Relationship Between Possible Indicators Of Disease Severity And Treatment Outcomes In Hodgkin Lymphoma
Keywords:
survival, absolute neutrophil count, treatment outcome, prognosis, lymphoma, HodgkinAbstract
Aims and objectives: To assess the relationship between some possible indicators of disease severity and the treatment outcomes in Hodgkin lymphoma.
Materials and Methods: This was a prospective study of patients histologically diagnosed with Hodgkin lymphoma from July 2016 to July 2019 in three tertiary hospitals in Nigeria.
Results: The patients included 20 males and 20 females, aged 17 to 76 years. Median values at diagnosis were; haemoglobin concentration (Hb) varied from 9.5g/dL (range 10, 95% CI), leucocyte count was 7.5 x 10 9 /L (range 32.2, 95% CI), absolute neutrophil count (ANC) was 4.3x 10 9 /L (Range 29.4, CI 95%), platelet count was 238 x 109/L (Range 474, CI 95%). Two (5.4%) patients were positive for HIV. Splenomegaly was seen in (8/33) 24.2 % of the patients at diagnosis. Neither age nor spleen size were noted to be associated with survival (r = -0.146; p= 0.474 and r =0.043; 0.967, respectively). Nodular sclerosis HL was the most prevalent (50%), with higher mortality (p=0.001). The mean absolute neutrophil count (ANC) at diagnosis was 4.3±7.8 x 109/L and was related to an increased risk of death (F = 585.9; p = 0.002). The mean haemoglobin concentration at diagnosis was 9.5 ± 2.5 g/dL and this had a direct relationship with the duration of survival (r = 0.637; p = 0.011). Twenty patients (57.1%) had AnnArbor Stage IV disease, while 5 (12.5%) had B symptoms. The relationship between ANC and duration of follow-up was not significant. Combination chemotherapy - ABVD, was used in 75% of the patients out of which 20% relapsed or failed treatment. High serum conjugated bilirubin and alkaline phosphatase were associated with poorer outcomes (r = -0.593; p=0.018 and r = -0.753; 0.019, respectively).
Conclusion: At presentation, haemoglobin concentration had a direct relationship with the duration of survival, while a high absolute neutrophil count and the nodular sclerosis HL subtype were associated with higher risk of death. There is, therefore, a need for more studies to corroborate these findings in larger patient groups.
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References
Hodgkin. On some Morbid Appearances of the Absorbent Glands and Spleen. Med Chir Trans. 1832; 17: 68–114.
Lukes RJ, Butler JJ, Hicks EB. Natural history of Hodgkin’s disease as related to its pathologic picture. Cancer 1966; 19(3): 317–344.
Chen B-J, Chen DY-T, Kuo C-C, Chuang S-S. EBV-associated but HHV8-unrelated double-hit effusion-based lymphoma. Diagn Cytopathol. 2017; 45(3): 257–261.
Armstrong AA, Alexander FE, Cartwright R, Angus B, Krajewski AS, Wright DH, et al. Epstein-Barr virus and Hodgkin’s disease: further evidence for the three disease hypothesis. Leukemia 1998; 12(8):1272–1276.
Clarke CA, Glaser SL, Gomez SL, Wang SS, Keegan TH, Yang J, et al. Lymphoid malignancies in U.S. Asians: incidence rate differences by birthplace and acculturation. Cancer Epidemiol Biomarkers Prev. 2011; 20(6): 1064–1077.
Clarke CA, Glaser SL, Keegan THM, Stroup A. Neighborhood socioeconomic status and Hodgkin’s lymphoma incidence in California. Cancer Epidemiol Biomarkers Prev. 2005; 14(6): 1441–1447.
Chang ET, Zheng T, Weir EG, Borowitz M, Mann RB, Spiegelman D, et al. Childhood social environment and Hodgkin’s lymphoma: new findings from a population-based case-control study. Cancer Epidemiol Biomarkers Prev. 2004; 13(8): 1361–13670.
Mani H, Jaffe ES. Hodgkin lymphoma: an update on its biology with new insights into classification. Clin Lymphoma Myeloma 2009; 9(3): 206–216.
Bröckelmann PJ, Angelopoulou MK, Vassilakopoulos TP. Prognostic factors in Hodgkin lymphoma. Semin Hematol. 2016; 53(3): 155–164.
Adams HJA, Kwee TC. Controversies on the prognostic value of interim FDG-PET in advanced-stage Hodgkin lymphoma. Eur J Haematol. 2016; 97(6): 491–498.
Adams HJA, Nievelstein RAJ, Kwee TC. Systematic review and meta-analysis on the prognostic value of complete remission status at FDG-PET in Hodgkin lymphoma after
completion of first-line therapy. Ann Hematol. 2016; 95(1): 1–9.
