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脊髓低级别星形细胞瘤患者的长期生存及功能状态

Long-term survival and functional status of patients with low-grade astrocytoma of spinal cord.

作者信息

Robinson Clifford G, Prayson Richard A, Hahn Joseph F, Kalfas Iain H, Whitfield Melvin D, Lee Shih-Yuan, Suh John H

机构信息

Department of Radiation Oncology, Brain Tumor Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2005 Sep 1;63(1):91-100. doi: 10.1016/j.ijrobp.2005.01.009.

Abstract

PURPOSE

To determine survival and changes in neurologic function and Karnofsky performance status (KPS) in a series of patients treated for low-grade astrocytoma of the spinal cord during the past two decades.

METHODS

This study consisted of 14 patients with pathologically confirmed low-grade astrocytoma of the spinal cord who were treated between 1980 and 2003. All patients underwent decompressive laminectomy followed by biopsy (n = 7), subtotal resection (n = 6), or gross total resection (n = 1). Ten patients underwent postoperative radiotherapy (median total dose 50 Gy in 28 fractions). The overall survival, progression-free survival, and changes in neurologic function and KPS were measured.

RESULTS

The overall survival rate at 5, 10, and 20 years was 100%, 75%, and 60%, respectively. The progression-free survival rate at 5, 10, and 20 years was 93%, 80%, and 60%, respectively. Neither overall survival nor progression-free survival was clearly correlated with any patient, tumor, or treatment factors. Neurologic function and KPS worsened after surgery in 8 (57%) of 14 and 9 (69%) of 13 patients, respectively. At a mean follow-up of 10.2 years, neurologic function had stabilized or improved in 8 (73%) of 11 remaining patients, but the KPS had worsened in 5 (50%) of 10. Most patients who were employed before surgery were working at last follow-up.

CONCLUSION

Patients who undergo gross total resection of their tumor may be followed closely. Patients who undergo limited resection should continue to receive postoperative RT (50.4 Gy in 1.8-Gy fractions). The functional measures should be routinely evaluated to appreciate the treatment outcomes.

摘要

目的

确定在过去二十年中接受脊髓低级别星形细胞瘤治疗的一系列患者的生存率、神经功能变化及卡氏功能状态评分(KPS)。

方法

本研究纳入了1980年至2003年间接受治疗的14例经病理确诊的脊髓低级别星形细胞瘤患者。所有患者均接受了减压性椎板切除术,随后进行活检(n = 7)、次全切除(n = 6)或全切除(n = 1)。10例患者接受了术后放疗(中位总剂量50 Gy,分28次)。测量总生存率、无进展生存率以及神经功能和KPS的变化。

结果

5年、10年和20年的总生存率分别为100%、75%和60%。5年、10年和20年的无进展生存率分别为93%、80%和60%。总生存率和无进展生存率均与任何患者、肿瘤或治疗因素无明显相关性。14例患者中有8例(57%)、13例患者中有9例(69%)术后神经功能和KPS分别恶化。在平均10.2年的随访中,11例剩余患者中有8例(73%)神经功能稳定或改善,但10例患者中有5例(50%)KPS恶化。大多数术前工作的患者在最后一次随访时仍在工作。

结论

肿瘤接受全切除的患者可密切随访。接受有限切除的患者应继续接受术后放疗(1.8 Gy分割,共50.4 Gy)。应常规评估功能指标以了解治疗效果。

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