Soft Tissue Sarcomas of Childhood and Adolescence: The Prognostic Role of Tumor Size in Relation to Patient Body Size

2009 ◽  
Vol 2009 ◽  
pp. 184
Author(s):  
C.P. Beauchamp
2009 ◽  
Vol 27 (3) ◽  
pp. 371-376 ◽  
Author(s):  
Andrea Ferrari ◽  
Rosalba Miceli ◽  
Cristina Meazza ◽  
Elena Zaffignani ◽  
Alessandro Gronchi ◽  
...  

Purpose Tumor size is a key prognostic variable for soft tissue sarcomas (STS), and a tumor diameter of 5 cm is generally used as a cutoff for risk grouping purposes. This study aimed to investigate the prognostic effect of tumor size on overall survival and whether such an effect was influenced by the patient's size, expressed as body-surface area (BSA), in a series of 553 pediatric patients with localized STS. Patients and Methods Multivariable Cox models were used in which the effect of tumor size was adjusted for patients age, tumor site, histologic subtype, and Intergroup Rhabdomyosarcoma Study grouping, and the interaction between size and BSA was included. Results Tumor size was confirmed as a significant prognostic factor. Interaction between size and BSA meant that, for a given tumor size, the mortality increased from the larger to the smaller BSA. Conversely, the mortality risk associated with a patient with a BSA of 1.75 m2 and a 5-cm tumor was the same as for a 0.6 m2 child with a 2.8-cm tumor. Conclusion Tumor and body size are jointly informative on outcome. The risk associated with a given tumor size is not the same in patients of different body size, so it may be wrong to use the same 5-cm cutoff for tumor size in risk stratification.


2020 ◽  
Vol 31 ◽  
pp. S988-S989
Author(s):  
P. Teterycz ◽  
A.M.M. Czarnecka ◽  
A. Szmajdzinska ◽  
M. Kalejta ◽  
M. Zdzienicki ◽  
...  

2010 ◽  
Vol 42 (3) ◽  
pp. 144 ◽  
Author(s):  
Byoung Yong Shim ◽  
Jinyoung Yoo ◽  
Yeon-Soo Lee ◽  
Young Sun Hong ◽  
Hoon-Kyo Kim ◽  
...  

2014 ◽  
Vol 25 (5) ◽  
pp. 1073-1074 ◽  
Author(s):  
M. Campiglio ◽  
M. Sandri ◽  
M. Sasso ◽  
F. Bianchi ◽  
A. Balsari ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (12) ◽  
pp. e0189127 ◽  
Author(s):  
Anaid Anna Kasangian ◽  
Giorgio Gherardi ◽  
Elena Biagioli ◽  
Valter Torri ◽  
Anna Moretti ◽  
...  

2021 ◽  
Vol 32 ◽  
pp. S1125-S1126
Author(s):  
R.W. Hamacher ◽  
X. Liu ◽  
M.K. Schuler ◽  
L. Hentschel ◽  
P. Schöffski ◽  
...  

2005 ◽  
Vol 3 (2) ◽  
pp. 198-205
Author(s):  
Margaret von Mehren

Medical management of soft tissue sarcomas (STS) has been restricted by the limited availability of active drugs. A plethora of new oncologic agents are now available, many of which have specific therapeutic targets. Gemcitabine and docetaxel is a combination of drugs that have limited single-agent activity. Yondelis, a novel chemotherapeutic that binds DNA and functions partially by inhibiting transcription, is being tested alone and in combination with doxorubicin. Inhibitors of mTOR, a serine/threonine kinase that regulates cell cycle activation and cell growth, are also being tested. Growth factor receptor inhibitors are being evaluated in a variety of sarcomas that have been found to express the targets. In addition, a variety of agents are being assessed in gastrointestinal stromal tumors (GIST). Single agents and agents combined with imatinib are being tested in imatinib-refractory and in metastatic GIST. The increased use of targeted agents underscores the need for understanding sarcoma biology.


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