Challenges with defining response to antitumor agents in pediatric neuro-oncology: a report from the response assessment in pediatric neuro-oncology (RAPNO) working group
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Challenges with defining response to antitumor agents in pediatric neuro-oncology: a report from the response assessment in pediatric neuro-oncology (RAPNO) working group. / Warren, Katherine E; Poussaint, Tina Y; Vezina, Gilbert; Hargrave, Darren; Packer, Roger J; Goldman, Stewart; Wen, Patrick Y; Pollack, Ian F; Zurakowski, David; Kun, Larry E; Prados, Michael D; Rutkowski, Stefan; Kieran, Mark W.
In: PEDIATR BLOOD CANCER, Vol. 60, No. 9, 01.09.2013, p. 1397-401.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Challenges with defining response to antitumor agents in pediatric neuro-oncology: a report from the response assessment in pediatric neuro-oncology (RAPNO) working group
AU - Warren, Katherine E
AU - Poussaint, Tina Y
AU - Vezina, Gilbert
AU - Hargrave, Darren
AU - Packer, Roger J
AU - Goldman, Stewart
AU - Wen, Patrick Y
AU - Pollack, Ian F
AU - Zurakowski, David
AU - Kun, Larry E
AU - Prados, Michael D
AU - Rutkowski, Stefan
AU - Kieran, Mark W
N1 - Copyright © 2013 Wiley Periodicals, Inc.
PY - 2013/9/1
Y1 - 2013/9/1
N2 - Criteria for new drug approval include demonstration of efficacy. In neuro-oncology, this is determined radiographically utilizing tumor measurements on MRI scans. Limitations of this method have been identified where drug activity is not reflected in decreased tumor size. The RANO (Response Assessment in Neuro-Oncology) working group was established to address limitations in defining endpoints for clinical trials in adult neuro-oncology and to develop standardized response criteria. RAPNO was subsequently established to address unique issues in pediatric neuro-oncology. The aim of this paper is to delineate response criteria issues in pediatric clinical trials as a basis for subsequent recommendations.
AB - Criteria for new drug approval include demonstration of efficacy. In neuro-oncology, this is determined radiographically utilizing tumor measurements on MRI scans. Limitations of this method have been identified where drug activity is not reflected in decreased tumor size. The RANO (Response Assessment in Neuro-Oncology) working group was established to address limitations in defining endpoints for clinical trials in adult neuro-oncology and to develop standardized response criteria. RAPNO was subsequently established to address unique issues in pediatric neuro-oncology. The aim of this paper is to delineate response criteria issues in pediatric clinical trials as a basis for subsequent recommendations.
KW - Adolescent
KW - Adult
KW - Antineoplastic Agents
KW - Child
KW - Child, Preschool
KW - Clinical Trials as Topic
KW - Female
KW - Humans
KW - Infant
KW - Infant, Newborn
KW - Male
KW - Neoplasms, Nerve Tissue
U2 - 10.1002/pbc.24562
DO - 10.1002/pbc.24562
M3 - SCORING: Journal article
C2 - 23625747
VL - 60
SP - 1397
EP - 1401
JO - PEDIATR BLOOD CANCER
JF - PEDIATR BLOOD CANCER
SN - 1545-5009
IS - 9
ER -