Literature DB >> 9655307

Treatment of diencephalic syndrome with chemotherapy: growth, tumor response, and long term control.

A L Gropman1, R J Packer, H S Nicholson, L G Vezina, R Jakacki, R Geyer, J M Olson, P Phillips, M Needle, E H Broxson, G Reaman, J Finlay.   

Abstract

BACKGROUND: The diencephalic syndrome (DS), which is manifested by progressive emaciation and failure to thrive in an apparently alert, cheerful infant, usually is due to a low grade hypothalamic glioma. Treatment with aggressive surgery and/or radiotherapy is variably successful in controlling disease and may result in severe neurologic sequelae. Chemotherapy recently has been shown to be effective in patients with low grade gliomas of childhood, but it is used infrequently in those with DS.
METHODS: The authors evaluated the efficacy of a regimen of carboplatin and vincristine on improving weight, causing tumor shrinkage, and delaying the need for alternative therapies in seven children (ages 9-20 months; median age, 11 months) with DS. Five patients weighed less than the 5th percentile for their age at the start of the study, one weighed within the 10th percentile, and one weighed within the 25th percentile.
RESULTS: At follow-up (range, 6-54 months; median, 28 months), the patients' weights had increased by 66-95% (median, 80%). On magnetic resonance imaging, four patients had a >50% reduction in tumor mass, one had a 25-50% reduction, and two had stable disease. In those patients with radiographic response to treatment, weight gain was accomplished with oral feedings in four of five patients, whereas those with stable disease required nasogastric, nasojejunal, or gastrostomy tube supplementation to maintain weight. Disease progression occurred at a median of 24 months after initiation of chemotherapy, and two patients remained free of progressive disease at last follow-up. Five patients were alive a median of 59 months from diagnosis. The need for radiation or other therapies was delayed in six of seven children. Therapy was tolerated without significant toxicities.
CONCLUSION: The authors conclude that treatment of DS with a carboplatin and vincristine regimen results in demonstrable weight gain, may result in tumor shrinkage, and in some cases, significantly delays the need for alternative therapies.

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Year:  1998        PMID: 9655307     DOI: 10.1002/(sici)1097-0142(19980701)83:1<166::aid-cncr22>3.0.co;2-u

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  16 in total

1.  Delayed presentation of diencephalic syndrome associated with leptomeningeal dissemination in a child.

Authors:  John Ross Crawford; Katayoon Shayan; Michael L Levy
Journal:  BMJ Case Rep       Date:  2013-06-16

2.  Case 3: An eight-month-old boy with failure to thrive.

Authors:  Andrea Human; Kamal Eltobgy; Carolyn E Beck
Journal:  Paediatr Child Health       Date:  2014-11       Impact factor: 2.253

Review 3.  Considerations on the role of chemotherapy and modern radiotherapy in the treatment of childhood low grade glioma.

Authors:  Giorgio Perilongo
Journal:  J Neurooncol       Date:  2005-12       Impact factor: 4.130

4.  Successful treatment with a low-dose cisplatin--etoposide regimen for patients with diencephalic syndrome.

Authors:  Iacopo Sardi; Cecilia Bresci; Elisabetta Schiavello; Veronica Biassoni; Valentina Fratoni; Stefania Cardellicchio; Lorenzo Genitori; Maurizio Aricò; Maura Massimino
Journal:  J Neurooncol       Date:  2012-06-21       Impact factor: 4.130

5.  Disseminated pilocytic astrocytoma involving brain stem and diencephalon: a history of atypical eating disorder and diagnostic delay.

Authors:  Felix Distelmaier; Gisela Janssen; Ertan Mayatepek; Jörg Schaper; Ulrich Göbel; Thorsten Rosenbaum
Journal:  J Neurooncol       Date:  2006-04-06       Impact factor: 4.130

6.  Management of childhood brain tumors: consensus report by the Pediatric Hematology Oncology (PHO) Chapter of Indian Academy of Pediatrics (IAP).

Authors:  Sunil Bhat; Satya Prakash Yadav; Vaishali Suri; Rana Patir; Purna Kurkure; Stewart Kellie; Anupam Sachdeva
Journal:  Indian J Pediatr       Date:  2011-06-22       Impact factor: 1.967

7.  Favorable survival and metabolic outcome for children with diencephalic syndrome using a radiation-sparing approach.

Authors:  John-Paul Kilday; Ute Bartels; Annie Huang; Mary Barron; Mary Shago; Matthew Mistry; Nataliya Zhukova; Normand Laperriere; Peter Dirks; Cynthia Hawkins; Eric Bouffet; Uri Tabori
Journal:  J Neurooncol       Date:  2013-11-12       Impact factor: 4.130

8.  Diencephalic syndrome as sign of tumor progression in a child with neurofibromatosis type 1 and optic pathway glioma: a case report.

Authors:  Maria Elena Cavicchiolo; Enrico Opocher; Marco Daverio; Matteo Bendini; Elisabetta Viscardi; Gianni Bisogno; Giorgio Perilongo; Liviana Da Dalt
Journal:  Childs Nerv Syst       Date:  2013-04-25       Impact factor: 1.475

9.  New Treatments in Pediatric Brain Tumors.

Authors:  Roger J. Packer; Alyssa Reddy
Journal:  Curr Treat Options Neurol       Date:  2004-09       Impact factor: 3.598

10.  Successful high-dose chemotherapy for widespread neuroaxis dissemination of an optico-hypothalamic juvenile pilocytic astrocytoma in an infant: a case report.

Authors:  Teruyoshi Kageji; Shinji Nagahiro; Hidehisa Horiguchi; Tsutomu Watanabe; Hiroko Suzuya; Yasuhiro Okamoto; Yasuhiro Kuroda
Journal:  J Neurooncol       Date:  2003-05       Impact factor: 4.130

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