• Journal of Korean Neurosurgical Society
• /
• 제54권6호
• /
• pp.489-495
• /
• 2013

Objective : To evaluate the efficacy of temozolomide (TMZ) chemotherapy for recurrent anaplastic oligodendroglioma (AO) and anaplastic oligoastrocytoma (AOA). Methods : A multi-center retrospective trial enrolled seventy-two patients with histologically proven AO/AOA who underwent TMZ chemotherapy for their recurrent tumors from 2006 to 2010. TMZ was administered orally (150 to 200 $mg/m^2/day$) for 5 days per 28 days until unacceptable toxicity occurred or tumor progression was observed. Results : TMZ chemotherapy cycles administered was median 5.3 (range, 1-41). The objective response rate was 24% including 8 cases (11%) of complete response and another 23 patients (32%) were remained as stable disease. Severe side effects (${\geq}$grade 3) occurred only in 9 patients (13%). Progression-free survival (PFS) of all patients was a median 8.0 months (95% confidence interval, 6.0-10.0). The time to recurrence of a year or after was a favorable prognostic factor for PFS (p<0.05). Overall survival (OS) was apparently differed by the patient's histology, as AOA patients survived a median OS of 18.0 months while AO patients did not reach median OS at median follow-up of 11.5 months (range 2.7-65 months). Good performance status of Eastern Cooperative Oncology Group 0 and 1 showed prolonged OS (p<0.01). Conclusion : For recurrent AO/AOA after surgery followed by radiation therapy, TMZ could be recommended as a salvage therapy at the estimated efficacy equal to procarbazine, lomustine, and vincristine (PCV) chemotherapy at first relapse. For patients previously treated with PCV, TMZ is a favorable therapeutic option as 2nd line salvage chemotherapy with an acceptable toxicity rate.

• Journal of Korean Neurosurgical Society
• /
• 제30권7호
• /
• pp.925-927
• /
• 2001

Multiple intracranial tumors of different cell types are rare. We report a case of double primary intracranial tumors of different histologic types : oligodendroglioma, and pituitary adenoma. Von Recklinghausen's disease or other etiologic factors supposedly associated with multiple brain tumors were not recognized in this 36-year-old male patient.

• 대한자기공명의과학회:학술대회논문집
• /
• 대한자기공명의과학회 2003년도 제8차 학술대회 초록집
• /
• pp.21-21
• /
• 2003

목적： 악성뇌종양 주변부위의 역동자기공명영상에서의 시간신호강도곡선 양상으로 종양의 성장 양상이나 예후를 판단할 수 있는지를 알고자 한다. 대상 및 방법： Anaplastic oligodendroglioma 3예, Anaplastic astrocytoma 1예, Glioblastoma multiforme 1예, Malignant ependymoma 2예, Medulloblastorna 1예로서, 총 8예의 종양절제전, 혹은 후의 잔류 종양을 대상으로 하였다. Routine MRI에 추가하여 종양부위에서 Turbo spin echo T1 강조 역동자기공명영상을 하였으며, Gd-DTPA 0.1 mmol/kg를 급속 주사 한 후, TR/TE, 350/15, slice thickness 6 mm, slice number 3, NEX 2회, scan time은 15 초로 하여 5 분 동안 20회 영상을 얻었다. 가시적으로 조영증강이 없는 종양의 주변부위나 수술경계부위에 관심영역을 그려서 시간신호강도곡선을 얻었으며, 첫 회 조영제 통과시의 peak 이후에 신호가 감소하는 경우를 Normal pattern으로, peak 이후에 신호가 계속 유지되거나 증가하는 경우를 Tumor pattern으로 하였으며, Normal pattern과 Tumor pattern을 보인 예들을 구분하여 종양의 재성장 상태와 환자의 생존 기간을 비교 관찰하였다.

