CC BY-NC-ND 4.0 · J Lab Physicians 2021; 13(02): 134-138
DOI: 10.1055/s-0041-1730752
Original Article

Isolated CNS Relapse in Acute Lymphoblastic Leukemia (ALL): An Experience from a Tertiary Care Center

Manvir Singh Tevatia
1   Department of Pathology, Command Hospital, Pune, Maharashtra, India
,
Isha Sharma
2   Department of Pathology, Armed Forces Medical College, Pune, Maharashtra, India
,
Toyaja Jadhav
2   Department of Pathology, Armed Forces Medical College, Pune, Maharashtra, India
,
3   Department of Lab Sciences and Mol Medicine, Army Hospital (R&R), Delhi, India
,
Sanjeevan Sharma
4   Department of Medicine and of Haematology, Command Hospital, Lucknow, Uttar Pradesh, India
› Author Affiliations

Abstract

Aims and Objectives In this study the various parameters of acute lymphoblastic leukemia (ALL), including the clinical features, peripheral blood and bone marrow (BM) findings, immunophenotypic and cytogenetic details in ALL cases who had isolated relapse involving the central nervous system (CNS), were studied.

Patients/Materials and Methods Duration of the study is from 2015 to 2019 in which 5 ALL cases were presented to this tertiary care center. The presenting symptoms varied from headache, fever, and distension of abdomen. These cases were either on therapy or post completion of chemotherapy. The diagnosis of CNS relapse followed after the examination of cerebrospinal fluid (CSF). Patients also underwent BM examination to rule out systemic relapse.

Results Age of patients ranged from 7 months to 42 years. There were three female patients. Two patients had isolated CNS relapse 3.5 years after completing therapy and succumbed to their illness. Two patients had t(9;22) while one patient had t(1;14) cytogenetic abnormality at diagnosis. One patient was diagnosed as T-ALL. Treatment offered was German Multicentre ALL protocol for induction along with 10 cycles of maintenance.

Conclusion The most common hematolymphoid malignancy in children namely ALL accounts for 75% of childhood leukemias. Complete remission rates reach up to 70 to 80%. CNS involvement is known to occur in these cases. CNS relapse may occur alone or with systemic relapse. Advances in therapeutic protocols along with CNS prophylaxis have drastically brought down the rates of CNS relapse. It is essential to maintain a high degree of suspicion so that these cases of isolated CNS relapse can be identified at the earliest and definitive therapy can be offered.



Publication History

Article published online:
15 June 2021

© 2021. The Indian Association of Laboratory Physicians. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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  • References

  • 1 Borowitz MJ, Chan JKC, Downing JR, Lebeau MM, Arber DA. B- lymphoblastic leukaemia/lymphoma, not otherwise specified (NOS). In: Swerdlow SH, Campo E, eds. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Cours Albert Thomas, Lyon:. International Agency For Research on Cancer 2017; 200-202
  • 2 Redaelli A, Laskin BL, Stephens JM, Botteman MF, Pashos CL. A systematic literature review of the clinical and epidemiological burden of acute lymphoblastic leukaemia (ALL). Eur J Cancer Care (Engl) 2005; 14 (01) 53-62
  • 3 Maitra A, McKenna RW, Weinberg AG, Schneider NR, Kroft SH. Precursor B-cell lymphoblastic lymphoma. A study of nine cases lacking blood and bone marrow involvement and review of the literature. Am J Clin Pathol 2001; 115 (06) 868-875
  • 4 Borowitz MJ, Chan JKC, Bene MC, Arber DA. T-lymphoblastic leukaemia/lymphoma. In: Swerdlow SH, Campo E, eds. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Cours Albert Thomas, Lyon:. International Agency For Research on Cancer 2017; 209-212
  • 5 Dass J, Dayama A, Mishra PC. et al. Higher rate of central nervous system involvement by flow cytometry than morphology in acute lymphoblastic leukemia. Int J Lab Hematol 2017; 39 (05) 546-551
  • 6 Surapaneni UR, Cortes JE, Thomas D. et al. Central nervous system relapse in adults with acute lymphoblastic leukemia. Cancer 2002; 94 (03) 773-779
  • 7 Hormigo A, Abrey L, Heinemann MH, DeAngelis LM. Ocular presentation of primary central nervous system lymphoma: diagnosis and treatment. Br J Haematol 2004; 126 (02) 202-208
  • 8 Jahnke K, Thiel E, Martus P. et . German Primary Central Nervous System Lymphoma Study Group. Relapse of primary central nervous system lymphoma: clinical features, outcome and prognostic factors. J Neurooncol 2006; 80 (02) 159-165
  • 9 Simone JV. History of the treatment of childhood ALL: a paradigm for cancer cure. Best Pract Res Clin Haematol 2006; 19 (02) 353-359
  • 10 Cortes J, O’Brien SM, Pierce S, Keating MJ, Freireich EJ, Kantarjian HM. The value of high-dose systemic chemotherapy and intrathecal therapy for central nervous system prophylaxis in different risk groups of adult acute lymphoblastic leukemia. Blood 1995; 86 (06) 2091-2097
  • 11 Hoelzer D, Gökbuget N. Treatment of lymphoblastic lymphoma in adults. Best Pract Res Clin Haematol 2002; 15 (04) 713-728
  • 12 Hollender A, Kvaloy S, Nome O, Skovlund E, Lote K, Holte H. Central nervous system involvement following diagnosis of non-Hodgkin’s lymphoma: a risk model. Ann Oncol 2002; 13 (07) 1099-1107
  • 13 Feugier P, Virion JM, Tilly H. et al. Incidence and risk factors for central nervous system occurrence in elderly patients with diffuse large-B-cell lymphoma: influence of rituximab. Ann Oncol 2004; 15 (01) 129-133
  • 14 Badr MA, Hassan TH, El-Gerby KM, Lamey ME. Magnetic resonance imaging of the brain in survivors of childhood acute lymphoblastic leukemia. Oncol Lett 2013; 5 (02) 621-626
  • 15 Mahmoud HH, Rivera GK, Hancock ML. et al. Low leukocyte counts with blast cells in cerebrospinal fluid of children with newly diagnosed acute lymphoblastic leukemia. N Engl J Med 1993; 329 (05) 314-319
  • 16 Smith M, Arthur D, Camitta B. et al. Uniform approach to risk classification and treatment assignment for children with acute lymphoblastic leukemia. J Clin Oncol 1996; 14 (01) 18-24
  • 17 Pui CH, Campana D, Pei D. et al. Treating childhood acute lymphoblastic leukemia without cranial irradiation. N Engl J Med 2009; 360 (26) 2730-2741
  • 18 Pui CH, Evans WE. Treatment of acute lymphoblastic leukemia. N Engl J Med 2006; 354 (02) 166-178
  • 19 Dennis AC. Acute leukemia and myelodysplastic syndromes. In: Mary CT, ed. Lippincott Manual of Oncology. Philadelphia, PA:. Wolters Kluwer 2008; 840