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December, 2017 >>

Clinical presentation of acute myeloid leukaemia ó A decade-long institutional follow-up

Bibi Kulsoom  ( National Institute of Blood Disease & Bone Marrow Transplantation, Karachi, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia, )

Tahir Sultan Shamsi  ( National Institute of Blood Disease & Bone Marrow Transplantation, Karachi, )

Nikhat Ahmed  ( College of Medicine, Ziauddin University, Clifton, Karachi, )

Syed Nazrul Hasnain  ( (Retired) Dow International Medical College, Karachi, Pakistan. )

Abstract

Objective: To analyse a decade-long pattern of clinical presentation of acute myeloid leukaemia patients and compare it with contemporary data. 
Methods: The retrospective cohort study was conducted at the National Institute of Blood Diseases and Bone Marrow Transplantation, Karachi, and comprised of medical record of acute myeloid leukaemia patients from March 2006 to October 2016. Data noted age at presentation, gender, medical history, physical examination, blood and bone marrow investigations such as, haemoglobin levels, blood cell count myeloperoxidase activity, periodic acid-Schiff and reticulin staining as well as final diagnosis. Comparison, where possible, was done with contemporary literature. SPSS 19 was used for data analysis 
Results: Of the 626 subjects, 248(39.6%) were females and 378(60.4%) males. The overall mean age was 35.3¬Ī17.1 years. The most common age group was 15-40 years with 354(56.5%) patients. The most common subtype was acute myeloid leukaemia with maturation 183(33.6%). Myeloperoxidase activity was positive for the majority of the acute myeloid leukaemia patients. Periodic acid-Schiff test, done on only selected patients, was mostly negative. Reticulin staining was positive for 113(65.3%) patients. The most common presenting complaints were fever 266(71.9%) and weakness 168(45.4%). Mean haemoglobin and red blood cell count were 8.3 ¬Ī 2.4 g/dL and 2.9 ¬Ī 1.2 1012/L, respectively.¬†
Conclusion: Acute myeloid leukaemia was found to be a highly variable disease that presented with non-specific signs and symptoms. 
Keywords: AML presentation, AML epidemiology, AML in Pakistan, Myeloperoxidase, AML-M2. (JPMA 67: 1837; 2017)

Introduction

Acute myeloid leukaemia (AML) is a group of heterogeneous malignant disorders. It primarily results from aberrant differentiation that leads to uncontrolled proliferation of immature myeloid cells.1 AML is more frequently observed in adults.2AML patients may present with signs and symptoms related to pancytopenia, which include infections, fever, weakness, fatigue and haemorrhagic findings like petechiae, menorrhagia and epistaxis. This is because the proliferation of malignant cells gradually takes over the normal blood cell in bone marrow. Occasionally, there is sternal discomfort or tenderness and pain in lower extremities. There may be cutaneous or gingival infiltration by leukaemia cells. Physical examination may reveal pallor, lymph node enlargement, hepatomegaly and splenomegaly.3
AML classification is based on criteria defined in World Health Organisation's (WHO) or French-American-British (FAB) classifications.1 In the WHO classification, genetic mutations, karyotyping abnormalities, different stages of maturation and blast cell subtypes are taken into account.4 Thus, it points towards diverse underlying mechanisms in the development of AML. Therefore, more studies are required to report the common and rare presentations of AML at clinic as it will help in prompt diagnosis and timely management.It is essential to specify AML subtype as investigations, treatment and prognosis may be different.5 One good example is that of acute promyelocytic leukaemia (APL) which has very different management than other AML subtypes.6,7 In APL, complete remission (CR) rate after chemotherapy is above 90% and the prognosis has greatly improved as manifested by a lower relapse rate, and longer disease-free survival (DFS) as well as overall survival (OS) rates.6 However, different contemporary studies have reported differences in terms of various characteristics, such as, gender, age, presenting complaints, investigation profile and diagnosis.2,8-12 The current study was conducted to report the clinical presentations of AML patients at the time of diagnosis to fill in any existing gaps in global clinical literature.

