Feasibility, toxicity and response of upfront metaiodobenzylguanidine therapy therapy followed by German Pediatric Oncology Group Neuroblastoma 2004 protocol in newly diagnosed stage 4 neuroblastoma patients

Publication date: May 2017
Source:European Journal of Cancer, Volume 76
Author(s): K.C.J.M. Kraal, G.M. Bleeker, B.L.F. van Eck-Smit, N.K.A. van Eijkelenburg, F. Berthold, M.M. van Noesel, H.N. Caron, G.A.M. Tytgat
Aim of the studyRadiolabelled meta-iodobenzylguanidine (MIBG) is an effective option in treatment of neuroblastoma (NBL) tumours. We studied feasibility, toxicity and efficacy of upfront ¹³¹I-MIBG and induction treatment in stage 4 NBL patients.Patients and methodsRetrospective, multi-centre (AMC and EMC) pilot regimen (1/1/2005–2011). Newly diagnosed stage 4 NBL patients, were treated with 2 courses of ¹³¹I-MIBG, GPOH 2004 NBL protocol, myeloablative therapy (MAT) and autologous stem cell rescue (ASCT). ¹³¹I-MIBG was administered in a fixed dose. Response rate (RR) was defined as complete remission, very good partial response and partial response.ResultsThirty-two patients, (median age [range] 2.9 [0–11.4] years), 21 received ¹³¹I-MIBG therapy, 11 did not because of: MIBG non-avid (N = 5) and poor clinical condition (N = 6). In 95% of eligible patients ¹³¹I-MIBG treatment was feasible within 2 weeks from diagnosis. Interval between chemotherapy courses was 25 days (¹³¹I-MIBG group) versus 22 days (chemotherapy group). No stem cell support was needed after ¹³¹I-MIBG therapy. Stem cell harvest in both groups was feasible, neutrophil recovery was comparable, but platelet recovery post MAT, ASCT was slower for ¹³¹I-MIBG-treated patients. RR post ¹³¹I-MIBG was 38%, post MAT + ASCT was 71% (¹³¹I-MIBG group), 36% (chemotherapy group) and overall 59%.ConclusionsInduction therapy with ¹³¹I-MIBG before the HR GPOH NB 2004 protocol is feasible, tolerable and effective in newly diagnosed stage 4 NBL patients. ¹³¹I-MIBG upfront therapy induces early responses.



http://ift.tt/2nTmpPI