East meets West for the treatment of glioma: A discussion of real-world cases

Glioma Pub Date : 2020-01-01 DOI:10.4103/glioma.glioma_29_19
H. Piao, Ye Zhang, Chengcheng Guo, Li Zhu, Lina Liu, U. Herrlinger, F. Sahm, Zhongping Chen
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He had undergone a biopsy and was diagnosed with an oligodendroglioma 3 years previously. He underwent chemoradiotherapy followed by 12 cycles of chemotherapy with temozolomide (TMZ), and complete remission was achieved. However, the tumor recurred within a short period of time and was resected by a second surgery. The pathologic diagnosis of the recurrent tumor was a glioblastoma because 1p/19q was intact when detected by sequencing. Pathologic consultation from another hospital still considered an anaplastic oligodendroglioma based on the positive result of 1p19q loss of heterozygosity (LOH) determined by fluorescence in situ hybridization. Patient 2 was a 50-year-old man with a left temporal glioblastoma. He underwent tumor resection but no radiotherapy. After seven cycles of TMZ (5/28-day regimen), his symptoms deteriorated, and his treatment was changed to a TMZ dose-dense regimen (7 days on/7 days off) and bevacizumab (7.5 mg/kg every 2 weeks), plus tumor-treating field therapy. Consultation Results: The pathological diagnosis based on biopsy for Patient 1 was an oligodendroglioma (World Health Organization Grade II), whereas the result of the second surgical sample was glioblastoma or anaplastic oligodendroglioma (questionable). Although the accuracy of fluorescence in situ hybridization for the detection of 1p/19q LOH requires improvement, 1p/19q LOH is typically not reconstituted in oligodendroglioma. More likely, it was due to sampling; a positive observation field may be missed with consequent negative results, and both oligodendroglioma (with 1p/19q co-deletion and isocitrate dehydrogenase mutation) and astrocytoma (without 1p/19q co-deletion) may exist. With respect to further treatment for cases such as Patient 1, both Chinese and European experts agree that procarbazine + lomustine chemotherapy is appropriate, while re-irradiation is suggested only if the tumor recurs outside the original radiotherapy field or within the radiotherapy field in the future. Considering the medical history, the rapid tumor regrowth without postoperative radiotherapy in Patient 2 was not surprising. After application of a rescue treatment regimen, the general condition of the patient improved, which may have resulted from the bevacizumab. A consensus was reached between the Chinese and European experts regarding subsequent treatment of Patient 2. Continuation of TMZ and bevacizumab was suggested until further deterioration. Whether tumor-treating field therapy should play a role in this patient could not be evaluated. However, some other molecular targeted agents (e.g. vascular endothelial growth factor receptor tyrosine kinase inhibitors such as regorafenib or apatinib) after bevacizumab failure, the effectiveness of these drugs remains unclear. Conclusion: In clinical practice, although we should follow established guidelines, the final treatment regimen requires informed consent from the patient. Thus, some real-world cases may deviate from the established guidelines. When patients reach end-stage disease with a marked decrease in their performance status and no standard treatment options, active antitumor treatment might be more likely to be attempted in China, while symptomatic treatment is more frequently performed in Europe. Although treatment philosophies for patients with glioma are slightly different between Eastern and Western medical experts, any treatment strategies should satisfy these patients.","PeriodicalId":12731,"journal":{"name":"Glioma","volume":"3 1","pages":"24 - 29"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Glioma","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/glioma.glioma_29_19","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background and Aim: The standard of care for patients with gliomas should follow established guidelines. In real-world management, however, the management sometimes deviates from these guidelines. We organized a discussion of real-world clinical cases and summarized different considerations from Chinese and European specialists.Case Presentation: A multidisciplinary team comprising experts from Europe and China discussed two patients with glioma treated at Sun Yat-sen University Cancer Center and Liaoning Cancer Hospital and Institute, China. Patient 1 was a 43-year-old man with a recurrent oligodendroglioma in the left frontal lobe diagnosed based on histology alone. He had undergone