CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2018; 39(03): 301-306
DOI: 10.4103/ijmpo.ijmpo_9_17
Original Article

Five-Year Survival Rate and the Factors for Risk-Directed Therapy in Acute Lymphoblastic Leukemia

Bibin Varghese
Department of Paediatrics, Institute of Child Health, Kottayam, Kerala, India
,
Austoria Abzalon Joobomary
Department of Community Medicine, Government Medical College, Kottayam, Kerala, India
,
P Savida
Department of Paediatrics, Institute of Child Health, Kottayam, Kerala, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

Background: Acute lymphoblastic leukemia (ALL) has 5-year survival of more than 90% in many advanced cancer research institutes. However, advanced cancer care is not available to majority of poor in developing countries. The experience of treating such patients in a resource-scarce setting is described herewith. Of the 75 individuals studied, 11% of the children were stunted, >21% were underweight, and 16% of the under-five children had acute malnutrition. Massive hepatosplenomegaly and lymphadenopathy were present in 75% and 77% children, respectively. About 71% patients achieved complete remission (CR). A total of 30 (40%) children lived for >5 years after diagnosis and 21 (28%) of them had event-free 5 years. Weight for height for under-five children (P = 0.029) and total count (P = 0.019) were found to be significantly associated with deaths during induction. Weight for age (P = 0.024), weight for height of under-five children (P = 0.009), and lymphadenopathy (P = 0.049) had a strong association with 5-year event-free survival. Using multivariate model, only weight for height among under five remained significantly associated with induction deaths (P = 0.021) and absence of lymphadenopathy with event-free 5-year survival (P = 0.042). Context: ALL has 5-year survival of >90% in many advanced cancer research institutes. However, advanced care is not available to majority of poor in the periphery of developing countries. Data available on the survival and the factors affecting the outcome among patients treated in poor resource settings are limited. Aims: This study aims to find the 5-year survival rate and the factors for risk-directed therapy in the region. Settings and Design: Cross-sectional analytical study at a tertiary center of public health in central Kerala. Subjects and Methods: Retrospective analysis of case sheets of 75 children who were treated at the institute from March 2006 to March 2011. Statistical Analysis Used: Univariate and Multivariate analysis using IBM SPSS Statistics for Windows, Version 20.0. Results:: Of the 75 individuals studied, 11% of the children were stunted, >21% were underweight, and 16% of the under-five children had acute malnutrition. Massive hepatosplenomegaly and lymphadenopathy were present in 75% and 77% children, respectively. About 71% patients achieved CR. A total of 30 (40%) children lived for >5 years after diagnosis and 21 (28%) of them had event-free 5 years. Weight for height for under-five children (P = 0.029) and total count (P = 0.019) were found to be significantly associated with deaths during induction. Weight for age (P = 0.024), weight for height of under-five children (P = 0.009), and lymphadenopathy (P = 0.049) had a strong association with 5-year event-free survival. Using multivariate model, only weight for height among under five remained significantly associated with induction deaths (P = 0.021) and absence of lymphadenopathy with event-free 5-year survival (P = 0.042). Conclusions: Overall survival was 40% and event-free survival was 28%. Children with acute malnutrition and a higher white blood cell count were more likely to die during induction. Underweight children, malnourished children, and children with lymphadenopathy had significantly poor chances of surviving 5 years' event free.



