TY - JOUR
T1 - Outcome after surgery alone or with restricted use of chemotherapy for patients with low-risk neuroblastoma
T2 - Results of Children's Oncology Group study P9641
AU - Strother, Douglas R.
AU - London, Wendy B.
AU - Schmidt, Mary Lou
AU - Brodeur, Garrett M.
AU - Shimada, Hiroyuki
AU - Thorner, Paul
AU - Collins, Margaret H.
AU - Tagge, Edward
AU - Adkins, Stanton
AU - Reynolds, C. Patrick
AU - Murray, Kevin
AU - Lavey, Robert S.
AU - Matthay, Katherine K.
AU - Castleberry, Robert
AU - Maris, John M.
AU - Cohn, Susan L.
PY - 2012/5/20
Y1 - 2012/5/20
N2 - Purpose: The primary objective of Children's Oncology Group study P9641 was to demonstrate that surgery alone would achieve 3-year overall survival (OS) ≥ 95% for patients with asymptomatic International Neuroblastoma Staging System stages 2a and 2b neuroblastoma (NBL). Secondary objectives focused on other low-risk patients with NBL and on those who required chemotherapy according to protocol-defined criteria. Patients and Methods: Patients underwent maximally safe resection of tumor. Chemotherapy was reserved for patients with, or at risk for, symptomatic disease, with less than 50% tumor resection at diagnosis, or with unresectable progressive disease after surgery alone. Results: For all 915 eligible patients, 5-year event-free survival (EFS) and OS were 89% ± 1% and 97% ±1%, respectively. For patients with asymptomatic stage 2a or 2b disease, 5-year EFS and OS were 87% ± 2% and 96% ± 1%, respectively. Among patients with stage 2b disease, EFS and OS were significantly lower for those with unfavorable histology or diploid tumors, and OS was significantly lower for those ≥ 18 months old. For patients with stage 1 and 4s NBL, 5-year OS rates were 99% ± 1% and 91% ± 1%, respectively. Patients who required chemotherapy at diagnosis achieved 5-year OS of 98% ± 1%. Of all patients observed after surgery, 11.1% experienced recurrence or progression of disease. Conclusion: Excellent survival rates can be achieved in asymptomatic low-risk patients with stages 2a and 2b NBL after surgery alone. Immediate use of chemotherapy may be restricted to a minority of patients with low-risk NBL. Patients with stage 2b disease who are older or have diploid or unfavorable histology tumors fare less well. Future studies will seek to refine risk classification.
AB - Purpose: The primary objective of Children's Oncology Group study P9641 was to demonstrate that surgery alone would achieve 3-year overall survival (OS) ≥ 95% for patients with asymptomatic International Neuroblastoma Staging System stages 2a and 2b neuroblastoma (NBL). Secondary objectives focused on other low-risk patients with NBL and on those who required chemotherapy according to protocol-defined criteria. Patients and Methods: Patients underwent maximally safe resection of tumor. Chemotherapy was reserved for patients with, or at risk for, symptomatic disease, with less than 50% tumor resection at diagnosis, or with unresectable progressive disease after surgery alone. Results: For all 915 eligible patients, 5-year event-free survival (EFS) and OS were 89% ± 1% and 97% ±1%, respectively. For patients with asymptomatic stage 2a or 2b disease, 5-year EFS and OS were 87% ± 2% and 96% ± 1%, respectively. Among patients with stage 2b disease, EFS and OS were significantly lower for those with unfavorable histology or diploid tumors, and OS was significantly lower for those ≥ 18 months old. For patients with stage 1 and 4s NBL, 5-year OS rates were 99% ± 1% and 91% ± 1%, respectively. Patients who required chemotherapy at diagnosis achieved 5-year OS of 98% ± 1%. Of all patients observed after surgery, 11.1% experienced recurrence or progression of disease. Conclusion: Excellent survival rates can be achieved in asymptomatic low-risk patients with stages 2a and 2b NBL after surgery alone. Immediate use of chemotherapy may be restricted to a minority of patients with low-risk NBL. Patients with stage 2b disease who are older or have diploid or unfavorable histology tumors fare less well. Future studies will seek to refine risk classification.
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U2 - 10.1200/JCO.2011.37.9990
DO - 10.1200/JCO.2011.37.9990
M3 - Article
C2 - 22529259
SN - 0732-183X
VL - 30
SP - 1842
EP - 1848
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 15
ER -