Introduction
Hematological malignancies (HM) are neoplasia developed at the expense of hematopoietic tissue and lymph nodes. According to WHO International Classification of Diseases for Oncology 2001, this includes all syndromes that develop from bone marrow stem cells. They may present clinically as leukemias, solid tumors called sarcomas or lymphomas [
1,
2].
There would be an East–West gradient in geographical distribution and disparities, especially in developed countries. Asian countries such as Korea [
3], Singapore, and China had lower incidence and mortality rates than Western countries [
4]. Within a country, disparities could also be observed among ethnic groups, such as in metropolitan France or the United States, with lower incidences in particular among Asians or Caucasians and higher incidences among African-descent [
5‐
9].
Recent decades’ data in the literature have shown an overall increase in incidence and mortality rates for HM, with age in both sexes, but with notable geographical distributions and disparities. According to the GLOBOCAN 2018 statistics [
10], these worldwide rates would be significantly higher than the GLOBOCAN 2012 statistics [
11]. Each category had heterogeneous evolutionary patterns, prognosis, patterns of occurrence, and global distribution frequencies.
Martinique, French Caribbean Island whose population is mainly of African origin, had no exception to the rule. General Cancer Registry of Martinique (GCRM) had already recorded an increase in standardized incidence ratios during the period 2007–2014 [
9].
In order to update epidemiological data and characteristics of HM, we have performed, through the GCRM database, an analysis of HM between 2009 to 2018.
Materials and methods
Population and design
This retrospective study included all cases registered by the GCRM of diagnosed HM (ICD-O-3/ codes:9590–9597, 9670–9719, 9724–9729, 9832–9838, 9650–9667, 9731–9734, 9760–9764, 9840, 9860, 9861, 9866, 9867, 9870–9874, 9891–9931, 9984, 9805, 9806–9809, 9865, 9869, 9911, 9898) between January 1, 2009, and December 31, 2018.
Data sources/collection
Data were recorded in the GCRM in strict compliance with international standards set by International Agency for Research on Cancer, French FRANCIM network, and European Network of Cancer Registries (ENCR). Registry procedures and data quality control, through data cross-checking and analysis across all available data sources, are in full accordance with national and international guidelines for cancer registries and are approved by the General Data Protection Regulation (GDPR). GCRM provides high-quality information on cancer in Martinique and collaborates with various local organizations to provide a complete data collection circuit.
Incidence data for HM were classified into four categories and presented by sex: (i) Multiple Myeloma and Immunoproliferative diseases (MM), (ii) Non-Hodgkin's malignant lymphoma (LMNH), (iii) Acute myeloid leukemia (LAM), and (iv) Hodgkin's lymphoma. This classification within the FRANCIM network is a particularity of the French Cancer Registries in the Caribbean area. It was adopted because of the over-incidence of MM compared with France.
Data on patients' deaths in Martinique were obtained from the French Epidemiology Center on Medical Causes of Death (CépiDc), ensuring complete information on deaths. Mortality data are coded according to the 10th International Classification of Diseases, CIM-10 (Hodgkin's disease and lymphomas: C81-C86, Other malignant tumors of lymphoid and hematopoietic tissues: C88, C90, C96, and Leukemia: C91-C95).
Statistical analysis
Patient characteristics are described as mean ± standard deviation for quantitative variables. Descriptive analysis was performed for all the HM over the period 2009–2018. Age-specific incidence rates of HM were assessed in the following five age groups: “0–4”, “5–9” “10–14”, “15–19”, “20–24”, “25–29”, “30–34”, “35–39” “40–44”, “45–49”, “50–54”, “55–59”, “60–64”, “65–69”, “70–74”, “75–79”, “80–84”, “85 and over”. Incidence standardized rates were calculated as the observed number of the main HM cases divided by the number of population over the period 2009–2018 (with 95% confidence intervals). Mortality rate were calculated as the ratio of the number of deaths during the year to the average total population for the year. We have calculated the cumulative rate, which is the sum, for each year of age, of the age-specific incidence rates from birth to age 74 for the 0–74 rate. It can be interpreted as an approximation of the cumulative risk. Cumulative risk is the risk that an individual would have of developing a hematological malignancy during the 0–74 period if no other cause of death were involved [
12]. Standardized rates were calculated using the standard world population of WHO as standard. Incidence and mortality rates were expressed in person-time.