Patients and Methods


This retrospective cohort study was conducted at the National Institute of Blood Diseases and Bone Marrow Transplantation (NIBD & BMT), Karachi, and comprised of medical records of AML patients from March 2006 to October 2016. Institutional ethics review board approved the study.
Data collected included age at presentation, gender, medical history, physical examination, blood and bone marrow investigations done as diagnostic workup for AML patients such as, haemoglobin levels, blood cell count myeloperoxidase (MPO) activity, periodic acid-Schiff (PAS) and reticulin staining as well as the final diagnosis. Patients were divided into four age groups of <15 years, 15-40 years, 41-60 years and >60 years.
Data was entered in Microsoft Excel. SPSS 19 was used for data analysis. All discrete data, such as number of patients in a category, were given as frequency and percentage. Continuous data, such as haemoglobin levels and other haematological parameters, were given as mean and standard deviation (SD) or median and interquartile range (IQR) where appropriate. An attempt was made to compare our data with contemporary literature where appropriate.

Results


Of the 626 participants, 248(39.6%) were females and 378(60.4%) males with an overall mean age of 35.3¬Ī17.1 years while the median age was 35 years (IQR: 1-86 years). The most common age group was 15-40 years with 354(56.5%) patients, followed by 41-60 years with 168(26.8%). The number of patients in <15 and >60-year age groups was 53(8.5%) and 51(8.1%), respectively.
AML subtypes were available for 545(87.1%) patients. The most common AML subtype according to latest WHO classification was "AML with maturation" (M2) having 183(33.6%) patients, followed by "AML without maturation" (M1) with 141(25.9%). APL was the third-most frequent pathology with 62(11.4%) cases, followed by acute monocytic leukaemia 53(9.7%). Two (0.3%) cases of chronic myeloid leukaemia (CML) blast crisis were excluded.
MPO activity was reported for 336(53.7%) patients, out of which 316(94.1%) patients were found positive. PAS staining data was available only for 42(6.7%) patients, out of which 13(31%) patients were positive. Reticulin staining data was reported for 173(27.6%) patients, out of which it was positive for 113(65.3%) patients (Table-1; Figure-1).





Most frequent clinical features at presentation included fever 266(71.9%), weakness 168(45.4%) and bleeding tendency 171(19.2%). A significant number of patients had presented with bodyaches, respiratory complaints and hepatosplenomegaly or other abdominal complaints (Table-2).



Normal blood cell counts were available for a majority of the patients, but due to extreme values (for example, leukocyte count) secondary to underlying pathology, we considered median levels in this case. Median haemoglobin levels was 8.1 g/dl (IQR: 2.1 - 17), whereas median counts for red blood cells (RBC), white blood cells (WBC), platelets and blasts were 2.9 1012/L (IQR: 0-23), 9.6 109/L (IQR: 2-234000), 36 109/L (IQR: 0-100000) and 48% (IQR: 1-100), respectively (Table-3).



We carried out subgroup analysis to find any significant difference between blood counts, clinical presentation and other investigation results according to gender, age group and AML type. Pearson's correlation revealed that AML patients in older age groups tended to present with lower haemoglobin levels and RBC count compared to young patients (r= -0.106, p=0.01; and r= -0.103, p=0.01, respectively). Although the difference did not reach statistical significance, a clear downward trend could be noted as measured by Mantel-Haenszel test of trend (p=0.01). Such observation was not seen when gender or other factors were used to do similar subgroup analysis. Similarly, MPO activity being positive was more often seen in older age groups of patients with a significant positive trend (Mantel-Haenszel p=0.002). Other subgroup analyses yielded no significant differences (Figure-2).



Discussion


Our study is unique from this region, as it reports findings from a large group of patients who presented during a period of 11 years. We found extensive data in a large group of patients. Further, an attempt has been made to compare our data with contemporary literature published during the same period. This approach has revealed certain differences between different data sets. Our study included the largest number of patients, except that reported by Wakui et al. (Table-3).10 Various aspects were compared between our findings and other reported studies. Female-to-male ratio is similar to those reported from different parts of Pakistan (Table-4).



