Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert pane". Blood 110 (4): 1092–7. doi:10.1182/blood-2007-04-083501. PMID 17488875. 
  7. ^ Nowell PC (2007). "Discovery of the Philadelphia chromosome: a personal perspective". Journal of Clinical Investigation 117 (8): 2033–5. doi:10.1172/JCI31771. PMC 1934591. PMID 17671636. 
  8. ^ a b Faderl S, Talpaz M, Estrov Z, Kantarjian HM (1999). "Chronic myelogenous leukemia: biology and therapy". Annals of Internal Medicine 131 (3): 207–219. doi:10.7326/0003-4819-131-3-199908030-00008. PMID 10428738. 
  9. ^ a b Hehlmann R, Hochhaus A, Baccarani M; European LeukemiaNet (2007). "Chronic myeloid leukemia". Lancet 370 (9584): 342–50. doi:10.1016/S0140-6736(07)61165-9. PMID 17662883. 
  10. ^ Kantarjian H, Dixon D, Keating M, Talpaz M, Walters R, McCredie K, Freireich E (1988). "Characteristics of accelerated disease in chronic myelogenous leukemia". Cancer 61 (7): 1441–6. doi:10.1002/1097-0142(19880401)61:7<1441::AID-CNCR2820610727>3.0.CO;2-C. PMID 3162181. 
  11. ^ Sokal J, Baccarani M, Russo D, Tura S (1988). "Staging and prognosis in chronic myelogenous leukemia". Semin Hematol 25 (1): 49–61. PMID 3279515. 
  12. ^ Vardiman J, Harris N, Brunning R (2002). "The World Health Organization (WHO) classification of the myeloid neoplasms". Blood 100 (7): 2292–302. doi:10.1182/blood-2002-04-1199. PMID 12239137. Retrieved 2007-09-22. 
  13. ^ Karbasian Esfahani M, Morris EL, Dutcher JP, Wiernik PH (2006). "Blastic phase of chronic myelogenous leukemia". Current Treatment Options in Oncology 7 (3): 189–199. doi:10.1007/s11864-006-0012-y. PMID 16615875. 
  14. ^ a b Besa, EC; Buehler, B; Markman, M; Sacher, RA (27 December 2013). "Chronic Myelogenous Leukemia Treatment & Management". In Krishnan, K. Medscape Reference. WebMD. Retrieved 4 January 2014. 
  15. ^ Kufe DW; Pollack RE; Weichselbau RR et al., eds. (2003). "Tyrosine Kinase Inhibitors: Targeting Considerations". Holland-Frei Cancer Medicine (NCBI bookshelf book) (6th ed.). Hamilton, Ontario: BC Decker. ISBN 1-55009-213-8. Retrieved October 27, 2012 
  16. ^ Besa, EC; Buehler, B; Markman, M; Sacher, RA (27 December 2013). "Chronic Myelogenous Leukemia". In Krishnan, K. Medscape Reference. WebMD. Retrieved 3 January 2014. 
  17. ^ DeAngelo, DJ; Ritz, J (January 2004). "Imatinib Therapy for Patients with Chronic Myelogenous Leukemia: Are Patients Living Longer?" (PDF). Clinical Cancer Research 10 (1 Pt. 1): 1–3. doi:10.1158/1078-0432.CCR-1218-3. PMID 14734443. 
  18. ^ a b Gambacorti-Passerini, C.; Antolini, L.; Mahon, F. -X.; Guilhot, F.; Deininger, M.; Fava, C.; Nagler, A.; Della Casa, C. M.; Morra, E.; Abruzzese, E.; d'Emilio, A.; Stagno, F.; Le Coutre, P.; Hurtado-Monroy, R.; Santini, V.; Martino, B.; Pane, F.; Piccin, A.; Giraldo, P.; Assouline, S.; Durosinmi, M. A.; Leeksma, O.; Pogliani, E. M.; Puttini, M.; Jang, E.; Reiffers, J.; Valsecchi, M. G.; Kim, D. -W. (2011). "Multicenter Independent Assessment of Outcomes in Chronic Myeloid Leukemia Patients Treated with Imatinib". JNCI Journal of the National Cancer Institute 103 (7): 553–561. doi:10.1093/jnci/djr060. PMID 21422402.  edit
  19. ^ Jabbour, E.; Cortes, J. E.; Giles, F. J.; O'Brien, S.; Kantarjian, H. M. (2007). "Current and emerging treatment options in chronic myeloid leukemia". Cancer 109 (11): 2171–2181. doi:10.1002/cncr.22661. PMID 17431887.  edit
  20. ^ Kimura, S.; Ashihara, E.; Maekawa, T. (2006). "New tyrosine kinase inhibitors in the treatment of chronic myeloid leukemia". Current pharmaceutical biotechnology 7 (5): 371–379. doi:10.2174/138920106778521532. PMID 17076652.  edit
  21. ^ "Homoharringtonine (Omacetaxine Mepesuccinate) in Treating Patients With Chronic Myeloid Leukemia (CML) With the T315I BCR-ABL Gene Mutation". ClinicalTrial.gov (database recprd). Retrieved October 27, 2012 
  22. ^ FDA approves Synribo for chronic myelogenous leukemia (press release). U.S. Food and Drug Administration. October 26, 2012. Retrieved October 27, 2012 
  23. ^ FDA approves new orphan drug for chronic myelogenous leukemia (press re;ease). U.S. Food and Drug Administration. September 4, 2012. Retrieved October 27, 2012 
  24. ^ Shapira T, Pereg D, Lishner M (September 2008). "How I treat acute and chronic leukemia in pregnancy". Blood Rev. 22 (5): 247–59. doi:10.1016/j.blre.2008.03.006. PMID 18472198. 
  25. ^ Bocchia, M.; Gentili, S.; Abruzzese, E.; Fanelli, A.; Iuliano, F.; Tabilio, A.; Amabile, M.; Forconi, F.; Gozzetti, A.; Raspadori, D.; Amadori, S.; Lauria, F. (2005). "Effect of a p210 multipeptide vaccine associated with imatinib or interferon in patients with chronic myeloid leukaemia and persistent residual disease: A multicentre observational trial". The Lancet 365 (9460): 657–662. doi:10.1016/S0140-6736(05)17945-8. PMID 15721470.  edit
  26. ^ Druker BJ; Guilhot F; O'Brien SG et al. (2006). "Five-Year Follow-up of Patients Receiving Imatinib for Chronic Myeloid Leukemia". New England Journal of Medicine 355 (20): 2408–17. doi:10.1056/NEJMoa062867. PMID 17151364. 

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