TY - JOUR
T1 - Consensus recommendations to accelerate clinical trials for neurofibromatosis type 2
AU - Evans, D. Gareth
AU - Kalamarides, Michel
AU - Hunter-Schaedle, Kim
AU - Blakeley, Jaishri
AU - Allen, Jeffrey
AU - Babovic-Vuskanovic, Dusica
AU - Belzberg, Allan
AU - Bollag, Gideon
AU - Chen, Ruihong
AU - DiTomaso, Emmanuelle
AU - Golfinos, John
AU - Harris, Gordon
AU - Jacob, Abraham
AU - Kalpana, Ganjam
AU - Karajannis, Matthias
AU - Korf, Bruce
AU - Kurzrock, Razelle
AU - Law, Meng
AU - McClatchey, Andrea
AU - Packer, Roger
AU - Roehm, Pamela
AU - Rubenstein, Allan
AU - Slattery, William
AU - Tonsgard, James H.
AU - Welling, D. Bradley
AU - Widemann, Brigitte
AU - Yohay, Kaleb
AU - Giovannini, Marco
PY - 2009/8/15
Y1 - 2009/8/15
N2 - Purpose: Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder associated primarily with bilateral schwannomas seen on the superior vestibular branches of the eighth cranial nerves. Significant morbidity can result from surgical treatment of these tumors. Meningiomas, ependymomas, and other benign central nervous system tumors are also common in NF2. The lack of effective treatments for NF2 marks an unmet medical need. Experimental Design: Here, we provide recommendations from a workshop, cochaired by Drs. D. Gareth Evans and Marco Giovannini, of 36 international researchers, physicians, representatives of the biotechnology industry, and patient advocates on how to accelerate progress toward NF2 clinical trials. Results: Workshop participants reached a consensus that, based on current knowledge, the time is right to plan and implement NF2 clinical trials. Obstacles impeding NF2 clinical trials and how to address them were discussed, as well as the candidate therapeutic pipeline for NF2. Conclusions: Both phase 0 and phase II NF2 trials are near-term options for NF2 clinical trials. The number of NF2 patients in the population remains limited, and successful recruitment will require ongoing collaboration efforts between NF2 clinics.
AB - Purpose: Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder associated primarily with bilateral schwannomas seen on the superior vestibular branches of the eighth cranial nerves. Significant morbidity can result from surgical treatment of these tumors. Meningiomas, ependymomas, and other benign central nervous system tumors are also common in NF2. The lack of effective treatments for NF2 marks an unmet medical need. Experimental Design: Here, we provide recommendations from a workshop, cochaired by Drs. D. Gareth Evans and Marco Giovannini, of 36 international researchers, physicians, representatives of the biotechnology industry, and patient advocates on how to accelerate progress toward NF2 clinical trials. Results: Workshop participants reached a consensus that, based on current knowledge, the time is right to plan and implement NF2 clinical trials. Obstacles impeding NF2 clinical trials and how to address them were discussed, as well as the candidate therapeutic pipeline for NF2. Conclusions: Both phase 0 and phase II NF2 trials are near-term options for NF2 clinical trials. The number of NF2 patients in the population remains limited, and successful recruitment will require ongoing collaboration efforts between NF2 clinics.
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U2 - 10.1158/1078-0432.CCR-08-3011
DO - 10.1158/1078-0432.CCR-08-3011
M3 - Review article
C2 - 19671848
AN - SCOPUS:68149180536
SN - 1078-0432
VL - 15
SP - 5032
EP - 5039
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 16
ER -