Literature DB >> 28791452

Long-term daily temozolomide with dose-dependent efficacy in MGMT promotor methylation negative recurrent high-grade astrocytoma.

Zhengqiu Zhou1, Tracy A Howard1, John L Villano2,3.   

Abstract

Temozolomide (TMZ) for malignant gliomas is traditionally dosed in 5 out of a 28-day cycle, however alternative regimens exist, including dose-dense. Continuous daily dosing is available, but the acceptable dose and duration of therapy is unknown. We document a 40-year-old male with recurrent anaplastic astrocytoma, IDH mutant and MGMT promotor methylation negative, who has well-tolerated continuous daily TMZ for 20 months at 100 mg per day for nearly the length of this period. A trial at 80 mg per day demonstrated disease progression with response upon return to 100 mg per day. Prior to the daily TMZ, the patient underwent three surgical resections, radiation therapy with concurrent TMZ according to the EORTC-NCIC protocol, and subsequently bevacizumab in combination with use of the Optune device. Long-term survival of patients with recurrent malignant gliomas is uncommon, and currently no standard treatment strategies exist for these patients. We present this case to demonstrate the tolerability and dose dependency of prolonged daily TMZ dosing as a therapeutic option for recurrent anaplastic astrocytomas.

Entities:  

Keywords:  Anaplastic astrocytoma; Dose dependence; Dose-dense; High-grade astrocytoma; Long-term daily dosing; Temozolomide

Mesh:

Substances:

Year:  2017        PMID: 28791452     DOI: 10.1007/s00280-017-3415-5

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  3 in total

1.  Dose-dense temozolomide for recurrent high-grade gliomas: a single-center retrospective study.

Authors:  Catherine R Garcia; Stacey A Slone; Rachael M Morgan; Lindsey Gruber; Sameera S Kumar; Donita D Lightner; John L Villano
Journal:  Med Oncol       Date:  2018-08-28       Impact factor: 3.064

2.  PI3Kγ inhibition suppresses microglia/TAM accumulation in glioblastoma microenvironment to promote exceptional temozolomide response.

Authors:  Jie Li; Megan M Kaneda; Jun Ma; Ming Li; Ryan M Shepard; Kunal Patel; Tomoyuki Koga; Aaron Sarver; Frank Furnari; Beibei Xu; Sanjay Dhawan; Jianfang Ning; Hua Zhu; Anhua Wu; Gan You; Tao Jiang; Andrew S Venteicher; Jeremy N Rich; Christopher K Glass; Judith A Varner; Clark C Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2021-04-20       Impact factor: 11.205

3.  Combination chemoradiotherapy with temozolomide, vincristine, and interferon-β might improve outcomes regardless of O6-methyl-guanine-DNA-methyltransferase (MGMT) promoter methylation status in newly glioblastoma.

Authors:  Kenichiro Asano; Toshio Fumoto; Masashi Matsuzaka; Seiko Hasegawa; Naoya Suzuki; Kenichi Akasaka; Kosuke Katayama; Akihisa Kamataki; Akira Kurose; Hiroki Ohkuma
Journal:  BMC Cancer       Date:  2021-07-28       Impact factor: 4.430

  3 in total

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