Durable complete response to chemotherapy in an infant with a clival chordoma

Chordomas are rare bone tumors of notochord remnants that may occur anywhere within the axial skeleton. The standard of care is complete surgical removal. Proton beam irradiation is commonly used when the tumor is inaccessible or has recurred. Chemotherapy has been used in the treatment of patients...

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Veröffentlicht in:Pediatric blood & cancer 2012-08, Vol.59 (2), p.323-325
Hauptverfasser: Al-Rahawan, Mohamad M., Siebert, James D., Mitchell, Craig S., Smith, Stephen D.
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container_issue 2
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container_title Pediatric blood & cancer
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creator Al-Rahawan, Mohamad M.
Siebert, James D.
Mitchell, Craig S.
Smith, Stephen D.
description Chordomas are rare bone tumors of notochord remnants that may occur anywhere within the axial skeleton. The standard of care is complete surgical removal. Proton beam irradiation is commonly used when the tumor is inaccessible or has recurred. Chemotherapy has been used in the treatment of patients at relapse but it has been generally proven ineffective. We report a 7‐month‐old infant with a clival chordoma who responded to combination chemotherapy consisting of cycles of vincristine/cyclophosphamide/doxorubicin alternating with etoposide/ifosfamide. She has been off chemotherapy for 2 years and is well at age 5. Pediatr Blood Cancer 2012;59:323–325. © 2011 Wiley Periodicals, Inc.
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Brain Mapping
chemotherapy
child
chordoma
Chordoma - diagnosis
Chordoma - drug therapy
clivus
Cyclophosphamide - administration & dosage
Doxorubicin - administration & dosage
Etoposide - administration & dosage
Humans
Ifosfamide - administration & dosage
Infant
Magnetic Resonance Imaging
Male
Remission Induction
Skull Base Neoplasms - diagnosis
Skull Base Neoplasms - drug therapy
Vincristine - administration & dosage
title Durable complete response to chemotherapy in an infant with a clival chordoma
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