CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2019; 40(S 01): S13-S15
DOI: 10.4103/ijmpo.ijmpo_213_17
Original Article

Treatment Refusal and Abandonment Remain Major Concerns Despite Good Outcomes with Multi-Modality Management in Pediatric Medulloblastoma: Experience from a Cancer Center in Eastern India

Anirban Das
Departments of Paediatric Haematology-Oncology, Tata Medical Centre, Kolkata, West Bengal, India
,
Rimpa Basu Achari
Departments of Radiation Oncology, Tata Medical Centre, Kolkata, West Bengal, India
,
Lateef Zameer
Departments of Histopathology, Tata Medical Centre, Kolkata, West Bengal, India
,
Saugata Sen
Departments of Radiology, Tata Medical Centre, Kolkata, West Bengal, India
,
Shekhar Krishnan
Departments of Paediatric Haematology-Oncology, Tata Medical Centre, Kolkata, West Bengal, India
,
Arpita Bhattacharyya
Departments of Paediatric Haematology-Oncology, Tata Medical Centre, Kolkata, West Bengal, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

Context: Survival in medulloblastoma, the most common pediatric brain tumor, has lagged behind in developing countries in comparison to the West. Aim: The aim of this study was to analyze the clinical profile and outcome in a cancer center in Eastern India. Methods: Twenty-nine children were retrospectively analyzed over 6 years. Results: Vomiting (79%), headache (69%), and unsteadiness (55%) were the presenting complaints. The majority (67%) had classical histology. High-risk (HR) disease (61.6%) exceeded average-risk (AR) (38.4%) disease in numbers. Treatment-refusal (27.6%) and abandonment (6.9%) were major concerns. Four-year EFS was 81% and 52%, excluding and including refusal/abandonment, respectively. There was no relapse/progression among AR patients. Four-year EFS in HR was 63%. Posterior fossa syndrome (37.5%), febrile neutropenia (29%), and ototoxicity (16.7%) were the main treatment-related morbidities. Implications: Following this audit, patient tracking to reduce abandonment, coordination to limit delay in postsurgical referral, developing strategies for molecular subgrouping, and reducing cumulative cisplatin exposure were measures adopted to improve outcome in the unit.



Publication History

Article published online:
24 May 2021

© 2019. 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 Gupta T, Sarkar C, Rajshekhar V, Chatterjee S, Shirsat N, Muzumdar D. et al. Indian Society of Neuro-Oncology consensus guidelines for the contemporary management of medulloblastoma. Neurol India 2017; 65: 315-32
  • 2 Gajjar A, Chintagumpala M, Ashley D, Kellie S, Kun LE, Merchant TE. et al. Risk-adapted craniospinal radiotherapy followed by high-dose chemotherapy and stem-cell rescue in children with newly diagnosed medulloblastoma (St. Jude Medulloblastoma-96): Long-term results from a prospective, multicentre trial. Lancet Oncol 2006; 7: 813-20
  • 3 Menon G, Nair S, Muthurethinam T, Krishnakumar K, Bhattacharya RN. Medulloblastoma in children: Prognostic factors and predictors of outcome. J Pediatr Neurosci 2006; 1: 16-20
  • 4 Muzumdar D, Deshpande A, Kumar R, Sharma A, Goel N, Dange N. et al. Medulloblastoma in childhood-King Edward memorial hospital surgical experience and review: Comparative analysis of the case series of 365 patients. J Pediatr Neurosci 2011; 6: S78-85
  • 5 Gupta T, Jalali R, Goswami S, Nair V, Moiyadi A, Epari S. et al. Early clinical outcomes demonstrate preserved cognitive function in children with average-risk medulloblastoma when treated with hyperfractionated radiation therapy. Int J Radiat Oncol Biol Phys 2012; 83: 1534-40
  • 6 Kumar LP, Deepa SF, Moinca I, Suresh P, Naidu KV. Medulloblastoma: A common pediatric tumor: Prognostic factors and predictors of outcome. Asian J Neurosurg 2015; 10: 50
  • 7 Gaur S, Kumar SS, Balasubramaniam P. An analysis of medulloblastoma: 10 year experience of a referral institution in South India. Indian J Cancer 2015; 52: 575-8
  • 8 Rajagopal R, Abd-Ghafar S, Ganesan D, Bustam Mainudin AZ, Wong KT, Ramli N. et al. Challenges of treating childhood medulloblastoma in a country with limited resources: 20 years of experience at a single tertiary center in Malaysia. J Glob Oncol 2017; 3: 143-56
  • 9 Wang C, Yuan XJ, Jiang MW, Wang LF. Clinical characteristics and abandonment and outcome of treatment in 67 Chinese children with medulloblastoma. J Neurosurg Pediatr 2016; 17: 49-56
  • 10 Friedrich P, Lam CG, Kaur G, Itriago E, Ribeiro RC, Arora RS. et al. Determinants of treatment abandonment in childhood cancer: Results from a global survey. PLoS One 2016; 11: e0163090
  • 11 Nageswara Rao AA, Wallace DJ, Billups C, Boyett JM, Gajjar A, Packer RJ. et al. Cumulative cisplatin dose is not associated with event-free or overall survival in children with newly diagnosed average-risk medulloblastoma treated with cisplatin based adjuvant chemotherapy: Report from the Children’s Oncology Group. Pediatr Blood Cancer 2014; 61: 102-6