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低剂量全脑全脊髓放疗后髓母细胞瘤的复发模式

Pattern of recurrence of medulloblastoma after low-dose craniospinal radiotherapy.

作者信息

Wara W M, Le Q T, Sneed P K, Larson D A, Prados M D, Levin V A, Edwards M S, Weil M D

机构信息

Department of Radiation Oncology, University of California, San Francisco 94143-0226.

出版信息

Int J Radiat Oncol Biol Phys. 1994 Oct 15;30(3):551-6. doi: 10.1016/0360-3016(92)90940-j.

Abstract

PURPOSE

We retrospectively evaluated relapse of medulloblastoma after low- or high-dose craniospinal radiotherapy, and after conventional or hyperfractionated posterior fossa irradiation.

METHODS AND MATERIALS

Ninety-two pediatric patients were treated postoperatively since 1970 at the University of California, San Francisco. Until 1989, we employed conventional fractionation with low (< or = 30 Gy) or high-dose craniospinal fields and low-dose (< or = 56 Gy) posterior fossa boosts. Recently, hyperfractionation delivered low- or high-dose to the craniospinal axis and high-dose to the posterior fossa. Most patients treated after 1979 received chemotherapy.

RESULTS

Median follow-up was 70 months. Five-year disease-free survival was 36% (22% for poor-risk vs. 59% for good-risk patients). Five-year overall survival was 52% (43% for poor vs. 68% for good-risk). Neither the dose to the posterior fossa nor the craniospinal axis was statistically related to recurrence. Failure in the posterior fossa occurred despite boosts greater than 56 Gy. Females, over the age of 6 years, had significantly better relapse-free survival than males of the same age. Six of the 54 patients who relapsed were long-term survivors.

CONCLUSIONS

Low-dose craniospinal radiotherapy, where the majority of patients received chemotherapy, was not associated with increased failure. High-dose posterior fossa hyperfractionation did not improve control. Long-term survival was noted in a number of patients after relapse. We recommend 60 Gy or greater with conventional fractions to the primary area, and continued study of low-dose craniospinal irradiation with adjuvant chemotherapy.

摘要

目的

我们回顾性评估了髓母细胞瘤在低剂量或高剂量颅脊髓放疗后,以及在传统或超分割后颅窝照射后的复发情况。

方法和材料

自1970年以来,92例儿科患者在加利福尼亚大学旧金山分校接受了术后治疗。直到1989年,我们采用传统分割方式,对颅脊髓野进行低剂量(≤30 Gy)或高剂量照射,并对后颅窝进行低剂量(≤56 Gy)推量照射。最近,超分割方式是对颅脊髓轴进行低剂量或高剂量照射,对后颅窝进行高剂量照射。1979年后接受治疗的大多数患者接受了化疗。

结果

中位随访时间为70个月。5年无病生存率为36%(低危患者为22%,高危患者为59%)。5年总生存率为52%(低危患者为43%,高危患者为68%)。后颅窝或颅脊髓轴的照射剂量与复发均无统计学关联。尽管推量照射剂量大于56 Gy,但后颅窝仍出现了复发。6岁以上女性的无复发生存率明显优于同龄男性。54例复发患者中有6例是长期幸存者。

结论

在大多数患者接受化疗的情况下,低剂量颅脊髓放疗与失败率增加无关。高剂量后颅窝超分割并未改善控制效果。一些患者在复发后仍实现了长期生存。我们建议对原发区域采用传统分割方式给予60 Gy或更高剂量,并继续研究低剂量颅脊髓照射联合辅助化疗。

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