Neuroblastoma With Opsoclonus-Myoclonus-Ataxia Syndrome: Role of Chemotherapy in the Management: Experience From a Tertiary Care Center in a Resource-limited Setting. Issue 7 (23rd October 2021)
- Record Type:
- Journal Article
- Title:
- Neuroblastoma With Opsoclonus-Myoclonus-Ataxia Syndrome: Role of Chemotherapy in the Management: Experience From a Tertiary Care Center in a Resource-limited Setting. Issue 7 (23rd October 2021)
- Main Title:
- Neuroblastoma With Opsoclonus-Myoclonus-Ataxia Syndrome: Role of Chemotherapy in the Management: Experience From a Tertiary Care Center in a Resource-limited Setting
- Authors:
- Anand, Sachit
Agarwala, Sandeep
Jain, Vishesh
Bakhshi, Sameer
Dhua, Anjan
Gulati, Sheffali
Seth, Rachna
Srinivas, Maddur
Jana, Manisha
Kandasamy, Devasenathipathy
Bhatnagar, Veereshwar - Abstract:
- Abstract : Supplemental Digital Content is available in the text. Abstract : Children with neuroblastoma (NB) and opsoclonus-myoclonus-ataxia syndrome (OMAS) have a favorable oncologic outcome and overall survival. In contrast, despite intensive multidrug immunomodulation, the neurologic outcome is complicated by the relapsing nature of the neurologic symptoms and long-term neurobehavioral sequelae. Being associated with low-risk NB, there exists an ambiguity in the current literature regarding the administration of chemotherapy in these children. We reviewed our archives for children with NB-OMAS over a 22-year (January 1996 to January 2018) period. Eighteen children (10 female) with a median age at diagnosis of 23 months had NB-OMAS and were included. They had stage 1 (9/18; 50%), 2 (1/18; 5.5%), 3 (7/18; 39%), and 4 (1/18; 5.5%) disease according to the International Neuroblastoma Staging System. Multimodality therapy included surgery (16/18; 89%), chemotherapy (11/18; 61%), and immunomodulatory therapy (10/18; 55%). Complete oncologic remission was achieved in all children. Relapse of OMAS and presence of neurologic sequelae were observed in 1 (5.5%) and 5 (28%) cases, respectively. Presence of neurologic sequelae was significantly associated with low-tumor stage ( P =0.036) and treatment without chemotherapy ( P =0.003). Chemotherapy administration was the only variable significantly predicting a favorable neurologic outcome (95% confidence interval: 0.26-1.40, PAbstract : Supplemental Digital Content is available in the text. Abstract : Children with neuroblastoma (NB) and opsoclonus-myoclonus-ataxia syndrome (OMAS) have a favorable oncologic outcome and overall survival. In contrast, despite intensive multidrug immunomodulation, the neurologic outcome is complicated by the relapsing nature of the neurologic symptoms and long-term neurobehavioral sequelae. Being associated with low-risk NB, there exists an ambiguity in the current literature regarding the administration of chemotherapy in these children. We reviewed our archives for children with NB-OMAS over a 22-year (January 1996 to January 2018) period. Eighteen children (10 female) with a median age at diagnosis of 23 months had NB-OMAS and were included. They had stage 1 (9/18; 50%), 2 (1/18; 5.5%), 3 (7/18; 39%), and 4 (1/18; 5.5%) disease according to the International Neuroblastoma Staging System. Multimodality therapy included surgery (16/18; 89%), chemotherapy (11/18; 61%), and immunomodulatory therapy (10/18; 55%). Complete oncologic remission was achieved in all children. Relapse of OMAS and presence of neurologic sequelae were observed in 1 (5.5%) and 5 (28%) cases, respectively. Presence of neurologic sequelae was significantly associated with low-tumor stage ( P =0.036) and treatment without chemotherapy ( P =0.003). Chemotherapy administration was the only variable significantly predicting a favorable neurologic outcome (95% confidence interval: 0.26-1.40, P =0.01). To conclude, our study including a limited cohort of patients highlights a favorable neurologic outcome associated with chemotherapy administration in children with NB-OMAS. However, further studies with larger sample size need to be conducted before drawing any definite conclusions. … (more)
- Is Part Of:
- Journal of pediatric hematology/oncology. Volume 43:Issue 7(2021)
- Journal:
- Journal of pediatric hematology/oncology
- Issue:
- Volume 43:Issue 7(2021)
- Issue Display:
- Volume 43, Issue 7 (2021)
- Year:
- 2021
- Volume:
- 43
- Issue:
- 7
- Issue Sort Value:
- 2021-0043-0007-0000
- Page Start:
- e924
- Page End:
- e929
- Publication Date:
- 2021-10-23
- Subjects:
- Neuroblastoma -- opsoclonus-myoclonus-ataxia -- chemotherapy -- immunomodulatory therapy -- neurologic outcome
Pediatric hematology -- Periodicals
Tumors in children -- Periodicals
618.9215 - Journal URLs:
- http://journals.lww.com/jpho-online/pages/default.aspx ↗
http://gateway.tx.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00043426-000000000-00000 ↗
http://www.jpho-online.com/ ↗
http://journals.lww.com/jpho-online/pages/default.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MPH.0000000000002131 ↗
- Languages:
- English
- ISSNs:
- 1077-4114
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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