Taal Walter, van der Rijt Carin C D, Dinjens Winand N M, Sillevis Smitt Peter A E, Wertenbroek Agnes A A C M, Bromberg Jacoline E C, van Heuvel Irene, Kros Johan M, van den Bent Martin J
Department of Neuro-Oncology/Neurology, Erasmus MC Cancer Institute, Erasmus MC University Medical Center, Groene Hilledijk 301, 3075 EA, Rotterdam, The Netherlands,
J Neurooncol. 2015 Jan;121(2):365-72. doi: 10.1007/s11060-014-1641-9. Epub 2014 Oct 26.
We treated patients with newly diagnosed and large low-grade oligodendroglial tumors with upfront procarbazine, CCNU and vincristine (PCV) in order to delay radiotherapy. Patients were treated with PCV for a maximum of 6 cycles. The response to treatment was defined according to the RANO criteria; in addition change over time of mean tumor diameters (growth kinetics) was calculated. Thirty-two patients were treated between 1998 and 2006, 18 of which were diagnosed with 1p/19q co-deleted tumors. Median follow-up duration was 8 years (range 0.5-13 years). The median overall survival (mOS) was 120 months and the median progression-free survival (mPFS) was 46 months. Growth kinetics showed an ongoing decrease of the mean tumor diameter after completion of chemotherapy, during a median time of 35 months, but an increase of the mean tumor diameter did not herald progression as detected by RANO criteria. 1p/19q co-deletion was associated with a significant increase in OS (mOS 83 months versus not reached for codeleted tumors; p = 0.003)) and PFS (mPFS 35 months versus 67 months for codeleted tumors; p = 0.024). Patients with combined 1p/19q loss had a 10 year PFS of 34 % and the radiotherapy in these patients was postponed for a median period of more than 6 years. This long-term follow-up study indicates that upfront PCV chemotherapy is associated with long PFS and OS and delays radiotherapy for a considerable period of time in patients with low-grade oligodendroglial tumors, in particular with combined 1p/19q loss.
我们对新诊断的大型低度少突胶质细胞瘤患者采用丙卡巴肼、洛莫司汀和长春新碱(PCV)进行初始治疗,以推迟放疗。患者接受PCV治疗最多6个周期。根据RANO标准定义治疗反应;此外,计算平均肿瘤直径随时间的变化(生长动力学)。1998年至2006年间共治疗了32例患者,其中18例被诊断为1p/19q共缺失肿瘤。中位随访时间为8年(范围0.5 - 13年)。中位总生存期(mOS)为120个月,中位无进展生存期(mPFS)为46个月。生长动力学显示化疗完成后平均肿瘤直径持续下降,中位时间为35个月,但根据RANO标准,平均肿瘤直径增加并不预示疾病进展。1p/19q共缺失与总生存期(mOS 83个月,而共缺失肿瘤未达到;p = 0.003)和无进展生存期(mPFS 35个月,而共缺失肿瘤为67个月;p = 0.024)的显著增加相关。1p/19q联合缺失的患者10年无进展生存率为34%,这些患者的放疗推迟中位时间超过6年。这项长期随访研究表明,初始PCV化疗与低度少突胶质细胞瘤患者的长无进展生存期和总生存期相关,并在相当长一段时间内推迟放疗,尤其是对于1p/19q联合缺失的患者。