1. Building the bridge between rhabdomyosarcoma in children, adolescents and young adults: The road ahead 
J. Carlijn Van Gaal, Eveline S.J.M. De Bont, Suzanne E.J. Kaal, Yvonne Versleijen-Jonkers, Winette T.A. van der Graaf 
Critical Reviews in Oncology / Hematology 
Volume 82, Issue 3, Pages (June 2012)
DOI: /j.critrevonc
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2. Fig. 1
a. Incidence rates of all subtypes of RMS in patients 0–29 years of age [35,37]. *Data regarding patients with RMS >14 years in Europe were not available. b. Incidence of ERMS and ARMS in the childhood population.
Copied from Ognjanovic et al. [33]. Copyright 2011 American Cancer Society. This material is reproduced with permission of Wiley-Liss, Inc., a subsidiary of John Wiley & Sons, Inc.
Critical Reviews in Oncology / Hematology  , DOI: ( /j.critrevonc )
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3. Fig. 2
Clinical trial availability explicitly for sarcoma/RMS by phase (I/II/III), type of intervention (chemotherapy, targeted therapy, immune-related therapy, stem cell transplantation (SCT), radiotherapy, and others) and for each year of age 0–55 years over the 10-year period 1st January 2001–1st January It is of note that our search on sarcoma/rhabdomyosarcoma results in a major underestimation of phase I trials available in these patients of adult age, because this indication is often not mentioned explicitly in study description.
Critical Reviews in Oncology / Hematology  , DOI: ( /j.critrevonc )
Copyright © 2011 Elsevier Ireland Ltd Terms and Conditions