长期存活的多形性胶质母细胞瘤

A. Zaki, N. -, Yasmin Abdul Rashid, Adnan Abdul Jabbar
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引用次数: 0

摘要

背景:GBM是最常见、侵袭性最强的原发性恶性脑肿瘤。尽管采用多种方法治疗脑肿瘤,但GBM患者的生存率仍然很低。胶质母细胞瘤患者的中位生存期为˷12个月。然而,35%的患者存活超过3年,被称为长期幸存者。当疾病发生进展时,6个月无进展生存率(PFS)通常低于15%。病例介绍:一位68岁的男士于2011年3月在右侧额顶区出现占位性病变,显像显示空腔(实性增强4.3 × 4.2 × 2.7 cm,囊性成分3.6 × 3.5 × 3cm)。他接受开颅手术切除病变,术后扫描证实大体全切除。组织病理学显示为多形性胶质母细胞瘤。患者接受替莫唑胺75mg/ m2的同步放化疗(60gy / 30fr),随后每月使用替莫唑胺(1-5天,28天周期)。2011年7月至2015年7月,患者继续每月服用替莫唑胺,每月q3次影像学检查未发现残留病变。患者的原发肿瘤科医师被更换,由于没有残留疾病,也没有长期使用TMZ的证据,它被停止并置于监测之中。他的病情一直缓解到2017年9月,当时他出现了复发性疾病。2017年11月行右重开颅及SOL切除术。组织病理学显示为GBM。从2017年12月到2018年2月,患者开始每月服用替莫唑胺q,周期为28天,2月的中期扫描显示疾病进展,然后每周接受贝伐单抗和伊立替康q3,直到2018年4月,中期扫描显示当时疾病进展,他的临床状况也恶化,不适合任何进一步的全身治疗,因此建议进行缓和治疗,患者于2018年5月去世。这是一个罕见的病例,报告如此长的生存在GBM。结论:本病例预后较差,但预后较好。患者的肿瘤生物学可能是其不同结果的关键。
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Glioblastoma Multiforme with Long Term Survival
Background: GBM is the most common and aggressive primary malignant brain tumor. Despite multimodality approach in the treatment of brain tumor, survival of the patients with GBM remains poor. The median survival of glioblastoma patients is ˷12 months. However, 35% of the patients survives for more than 3 years and are referred to as long-term survivors. When disease progression occurs 6-month progression-free survival (PFS) is usually lower than 15%. Case Presentation: A 68-years-old gentleman presented with a space occupying lesion in right frontoparietal region in March 2011, work up showed space (solid enhancing 4.3 x 4.2 x 2.7 cm & cystic component 3.6 x 3.5 x 3 cm). He underwent craniotomy for excision of the lesion, Post-operaticve scan confirmed gross total resection. Histopathology revealed Glioblastoma Multiforme. He received concomitant chemoradiation (60 Gy/30 Fr) with Temozolomide 75mg/m 2 followed by monthly temozolomide (day 1-5 q 28 day cycle)., He was continued on monthly temozolomide (from July 2011- July 2015) with imaging Q 3 montly which revealed no residual disease. Patient primary oncologist was changed and since there was no residual disease and no evidence of prolong use of TMZ, it was stopped and was put on surveillance. He remained in remission till September 2017, when he developed recurrent disease. . He underwent right redo craniotomy & excision of SOL in November 2017. Histopathology revealed GBM. He was started on monthly temozolomide q 28day cycle from December 2017 till February 2018, interim scans in Feb shows disease progression he then received Bevacizumab and irrinotecan Q3weekly till April 2018 interim scans shows disease progression at his time his clinical condition also deteriorated and was not a candidate for any further systemic treatment hence advised palliative care and patient expired in May 2018. This is a rare case which reported such a long survival in GBM. Conclusion: GBM has poor prognosis however we describe a case with prolong outcome. Tumor biology of the patient might be the key to his differential outcome.
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