Keywords
Non Hodgkin lymphoma, Hodgkin lymphoma, Misan, Lymphoid cells, Iraq
Non Hodgkin lymphoma, Hodgkin lymphoma, Misan, Lymphoid cells, Iraq
The term lymphoma refers to a heterogeneous group of neoplasms that originate from lymphoid cells. The majority (85%) of lymphomas originate from mature B-cells, and 15% derive from the T-cell lineage1. Historically and clinically, lymphomas have been divided into two groups, Hodgkin’s lymphoma (HL) and non-Hodgkin’s lymphoma (NHL). HL is characterized by the presence of Reed–Sternberg cells, which arise in a single lymph node or chain of lymph nodes and typically spread in a stepwise fashion to anatomically contiguous nodes1. The crude incidence of HL among Europeans is 2.3 per 100,000 individuals2. Young adults aged 20 to 40 years are most commonly affected1. Histologically, classical HL accounts for 95% of all HL cases1. The subtypes of classical lymphomas include nodular sclerosis (the most common subtype, comprising 60–65% of cases), mixed cellularity (15–30%), lymphocyte-rich (5%), and lymphocyte-depleted (1%)1,3. HL patients present with peripheral lymphadenopathy, with nodes that are not tender, and with no overlying skin changes1,2. NHL are neoplastic transformations of mature B-, T-, or natural killer cells1. In children, diffuse large B-cell lymphoma (DLBCL), Burkitt’s lymphoma, and lymphoblastic lymphoma are most common2–4. DLBCL is the most common histological subtype in adults4. The incidence increases with age, while a family history of lymphoma, autoimmune disease, human immunodeficiency virus infection, hepatitis C virus seropositivity, and a high body-mass as a young adult have all been identified as risk factors of DLBCL4,5.
Here, we describe a study designed to show patterns of lymphoma among patients in Misan who presented at our center. Since this group of neoplasms are curable diseases, we need to obtain more information about them to get a significant and timely picture about the current lymphoma situation in Iraq, and in Misan in particular.
This was a retrospective, observational, single-center study carried out in Misan city, Iraq to identify any patterns in lymphoma prevalence in this governmental administrative area.
The study was conducted at Al-Shifaa Oncology Center, Al-Sadder Teaching Hospital, Faculty of Medicine, Misan University, Misan city, Iraq, from 1 April 2016 to 30 April, 2018 (Figure 1). The recruitment dates began on the tenth day of each month and continued to the thirtieth day of that month. The period from the first day of the month until the ninth day was the time of patient follow-up. Data were collected on the last day of each month of the study.
A total of 80 participants (48 men and 32 women) from Misan who were diagnosed with lymphoma were included in this study. The age of participants ranged from 10 years to 80 years. Each patient had been previously diagnosed with lymphoma and attended our center for chemotherapy. We included all patients diagnosed with lymphoma without any selectivity (the patients must live in Misan city). Sources of information included patient files, histopathology reports, and patient oncologist reports (these contained all of a patient’s data written by his/her oncologist). Participant follow-up was performed on any day of nine days following a chemotherapy cycle.
History and investigation results were documented and recorded for each participant in his/her file, including age, type of residency, occupation, sex, diagnosis, stage of lymphoma, subtype of lymphoma, and class of lymphoma.
The main sources of data were patient files and histopathology reports. Data written in the files included a patient’s baseline characteristics, lymphoma baseline characteristics, and all investigations done.
We obtained this number of participants because we included all individuals with lymphoma without any selection methods.
Written informed consent was obtained from all participants, or the parents of those aged less than 18 years, to participate in this study. The Medical Ethical Committee at Al-Shifaa Oncology Center, Al-Sadder Teaching Hospital, Faculty of Medicine, Misan University approved this study (code: 1000552).
All 80 participants included in this study were examined for eligibility and completion of follow-up. The mean age (±SD) of participants was 36±12.8 years. Half of the participants were in the 31–60 year age group, 24 (30%) of participants were aged >60 years, and just 16 (20%) belonged to the 10–30 year age group. Most participants (53; 67.5%) lived in rural areas, while 27 (32.5%) lived in urban regions. The majority of patients were employed (58; 72.5%). The male to female ratio was 1.5:1 (48 males and 32 females).