8,9,12,13 A lower ratio is observed in a large study from Japan10 while there seems to be no difference in male-to-female ratio from the United States.11,14 The mean age was 34 years for AML patients and a large number of patients (56.5%) fell into the age group of 15-40 years at presentation in clinic. The second-most common population of patient were from age group 41-60 years. Since AML is largely a disease of the adults, we found only 8.5% patients under 15 years of age. Our observations were consistent with most of the studies reporting age groups.8,9,11,15,16
As mentioned above, AML is a group of heterogeneous diseases which present with morphologically different subtypes.1,4 Although some cytogenetic abnormalities have been identified in relation with AML, it is expected that in future various morphological presentations could be related to specific cytogenetic abnormality and/or altered gene expression. This will give clear explanation of underlying mechanisms involved in malignant transformation. The most common AML subtype was AML with maturation (M2), followed by AML without maturation (M1). Similar findings have been reported by studies from the United States,11,14 India5 and a recent study from Karachi.17 Additionally, AML-M2 has been reported to be the most frequent subtype from Japan,10 and as the second-most common subtype in many other countries.2,12,13,16,18 Although we found APL as a frequent presentation, but it was not the most common presenting subtype as reported in studies from India and Iraq.2,16
AML patients present in clinic with a variety of non-specific and some specific signs and symptoms related to underlying pathology. In this study it was observed that most of the patients presented with fever and weakness. Such symptoms are highly non-specific and could be a source of delayed diagnosis.
MPO is the marker of myeloid lineage and its expression can help in determining need for treatment and bone marrow transplantation in AML patients.19 Only 59% of total AML patients had MPO activity ordered, out of which 94.1% were positive for it. Interestingly, MPO activity was more likely to be positive in older group of patients. The significance of this finding is not clear at present.
Similarly, PAS staining (for cell surface glycoproteins)was performed for 42 AML patients and only 13 were found positive for PAS, which included 5 patients of AML-M1 and 3 of AML-M2. PAS test is characteristically positive in leukaemias from lymphoid series, but sometimes it is also positive in AML patients.5 Additionally, matrix changes are also observed in AML. Reticulin staining is one of the matrix collagen testing,20 and is associated with poor prognosis.21 In our data, 173 patients were tested with reticulin staining and out of them 113(65.3%) were found positive. Among the positive cases, 51(45%) were AML-M2, 25(22%) were AML-M1 and 14(12.4%) were AML with myelodysplasia-related changes.
Haemoglobin levels and blood cell counts may be altered due to the fact that bone marrow is mostly populated by leukaemic blasts. Patients in our study presented with lower haemoglobin levels and RBC count. Others have also reported similar observations.8-10,13,15,22 However, we observed that older age group patients have a tendency to present with lower haemoglobin and RBC count as compared to younger age groups. The significance of this finding is unclear at present.
The current study had some limitations. Firstly, it was a single-centre study. Secondly, complete record was not present for all the subjects. Similarly, not all patients had their investigations done, apparently due to financial constraints, because the healthcare in Pakistan is largely borne privately by the public, whereas the management of malignant disorders is highly expensive. A low gross domestic product (GDP) further augments such constraints.

Conclusion

AML was found to be a highly variable disease that presented mostly with non-specific and wide variety of signs and symptoms. The most common age to present was 15-40 years, most frequent subtype was M2 and most common features included infection, weakness and bleeding tendency. Haemoglobin levels, RBC counts and MPO activity tended to differ with age groups.

Disclaimer:
The data was presented at HaemCon Conference, held in Lahore,
Pakistan from February 16 to 18, 2017, and at Cell Sciences Conference, held in Dubai, United Arab Emirates (UAE) from April 6 to 8, 2017.
Conflict of Interest: None.
Source of Funding: None.

