Survival following adjuvant PCV or temozolomide for anaplastic astrocytoma

被引:57
作者
Brandes, Alba A.
Nicolardi, Linda
Tosoni, Alicia
Gardiman, Marina
Iuzzolino, Paolo
Ghimenton, Claudio
Reni, Michele
Rotilio, Antonino
Sotti, Guido
Ermani, Mario
机构
[1] IRCCS Padova, Ist Oncol Veneto, Dept Med Oncol, I-35128 Padua, Italy
[2] IRCCS Padova, Ist Oncol Veneto, Dept Radiotherapy, I-35128 Padua, Italy
[3] Univ Padua, Azienda Osped, Dept Pathol, I-35128 Padua, Italy
[4] Univ Padua, Azienda Osped, Dept Neurosurg, I-35128 Padua, Italy
[5] Univ Padua, Azienda Osped, Dept Neurol Sci, I-35128 Padua, Italy
[6] Azienda Osped Belluno, Dept Pathol, I-32100 Belluno, Italy
[7] Osped San Raffaele, Dept Oncol, I-20132 Milan, Italy
关键词
adjuvant chemotherapy; anaplastic astrocytoma; clinical trials; PCV; temozolomide;
D O I
10.1215/15228517-2006-005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We compared survival in patients with anaplastic astrocytoma (AA) treated with adjuvant procarbazine, lomustine, and vincristine (PCV) with survival in patients treated with temozolomide. A retrospective analysis was made of patients with newly diagnosed AA treated with adjuvant postradiotherapy chemotherapy. Outcome analysis included progression-free survival and overall survival. The following prognostic factors were taken into account: patient age, extent of resection, performance status, presence of contrast enhancement in presurgical imaging, and type of adjuvant treatment. Among 109 AA patients, 49 were treated with PCV and 60 with temozolomide. The treatment groups were well matched for pretreatment characteristics, except for the presence of contrast enhancement. Age, extent of surgery, performance status, and presence of contrast enhancement were statistically significant prognostic factors according to the Cox model analysis of survival. Type of adjuvant chemotherapy was not a significant factor, either for progression-free survival or for overall survival. Hematological toxicity, nonhematological toxicity grades 3-4, and premature discontinuation due to toxicity were observed in 9%, 3% to 5%, and 37%, respectively, of cases in the PCV group versus 4% to 5%, 0, and 0, respectively, in the temozolomide group. Although the present study was not randomized, it was well designed, and it reports on two homogeneous and consecutive series of patients, for whom histology was verified to obtain survival data only for patients with AA following the recent WHO 2000 classification. Even if no survival advantage has been demonstrated for temozolomide versus PCV, we conclude that temozolomide should be preferred because of its greater tolerability.
引用
收藏
页码:253 / 260
页数:8
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