CC BY 4.0 · Indian J Med Paediatr Oncol 2024; 45(01): 022-027
DOI: 10.1055/s-0043-1768177
Original Article

Treatment Outcome of Burkitt's Lymphoma in Adolescents and Adults: A Retrospective Study

Sugeeth MT
1   Department of Medical Oncology, Regional Cancer Centre, Trivandrum, Kerala, India
,
Geetha Narayanan
1   Department of Medical Oncology, Regional Cancer Centre, Trivandrum, Kerala, India
,
1   Department of Medical Oncology, Regional Cancer Centre, Trivandrum, Kerala, India
,
Sreejith G Nair
1   Department of Medical Oncology, Regional Cancer Centre, Trivandrum, Kerala, India
,
Prakash NP
1   Department of Medical Oncology, Regional Cancer Centre, Trivandrum, Kerala, India
,
Jagathnath Krishna KM
2   Department of Epidemiology & Biostatistics, Regional Cancer Centre, Trivandrum, Kerala, India
,
Rekha A Nair
3   Department of Pathology, Regional Cancer Centre, Trivandrum, Kerala, India
› Institutsangaben
Funding None.

Abstract

Introduction Burkitt's lymphoma (BL) is a highly aggressive B cell non-Hodgkin lymphoma (NHL) having three distinct subtypes: endemic, sporadic, and immunodeficiency-associated BL. Sporadic BL accounts for only 1 to 2% of adult NHL.

Objectives The objective of this article was to study the clinical profile and treatment outcome of patients with BL.

Materials and Methods This was a retrospective study of 60 patients with BL conducted in the department of medical oncology at a tertiary cancer center in India during a 10-year period. Patients with BL/leukemia above 14 years of age diagnosed during the study period were included and their clinical presentation, treatment details, and outcome were studied.

Results Among 60 cases with BL, there were 41 males and 19 females. The median age at presentation was 42 years (range: 14–81 years). The main symptoms were lymphadenopathy, abdominal pain, and abdominal distension. Two patients each had paraparesis, breast lump, and jaw swelling and one patient had involvement of the cervix. Thirteen patients had features of tumor lysis at presentation. The Ann Arbor stage was I in 17, II in 16, III in 5, and IV in 22. Fifty-five patients received combination chemotherapy that included hyper-cyclophosphamide, vincristine, adriamycin, dexamethasone ± rituximab (hyper-CVAD ± R; 35), cyclophosphamide, adriamycin, vincristine, prednisolone/ cyclophosphamide, vincristine, prednisolone ± rituximab CHOP ± R (13), Berlin-Frankfurt-Munich protocol (4), and others (3). Thirty-four patients attained remission, 13 patients had progressive disease, and 8 patients died during chemotherapy. At a median follow-up of 113 months, 58% patients were alive.

Conclusions BL accounts for 1.57% of NHL above the age of 14 years with male preponderance. Intensive, short-duration chemotherapy is the standard treatment. Treatment with hyper-CVAD ± R gives 8-year progression-free survival and overall survival (OS) of 60%. Treatment with CHOP ± R is an alternative option in elderly frail patients with an 8-year OS of 46%.

Authors' Contributions

S.M.T. was involved in design, literature search, data acquisition, data analysis, statistical analysis, and manuscript preparation. G.N. contributed to conceptualization, designing, data acquisition, data analysis, manuscript preparation, manuscript editing, and manuscript review. A.T.M. helped in data acquisition and manuscript editing. S.G.N., P.N.P., and R.A.N. contributed to data acquisition. Jagathnath Krishna did statistical analysis.


Supplementary Material



Publikationsverlauf

Artikel online veröffentlicht:
24. April 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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