Methods for treating neuroblastoma

Abstract

The present invention provides methods and kits a) for preventing and/or treating neuroblastoma (e.g., high-risk neuroblastoma) that is linked, in part, to high levels of ODC activity and increased cellular polyamine content, b) for predicting cancer patient survival, especially cancer patients whose cancer is linked, in part, to high levels of ODC activity and increased cellular polyamine contents, and c) for selecting treatment options for such patients based on the allelic nucleotide sequence or SNP at positions +263 and/or +316 of the ODC1 gene. The invention also provides, cancer treatment methods comprising the determination of the ODC1 genotype at the +263 and/or +316 positions, as a means to guide treatment selection, which includes, in some aspects the administration of pharmaceutically effective amounts of α-difluoromethylornithine (DFMO), either as a monotherapy or in combination with one or more other drugs. In addition, the present invention provides methods for preventing and/or treating patients that have been determined to have cancer stem cells, such as patients in cancer remission that are at risk for relapse.

1 - 149 . (canceled) 
     
     
         150 . A method for preventing relapse of neuroblastoma in a patient at risk therefore, the method comprising administering to the patient an effective amount of a pharmaceutical therapy comprising α-difluoromethylornithine (DFMO) 
     
     
         151 . The method of  claim 150 , wherein the patient is in remission from high-risk neuroblastoma. 
     
     
         152 . The method of  claim 150 , wherein the patient has completed standard therapy for neuroblastoma. 
     
     
         153 . The method of  claim 150 , wherein the administration of DFMO is initiated within 120 days of completion of standard therapy. 
     
     
         154 . The method of  claim 150 , wherein the patient is a pediatric patient. 
     
     
         155 . The method of  claim 154 , wherein the patient is greater than 2 years old. 
     
     
         156 . The method of  claim 154 , wherein the patient is less than 2 years old. 
     
     
         157 . The method of  claim 150 , wherein the pharmaceutical therapy is administered orally. 
     
     
         158 . The method of  claim 150 , wherein the DFMO is administered in doses of 500-1500 mg/m 2 . 
     
     
         159 . The method of  claim 150 , wherein the pharmaceutical therapy is administered twice daily. 
     
     
         160 . The method of  claim 150 , wherein the pharmaceutical therapy is formulated as an oral liquid, an oral powder, a coated tablet, or a chewable tablet. 
     
     
         161 . The method of  claim 150 , wherein the patient has a T at rs2302616 of at least one allele of the ODC1 gene. 
     
     
         162 . The method of  claim 150 , wherein the patient has a TT or TG genotype at rs2302616 of the ODC1 gene. 
     
     
         163 . The method of  claim 150 , wherein the patient has a G at rs2302615 of at least one allele of the ODC1 gene. 
     
     
         164 . The method of  claim 150 , wherein the method prevents the formation of new neuroblastomas within the patient. 
     
     
         165 . The method of  claim 150 , wherein the DFMO is eflornithine hydrochloride monohydrate. 
     
     
         166 . The method of  claim 165 , wherein the eflornithine hydrochloride monohydrate is a racemic mixture of its two enantiomers.