• Radiation Oncology Journal
• /
• 제9권1호
• /
• pp.47-52
• /
• 1991

가톨릭의대 방사선치료실에서는 1983년 4월부터 1989년 4월 사이 6년 동안에 회돌기교종환자 21예를 외부방사선 치료하였다. 전예에 대하여, 연령 및 발병부위별 빈도와 임상증상과 CT소견 그리고 추적 가능하였던 20예의 생존율에 관한 후향적 분석을 하여 다음과 같은 성적을 얻었다. 1. 전예는 원발성 뇌종양으로 방사선치료 하였던 환자(246예)의 약 8%의 빈도를 보였으며, 연령 분포는 5~62세 (중앙값 38세)이고, 남녀의 비는 13:8이었다. 2. 임상주 증상은두통 18예(86%), 뇌운동신경마비 12예(57%), 오심구토 7예(33%), 경련 5예 (24%)등 순을 보였다. 3. 발병부위는 전두엽 10예(48%), 두정엽 10예(48%), 측두엽 7예(33%), 후두엽 2예(10%)그리고 뇌간 및 소뇌가 각각 1예 (5%)씩 이었다. 4. 조직학적 진단은 정위다방향 조직생검이 3예(14%), 종양의 수술적 제거 (부분 전체제거)에 의함이 18예(86%)이었다. 전예에서 전뇌 및 소부위에 3960~6480cGy15~8주 외부방사선 치료를 하였고, 6예 (29%)에서는 항암약물 치료도 병행하였다. 5. CT음영은 저, 고, 혼합 및 등가음영이 각각 13(62%), 3(14%), 3(14%), 2(10%), 예씩 이었고, 낭성종괴 7예(33%), 괴사 및 출혈성 종괴가 각각 1예(5%)씩 이었다. 석회와 음영은 14예 (67%)에서 관찰되었으며, 조영증강 유무는 9 : 12로 나타났다. 6. 평균생존기간은 38개월이었다.

• Investigative Magnetic Resonance Imaging
• /
• 제4권1호
• /
• pp.34-41
• /
• 2000

목적: 두개강내 종양의 감별진단에 있어서 확산강조자기공명영상(DWi: diffusion weighted MR imaging)의 임상적 유용성을 알아 보고자 하였다. 대상 및 방법: 19예의 두개강내 종양(전이암 10예, 고등급 교종 4예, 저등급 성상세포종 4예, 핍지교종 1예)을 대상으로 1.5T 장치를 이용하여 통상적인 자기공명영상과 EPI기법을 사용한 DWI(TR/TE=6500/107, b value 1000)를 얻었다. DWI에서 종%$\varepsilon$을 고형성분, 괴사나 낭성 부위, 주위 부종으로 나누어 신호강도(뇌설과 뇌실질을 기준으로 5등급으로 나눔)와 벙변과 반 대쪽 정상 뇌설질의 상대적 신호강도비(SIR: signal intensity ratio)를 구하였다. 이렇게 얻어진 종양간의 신호강도와 신호강도비의 차이를 독립표본 T 검정을 이용하여 비교 분석하였다. 결과: DWI에서 고형성분의 경우 전이암과 고등급 교종은 전예에서 뇌실질보다 고신호강도를 보 였으며, 저등급 성상세포종과 핍지교종은 뇌실질과 등신호 또는 약간 높은 신호강도를 보였다. 각각의 고형성분에서 평균 신호강도비는 전이암 1.52, 고등급 교종 1.48, 저등급 성상세포종 1.16, 핍지교종 1.31로 측정되어서 전반적으로 악성도가 증가할수록 높은 신호강도비를 보였다(P(0.05). 종양 주위 부종은 전이암 10예와 고등급 교종 4예에서 관찰되었으며 이중 전이암 7예, 고등급 교종 2예에서는 뇌실질과 유사한 신호강도를 보인 반면 나머지 5예들에서는 뇌실 질보다 높은 신호강도로 관찰되었다. 부종에서의 평균 신호강도비는 전이암이 1.14, 고등급 교종 1.31로 전이암에서 낮게 관찰되었지만 통계적 의의는 없었다(p >0.05). 괴사나 낭성부위의 평균 신호강도비는 0.63이였다. 조영증강되지 않았던 6예의 고형성분중 3예는 주위 부종보다 고신호강도를보여 종양의 경계가통상적인 자기공명영상에 비해 우수하였다. 결론: DWI에서 뇌종양의 고형성분의 신호강도는 종양의 악성도가 높을수록 고신호강도를 보였고 종양 주위 부종은 DWI기법에 기인된 고유효과인 "T2 shine through effect"와 혈관성 부종의 정도 간의 우열에 따라 다양한 소견을 보였으며, 또한 DWI에서 종양과 주위 부종과의 관계를 좀더 명확하게 구분 할 수 있었다.

