Conservative approach in localised rhabdomyosarcoma of the bladder and prostate: Results from International Society of Paediatric Oncology (SIOP) studies: Malignant mesenchymal tumour (MMT) 84, 89 and 95. Issue 2 (29th August 2013)
- Record Type:
- Journal Article
- Title:
- Conservative approach in localised rhabdomyosarcoma of the bladder and prostate: Results from International Society of Paediatric Oncology (SIOP) studies: Malignant mesenchymal tumour (MMT) 84, 89 and 95. Issue 2 (29th August 2013)
- Main Title:
- Conservative approach in localised rhabdomyosarcoma of the bladder and prostate: Results from International Society of Paediatric Oncology (SIOP) studies: Malignant mesenchymal tumour (MMT) 84, 89 and 95
- Authors:
- Jenney, Meriel
Oberlin, Odile
Audry, Georges
Stevens, Michael CG
Rey, Annie
Merks, Johannes HM
Kelsey, Anna
Gallego, Soledad
Haie‐Meder, Christine
Martelli, Hélène - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24727-sec-0001" sec-type="section"> <title>Background</title> <p>The three sequential SIOP MMT studies provide the largest dataset available to date, to define the patient and tumour characteristics, treatment modalities and event‐free and overall survival for children with non metastatic rhabdomyosarcoma (RMS) of the bladder and/or prostate (BP).</p> </sec> <sec id="pbc24727-sec-0002" sec-type="section"> <title>Procedure</title> <p>The combined dataset of 172 patients with BP RMS treated on the SIOP MMT 84, 89 and 95 studies was reviewed to determine tumour characteristics, details of treatment and outcome.</p> </sec> <sec id="pbc24727-sec-0003" sec-type="section"> <title>Results</title> <p>Median age at diagnosis was 2.5 years (range 2 months–17.8 years) and 138 (79%) were males. Median follow‐up was 11.4 years (range 3 months–22 years). The 5‐year overall survival of the combined cohort was 77% (CI 70–83%). The 5‐year event‐free survival was 63% and included 7 patients (4%) who did not achieve complete remission (CR), and 57 (33%) who relapsed. Age ≥ 10 years (RR 3.7) and alveolar pathology (RR 3.3) were identified as independent prognostic factors on multivariate analysis. Fifty‐nine (50%) of the 119 survivors were cured without significant local therapy, improving from 31% in MMT84 study to 61% in MMT95 study.</p> </sec> <sec id="pbc24727-sec-0004" sec-type="section"><abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24727-sec-0001" sec-type="section"> <title>Background</title> <p>The three sequential SIOP MMT studies provide the largest dataset available to date, to define the patient and tumour characteristics, treatment modalities and event‐free and overall survival for children with non metastatic rhabdomyosarcoma (RMS) of the bladder and/or prostate (BP).</p> </sec> <sec id="pbc24727-sec-0002" sec-type="section"> <title>Procedure</title> <p>The combined dataset of 172 patients with BP RMS treated on the SIOP MMT 84, 89 and 95 studies was reviewed to determine tumour characteristics, details of treatment and outcome.</p> </sec> <sec id="pbc24727-sec-0003" sec-type="section"> <title>Results</title> <p>Median age at diagnosis was 2.5 years (range 2 months–17.8 years) and 138 (79%) were males. Median follow‐up was 11.4 years (range 3 months–22 years). The 5‐year overall survival of the combined cohort was 77% (CI 70–83%). The 5‐year event‐free survival was 63% and included 7 patients (4%) who did not achieve complete remission (CR), and 57 (33%) who relapsed. Age ≥ 10 years (RR 3.7) and alveolar pathology (RR 3.3) were identified as independent prognostic factors on multivariate analysis. Fifty‐nine (50%) of the 119 survivors were cured without significant local therapy, improving from 31% in MMT84 study to 61% in MMT95 study.</p> </sec> <sec id="pbc24727-sec-0004" sec-type="section"> <title>Conclusion</title> <p>The clinical strategy of the MMT studies aims to minimise the burden of therapy whilst maintaining survival rates. Overall survival is comparable to that of other international groups, despite the lower use of radiotherapy and or radical surgery, although number of events experienced is higher. Further assessment of the late effects of therapy is required to confirm whether this approach results in lower morbidity in the long‐term. Pediatr Blood Cancer 2014;61:217–222. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 61:Issue 2(2014:Feb.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 61:Issue 2(2014:Feb.)
- Issue Display:
- Volume 61, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 61
- Issue:
- 2
- Issue Sort Value:
- 2014-0061-0002-0000
- Page Start:
- 217
- Page End:
- 222
- Publication Date:
- 2013-08-29
- 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.24727 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
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- 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:
- 4355.xml