TY - JOUR
T1 - Long-term treatment with temozolomide in malignant glioma
AU - Mannas, Jonathan P.
AU - Lightner, Donita D.
AU - Defrates, Sean R.
AU - Pittman, Thomas
AU - Villano, J. Lee
PY - 2014/1
Y1 - 2014/1
N2 - Six months of maintenance temozolomide (TMZ) following concurrent TMZ chemotherapy and radiation therapy has become the standard of care in the treatment of glioblastoma. In addition, TMZ has also been used to treat other forms of glioma although less evidence of efficacy exists. TMZ administration longer than 6 months is common in clinical practice, but it is unusual for the drug to be administered longer than 1 to 2 years. We report five patients who received long-term treatment with TMZ chemotherapy at normal dosing levels. One of these patients was diagnosed with glioblastoma, two with anaplastic astrocytoma, one with gliosarcoma, and one with oligo-astrocytoma. The length of treatment in our group of patients ranged from 45 to 85 cycles of TMZ. Common Terminology Criteria for Adverse Events (CTCAE) developed by The National Cancer Institute was used to classify toxicity. Two patients experienced no toxicity per CTCAE guidelines. One patient experienced grade I thrombocytopenia, one developed grade I leukopenia, and one experienced both grade I thrombocytopenia and grade I nausea, all which resolved with either withholding TMZ for 1 month or supportive treatment. Our report provides evidence that long-term TMZ chemotherapy is a therapeutic option when appropriately monitored.
AB - Six months of maintenance temozolomide (TMZ) following concurrent TMZ chemotherapy and radiation therapy has become the standard of care in the treatment of glioblastoma. In addition, TMZ has also been used to treat other forms of glioma although less evidence of efficacy exists. TMZ administration longer than 6 months is common in clinical practice, but it is unusual for the drug to be administered longer than 1 to 2 years. We report five patients who received long-term treatment with TMZ chemotherapy at normal dosing levels. One of these patients was diagnosed with glioblastoma, two with anaplastic astrocytoma, one with gliosarcoma, and one with oligo-astrocytoma. The length of treatment in our group of patients ranged from 45 to 85 cycles of TMZ. Common Terminology Criteria for Adverse Events (CTCAE) developed by The National Cancer Institute was used to classify toxicity. Two patients experienced no toxicity per CTCAE guidelines. One patient experienced grade I thrombocytopenia, one developed grade I leukopenia, and one experienced both grade I thrombocytopenia and grade I nausea, all which resolved with either withholding TMZ for 1 month or supportive treatment. Our report provides evidence that long-term TMZ chemotherapy is a therapeutic option when appropriately monitored.
KW - Brain tumors
KW - Malignant gliomas
KW - Temozolomide
KW - Toxicity
UR - http://www.scopus.com/inward/record.url?scp=84890557145&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84890557145&partnerID=8YFLogxK
U2 - 10.1016/j.jocn.2013.03.039
DO - 10.1016/j.jocn.2013.03.039
M3 - Article
C2 - 24063865
AN - SCOPUS:84890557145
SN - 0967-5868
VL - 21
SP - 121
EP - 123
JO - Journal of Clinical Neuroscience
JF - Journal of Clinical Neuroscience
IS - 1
ER -