textabstractBortezomib induced peripheral neuropathy is a dose-limiting side effect and a major concern in the treatment of multiple myeloma. To identify genetic risk factors associated with the development of this side effect in bortezomib treated multiple myeloma patients, a pharmacogenetic association study was performed using a discovery set (IFM 2005-01; n=238) and a validation set (HOVON65/GMMG-HD4 and a Czech dataset; n=231). After multiplicity correction, none of the 2,149 single nucleotide polymorphisms tested revealed any significant association with bortezomib induced peripheral neuropathy. However, 56 single nucleotide polymorphisms demonstrated an association with bortezomib induced peripheral neuropathy with pointwise, uncorre...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
Objective: Bortezomib is a new chemotherapeutic drug available for the treatment of lymphoid disorde...
The launch of novel chemotherapeutic agents—in particular, proteasome inhibitors and immunomodulator...
The proteasome-inhibitor bortezomib was introduced into the treatment of multiple myeloma more than ...
The introduction of proteasome inhibitors in the treatment of multiple myeloma (MM) patients has bee...
textabstractPurpose: Painful peripheral neuropathy is a frequent toxicity associated with bortezomib...
International audiencePurpose: Painful peripheral neuropathy is a frequent toxicity associated with ...
Purpose: To indentify genetic variation that can modulate and predict the risk of developing thalido...
Background: Based on the possible shared mechanisms of chemotherapy-induced peripheral neuropathy (C...
Purpose To indentify genetic variation that can modulate and predict the risk of developing thalidom...
Background Bortezomib-induced peripheral neuropathy is a dose-limiting toxicity in patients with mul...
Abstract Background Based on the possible shared mechanisms of chemotherapy-induced peripheral neuro...
Multiple myeloma (MM) is a B cell neoplasm characterized by uncontrolled growth of malignant plasma ...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
Objective: Bortezomib is a new chemotherapeutic drug available for the treatment of lymphoid disorde...
The launch of novel chemotherapeutic agents—in particular, proteasome inhibitors and immunomodulator...
The proteasome-inhibitor bortezomib was introduced into the treatment of multiple myeloma more than ...
The introduction of proteasome inhibitors in the treatment of multiple myeloma (MM) patients has bee...
textabstractPurpose: Painful peripheral neuropathy is a frequent toxicity associated with bortezomib...
International audiencePurpose: Painful peripheral neuropathy is a frequent toxicity associated with ...
Purpose: To indentify genetic variation that can modulate and predict the risk of developing thalido...
Background: Based on the possible shared mechanisms of chemotherapy-induced peripheral neuropathy (C...
Purpose To indentify genetic variation that can modulate and predict the risk of developing thalidom...
Background Bortezomib-induced peripheral neuropathy is a dose-limiting toxicity in patients with mul...
Abstract Background Based on the possible shared mechanisms of chemotherapy-induced peripheral neuro...
Multiple myeloma (MM) is a B cell neoplasm characterized by uncontrolled growth of malignant plasma ...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
A subanalysis of the GIMEMA-MMY-3006 trial was performed to characterize treatment-emergent peripher...
Objective: Bortezomib is a new chemotherapeutic drug available for the treatment of lymphoid disorde...
The launch of novel chemotherapeutic agents—in particular, proteasome inhibitors and immunomodulator...