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10.1245/ASO.2006.10.012
Annals of Surgical Oncology 13:238-244 (2006)
© 2006 Society of Surgical Oncology
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Original Article

The Influence of Biologic Factors on the Surgical Decision in Advanced Neuroblastoma

Wen-Ming Hsu, MD, PhD1, Yung-Ming Jen, MD2, Hsinyu Lee, PhD3, Min-Liang Kuo, PhD4, Po-Nien Tsao, MD, PhD5, Chiung-Nien Chen, MD, PhD1, Dar-Ming Lai, MD1, Ming-Tsan Lin, MD, DMSc1, Hong-Shiee Lai, MD, PhD1, Wei-Jao Chen, MD, MPH, DMSc1 and Fon-Jou Hsieh, MD6

1 Department of Surgery, National Taiwan University Hospital and National Taiwan University College of Medicine, #7 Chung-Shan South Road, Taipei 100, Taiwan
2 Department of Pathology, National Taiwan University Hospital and National Taiwan University College of Medicine, #7 Chung-Shan South Road, Taipei 100, Taiwan
3 Department of Life Science and Institute of Zoology, National Taiwan University, #1, Sec. 4, Roosevelt Road, Taipei 100, Taiwan
4 Institute of Toxicology, National Taiwan University College of Medicine, #1, Sec. 1, Jen-Ai Road, Taipei 100, Taiwan
5 Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, #7 Chung-Shan South Road, Taipei 100, Taiwan
6 Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, #7 Chung-Shan South Road, Taipei 100, Taiwan

Correspondence: Address correspondence and reprint requests to: Fon-Jou Hsieh, MD; E-mail: fjhsieh{at}ha.mc.ntu.edu.tw.

Background: Molecular markers greatly affect the outcome of neuroblastoma. This study evaluated the influence of Trk-A and myelocytomatosis viral-related oncogene, neuroblastoma-derived (MYCN) on the role of surgery in advanced neuroblastoma.

Methods: Ten stage 3 and 35 stage 4 neuroblastoma patients were included. Tumor resection was classified into gross total resection (GTR) and incomplete resection. Patients were classified into three biological risk groups according to Trk-A expression and myelocytomatosis viral-related oncogene, neuroblastoma-derived (MYCN) status in tumor tissues studied by immunohistochemistry and fluorescence in situ hybridization, respectively: low risk (positive Trk-A and normal MYCN), intermediate risk (negative Trk-A and normal MYCN), and high risk (positive or negative Trk-A and MYCN amplification). The effect of tumor resection on prognosis was studied and stratified according to the risk grouping.

Results: GTR was achieved in 21 patients (46.7%) with a higher complication rate (33% vs. 8% in the incomplete resection group, P = .036). GTR was easier to achieve in low-risk tumors than in intermediate- or high-risk tumors (12 of 13, 4 of 17, and 5 of 15, respectively; P < .001). GTR predicted a favorable prognosis for intermediate-risk patients (P = .037; log-rank test), but not for low- or high-risk patients because of the overall favorable and poor prognosis, respectively.

Conclusions: GTR carries a potentially higher possibility of complication. Although GTR can be achieved easily in low-risk neuroblastoma patients with a favorable prognosis, surgeons should do their best to achieve GTR for intermediate-risk patients to improve outcome. Nevertheless, sacrificing vital organs to achieve GTR for high-risk patients is not justified.

Key Words: Neuroblastoma • Surgery • Trk-A • MYCN




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W.-M. Hsu, H. Lee, H.-F. Juan, Y.-Y. Shih, B.-J. Wang, C.-Y. Pan, Y.-M. Jeng, H.-H. Chang, M.-Y. Lu, K.-H. Lin, et al.
Identification of GRP75 as an Independent Favorable Prognostic Marker of Neuroblastoma by a Proteomics Analysis
Clin. Cancer Res., October 1, 2008; 14(19): 6237 - 6245.
[Abstract] [Full Text] [PDF]




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