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High‐dose carboplatin–irinotecan–temozolomide: Treatment option for neuroblastoma resistant to topotecan
Author(s) -
Kushner Brian H.,
Kramer Kim,
Modak Shakeel,
Cheung NaiKong V.
Publication year - 2011
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.22855
Subject(s) - medicine , topotecan , irinotecan , carboplatin , mucositis , salvage therapy , chemotherapy , refractory (planetary science) , temozolomide , surgery , gastroenterology , regimen , absolute neutrophil count , oncology , cancer , neutropenia , colorectal cancer , cisplatin , physics , astrobiology
Background We report a retrospective study of a novel regimen for neuroblastoma (NB) resistant to standard induction or salvage chemotherapy which now routinely includes topotecan. Patients and Methods Forty‐five patients received carboplatin (500 mg/m 2 /day, 2×)–irinotecan (50 mg/m 2 /day, 5×)–temozolomide (250 mg/m 2 /day, 5×) (HD‐CIT). Only one course was planned. Patients with thrombocytopenia indicative of poor bone marrow (BM) reserve resulting from extensive prior therapy received peripheral blood stem cells (PBSCs) post‐HD‐CIT. Results Modest acute toxicity allowed outpatient treatment. Low‐grade diarrhea was common; there was no mucositis, nephrotoxicity, or cardiotoxicity. Myelosuppression was prolonged but uncomplicated. The absolute neutrophil count reached 500/µl on days 20–30 (median, 25) in 25 patients with satisfactory BM reserve, and on days 9–14 (median, 11) post‐PBSC infusion. Anti‐NB activity was common against refractory (non‐progressing) disease or new relapse occurring off therapy (68% objective response rate), but not against disease progressing on therapy. Seven of 26 patients treated for refractory NB are progression‐free and in complete remission following subsequent therapy, including anti‐G D2 immunotherapy, at ≥29+ months post‐HD‐CIT. Conclusions HD‐CIT is appealing as salvage or consolidative therapy because of anti‐NB activity and modest non‐hematologic toxicity. PBSC support is unnecessary when BM reserve is intact. The wide antineoplastic activity of its three components and their potential for activity against disease in the central nervous system support applicability to other cancers. Pediatr Blood Cancer 2011;56:403–408. © 2010 Wiley‐Liss, Inc.