Literature DB >> 21572345

Oxaliplatin, irinotecan, and gemcitabine: a novel combination in the therapy of progressed, relapsed, or refractory tumors in children.

Carolin Hartmann1, Peter Weinel, Hansjörg Schmid, Lorenz Grigull, Anette Sander, Christin Linderkamp, Karl Welte, Dirk Reinhardt.   

Abstract

Therapeutic options for unresectable neuroendocrine carcinomas and relapsed or refractory solid tumors are still limited in pediatric patients. We present a retrospective review of 12 children (3 to 16 y) in a case series treated with a novel combination of oxaliplatin, irinotecan, and gemcitabine (triple therapy). We defined its feasibility in a mainly outpatient setting and assessed its toxicity and effectiveness. Three patients with unresectable neuroendocrine carcinomas received triple therapy as first-line treatment; 9 children with relapsed or refractory solid tumors of different entities were assigned after failure of standard treatment protocols. The treatment schedule comprised oxaliplatin (85 mg/m²), irinotecan (175 mg/m²), and gemcitabine (1,000 mg/m²), the latter to be repeated on day 8. A median of 7 cycles was applied. Nine of 12 patients showed hematotoxicity 0-III degrees. Gastrointestinal toxicity I-II degrees were handled satisfactorily by supportive drugs. Tumor response was defined as partial response in 1 of 12 children, stable disease in 8 of 12 children, and progressive disease in 3 of 12 children with a median time of disease control of 7 months. We regard triple therapy as a well-tolerated outpatient treatment option offering children a high quality of life and showing considerable effectiveness in delaying tumor progress.

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Year:  2011        PMID: 21572345     DOI: 10.1097/MPH.0b013e31820994ec

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  5 in total

1.  5-aza-2'-deoxycytidine, a DNA methylation inhibitor, attenuates hyperoxia-induced lung fibrosis via re-expression of P16 in neonatal rats.

Authors:  Shi-Meng Zhao; Hong-Min Wu; Mei-Ling Cao; Dan Han
Journal:  Pediatr Res       Date:  2017-12-20       Impact factor: 3.756

2.  Convection-enhancement delivery of liposomal formulation of oxaliplatin shows less toxicity than oxaliplatin yet maintains a similar median survival time in F98 glioma-bearing rat model.

Authors:  Minghan Shi; David Fortin; Benoit Paquette; Léon Sanche
Journal:  Invest New Drugs       Date:  2016-03-09       Impact factor: 3.850

3.  Phase I clinical trial of ifosfamide, oxaliplatin, and etoposide (IOE) in pediatric patients with refractory solid tumors.

Authors:  Catherine G Lam; Wayne L Furman; Chong Wang; Sheri L Spunt; Jianrong Wu; Percy Ivy; Victor M Santana; Lisa M McGregor
Journal:  J Pediatr Hematol Oncol       Date:  2015-01       Impact factor: 1.289

4.  Acquired resistance to oxaliplatin is not directly associated with increased resistance to DNA damage in SK-N-ASrOXALI4000, a newly established oxaliplatin-resistant sub-line of the neuroblastoma cell line SK-N-AS.

Authors:  Emily Saintas; Liam Abrahams; Gulshan T Ahmad; Anu-Oluwa M Ajakaiye; Abdulaziz S H A M AlHumaidi; Candice Ashmore-Harris; Iain Clark; Usha K Dura; Carine N Fixmer; Chinedu Ike-Morris; Mireia Mato Prado; Danielle Mccullough; Shishir Mishra; Katia M U Schöler; Husne Timur; Maxwell D C Williamson; Markella Alatsatianos; Basma Bahsoun; Edith Blackburn; Catherine E Hogwood; Pamela E Lithgow; Michelle Rowe; Lyto Yiangou; Florian Rothweiler; Jindrich Cinatl; Richard Zehner; Anthony J Baines; Michelle D Garrett; Campbell W Gourlay; Darren K Griffin; William J Gullick; Emma Hargreaves; Mark J Howard; Daniel R Lloyd; Jeremy S Rossman; C Mark Smales; Anastasios D Tsaousis; Tobias von der Haar; Mark N Wass; Martin Michaelis
Journal:  PLoS One       Date:  2017-02-13       Impact factor: 3.240

Review 5.  Fifteen years of irinotecan therapy for pediatric sarcoma: where to next?

Authors:  Lars M Wagner
Journal:  Clin Sarcoma Res       Date:  2015-08-28
  5 in total

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