Literature DB >> 22493777

The significance of serial histopathology in a residual mass for outcome of intermediate risk stage 3 neuroblastoma.

Araz Marachelian1, Hiroyuki Shimada, Hideki Sano, Hollie Jackson, James Stein, Richard Sposto, Katherine K Matthay, David Baker, Judith G Villablanca.   

Abstract

BACKGROUND: To describe the serial histopathology of intermediate risk stage 3 neuroblastoma after chemotherapy, and correlate with residual mass at therapy completion and outcome. PROCEDURE: A retrospective review of intermediate risk stage 3 neuroblastoma patients treated 1989-2005 at Children's Hospital Los Angeles according to CCG 3881 or CCG 3961 protocols was performed, with central review of histopathology, radiology, and surgery.
RESULTS: Eighteen patients treated per CCG 3881 (n = 9) or CCG 3961 (n = 9), with including 1 (n = 5), 2 (n = 9), ≥ 3 (n = 3), or unknown number (n = 1) of surgical procedures were included. At therapy completion, 10 patients had residual tumor: <10% original size (n = 3), >10% original size (n = 6) (5 MIBG avid; 4 with elevated catecholamines), and CT non-measurable MIBG avid tumor (n = 1). Post-chemotherapy histology showed tumor regression (n = 4); or maturation with (n = 6) or without (n = 2) Schwannian development. Histologic changes correlated with median tumor shrinkage of 80% (regressing tumors) and <25% (maturing tumors). Tumor size increased in one patient with maturing tumor and Schwannian development. Overall survival was 100%.
CONCLUSION: Post-chemotherapy histopathology of intermediate risk stage 3 neuroblastoma was characterized by regression or maturation. Persisting residual and maturing tumors were not associated with tumor progression, despite MIBG uptake and/or elevated catecholamines, supporting observation only. Histopathology should be obtained in future studies to confirm these findings, and guide length of chemotherapy.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22493777     DOI: 10.1002/pbc.23250

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  4 in total

Review 1.  Neuroblastoma: clinical and biological approach to risk stratification and treatment.

Authors:  Vanessa P Tolbert; Katherine K Matthay
Journal:  Cell Tissue Res       Date:  2018-03-23       Impact factor: 5.249

Review 2.  Revisions to the International Neuroblastoma Response Criteria: A Consensus Statement From the National Cancer Institute Clinical Trials Planning Meeting.

Authors:  Julie R Park; Rochelle Bagatell; Susan L Cohn; Andrew D Pearson; Judith G Villablanca; Frank Berthold; Susan Burchill; Ariane Boubaker; Kieran McHugh; Jed G Nuchtern; Wendy B London; Nita L Seibel; O Wolf Lindwasser; John M Maris; Penelope Brock; Gudrun Schleiermacher; Ruth Ladenstein; Katherine K Matthay; Dominique Valteau-Couanet
Journal:  J Clin Oncol       Date:  2017-05-04       Impact factor: 44.544

3.  SIOP-PODC adapted risk stratification and treatment guidelines: Recommendations for neuroblastoma in low- and middle-income settings.

Authors:  Nehal S Parikh; Scott C Howard; Guillermo Chantada; Trijn Israels; Mohammed Khattab; Patricia Alcasabas; Catherine G Lam; Lawrence Faulkner; Julie R Park; Wendy B London; Katherine K Matthay
Journal:  Pediatr Blood Cancer       Date:  2015-03-21       Impact factor: 3.167

4.  Usefulness of fluorodeoxyglucose positron emission tomography/computed tomography for detection of a neuroblastic nodule in a ganglioneuroblastoma: a case report.

Authors:  Yuka Takeda; Hideki Sano; Asuka Kawano; Kazuhiro Mochizuki; Nobuhisa Takahashi; Shogo Kobayashi; Yoshihiro Ohara; Kazuhiro Tasaki; Mitusuaki Hosoya; Atsushi Kikuta
Journal:  J Med Case Rep       Date:  2018-05-03
  4 in total

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