van den Bent M J, Kros J M, Heimans J J, Pronk L C, van Groeningen C J, Krouwer H G, Taphoorn M J, Zonnenberg B A, Tijssen C C, Twijnstra A, Punt C J, Boogerd W
Department of Neuro-oncology, Dr. Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
Neurology. 1998 Oct;51(4):1140-5. doi: 10.1212/wnl.51.4.1140.
To determine the response rate and factors correlated with response of oligodendroglial tumors to procarbazine, lomustine (CCNU), and vincristine (PCV) chemotherapy.
Retrospective, observational multicenter study.
Patients treated with PCV or intensified PCV chemotherapy for a recurrent oligodendroglial tumor after surgery and radiation therapy with measurable disease were retrospectively evaluated for response. A 50% reduction in cross-sectional enhancing tumor area was considered a partial response. Stabilized or responding patients received six cycles of PCV unless unacceptable toxicity occurred.
Fifty-two patients were included; median time to progression (MTP) for the entire group was 10 months. In 17% of patients a complete response (MTP, 25 months) was obtained, and in 46% a partial response (MTP, 12 months) was obtained. Median overall survival was 20 months. Although treatment was discontinued for toxicity in seven patients, it was generally well tolerated. The intensified PCV regimen was more toxic. Patients initially presenting with seizures and patients with tumor necrosis in histologic specimens had a better response rate in contrast to patients who had their first relapse within 1 year of first treatment (surgery and radiation therapy).
Oligodendroglial tumors are chemosensitive, but most patients will have relapsed after 12 to 16 months. New studies must aim at improving initial treatment and second-line chemotherapy.
确定少突胶质细胞瘤对丙卡巴肼、洛莫司汀(CCNU)和长春新碱(PCV)化疗的反应率及相关因素。
回顾性观察性多中心研究。
对接受PCV或强化PCV化疗的患者进行回顾性评估,这些患者在手术和放疗后患有复发性少突胶质细胞瘤且疾病可测量。横断面增强肿瘤面积减少50%被视为部分缓解。病情稳定或有反应的患者接受六个周期的PCV治疗,除非出现不可接受的毒性反应。
纳入52例患者;整个组的中位进展时间(MTP)为10个月。17%的患者获得完全缓解(MTP,25个月),46%的患者获得部分缓解(MTP,12个月)。中位总生存期为20个月。尽管有7例患者因毒性反应而停止治疗,但总体耐受性良好。强化PCV方案毒性更大。与首次治疗(手术和放疗)后1年内首次复发的患者相比,最初出现癫痫发作的患者和组织学标本中有肿瘤坏死的患者反应率更高。
少突胶质细胞瘤对化疗敏感,但大多数患者在12至16个月后会复发。新的研究必须致力于改善初始治疗和二线化疗。