al-Mefty O, Borba L A
Department of Neurosurgery, University of Arkansas for Medical Sciences, Little Rock, USA.
J Neurosurg. 1997 Feb;86(2):182-9. doi: 10.3171/jns.1997.86.2.0182.
Because of their critical location, invasive nature, and aggressive recurrence, skull base chordomas are challenging and, at times, frustrating tumors to treat. Both radical surgical removal and high-dose radiation therapy, particularly proton beam therapy, reportedly are effective in tumor control and improve survival rates. The authors posit that these tumors are best treated with radical surgery and proton-photon beam therapy. During the last 5 years, they treated 25 patients (15 females and 10 males) who harbored pathologically diagnosed skull base chordomas. The mean age of the patients was 38.4 years (range 8-61 years). Previous surgery or radiation therapy was performed at other institutions in seven and two patients, respectively. The authors performed 33 surgical procedures on 23 patients. Radical removal (defined as absence of residual tumor on operative inspection and postoperative imaging) was achieved in 10 patients; subtotal resection (defined as resection of > 90% of the tumor) was achieved in 11 patients; and partial resection (defined as resection of < 90% of the tumor) was achieved in two patients. Radical surgical removal included not only the excision of soft-tumor tissue, but also extensive drilling of the adjacent bone. Adjuvant therapy consisted of postoperative combined proton-photon beam therapy (given to 17 patients and planned for one patient) and conventional radiation therapy (two patients); three patients received no adjunct therapy. To date, four patients have died. One patient who had undergone previous surgery and sacrifice of the internal carotid artery died postoperatively from a massive stroke; one patient died from adenocarcinoma of the pancreas without evidence of recurrence; and two patients died at 25 and 39 months of recurrent tumor. Permanent neurological complications included third cranial nerve palsy (one patient) and hemianopsia (one patient); radiation necrosis occurred in three patients. Of the 21 patients followed for more than 3 months after surgery, 16 have had no evidence of recurrence and five (including the two mortalities noted above) have had recurrent tumors (four diagnosed clinically and one radiologically). The mean disease-free interval was 14.4 months. A longer follow-up period will, hopefully, support the early indication that radical surgical removal and postoperative proton-photon beam therapy is an efficacious treatment. The use of skull base approaches based on the tumor classification introduced in this paper is associated with low mortality and morbidity rates.
由于其关键的位置、侵袭性本质以及侵袭性复发,颅底脊索瘤治疗起来具有挑战性,有时令人沮丧。据报道,根治性手术切除和高剂量放射治疗,尤其是质子束治疗,在肿瘤控制和提高生存率方面均有效。作者认为,这些肿瘤最好采用根治性手术和质子 - 光子束治疗。在过去5年中,他们治疗了25例经病理诊断为颅底脊索瘤的患者(15名女性和10名男性)。患者的平均年龄为38.4岁(范围8 - 61岁)。分别有7例和2例患者曾在其他机构接受过手术或放射治疗。作者对23例患者进行了33次手术。10例患者实现了根治性切除(定义为手术检查和术后影像学检查无残留肿瘤);11例患者实现了次全切除(定义为切除肿瘤的> 90%);2例患者实现了部分切除(定义为切除肿瘤的< 90%)。根治性手术切除不仅包括切除软组织肿瘤,还包括对相邻骨质的广泛钻孔。辅助治疗包括术后联合质子 - 光子束治疗(17例患者接受治疗,1例患者计划接受治疗)和传统放射治疗(2例患者);3例患者未接受辅助治疗。迄今为止,4例患者死亡。1例曾接受过手术且牺牲了颈内动脉的患者术后因大面积中风死亡;1例患者死于胰腺癌,无复发迹象;2例患者在复发肿瘤后25个月和39个月死亡。永久性神经并发症包括动眼神经麻痹(1例患者)和偏盲(1例患者);3例患者发生放射性坏死。在术后随访超过3个月的21例患者中,并五(包括上述2例死亡患者)有复发肿瘤(4例临床诊断,1例影像学诊断)。无病生存期的平均时间为14.4个月。希望更长的随访期能支持早期的迹象,即根治性手术切除和术后质子 - 光子束治疗是一种有效的治疗方法。基于本文介绍的肿瘤分类采用颅底入路,死亡率和发病率较低。