Publication History

Article published online:
17 June 2021

© 2018. Indian Society of Medical and Paediatric Oncology. 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 Frehling E, Ritchey AK, Tubergen DG, Bleyer A. Acute lymphoblastic leukaemia. In: Kliegman RM, Stanton B, Geme JS, Schor NF. editors Nelson Textbook of Paediatrics. 1st ed. South Asia: Elsevier Health Sciences; 2015
  • 2 Hunger SP, Lu X, Devidas M, Camitta BM, Gaynon PS, Winick NJ. et al. Improved survival for children and adolescents with acute lymphoblastic leukemia between 1990 and 2005: A report from the children's oncology group. J Clin Oncol 2012; 30: 1663-9
  • 3 Advani S, Pai S, Venzon D, Adde M, Kurkure PK, Nair CN. et al. Acute lymphoblastic leukemia in India: An analysis of prognostic factors using a single treatment regimen. Ann Oncol 1999; 10: 167-76
  • 4 Kapoor A, Kalwar A, Kumar N, Singhal MK, Beniwal S, Kumar HS. et al. Analysis of outcomes and prognostic factors of acute lymphoblastic leukemia patients treated by MCP841 protocol: A regional cancer center experience. J Res Med Sci 2016; 21: 15
  • 5 Menon J, Mathews L, Purushothaman KK. Treating leukemia in a resource poor setting. Indian Pediatr 2008; 45: 410-2
  • 6 Pui CH. Acute Lymphoblastic Leukemia Hong Kong J Paediatr (New Series) 1996;1:5-13 Available from: http://wwwhkjpaedorg/detailsasp?id=434&show=1234. [Last accessed on 2016 Dec 16]
  • 7 Sinha S, Pui CH, Crist WM. Biology and treatment of acute lymphoblastic leukemia. J Pediatr 1994; 124: 491-503
  • 8 Magrath I, Shanta V, Advani S, Adde M, Arya LS, Banavali S. et al. Treatment of acute lymphoblastic leukaemia in countries with limited resources; lessons from use of a single protocol in India over a twenty year period [corrected]. Eur J Cancer 2005; 41: 1570-83
  • 9 Arora RS, Eden TO, Kapoor G. Epidemiology of childhood cancer in India Indian J Cancer 2009; 46: 264-73
  • 10 Kuppuswamy B. Manual of Socioeconomic Status (urban). Delhi: Manasayan; 1981.
  • 11 Sharma R. Kuppuswamy's socioeconomic status scale – Revision for 2011 and formula for real-time updating. Indian J Pediatr 2012; 79: 961-2
  • 12 Indian Academy of Pediatrics Growth Charts Committee. Khadilkar V, Yadav S, Agrawal KK, Tamboli S, Banerjee M. et al. Revised IAP growth charts for height, weight and body mass index for 5- to 18-year-old Indian children. Indian Pediatr 2015; 52: 47-55
  • 13 Kulkarni KP, Arora RS, Marwaha RK. Survival outcome of childhood acute lymphoblastic leukemia in India: A resource-limited perspective of more than 40 years. J Pediatr Hematol Oncol 2011; 33: 475-9
  • 14 Yadav SP, Kalra M, Anjan M, Sachdeva A. Survival outcome in childhood acute lymphoblastic leukemia in India. Pediatr Blood Cancer 2010; 54: 178
  • 15 Lobato-Mendizábal E, Ruiz-Argüelles GJ, Marín-López A. Leukaemia and nutrition I: Malnutrition is an adverse prognostic factor in the outcome of treatment of patients with standard-risk acute lymphoblastic leukaemia. Leuk Res 1989; 13: 899-906
  • 16 Viana MB, Murao M, Ramos G, Oliveira HM, de Carvalho RI, de Bastos M. et al. Malnutrition as a prognostic factor in lymphoblastic leukaemia: A multivariate analysis. Arch Dis Child 1994; 71: 304-10
  • 17 Dutta U, Raina V, Garg PK, Gurbuxani S, Joshi YK, Bhargava M. et al. A prospective study on the incidence of hepatitis B & C infections amongst patients with lymphoproliferative disorders. Indian J Med Res 1998; 107: 78-82
  • 18 Nag S, Vadya S, Pai S. Hepatitis B viral infection in All. Indian J Haematol Bid Trans 1995; 13: 150-3
  • 19 Rubnitz JE, Lensing S, Zhou Y, Sandlund JT, Razzouk BI, Ribeiro RC. et al. Death during induction therapy and first remission of acute leukemia in childhood: The St Jude experience. Cancer 2004; 101: 1677-84
  • 20 Rajalekshmy KR, Abitha AR, Pramila R, Gnanasagar T, Shanta V. Immunophenotypic analysis of T-cell acute lymphoblastic leukaemia in Madras, India. Leuk Res 1997; 21: 119-24
  • 21 Mukhopadhyay A, Gangopadhyay S, Dasgupta S, Paul S, Mukhopadhyay S, Ray UK. et al. Surveillance and expected outcome of acute lymphoblastic leukemia in children and adolescents: An experience from Eastern India. Indian J Med Paediatr Oncol 2013; 34: 280-2
  • 22 Hunger SP, Sung L, Howard SC. Treatment strategies and regimens of graduated intensity for childhood acute lymphoblastic leukemia in low-income countries: A proposal. Pediatr Blood Cancer 2009; 52: 559-65
  • 23 Veerman AJ, Sutaryo S, Sumadiono S. Twinning: A rewarding scenario for development of oncology services in transitional countries. Pediatr Blood Cancer 2005; 45: 103-6