In addition, temporal trends of incidence and mortality rates were performed by sex across the study period for the main HM.
All analyses were performed using STATA version 18 (Stata Corp., College Station, Texas, USA).
Discussion
We described the characteristics of an epidemiological analysis of HM based on a population-based cancer registry in the French West Indies from 2009 to 2018. It is a main strength to carry out this work using data from GCRM, which is well established in the health care systems and essential in Caribbean public health.
In Martinique, incidence of all cancers combined was currently lower than mainland France but was following a negative trend, probably due to the aging population and the increased prevalence of lifestyle risk factors (sedentary lifestyle, overweight and obesity, smoking). According to the GCRM, more than 1,583 new cases of invasive cancer are recorded each year, with a male/female ratio of 1.5. Incidence of cancer observed from 2009 to 2018 differs from that of France, as higher incidences have been observed for MM in particular. However, median ages are similar [
9].
Over the study period in Martinique, temporal standardized incidence distribution of all HM had decreased and persistent after 2013 for all HM groups except for MM, which showed a notable increase in incidence since then. In Martinique, the incidence was still twice as high as in France [
9]. Our study showed that LMNH was diagnosed twice less often than in mainland France. LMNH was known to be 2.5 times more common in developed countries, particularly in France, which was among the European countries with the highest incidence [
11]. The year 2000 marked the beginning of the decline in the incidence of LMNH in mainland France. In Martinique, this decline was observed more recently in 2013 [
9,
13].
Concerning worldwide epidemiology, HM was the fourth most common location and the sixth leading cause of death for all cancers combined. Our results would reflect significant points of convergence with what was observed in the Pan-American area in the United States and in the rest of the world. In particular, male dominance of incidence and mortality was observed in all age groups. Incidence rates for LMNH, LH, and MM can range from 20 to 30 worldwide [
14‐
16]. LH incidence was higher in developed countries. Incidence by age varies between the industrialized countries of the Western world and the so-called developing countries [
10]. MM incidence rates were higher for both sexes in black African-descent populations in France and in the United States [
5].
More recently, a significant and original study used 2012–2017 vital statistics data and cancer mortality data from four states: California, Florida, Minnesota, and New York. These states provided a balance of West Africans, more common in New York, with East Africans, more common in Minnesota, and African-Caribbean, found mainly in Florida and New York. African-Americans born in the United States showed highest burden of cancer mortality for MM and LAM [
17]. In this study, there was a descending gradient in mortality for HM with a sex ratio in favor of males: African-American, African-Caribbean, and African. Analysis showed several similarities with this study of subgroups of African-Americans in the United States, namely a similar distribution in the frequency of diagnosed HM (MM, LAM, LMNH, and very few LH), associated with standardized incidence and mortality rates of MM that were among the highest in the world. It should be noted, however, that MM mortality rates observed in Martinique in men and women were systematically lower in comparison with the three subgroups of black ethnic groups in the USA [
9,
10,
16‐
18].
Available data from the Pan American zone is vital because it allows the GCRM to compare neighboring populations with shared cultures, customs, and origins. In Latin America, only 8% of population were covered by cancer registries [
19]. HOLA, a multi-center retrospective observational study (Hemato-Oncology Latin America), generated unprecedented data on patient's characteristics and treatment patterns with HM [
20]. Distribution frequencies and pathology characteristics were comparable to those observed in Europe or Asia and, therefore, different from those observed in Martinique and black populations since 57.7% of patients had LMNH, 29.5% had MM, and 12.7% had LAM. This work revealed that the median age of patients was younger than those observed in Martinique and France for MM (67.4 versus 72 years) and LMNH (58 versus 62 years) and comparable for LH and LAM. There was a slight predominance of males (54.2%) over females (45.8%), except for LMNH, which had a sex ratio in favor of females. The most frequent age categories for all subtypes of HM were also comparable with those observed in Martinique. As in the rest of the world, regional disparities were observed in this Pan-American region [
20]. Incidence and mortality rates were intermediate between Caucasian and Black populations in the USA [
9,
20].