References


1. Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick HR, et al. Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 1976; 33: 451-8.
2. Singh G, Parmar P, Kataria SP, Singh S, Sen R. Spectrum of acute and chronic leukemia at a tertiary care hospital, Haryana, India. Int J Res Med Sci 2016; 4: 1115-8.
3. Kufe DW, Raphael P, Weichselbaum RR,  Bast RC, Gansler TS, Holland JF, et al. Holland Frei Cancer Medicine. 6th ed. [Online] [Cited 2014 Sep 08]. Available from: URL: http://www.ncbi.nlm.nih.gov/books/NBK12354/).
4. Vardiman JW, Thiele J, Arber DA, Brunning RD, Borowitz MJ, PorwitA, et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 2009; 114: 937-51.
5.Salkar AB, Patrikar A, Bothale K, Malore S, Salkar A, Modani S. Clinicohematological evaluation of leukemias in a tertiary care hospital. IOSR-JDMS 2014; 13: 126-34.
6. Sanz MA, Montesinos P, Rayón C, Holowiecka A, de la Serna J, Milone G, et al. Risk-adapted treatment of acute promyelocyticleukemia based on all-trans retinoic acid and anthracycline with addition of cytarabine in consolidation therapy for high-risk patients: further improvements in treatment outcome. Blood 2010; 115: 5137-46.
7. D√∂hner H, Estey EH, Amadori S, Appelbaum FR, B√ľchner T, Burnett AK, et al. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European Leukemia Net. Blood 2010; 115: 453-74.
8. Sultan S, Zaheer HA, Irfan SM, Ashar S. Demographic and Clinical Characteristics of Adult Acute Myeloid Leukemia - Tertiary Care Experience. Demographical and Clinical Characteristics of Pakistani Adult AML Cases. Asian Pac J Cancer Prev 2016;17: 357-60.
9. Sultan S, Zaheer HA, Irfan SM, Ashar S. Acute Myeloid Leukemia: Clinical Spectrum of 125 Patients. Asian Pac J Cancer Prev 2016; 17: 369-72.
10. Wakui M, Kuriyama K, Miyazaki Y, Hata T, Taniwaki M, Ohtake S, et al. Diagnosis of acute myeloid leukemia according to the WHO classification in the Japan Adult Leukemia Study Group AML-97 protocol. Int J Hematol 2008; 87: 144-51.
11. Appelbaum FR, Gundacker H, Head DR, Slovak ML, Willman CL, Godwin JE, et al. Age and acute myeloid leukemia. Blood 2006; 107: 3481-5.
12. Kakepoto GN, Burney IA, Zaki S, Adil SN, Khurshid M. Long term outcome of acute myeloid leukemia in adults in Pakistan. J Pak Med Assoc 2002; 52: 482-6.
13. Harani MS, Adil SN, Shaikh MU, Kakepoto GN, Khurshid M. Frequency of FAB subtypes in acute myeloid leukemia patients at Aga Khan University Hospital Karachi. J Ayub Med Coll Abbottabad 2005; 17: 26-9.
14. Arber DA, Stein AS, Carter NH, Ikle D, Forman SJ, Slovak ML. Prognostic impact of acute myeloid leukemia classification. Importance of detection of recurring cytogenetic abnormalities and multilineage dysplasia on survival. Am J Clin Pathol 2003; 119: 672-80.
15. Asif N, Hassan K. Acute Myeloid Leukemia amongst Adults. JIMDC 2013; 2: 58-63.
16. Al-Husseiny AH.  Acute myeloid leukemia in adolescent and adult Iraqi patients clinical and haematological study. J Res Diyala Humanity 2008; 29: 1-11
17. Chang F, Shamsi TS, Waryah AM. Clinical and Hematological Profile of Acute Myeloid Leukemia (AML) Patients of Sindh. J Hematol Thrombo Dis 2016; 4: 239.
18. Hassan K, Ikram N, Shah SH. A morphological pattern of 234 cases of leukemias. J Pak Med Assoc 1994; 44: 145-8.
19. Kim Y, Yoon S, Kim SJ, Kim JS, Cheong JW, Min YH. Myeloperoxidase Expression in Acute Myeloid Leukemia Helps Identifying Patients to Benefit from Transplant. Yonsei Med J 2012; 53: 530-6.
20. Sundström G, Dahl  IM, Hultdin M, Lundström B, Wahlin A, Engström-Laurent A. Bone marrow hyaluronan distribution in patients with acute myeloid leukemia. Med Oncol 2005; 22: 71-8.
21. Kuter DJ, Bain B, Mufti G, Bagg A, Hasserjian RP. Bone marrow fibrosis: pathophysiology and clinical significance of increased bone marrow stromal fibres. Br J Haematol 2007; 139: 351-62.
22. Ali A, Siddique MK, Shakoori AR. Frequency of FLT3/ITD Mutations in Pakistani Acute Myeloid Leukemia Patients. Pak J Zool 2013; 45: 495-501.


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