Department of Medicine II, Tokyo Women's Medical University, 8-1, Kawadacho, Shinjuku-ku, Tokyo, 162-8666, Japan.
Horm Cancer. 2013 Apr;4(2):103-10. doi: 10.1007/s12672-013-0133-2. Epub 2013 Jan 30.
Choosing effective therapy for patients with malignant pheochromocytoma or paraganglioma (PPGL) is problematic and none of the options are curative. Although combination chemotherapy with cyclophosphamide, vincristine, and dacarbazine (CVD) is an established treatment option, only a limited number of case series have been reported in the literature. To determine the efficacy of CVD in patients treated at Tokyo Women's Medical University. Retrospective review of patients treated with CVD between 1989 and 2012 was conducted. Demographics, clinical presentation, imaging, and laboratory reports were reviewed and analyzed. Efficacy of CVD was ascertained from the biochemical and tumor responses. Twenty-three patients fulfilled study criteria and 6 of these were excluded due to inadequate follow-up or discontinuance by poor general condition or adverse effects. Thus, 17 cases were included in the study. The age and duration of the disease before initiation of CVD were 54.7 ± 12.0 years and 9.1 ± 8.1 years, respectively. The follow-up period after initiation of CVD ranged from 12 to 192 months (median, 60 months). Complete or partial biochemical and/or partial tumor response was achieved in 47.1 % (responders). No significant biochemical or tumor response was seen in 23.5 % and deterioration in biochemical and tumor outcomes was seen in 29.4 % (non-responders). No patient showed complete biochemical and tumor responses. In responders, these effects were documented within 4 months after initiation of CVD with a progression-free survival of 31 to 60 months (median, 40 months). Age at the first diagnosis with PPGL was younger (P < 0.05) and the lag time to eventual diagnosis of malignant disease was longer (P < 0.05) in responders than those in non-responders. The responders had improvements in hypertension and impaired glucose tolerance. Although CVD chemotherapy is not curative for patients with malignant PPGL, it does provide approximately half of the patients with biochemical, tumor, and hypertension benefits.
选择有效的治疗方法对患有恶性嗜铬细胞瘤或副神经节瘤(PPGL)的患者来说是一个问题,目前尚无任何治疗方法可以根治。虽然环磷酰胺、长春新碱和达卡巴嗪(CVD)联合化疗是一种既定的治疗选择,但文献中仅报道了有限数量的病例系列。为了确定东京女子医科大学治疗患者的 CVD 疗效,我们对 1989 年至 2012 年间接受 CVD 治疗的患者进行了回顾性研究。回顾了患者的人口统计学、临床表现、影像学和实验室报告,并进行了分析。通过生化和肿瘤反应来确定 CVD 的疗效。23 名患者符合研究标准,但由于随访不充分或因一般状况差或不良反应而中断,有 6 名患者被排除在外。因此,共有 17 例患者纳入研究。CVD 开始前患者的年龄和疾病持续时间分别为 54.7±12.0 岁和 9.1±8.1 年。CVD 开始后的随访时间为 12-192 个月(中位数为 60 个月)。47.1%(应答者)患者达到完全或部分生化和/或部分肿瘤缓解。23.5%的患者无明显生化或肿瘤反应,29.4%的患者生化和肿瘤结局恶化(无应答者)。没有患者表现出完全的生化和肿瘤反应。在应答者中,这些效果在 CVD 开始后 4 个月内得到证实,无进展生存期为 31-60 个月(中位数为 40 个月)。恶性疾病最终诊断的 PPGL 首次诊断年龄较小(P<0.05),且最终诊断恶性疾病的时间间隔较长(P<0.05)。应答者的高血压和葡萄糖耐量受损有所改善。尽管 CVD 化疗对恶性 PPGL 患者不能治愈,但它确实为大约一半的患者提供了生化、肿瘤和高血压方面的获益。