According to the literature in Martinique and mainland France, LH was a common pathology in young people; the median age is 39 in men and 33 in women. As observed in most African-descent populations worldwide, LH incidence rates in Martinique were lower (men/women: 1.2/1.4) than in France and Europe [
5,
9,
10]. Socioeconomic status has been shown to influence the epidemiology of LH. These observations led to the formulation of a late infection model, in which the absence of exposure to infectious agents in childhood increases the risk of LH in young adults [
21]. Concerning familial risk, epidemiological studies have shown that the risk is fourfold in first-degree relatives of LH patients [
22]. Other factors are also thought to increase the risk of LH, including eczema and autoimmune diseases [
23].
As observed in mainland France and more widely, LAM in Martinique was rare and mainly affected elderly subjects. Sex ratio reflecting similar incidence. Incidence rates were low and relatively stable over the study period as those observed in mainland France until 2010 [
9,
24] or United States [
25].
The origin of LMNH was multifactorial, involving genetic, viral, and environmental factors. The known risk factors for LMNH were primary immune deficiencies, organ transplants, and infectious agents such as Helicobacter Pylori, hepatitis C virus or T-cell lymphomas due to the human lymphotropic virus T-HTLV-1, autoimmune diseases such as Sjögren's syndrome and systemic lupus erythematous, family and personal history of HM [
26,
27].
Meta-analysis confirmed a link between occupational exposure to pesticides and LMNH subtypes [
28‐
30]. The French West Indies were characterized by high pesticide exposure, particularly to chlordecone (CLD), an insecticide used in banana plantations. MM, 1st HM in Guadeloupe and Martinique, was over-incidence compared to France. Information on pollutant contamination at an acceptable geographical level was available in the French West Indies. As part of the Chlordecone Plan implemented throughout the French West Indies, a study of the spatial distribution of cancers potentially linked to soil pollution by organochlorine pesticides was carried out in 2008 by the GCRM, with the support of the Regional Health Agency of Martinique. The study showed an excess incidence of MM in men living in communities with the highest levels of soil contamination, suggesting occupational exposure to organochlorine pesticides. Work on the banana worker cohort found a non-significant excess of deaths from non-Hodgkin's lymphoma and significant for multiple myeloma [
24,
31].
Overall incidence rate of myeloma has increased due to an aging population. MM were among the HM with higher incidence and mortality in French West Indies territories than in mainland France. Estimated incidence of MM in 2018 in France was slightly above the European average [
32] and slightly lower than in the United States [
25]. According to the literature, it was well known that this over incidence could be related to ethnicity.
Future epidemiological studies should allow the declination of the characteristics of the most frequent subtypes of HM in the Caribbean region and their degrees of heterogeneity. Nevertheless, all these results suggest that modern adapted therapies can increase the survival time of patients, especially for MM. For instance, hematopoietic stem cell autotransplantation by cryopreservation of grafts obtained by cytapheresis provides comprehensive access to care for patients with severe forms of myeloma and non-Hodgkin's lymphoma. This therapeutic procedure is complementary to high-dose chemotherapy, depending on the clinical indications, with preventive or curative aims [
33‐
36].
Conclusion
The results of this work would show a change in the evolution of the epidemiology of HM in Martinique with a clear downward trend in temporal trends, which has been confirmed in recent years. We also noted similarities with populations of African origin in the United States or the Pan-American zone, such as higher standardized incidence rates than in the rest of the world. Indeed, we have found a similar distribution of subtypes for HM associated with similar over-incidences. Differences in treatment and access to specific innovative techniques or therapeutic lines could explain these changes.
Ethno-geographical and socio-economic characteristics of this predominantly Afro-Caribbean population might explain some of its disparities. In addition, the role of infectious agents and environmental factors specific to the Caribbean region warrants specific research with neighboring territories that could help identify other risk factors. Finally, genome-wide association studies should also be implemented in the Caribbean to identify genetic variants that would influence the risk of genetic predisposition.
Conducting original studies in the Caribbean, characterized by atypical epidemiology and ecosystem, would provide a wide range of information on environmental exposure, co-infections with emerging viruses such as COVID-19, and the genetic variants of risk involved. Our results will contribute to expanding knowledge on the epidemiology of heterogeneous diseases such as HM disease in the Caribbean zone with a primary objective; to develop a regional strategy integrating aspects related to the patient's quality of life.
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