NHL was three-times more prevalent than HL, with 60 (75%) and 20 (25%) cases, respectively. Participants most frequently presented with stage IV, in 34 (42.5%) of cases, followed by stage III in 24 (32.5%), stage II in 12 (15%), and stage I in 8 (10%) cases. The classical subtypes of HL were most common, occurring in 14 (70%) cases compared with 6 (30%) cases who had nodular subtypes. The DLBCL subtype was most common among NHL subtypes, being recorded in 44 (73.3%) of cases. Classical HL was subdivided into nodular sclerosis (2; 14.3%), lymphatic-rich subtype (4; 28.6%), and mixed cellularity (8; 57.1%) (Table 1).
In our study, HL and NHL were recorded in 25% and 75% of cases, respectively, which is consistent with the results of a study conducted in Erbil city, in the north of Iraq6. The majority of HL cases presented as the classical subtype (70%), while 30% of cases encountered were of the nodular subtype (30%). The subtypes of classical HL included the nodular sclerosis (NS) subtype (14.3%) and the lymphocyte-rich subtype (28.6%), although the majority of cases comprised the mixed cellularity subtype (57.1%). The most frequent histological subtype of HL was mixed cellularity, which differs from earlier reports from the north of Iraq5,6, but is consistent with earlier reports from nearby countries and India7–17. This changing pattern differs from more recent reports from Saudi Arabia, Jordan, United Arab Emirates (UAE), and Kuwait, where higher relative rates of NS HL were reported, approaching levels seen in the USA and in European countries12–17.
With regard to NHL subtypes, we found that the majority comprised DLBCL, followed by mantle cell, follicular cell, peripheral T-cell, and Burkitt’s lymphoma. According to WHO classifications, DLBCL was also the most common diagnosis worldwide, at 52.2%, followed by T-cell rich lymphoma12. The relative proportion of DLBCL seen in the current study is almost twice the proportion seen in the USA and Europe, and is much higher than the proportion reported in India2,4,17,18, but is closer to figures reported from UAE14, Kuwait15, Jordan13, and Turkey19.
We found that the majority of lymphoma cases occurred in those aged 31 to 60 years, which was the same as findings in the USA and other countries15,18–20.
The majority of cases in our study presented at stage III or stage IV. Stage IV comprised 42.5% of cases and stage III 32.5%, while the remainder were stage II (15%) and stage I (10%). These results are in agreement with the results of a study by Robert et al.21.
Limitations of this study include that it was a single-centre study, with a small number of participants, and the participants represent residents of the Misan government administrative area only.
This study showed that in Misan city, Iraq, lymphoma occurs most frequently among males. NHL is more common than HL, and the most common histopathology of HL is mixed cellularity, while DLBCL is the most common histopathology for NHL. Most cases presented with stage III or IV, which reflects delays in diagnosis, and decreases the chance of complete recovery, reflecting a more aggressive course and behavior of the disease.
Zenodo: Lymphoma diseases patients patterns in Misan Government, http://doi.org/10.5281/zenodo.345880622.
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Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
No
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
No
Are all the source data underlying the results available to ensure full reproducibility?
No
Are the conclusions drawn adequately supported by the results?
Yes
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Epidemiology and pathology of hematologic neoplasms.
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
If applicable, is the statistical analysis and its interpretation appropriate?
Not applicable
Are all the source data underlying the results available to ensure full reproducibility?
No source data required
Are the conclusions drawn adequately supported by the results?
Partly
References
1. Perry AM, Diebold J, Nathwani BN, MacLennan KA, et al.: Non-Hodgkin lymphoma in the developing world: review of 4539 cases from the International Non-Hodgkin Lymphoma Classification Project.Haematologica. 101 (10): 1244-1250 PubMed Abstract | Publisher Full TextCompeting Interests: No competing interests were disclosed.
Reviewer Expertise: Pediatric and Young adult hematological malignancies, particularly Hodgkin and non Hodgkin lymphomas,
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | ||
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Version 1 09 Oct 19 |
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Provide sufficient details of any financial or non-financial competing interests to enable users to assess whether your comments might lead a reasonable person to question your impartiality. Consider the following examples, but note that this is not an exhaustive list:
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