• Radiation Oncology Journal
• /
• 제29권3호
• /
• pp.147-155
• /
• 2011

Purpose: This study was designed to determine the influencing factors and clinical course of pathologically proven cases of radiation-induced brain injury (RIBI). Materials and Methods: The pathologic records of twelve patients were reviewed; these patients underwent surgery following radiotherapy due to disease progression found by follow-up imaging. However, they were finally diagnosed with RIBI. All patients had been treated with 3-dimensional conventional fractionated radiotherapy and/or radiosurgery for primary or metastatic brain tumors with or without chemotherapy. The histological distribution was as follows: two falx meningioma, six glioblastoma multiform (GBM), two anaplastic oligodendroglioma, one low grade oligodendroglioma, and one small cell lung cancer with brain metastasis. Results: Radiation necrosis was noted in eight patients and the remaining four were diagnosed with radiation change. Gender (p = 0.061) and biologically equivalent dose $(BED)_3$ (p = 0.084) were the only marginally influencing factors of radiation necrosis. Median time to RIBI was 7.3 months (range, 0.5 to 61 months). Three prolonged survivors with GBM were observed. In the subgroup analysis of high grade gliomas, RIBI that developed <6 months after radiotherapy was associated with inferior overall survival rates compared to cases of RIBI that occurred ${\geq}6$ months (p = 0.085). Conclusion: Our study demonstrated that RIBI could occur in early periods after conventional fractionated brain radiotherapy within normal tolerable dose ranges. Studies with a larger number of patients are required to identify the strong influencing factors for RIBI development.

• 대한세포병리학회지
• /
• 제15권1호
• /
• pp.52-55
• /
• 2004

Secretory meningioma is a distinct subtype of meningioma. We describe the cytologic features of a secretory meningioma on squash preparations, in comparision with other cytologic mimickers. A 54-year-old woman presented with hearing loss, vertigo, tinnitus, and headache for seven years. A brain MRI study revealed a 4.5cm sized mass in the cerebellopontine angle, which showed homogenous signal intensity in T2-weighted image. The intraoperative squash smear showed some well-defined, thin rimmed intracytoplasmic inclusions, containing a finely granular eosinophilic core among less cohesive meningiomatous cells. Histologic sections revealed a meningothelial meningioma with scattered inclusions, with periodic acid-Schiff, carcinoembryonic antigen, and cytokeratin positivity. Identification of characteristic intracytoplasmic inclusions is helpful for diagnosing secretory meningiomas. On squash preparations, differential diagnoses included tumors with inclusions or cytoplasmic vacuolizations, such as metastatic mammary infiltrating ductal carcinoma, gastric adenocarcinoma, hepatocellular carcinoma, and clear cell ependymoma, oligodendroglioma, hemangioblastoma, chordoma, and other variants of meningiomas (clear cell, xanthomatous, microcytic, and chordoid variants). In addition, the possibilities of glioma with eosinophilic granular body, and metastatic tumors from mammary infiltrating ductal carcinoma, gastric adenocarcinoma, and hepatocellular carcinoma in meningioma should be considered.

