The specific features of renal lesion in Burkitt's lymphoma


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Abstract

Aim. To analyze the causes of renal lesion in patients with Burkitt's lymphoma (BL) and to develop optimal treatment policy. Materials and methods. The data of examination and treatment were analyzed in 20 patients with BL (14 men and 6 women aged 15 to 57 years (median age 24 years)) who had been followed up for renal lesion at the Hematology Research Center (HRC) in 2003 to 2011. When admitted to hospital, all the patients were found to have ureteric compression, renal parenchymal tumor infiltration, massive tumor cytolysis syndrome (MTCS). Polychemotherapy (PCT) was performed in accordance with the original intensive BL-M-04 protocol. The extent of the process was estimated according to the classification developed by S.B.Murphy: L3 variant B of acute lymphoblastic leukemia in 10 cases; Stage IV in 2; Stage III in 8. Acute renal failure (ARF) was identified in 13 patients. A control group comprised 36 patients with BL without ARF who had been followed up at the HRC in 2003 to 2011 and included into the BL-M-04 protocol. The ratio of patients with bone marrow lesion was 7:13 and 9:36 in the BL+ARF and BL-ARF groups, respectively. Results. Decreased urine specific gravity and proteinuria (0.4 to 1.3 g/l) were the first manifestations of renal lesion and were seen in approximately 50% of all cases both on admission to hospital and in the first stages of PCT (10 and 9, 8 and 7 of the 20 cases, respectively). Microhematuria more commonly developed after initiation of PCT (7 and 3 of the 20 cases, respectively). ARF was diagnosed in 13 patients (24% of the 55 BL patients followed up at HRC in 2003 to 2011). One female patient developed ARF after the start of PCT. Twelve patients developed this condition at the onset of disease; in 4 patients, ARF existing prior to PCT began progressing after drug administration. The etiology of ARF was generally mixed. At the onset of disease, MTCS (n=6) and specific renal parenchymal infiltration (n=6) were more common causes of ARF. Postrenal anuria was present in 2 cases. ARF after PCT initiation resulted from the toxic effects of methotrexate and MTCS (3 and 4 cases, respectively). ARF regressed in the early periods: in the prophase (n=4) and during or the first PCT block A (n=9). The BL patients with ARF, as compared to those without the latter, showed a statistically significant earlier onset of myelotoxic agranulocytosis (MTA): on day 3 of an intercourse interval (95 CI from 0 to 3 days) versus its day 5 (95% CI from 2 to 5 days) and a statistically significant longer duration of MTA - 12 days (95% CI from 7 to 16 days) versus 7 days (95% CI from 3 to 10 days); they were observed to have more severe mucositis. Despite the longer intercourse interval, 10 patients with ARF achieved remission; 4 patients died from therapy-refractory sepsis and 1 patient from thrombocytopenia. In the patients with ARF, mortality rates were significantly higher than in those without ARF (33% versus 10%; p=0.04). Conclusion. Although there is a high risk of worsening renal dysfunction, PCT is a necessary condition for ARF resolution in BL.

About the authors

A E Lukina

ФГБУ "Гематологический научный центр" Минздравсоцразвития России, Москва

Email: anna.lukina1@gmail.com

E A Bariakh

Email: ebaryakh@gmail.com

S K Kravchenko

Email: krav@blood.ru

L S Biriukova

Email: birjukova@blood.ru

É G Gemdzhian

Email: edstat@mail.ru

A U Magomedova

Email: maminat@mail.ru

A M Kremenetskaia

Email: Mtkalexandra@gmail.com

A I Vorob'ev

Email: tt@blood.ru

References

  1. Барях Е.А., Обухова Т.Н., Звонков Е.Е., Кравченко С.К. Лимфома Беркитта: клиника, диагностика и лечение. ГНЦ РАМН. Гематол и трансфузиол 2005; 6: 30-36.
  2. Барях Е.А., Валиев Т.Т., Звонков Е.Е. и др. Интенсивная терапия лимфомы Беркитта: описание двух клинических случаев. Гематол и трансфузиол 2007; 1: 41-45.
  3. Siegel M.B., Alexander E.A., Wintraub L., Idelson B.A. Renal failure in Burkitt's lymphoma. Clin Nephrol 1977; 7: 279-283.
  4. Stapleton F.B., Strother D.R., Roy S. et al. Acute renal failure at onset of therapy for advanced stage Burkitt lymphoma and B-cell acute lymphoblastic lymphoma. Memphis. Pediatrics 1988; 82: 6.
  5. Castellano I., Hernandez M.T., Gomez-Martino J.R. et al. Acute renal failure as presentation of a Burkitt's lymphoma. Am J Kidney Dis 2000; 36: E32.
  6. Mantadakis E., Aquino V.M., Strand W.R., Quigley R. Acute renal failure due to obstruction in Burkitt lymphoma. Pediatr Nephrol 1999; 13: 237-240.
  7. Olowu W.A. Hypertension and acute renal failure in Nigerian children with Burkitts lymphoma: report of three cases and review. Ann Trop Paediatr 1997; 17: 169-174.
  8. Romeril K.R., Concannon A.J., Biggs J.C. Metabolic abnormalities in adult acute lymphoblastic leukemia (Burkitt cell type): case report. N Z Med J 1981; 94: 299-301.
  9. Ворожеикина Е.Г., Бирюкова Л.С., Савченко В.Г. Синдром массивного цитолиза опухоли. Тер арх 2006; 7: 99-103.
  10. Seidemann K., Meyer U., Jansen P. Impaired renal function and tumor lysis syndrome in pediatric patients with non-Hodgkin's lymphoma and B-ALL. Observations from the BFM-trials. Klin Pädiatr 1998; 210 (4): 279-284.
  11. Kagu M.В, Ahmed S.G, Bukar A.A. Pre-treatment tumor lysis syndrome and acute renal failure in adult Iigerians with Burkitt's lymphoma: report of tree cases and literature review. Afr J Med Med Sci 2005; 34 (4): 399-402.
  12. Atamer T., Artim-Esen B., Yavuz S. et al. Massive post-obstructive diuresis in a patient with Burkitt's lymphoma. Nephrol Dial Transplant 2005; 20 (9): 1991-1993.
  13. Olowu W.A., Elusiyan J.B, Badejo S.A et al. Acute renal failure in African children with Burkitt's lymphoma: a comparison of two treatment regimens. Pediatr Blood Cancer 2006; 46 (4): 446-453.
  14. Humphreys B.D., Robert J. Renal Failure Associated with Cancer and Its Treatment: An Update. J Am Soc Nephrol 2005: 16: 151-161.
  15. Biggar R.J., Nkrumah F.K. Tumour site and renal dysfunction as factors influencing leucopenia after chemotherapy for Burkitt's lymphoma. Br J Cancer 1979; 40 (1): 152-155.

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