Abstract
While highly curable in developed countries, Hodgkin's lymphoma (HL), remains a significant challenge for resource-limited ones. This study aimed to describe the profile of HL in Togo. This was a retrospective, descriptive study conducted at the Clinical Hematology Department of the Campus University Hospital Center in Lome, Togo. It focused on patient records diagnosed with HL between January 1, 2006, and December 31, 2022. Various variables such as age, gender, histological type of HL, Ann Arbor stage, prognostic classification, therapeutic protocol used, and patient outcomes were examined. The annual incidence of HL was 1.5 with a mean age of 38.7 years (range 12-63). Lymph node enlargement was the primary clinical sign (100%). Histologically, classical HL was found in 21 patients (87.5%). Staging was conducted for 16 (66.7%) patients, among whom 11 (66.7%) were at an advanced stage, and 6 (37.5%) had an unfavorable prognosis. The ABVD protocol was used in 13 patients (54.2%), receiving between 1 and 6 cycles. One patient achieved complete remission (4.1%), three deceased (12.5%), and 17 (71%) were lost to follow-up. Hodgkin's lymphoma prognosis remains unfavorable with low remission rates in Togo. Improving the technical facilities will ensure better management of this lymphoma.
Author Contributions
Copyright© 2024
Padaro Essohana, et al.
License
This work is licensed under a Creative Commons Attribution 4.0 International License.
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Competing interests The authors have declared that no competing interests exist.
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Introduction
First reported by Thomas Hodgkin from the Guy’s hospital in London in 1832, Hodgkin lymphoma are a family of unique lymphoma subtypes, in which the nature of the neoplastic cell was enigmatic for many years
Results
In total, 24 records were included. HL accounted for 18.1% of lymphoid neoplasms (24/132) and 3.8% of malignant hematologic disorders (24/748) during the study period. The annual incidence was 1.5. The mean age of patients was 38.7 years (12-63), with a male predominance and a sex ratio of 1.7. The main presenting circumstance of Hodgkin's lymphoma (HL) was lymph node enlargement, present in all patients (100%). Patients also exhibited night sweats (6/24), prolonged fever (6/24), fatigue (1/24), and persistent pruritus (1/24). Physical signs were predominantly characterized by lymph node enlargement, averaging 7cm (range 2-15). These were peripheral in 21 patients and cervical in 17. A quarter of the patients also presented with hepatomegaly, and four had splenomegaly. Histologically, classical HL constituted most histological types, diagnosed in 21 (87.5%) patients. Sixteen patients underwent staging (66.7%). Among these patients, five (33.3%) were at an early stage at diagnosis, with two patients presenting a bulky mass, and eleven (67.7%) were at an advanced stage ( In terms of treatment, the frontline protocol used was the combination chemotherapy regimen of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD). Thirteen patients, accounting for a ratio of 54.2%, initiated this treatment. They received between 1 and 6 cycles.
Classical HL
21
87,5
Nodular sclerosis HL
10
41,6
Mixed cellularity classical HL
6
25
Lymphocyte-rich classical HL
3
12,5
Lymphocyte-depleted classical HL
1
4,2
Not specified
1
4,2
Nodular lymphocyte predominant HL
3
12,5
Favorable
4
80
Unfavorable
1
20
Favorable
3
27,3
Unfavorable
8
72,7
Favorable
4
80
Unfavorable
1
20
Favorable
3
27,3
Unfavorable
8
72,7
Discussion
In comparison to other malignant hematologic disorders, Hodgkin's lymphoma is relatively rare, as demonstrated by the prevalence found in our study. With approximately 1,500 new cases per year in France, Hodgkin's lymphoma accounts for only 10 to 15% of lymphomas and 0.5 to 1% of new cancer cases All patients presented with lymph node enlargement, predominantly peripheral and cervical. Indeed, at the time of diagnosis, most Hodgkin's lymphoma patients present with supradiaphragmatic lymphadenopathy. Patients frequently exhibit involvement of cervical, anterior mediastinal, supraclavicular, and axillary lymph nodes, while inguinal regions are less commonly affected. About a third of patients present systemic symptoms such as fever, night sweats, and weight loss Classical HL is the most found subtype, accounting for nearly 90% of HL cases Only 16 patients (66.67%) underwent staging. This is mostly due to the patients' low socioeconomic status. Undergoing a scan cost approximately $133 USD, approximately 2.3 times the minimum wage during the study period ($58 USD). Long delays in specialized consultations, associated with diagnostic errors, and the difficulty in accessing the country's only public clinical hematology service account for the prevalence of advanced stages and poor prognoses in our study. The indicated first-line treatment in our study was the ABVD protocol with six cycles, due to the unavailability of PET-CT at CHU and radiotherapy, which could have reduced the number of chemotherapy cycles based on the therapeutic response to systemic treatment. Only one patient achieved complete remission, and 17 (71%) were lost to follow-up. This high rate of loss to follow-up and low rate of remission reflects the financial precariousness of patients, most of whom did not initiate or complete the treatment. Indeed, Hodgkin's lymphoma is a highly curable hematologic malignancy, and the ABVD protocol is a validated treatment supported by several studies. It is used in combined therapy with radiotherapy or as a single modality due to the late toxicity of radiotherapy
Conclusion
Hodgkin's lymphoma is an infrequent lymphoma in our daily practice, even though its incidence is increasing. Its diagnosis is straightforward, relying on histology coupled with immunohistochemistry. Although the treatment is well-defined by various international recommendations, it poses similar challenges for practitioners in resource-limited countries, including prolonged diagnostic delays resulting in advanced disease and poor prognosis, inaccessibility to modern prognostic tools, and difficulty accessing standard or innovative therapies. All these factors lead to a low remission rate. Improvement in technical facilities and better social coverage will likely enable a more effective management of Hodgkin's lymphoma in Togo.