• Journal of Korean Neurosurgical Society
• /
• 제30권5호
• /
• pp.638-641
• /
• 2001

Carboplatin intra-arterial chemotherapy(IAC) has an advantage of increased uptake during the first passage of the drugs through tumor capillaries. Although not common, this type of therapy is known to cause neurological complications, myelosuppression, and ototoxicity. However, the incidence of ocular toxicity is reported to be rare. Eleven of our patients with glioma(Grade II Astrocytoma : 3, Grade III Astrocytoma : 1, Grade IV Astrocytoma : 5, Gliofibroma : 1, Oligodendroglioma : 1) underwent IAC regimen with carboplatin($300mg/m^2$) which were administrated after blood-brain barrier disruption. Of there, 3 patients had ocular complications after supra-ophthalmic IAC injection of carboplatin but fully recovered following steroid therapy. Although our results from IAC seem to be favorable for these patients, we suggest that its complications, such as ocular toxicity, need to be carefully considered prior to treatment.

• 대한한의학회지
• /
• 제41권3호
• /
• pp.247-259
• /
• 2020

Objectives: This review aims to investigate clinical studies related to bee venom pharmacopuncture for cancer patients and to analyze the research trend for further study. Methods: We searched for clinical studies using bee venom pharmacopuncture therapy on patients with cancer through the electronic databases including Pubmed, Cochrane library, OASIS, KISS, NDSL, and KMBASE. There was no restriction on language and publication date, and after selection/exclusion process, the study design, target disease, intervention details including acupoints, treatment frequency and period, outcomes, study results and adverse events were extracted. Results: Thirteen clinical studies were finally selected. There were a randomized controlled trial RCT about the effect of sweet bee venom pharmacopuncture on cancer-related pain, and three case series about chemotherapy-induced peripheral neuropathy. In case reports, there were nine studies about oligodendroglioma, plexiform neurofibroma, breast cancer, prostate cancer, lung cancer, urachal adenocarcinoma, malignant melanoma, and atypical squamous cells of undetermined significance. The bee venom therapy affected the improvement of outcomes such as symptoms, quality of life, tumor response, and lab findings. Conclusions: The present study found that bee venom therapy is applicable to the treatment of cancer patients, and showed some effect on various symptoms. However, due to insufficient number and quality of studies, well designed and high-quality clinical trials are necessary to confirm the effectiveness and safety of bee venom pharmacopuncture therapy in patients with cancer.

• Asian Pacific Journal of Cancer Prevention
• /
• 제14권12호
• /
• pp.7261-7264
• /
• 2013

Recent genome wide sequencing has identified mutations in IDH1/IDH2 predominantly in grade II-III gliomas and secondary glioblastomas which are associated with favorable clinical outcome. These mutations have become molecular markers of significant diagnostic and prognostic relevance in the assessment of human gliomas. In the current study we evaluated IDH1 (R132) and IDH2 (R172) in 32 gliomas of various grades and tumor subtypes. Sequencing analysis revealed R132H mutations in 18.7% tumors, while none of the cases showed IDH2 (R172) mutations. The frequency of IDH1 mutations was higher in females (21.4%) than males (11.1%), and it was significantly higher in younger patients. Histological analyses demonstrated presence of necrosis and micro vascular proliferation in 69% and 75% respectively. Interestingly, IDH1 mutations were predominantly present in non-necrotic tumors as well as in cases showing microvascular proliferation. Of the six IDH1 positive cases, three were glioblastomas (IV), and one each were anaplastic oligoastrocytoma (III), anaplastic oligodendroglioma III (n=1) and diffuse astrocytoma. In conclusion, IDH1 mutations are quite frequent in Indian glioma patients while IDH2 mutations are not observed. Since IDH mutations are associated with good prognosis, their use in routine clinical practice will enable better risk stratification and management of glioma patients.