a biopsy and was diagnosed with an oligodendroglioma 3 years previously. He underwent chemoradiotherapy followed by 12 cycles of chemotherapy with temozolomide (TMZ), and complete remission was achieved. However, the tumor recurred within a short period of time and was resected by a second surgery. The pathologic diagnosis of the recurrent tumor was a glioblastoma because 1p/19q was intact when detected by sequencing. Pathologic consultation from another hospital still considered an anaplastic oligodendroglioma based on the positive result of 1p19q loss of heterozygosity (LOH) determined by fluorescence in situ hybridization. Patient 2 was a 50-year-old man with a left temporal glioblastoma. He underwent tumor resection but no radiotherapy. After seven cycles of TMZ (5/28-day regimen), his symptoms deteriorated, and his treatment was changed to a TMZ dose-dense regimen (7 days on/7 days off) and bevacizumab (7.5 mg/kg every 2 weeks), plus tumor-treating field therapy. Consultation Results: The pathological diagnosis based on biopsy for Patient 1 was an oligodendroglioma (World Health Organization Grade II), whereas the result of the second surgical sample was glioblastoma or anaplastic oligodendroglioma (questionable). Although the accuracy of fluorescence in situ hybridization for the detection of 1p/19q LOH requires improvement, 1p/19q LOH is typically not reconstituted in oligodendroglioma. More likely, it was due to sampling; a positive observation field may be missed with consequent negative results, and both oligodendroglioma (with 1p/19q co-deletion and isocitrate dehydrogenase mutation) and astrocytoma (without 1p/19q co-deletion) may exist. With respect to further treatment for cases such as Patient 1, both Chinese and European experts agree that procarbazine + lomustine chemotherapy is appropriate, while re-irradiation is suggested only if the tumor recurs outside the original radiotherapy field or within the radiotherapy field in the future. Considering the medical history, the rapid tumor regrowth without postoperative radiotherapy in Patient 2 was not surprising. After application of a rescue treatment regimen, the general condition of the patient improved, which may have resulted from the bevacizumab. A consensus was reached between the Chinese and European experts regarding subsequent treatment of Patient 2. Continuation of TMZ and bevacizumab was suggested until further deterioration. Whether tumor-treating field therapy should play a role in this patient could not be evaluated. However, some other molecular targeted agents (e.g. vascular endothelial growth factor receptor tyrosine kinase inhibitors such as regorafenib or apatinib) after bevacizumab failure, the effectiveness of these drugs remains unclear. Conclusion: In clinical practice, although we should follow established guidelines, the final treatment regimen requires informed consent from the patient. Thus, some real-world cases may deviate from the established guidelines. When patients reach end-stage disease with a marked decrease in their performance status and no standard treatment options, active antitumor treatment might be more likely to be attempted in China, while symptomatic treatment is more frequently performed in Europe. Although treatment philosophies for patients with glioma are slightly different between Eastern and Western medical experts, any treatment strategies should satisfy these patients.
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东西方结合治疗胶质瘤:对现实世界病例的讨论
背景和目的:胶质瘤患者的护理标准应遵循既定的指南。然而,在实际管理中,管理层有时会偏离这些指导方针。我们组织了对真实世界临床病例的讨论,并总结了中国和欧洲专家的不同考虑。病例介绍:一个由来自欧洲和中国的专家组成的多学科小组讨论了在中山大学肿瘤中心和中国辽宁肿瘤医院和肿瘤研究所治疗的两名胶质瘤患者。患者1是一名43岁男性,左额叶复发性少突胶质细胞瘤,仅根据组织学诊断。他曾接受活组织检查,3年前被诊断为少突胶质细胞瘤。患者接受放化疗,随后用替莫唑胺(TMZ)化疗12个周期,完全缓解。然而,肿瘤在短时间内复发,并通过第二次手术切除。该复发肿瘤的病理诊断为胶质母细胞瘤,因为测序检测到1p/19q是完整的。根据荧光原位杂交检测的1p19q杂合性缺失(LOH)阳性结果,另一家医院的病理会诊仍认为是间变性少突胶质细胞瘤。患者2是一位50岁的男性,患有左侧颞叶胶质母细胞瘤。他接受了肿瘤切除术,但没有接受放疗。TMZ治疗7个周期(5/28天方案)后,患者症状恶化,改为TMZ剂量密集方案(7天开/7天停)+贝伐单抗(7.5 mg/kg /2周)+肿瘤治疗现场治疗。会诊结果:患者1的活检病理诊断为少突胶质细胞瘤(世界卫生组织二级),而第二个手术样本的结果是胶质母细胞瘤或间变性少突胶质细胞瘤(可疑)。虽然荧光原位杂交检测1p/19q LOH的准确性有待提高,但在少突胶质细胞瘤中通常无法重建1p/19q LOH。更有可能的是,这是由于抽样;可能会错过阳性的观察视野而导致阴性结果,并且可能存在少突胶质细胞瘤(1p/19q共缺失和异柠檬酸脱氢酶突变)和星形细胞瘤(不存在1p/19q共缺失)。对于患者1等病例的进一步治疗,中国和欧洲专家一致认为丙卡嗪+洛莫司汀化疗是合适的,只有肿瘤在原放疗场外复发或将来在放疗场内复发时才建议再照射。考虑到患者2的病史,术后未进行放疗的快速肿瘤再生并不奇怪。应用抢救治疗方案后,患者的一般情况得到改善,这可能是贝伐单抗的结果。中欧专家就患者2的后续治疗达成共识。建议继续使用TMZ和贝伐单抗,直到病情进一步恶化。肿瘤治疗野疗法是否应在该患者中发挥作用尚无法评估。然而,其他一些分子靶向药物(如血管内皮生长因子受体酪氨酸激酶抑制剂如reorafenib或apatinib)在贝伐单抗失败后,这些药物的有效性尚不清楚。结论:在临床实践中,虽然我们应该遵循既定的指导方针,但最终的治疗方案需要患者的知情同意。因此,一些实际情况可能会偏离既定的指导方针。当患者达到终末期,表现明显下降且无标准治疗选择时,在中国可能更倾向于尝试积极的抗肿瘤治疗,而在欧洲则更常进行对症治疗。尽管东西方医学专家对神经胶质瘤患者的治疗理念略有不同,但任何治疗策略都应该满足这些患者。
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