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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-19-22</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-19-3-8</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Brain Neoplasms</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Postoperative Chemotherapy for Medulloblastoma</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Children&#x0027;s Memorial Hospital, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>03</month>
<year>2005</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>03</month>
<year>2016</year>
</pub-date>
<volume>19</volume>
<issue>3</issue>
<fpage>22</fpage>
<lpage>23</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2005 The Author(s)</copyright-statement>
<copyright-year>2005</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="doi" xlink:href="10.1056/NEJMoa042176" vol="352" page="978">
<article-title>Treatment of early childhood medulloblastoma by postoperative chemotherapy alone</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The survival rate and cognitive function of 43 children, age &#x003C;3 years, with medulloblastoma treated with intensive postoperative chemotherapy alone, without radiotherapy, were determined at the University of Wurzburg and other centers in Germany Chemotherapy consisted of three two-month cycles of cyclophosphamide, methotrexate, vincristine, carboplatin, and etoposide.</p>
</abstract>
<kwd-group>
<kwd>Postoperative Chemotherapy</kwd>
<kwd>Medulloblastoma</kwd>
<kwd>Asymptomatic Leukoencephalopathy</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The survival rate and cognitive function of 43 children, age &#x003C;3 years, with medulloblastoma treated with intensive postoperative chemotherapy alone, without radiotherapy, were determined at the University of Wurzburg and other centers in Germany Chemotherapy consisted of three two-month cycles of cyclophosphamide, methotrexate, vincristine, carboplatin, and etoposide. Intraventricular methotrexate was also administered in 36 doses through an implanted subcutaneous reservoir, beginning 2 to 4 weeks after surgery. The five-year progression-free and overall survival rates (+/-SE) were 82+/-9% and 93+/-6% for 17 patients with complete resection, 50+/-13% and 56+/-14% for 14 with residual tumor, 33+/-14% and 38+/-15% for 12 with macroscopic metastases, and 68+/-8% and 77+/-8% in 31 patients without macroscopic metastases. Tumor relapse occurred in 9 of 29 patients without residual disease after chemotherapy. Independent risk factors for tumor relapse were desmoplastic form of medulloblastoma (20 patients), metastatic disease, and age younger than 2 years. Asymptomatic leukoencephalopathy was detected by MRI in 19 of 23 patients. After treatment with chemotherapy, the mean IQ was significantly lower than that of healthy controls of the same age but higher than that of patients treated by radiotherapy in a previous trial. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Intensive postoperative chemotherapy that includes intraventricular methotrexate provides long remissions in children with medulloblastoma, and results are especially promising for patients without initial metastases. Except in cases of relapse, radiotherapy with its adverse side effects may be avoided in the very young patient with medulloblastoma. [<xref ref-type="bibr" rid="CIT0002">2</xref>]</p>
</body>
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