Perry AM, Diebold J, Nathwani BN, MacLennan KA, Müller-Hermelink HK, Bast M, et al. NonHodgkin lymphoma in the developing world: review of 4539 cases from the International Non-Hodgkin Lymphoma Classification Project. Haematologica 2016; 101(10): 1244–1250.
Bittencourt AL, Andrade AC, Requião C, Arruda M da GB, Araújo I. Prolonged lymphocytosis as the first manifestation of Hodgkin-like adult Tcell leukemia/lymphoma. Braz J Infect Dis. 2017; 21(1): 119–122.
Bari A, Marcheselli L, Marcheselli R, Pozzi S, Cox MC, Baldessari C, et al. Absolute monocyte count at diagnosis could improve the prognostic role of early FDG‐PET in classical Hodgkin lymphoma patients. Br J Haematol. 2018; 180(4): 600–602.
Key Statistics for Hodgkin Lymphoma [Internet]. [cited 2020 May 24]. Available from: https://www.cancer.org/cancer/hodgkinlymphoma/about/key-statistics.html
Zhou L, Deng Y, Li N, Zheng Y, Tian T, Zhai Z, et al. Global, regional, and national burden of Hodgkin lymphoma from 1990 to 2017: estimates from the 2017 Global Burden of Disease study. J. Hematol & Oncol. 2019; 12(1): 107.
Shenoy P, Maggioncalda A, Malik N, Flowers CR. Incidence Patterns and Outcomes for Hodgkin Lymphoma Patients in the United States [Internet]. Advances in Hematology. 2011; 2011: e725219.
Salati M, Cesaretti M, Macchia M, Mistiri ME, Federico M. Epidemiological Overview of Hodgkin Lymphoma across the Mediterranean Basin. Mediterr J Hematol Infect Dis. 2014; 6(1) DOI: 10.4084/MJHID.2014.048
MacMahon B. Epidemiology of Hodgkin’s Disease. Cancer Res. 1966; 26(6 Part 1): 1189– 1200.
Nigeria | UNAIDS [Internet]. [cited 2020 May 25]. Available from: https://www.unaids.org/en/regionscountries/cou ntries/nigeria
Malik IA, Khan WA, Aziz Z, Karim M. Selfadministered antibiotic therapy for chemotherapy-induced, low-risk febrile neutropenia in patients with nonhematologic neoplasms. Clin Infect Dis. 1994; 19(3): 522– 527.
Wang H-W, Balakrishna JP, Pittaluga S, Jaffe ES. Diagnosis of Hodgkin lymphoma in the modern era. Br J Haematol. 2019; 184(1): 45– 59.
Crawford J, Dale DC, Lyman GH. Chemotherapy-induced neutropenia: risks, consequences, and new directions for its management. Cancer. 2004; 100(2): 228–237.
Allemani C, Sant M, De Angelis R, MarcosGragera R, Coebergh JW, EUROCARE Working Group. Hodgkin disease survival in Europe and the U.S.: prognostic significance of morphologic groups. Cancer. 2006; 107(2): 352–360.
Wijlhuizen TJ, Vrints LW, Jairam R, Breed WP, Wijnen JT, Bosch LJ, et al. Grades of nodular sclerosis (NSI-NSII) in Hodgkin’s disease. Are they of independent prognostic value? Cancer 1989; 63(6): 1150–1153.
Josting A, Franklin J, May M, Koch P, Beykirch MK, Heinz J, et al. New prognostic score based on treatment outcome of patients with relapsed Hodgkin’s lymphoma registered in the database of the German Hodgkin’s lymphoma study group. J Clin Oncol. 2002 J; 20(1): 221–230.
Mauch P, Larson D, Osteen R, Silver B, Yeap B, Canellos G, et al. Prognostic factors for positive surgical staging in patients with Hodgkin’s disease. J Clin Oncol. 1990; 8(2): 257–265.
Pendlebury SC, Koutts J, Boyages J. Hodgkins disease: clinical and radiological prognostic factors in a laparotomy series. Australas Radiol. 1994; 38(2): 123–126.
Naresh KN, Agarwal B, Sangal BC, Basu DD, Kothari AS, Soman CS. Regional variation in the distribution of subtypes of lymphoid neoplasms in India. Leuk Lymphoma 2002; 43(10): 1939– 1943.
Rafiq M, Hayward A, Warren-Gash C, Denaxas S, Gonzalez-Izquierdo A, Lyratzopoulos G, et al. Socioeconomic deprivation and regional variation in Hodgkin’s lymphoma incidence in the UK: a population-based cohort study of 10 million individuals. BMJ Open 2019; 9(9): e029228.
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