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Response to N7 induction chemotherapy in children more than one year of age diagnosed with metastatic neuroblastoma treated in UKCCSG centers
Author(s) -
Kohler J.A.,
Ellershaw C.,
Machin D.
Publication year - 2007
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.21139
Subject(s) - medicine , induction chemotherapy , neuroblastoma , chemotherapy , induction therapy , clearance , response evaluation criteria in solid tumors , complete response , progressive disease , oncology , surgery , nuclear medicine , urology , biology , genetics , cell culture
Background The highest reported metastatic response rate to induction chemotherapy in patients with neuroblastoma has been achieved by Kushner et al. [Kushner et al.: J Clin Oncol 12:2607–2613,1994; Cheung et al.: Med Pediatr Oncol 36: 227–230, 2001; Kushner et al.: J Clin Oncol 22:4888‐4892, 2004] using their N6 and subsequently N7 protocols. This N7 induction was adopted by UKCCSG for new patients in 1999. Methods Forty‐seven children with metastatic neuroblastoma were recruited between 1999 and 2002. They received the N7 intensive chemotherapy protocol, after full staging including evaluation by I 123 mIBG imaging where possible. Results Thirty patients with positive mIBG scans were evaluable for response, and complete resolution of metastatic disease was obtained in 16 (53.3%). Fourteen patients without positive mIBG scans were evaluated for response according to bone marrow and bone scan data and 11 (78.6%) cleared metastatic disease. The toxicity of this induction therapy was similar to that seen in previous UK protocols, although 14 patients had Brock grade 3 or 4 ototoxicity. Thirty‐three patients proceeded to high‐dose therapy with no unanticipated toxicities. For the whole group of 44 evaluable patients, the 3‐year event‐free survival (EFS) and overall survival (OS) were 38.3 and 46.7%, respectively. Conclusions Although feasible in terms of delivery, when used in the UKCCSG centers, this protocol achieved a much lower response rate than in the previously published series in the US [Kushner et al.: J Clin Oncol 12:2607–2613,1994; Cheung et al.: Med Pediatr Oncol 36: 227–230, 2001; Kushner et al.: J Clin Oncol 22:4888‐4892, 2004]. Pediatr Blood Cancer 2007;49:234–239. © 2007 Wiley‐Liss, Inc.