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Article: Surgical outcomes of patients with neuroblastoma in a tertiary centre in Hong Kong: A 12-year experience
Title | Surgical outcomes of patients with neuroblastoma in a tertiary centre in Hong Kong: A 12-year experience |
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Authors | |
Keywords | Neuroblastoma Surgical excision Survival |
Issue Date | 2009 |
Publisher | Medcom Limited. The Journal's web site is located at http://www.hkjpaed.org/index.asp |
Citation | Hong Kong Journal of Paediatrics, 2009, v. 14 n. 3, p. 186-193 How to Cite? |
Abstract | Introduction: Neuroblastoma has a heterogeneous clinical course. The prognosis varies widely depending on the age of diagnosis, extent of disease and tumour biology. However, the specific clinical outcome of this disease in Hong Kong has not been well characterised thus far. Complete tumour excision has been demonstrated to confer survival benefit on patients with advanced disease even if there is metastasis. Since year 2004, we have adopted a revised, more aggressive surgical approach in managing these patients. Here, we aim to review our experience in the management of this disease. Methods: A retrospective review was performed for the past 12 years to include all patients who presented with neuroblastoma in our institution. Data such as the survival, age at diagnosis, MYCN amplification status, the extent of tumour excision, and stage of the disease were recorded and analysed. Results: 37 patients were included in this study. Overall survival of our patients was 67.6%. Patients with Stage 1, 2 and 4S have 100% survival whereas stage 4 patients only have 41.4% survival. Since our revised surgical approach in 2004, patients who had been operated had a better survival. Survival of stage 4 patients with operation after 2004 was 57.1% whereas the survival of patients at the same stage before 2004 was only 30%. Age at diagnosis, completeness of tumour excision and stage of disease are also correlated with overall prognosis. Further, patients with the presence of MYCN gene amplification have apparently poorer survival but it is not statistically significant due to the small sample size. Conclusion: The management of patients with neuroblastoma remains a challenge. Advanced stage of disease, incomplete tumour excision and increased age at diagnosis were all associated with poor survival. We demonstrated a better survival for those who underwent a more aggressive surgical approach, though this is a technically demanding and time consuming procedure. Thus, the management of advanced neuroblastoma should be centralised in a centre with combined surgical, oncological and paediatric intensive care expertise. |
Persistent Identifier | http://hdl.handle.net/10722/92367 |
ISSN | 2023 Impact Factor: 0.1 2023 SCImago Journal Rankings: 0.117 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chan, IHY | en_HK |
dc.contributor.author | Wong, KKY | en_HK |
dc.contributor.author | Chan, GCF | en_HK |
dc.contributor.author | Tam, PKH | en_HK |
dc.date.accessioned | 2010-09-17T10:43:57Z | - |
dc.date.available | 2010-09-17T10:43:57Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Hong Kong Journal of Paediatrics, 2009, v. 14 n. 3, p. 186-193 | en_HK |
dc.identifier.issn | 1013-9923 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/92367 | - |
dc.description.abstract | Introduction: Neuroblastoma has a heterogeneous clinical course. The prognosis varies widely depending on the age of diagnosis, extent of disease and tumour biology. However, the specific clinical outcome of this disease in Hong Kong has not been well characterised thus far. Complete tumour excision has been demonstrated to confer survival benefit on patients with advanced disease even if there is metastasis. Since year 2004, we have adopted a revised, more aggressive surgical approach in managing these patients. Here, we aim to review our experience in the management of this disease. Methods: A retrospective review was performed for the past 12 years to include all patients who presented with neuroblastoma in our institution. Data such as the survival, age at diagnosis, MYCN amplification status, the extent of tumour excision, and stage of the disease were recorded and analysed. Results: 37 patients were included in this study. Overall survival of our patients was 67.6%. Patients with Stage 1, 2 and 4S have 100% survival whereas stage 4 patients only have 41.4% survival. Since our revised surgical approach in 2004, patients who had been operated had a better survival. Survival of stage 4 patients with operation after 2004 was 57.1% whereas the survival of patients at the same stage before 2004 was only 30%. Age at diagnosis, completeness of tumour excision and stage of disease are also correlated with overall prognosis. Further, patients with the presence of MYCN gene amplification have apparently poorer survival but it is not statistically significant due to the small sample size. Conclusion: The management of patients with neuroblastoma remains a challenge. Advanced stage of disease, incomplete tumour excision and increased age at diagnosis were all associated with poor survival. We demonstrated a better survival for those who underwent a more aggressive surgical approach, though this is a technically demanding and time consuming procedure. Thus, the management of advanced neuroblastoma should be centralised in a centre with combined surgical, oncological and paediatric intensive care expertise. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Medcom Limited. The Journal's web site is located at http://www.hkjpaed.org/index.asp | en_HK |
dc.relation.ispartof | Hong Kong Journal of Paediatrics | en_HK |
dc.subject | Neuroblastoma | en_HK |
dc.subject | Surgical excision | en_HK |
dc.subject | Survival | en_HK |
dc.title | Surgical outcomes of patients with neuroblastoma in a tertiary centre in Hong Kong: A 12-year experience | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1013-9923&volume=14&issue=3&spage=186&epage=193&date=2009&atitle=Surgical+outcomes+of+patients+with+neuroblastoma+in+a+tertiary+centre+in+Hong+Kong:+A+12-year+experience | - |
dc.identifier.email | Wong, KKY: kkywong@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, GCF: gcfchan@hkucc.hku.hk | en_HK |
dc.identifier.email | Tam, PKH: paultam@hkucc.hku.hk | en_HK |
dc.identifier.authority | Wong, KKY=rp01392 | en_HK |
dc.identifier.authority | Chan, GCF=rp00431 | en_HK |
dc.identifier.authority | Tam, PKH=rp00060 | en_HK |
dc.description.nature | published_or_final_version | en_US |
dc.identifier.scopus | eid_2-s2.0-71649101766 | en_HK |
dc.identifier.hkuros | 160464 | - |
dc.identifier.hkuros | 175235 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-71649101766&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 14 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 186 | en_HK |
dc.identifier.epage | 193 | en_HK |
dc.publisher.place | Hong Kong | en_HK |
dc.identifier.scopusauthorid | Chan, IHY=36344597900 | en_HK |
dc.identifier.scopusauthorid | Wong, KKY=24438686400 | en_HK |
dc.identifier.scopusauthorid | Chan, GCF=16160154400 | en_HK |
dc.identifier.scopusauthorid | Tam, PKH=7202539421 | en_HK |
dc.identifier.issnl | 1013-9923 | - |