PMID- 8515721 OWN - NLM STAT- MEDLINE DCOM- 19930720 LR - 20190905 IS - 0098-1532 (Print) IS - 0098-1532 (Linking) VI - 21 IP - 6 DP - 1993 TI - Critical observations on neuroblastoma treatment with 131-I-metaiodobenzylguanidine at diagnosis. PG - 411-5 AB - Results of treatment with 131-I-Metaiodobenzylguanidine (131-I-MIBG) in patients with resistant neuroblastoma appear encouraging if one considers that most of the patients had far advanced, intensively pre-treated disease. To further explore the potential role of this new drug in untreated patients, we treated 3 children with stage III neuroblastoma. All three of our cases received 131-I-MIBG at relatively low dose with the complete disappearance of the tumor mass in case 1, whereas in cases 2 and 3 CT scan showed a significant reduction of the tumor mass and, interestingly enough, no evidence of 131-I-MIBG uptake of a tracer dose in the remaining tumor. Particularly, in case 2, the persistence and subsequent progression of part of the tumor mass without 131-I-MIBG uptake after a therapeutic dose of 131-I-MIBG, which apparently destroyed the 131-I-MIBG-positive cell population, clearly suggest heterogeneity at diagnosis, with a dual neuroblastoma cell population, one with 131-I-MIBG uptake and the other without. Besides the biological implications of the 131-I-MIBG uptake heterogeneity in neuroblastoma at diagnosis, our findings suggest that in stage III neuroblastoma patients even a relatively small dose of 131-I-MIBG administered at diagnosis is sufficient to destroy either the primary tumor completely (case 1) or the part of the tumor (case 2 and 3) which shows 131-I-MIBG uptake, without any significant hematologic toxicity. Furthermore, a single course of 131-I-MIBG at the dosage employed does not appear to jeopardize the subsequent use of chemotherapy. In conclusion, if our data are confirmed by further investigation, 131-I-MIBG may be included as a front line drug shortly followed by chemotherapy in future treatment strategies of advanced neuroblastoma without or with minimal bone marrow infiltration. FAU - Mastrangelo, R AU - Mastrangelo R AD - Division of Pediatric Oncology, Catholic University of the Sacred Heart, Rome, Italy. FAU - Lasorella, A AU - Lasorella A FAU - Iavarone, A AU - Iavarone A FAU - Rufini, V AU - Rufini V FAU - Troncone, L AU - Troncone L FAU - Danza, F AU - Danza F FAU - Riccardi, R AU - Riccardi R LA - eng PT - Case Reports PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review PL - United States TA - Med Pediatr Oncol JT - Medical and pediatric oncology JID - 7506654 RN - 0 (Iodine Radioisotopes) RN - 0 (Iodobenzenes) RN - 35MRW7B4AD (3-Iodobenzylguanidine) SB - IM MH - 3-Iodobenzylguanidine MH - Child, Preschool MH - Female MH - Humans MH - Infant MH - Iodine Radioisotopes/*therapeutic use MH - Iodobenzenes/*therapeutic use MH - Male MH - Neuroblastoma/diagnosis/*radiotherapy RF - 17 EDAT- 1993/01/01 00:00 MHDA- 1993/01/01 00:01 CRDT- 1993/01/01 00:00 PHST- 1993/01/01 00:00 [pubmed] PHST- 1993/01/01 00:01 [medline] PHST- 1993/01/01 00:00 [entrez] AID - 10.1002/mpo.2950210604 [doi] PST - ppublish SO - Med Pediatr Oncol. 1993;21(6):411-5. doi: 10.1002/mpo.2950210604.