A retrospective analysis of recurrent intracranial ependymoma. Issue 7 (24th February 2014)
- Record Type:
- Journal Article
- Title:
- A retrospective analysis of recurrent intracranial ependymoma. Issue 7 (24th February 2014)
- Main Title:
- A retrospective analysis of recurrent intracranial ependymoma
- Authors:
- Antony, Reuben
Wong, Kenneth E.
Patel, Moneil
Olch, Arthur J.
McComb, Gordon
Krieger, Mark
Gilles, Floyd
Sposto, Richard
Erdreich‐Epstein, Anat
Dhall, Girish
Gardner, Sharon
Finlay, Jonathan L. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc24996-sec-0001" sec-type="section"> <title>Background</title> <p>Recurrence occurs in almost 50% of patients with intracranial ependymoma, and their outcome following recurrence is poor.</p> </sec> <sec id="pbc24996-sec-0002" sec-type="section"> <title>Methods</title> <p>We retrospectively reviewed the medical records of 22 patients with intracranial ependymoma and subsequent relapse(s) (59 recurrences) treated at Children's Hospital Los Angeles or New York University between January 1997 and December 2012.</p> </sec> <sec id="pbc24996-sec-0003" sec-type="section"> <title>Results</title> <p>Median duration of follow‐up was 52 months (7–171 months). Median age at initial diagnosis was 4 years (0.3–19 years) with 8 patients younger than 3 years at presentation. Eleven patients had anaplastic and 11 cellular pathologies. Eighteen patients had infratentorial tumors at diagnosis and 3 (all infratentorial) had metastatic spinal cord involvement at presentation. Cerebrospinal fluid involvement was not identified at diagnosis or relapse. Median time to first recurrence was 16 months (1.3 to 115 months). The number of recurrences in each patient ranged from 1 to 9 (median = 2). Thirty‐seven recurrences (63%) were detected asymptomatically by surveillance imaging. Fifteen recurrences (26%) arose outside the initial tumor site. Recurrences were treated by surgical resection (45), with<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc24996-sec-0001" sec-type="section"> <title>Background</title> <p>Recurrence occurs in almost 50% of patients with intracranial ependymoma, and their outcome following recurrence is poor.</p> </sec> <sec id="pbc24996-sec-0002" sec-type="section"> <title>Methods</title> <p>We retrospectively reviewed the medical records of 22 patients with intracranial ependymoma and subsequent relapse(s) (59 recurrences) treated at Children's Hospital Los Angeles or New York University between January 1997 and December 2012.</p> </sec> <sec id="pbc24996-sec-0003" sec-type="section"> <title>Results</title> <p>Median duration of follow‐up was 52 months (7–171 months). Median age at initial diagnosis was 4 years (0.3–19 years) with 8 patients younger than 3 years at presentation. Eleven patients had anaplastic and 11 cellular pathologies. Eighteen patients had infratentorial tumors at diagnosis and 3 (all infratentorial) had metastatic spinal cord involvement at presentation. Cerebrospinal fluid involvement was not identified at diagnosis or relapse. Median time to first recurrence was 16 months (1.3 to 115 months). The number of recurrences in each patient ranged from 1 to 9 (median = 2). Thirty‐seven recurrences (63%) were detected asymptomatically by surveillance imaging. Fifteen recurrences (26%) arose outside the initial tumor site. Recurrences were treated by surgical resection (45), with irradiation (30), and with various oral chemotherapies (23) with (7) or without (16) conventional chemotherapy. The 5 and 10 year overall survival rates from first recurrence were 0.37 ± 0.14 and 0.25 ± 0.14.</p> </sec> <sec id="pbc24996-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Prolonged (5–10 year) survival from first relapse was noted in over one‐quarter of our patients. It remains unclear whether early radiographic diagnosis, differing treatment modalities beyond radical surgical resection or possibly unrecognized biological differences contributed towards this prolonged survival. Pediatr Blood Cancer 2014;61:1195–1201. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 61:Issue 7(2014:Jul.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 61:Issue 7(2014:Jul.)
- Issue Display:
- Volume 61, Issue 7 (2014)
- Year:
- 2014
- Volume:
- 61
- Issue:
- 7
- Issue Sort Value:
- 2014-0061-0007-0000
- Page Start:
- 1195
- Page End:
- 1201
- Publication Date:
- 2014-02-24
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.24996 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3976.xml