• Journal of Korean Neurosurgical Society
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• 제59권4호
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• pp.392-399
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• 2016

Objective : Brain metastases in gynecologic cancer (ovarian, endometrial, and cervical cancer) patients are rare, and the efficacy of Gamma Knife Radiosurgery (GKRS) to treat these had not been evaluated. We assessed the efficacy of GKRS and prognostic factors for tumor control and survival in brain metastasis from gynecologic cancers. Methods : This retrospective study was approved by the institutional review board. From May 1995 to October 2012, 26 women (mean age 51.3 years, range 27-70 years) with metastatic brain tumors from gynecologic cancer were treated with GKRS. We reviewed their outcomes, radiological responses, and clinical status. Results : In total 24 patients (59 lesions) were available for follow-up imaging. The median follow-up time was 9 months. The mean treated tumor volume at the time of GKRS was $8185mm^3$ (range $10-19500mm^3$), and the median dose delivered to the tumor margin was 25 Gy (range, 10-30 Gy). A local tumor control rate was 89.8% (53 of 59 tumors). The median overall survival was 9.5 months after GKRS (range, 1-102 months). Age-associated multivariate analysis indicated that the Karnofsky performance status (KPS), the recursive partitioning analysis (RPA) classification, and the number of treated lesions were significant prognostic factors for overall survival (HR=0.162, p=0.008, HR=0.107, p=0.038, and HR=2.897, p=0.045, respectively). Conclusion : GKRS is safe and effective for the management of brain metastasis from gynecologic cancers. The clinical status of the patient is important in determining the overall survival time.

• Radiation Oncology Journal
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• 제31권3호
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• pp.162-170
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• 2013

Purpose: To analyze the outcome of adjuvant postoperative external beam radiotherapy (EBRT) in well-differentiated thyroid cancer (WDTC). Materials and Methods: We identified 84 patients treated with EBRT for WDTC from February 1981 to December 2010. Among them, we analyzed 39 patients who received EBRT after initial radical surgery. Twenty-four females and 15 males were included. The median age was 49 years (range, 16 to 72 years). There were 34 papillary thyroid carcinomas and 5 follicular thyroid carcinomas. Most patients showed pathologic T3/T4 stage (54%/26%). Ten patients (25.6%) had gross residual tumors. Five patients (12.8%) had tumor cells at the margin. The median EBRT dose and fraction size were 62.6 Gy and 1.8 to 2.0 Gy, respectively. Results: The median follow-up was 73 months (range, 21 to 372 months). The five-year overall survival (OS) and locoregional recurrence free survival (LRFS) were 97.4% and 86.9%, respectively. Locoregional failures occurred in 5 and all failure sites were the neck node area. In univariate analysis, OS was significantly influenced by invasion of the trachea (p = 0.016) or esophagus (p = 0.006). LRFS was significantly decreased by male (p = 0.020), gross residuum after resection (p = 0.002), close or positive tumor at surgical margin involvement (p = 0.044), and tracheal invasion (p = 0.040). No significant prognostic factor was identified in the multivariate analysis. No patient experienced the Radiation Therapy Oncology Group grade 3 or more toxicity. Conclusion: Our locoregional control rate of 87.2% is comparable to historical controls with surgery alone, even though our study had a large proportion of advanced stage. Adjuvant EBRT may an effective and safe treatment option in patients with WDTC.

• Radiation Oncology Journal
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• 제14권3호
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• pp.201-209
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• 1996

목적 : FIGO 병기 Ib 자궁경부편평상피암 환자에서 고선량율 강내치료를 이용한 방사선치료후 환해율, 5년 국소제어을, 5년 생존율 및 예후인자, 방사선 합병증을 분석하여 고선량율 강내치료의 효용성을 평가하고자 하였다. 그리고 심각한 후기 합병증 없이 만족스런 국소 제어율을 얻기 위한 외부방사선선량과 강내치료선량의 최적 선량배합을 알아보고자 하였다. 대상 및 방법 : 1979. 5 - 1990. 12월 까지 연세암센타 치료방사선과에서 자궁경부 편평상피암 FlGO 병기 Ib로 진단된후 근치적 목적하에 외부 및 강내치료를 받은 162명의 환자들을 대상으로 치료 결과를 후향적 분석하였다. 외부 방사선 치료는 LINAC 10MV X-ray를 이용해 180-200cGy/fr씩 4000-4600cGy14.5-5주를 전골반 부위에 시행하였근데, 일부환자에서 2000-4000 cGy에서 중앙차폐(midline block)를 시행하였다. 코발트 선원을 이용한 원격 조정 아프터 로딩 고선량율 강내치료를 A점에 1회당 300cGy씩 주 3회, 총 10-13회 (3000-3900 cGy)실시하여 A 점에 들어간 총방사선 조사량은 6420 - 9500cGy 으로 평균 8394 cGy 였다. 결과 : 방사선 치료후 완전 관해율은 $99.4\%$ 였다. 5년 전체생존율은 $91.1\%$이고, 5년 무병생존율은 $90.9\%$였다. 추적 관찰 기간동안 치료 실패 양상을 관찰해 보면 국소 실패만 보인 경우는 7명이었고 원격전이만 보인경우가 6명이었으며, 국소 및 원격전이가 모두 발생한 경우가 1예 있어서 국소제어 실괘율은 $4.9\%$(8/163), 원격전이율은 $4.3\%$(7/164)였다. 후기 합병증은 38명 ($23.5\%$)에서 발생하였초, 그 중 30병 직장 합병증으로 $18.5\%$ 후기 합병증 발생율을 보였고, 방광 합병증은 8명에서 발생하여 $4.9\%$ 후기 합병증 발생율을 보였다. 직장 합병증이 생긴 환자관에서 직장에 소사된 방사선량은 평균 7887 cGy 이었고, 합병증이 발생하지 않은 환자군의 평균조사량은 7488 cGy이었다. 결론 : 근치적 목적으로 외부 방사선 치료 및 고선량률 강내 치료는 FIGO병기 Ib 자궁경 부편평상피암을 치료하는데 매우 효과석이라 생각하였고, 외부방사선치료중 중앙차폐를 시행하여 A점 선량이 75Gy를 넘지 않게 방사선치료 설계를 하면 심각 합병증없이 좋은 치료성적을 얻을 수 있겠다.

• Radiation Oncology Journal
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• 제23권2호
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• pp.92-97
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• 2005

목적 : 원발성 간암에서 근치적 목적의 방사선치료 결과엔 대한 문헌상 보고는 드물다. 이에 저자들이 경험한 원발성 간암의 분할 정위방사선치료에 대한 결과를 보고하고자 하였다. 대상 및 방법 : 1999년 7월부터 2002년 3월까지 원발성 간암으로 조직학적 진단을 받은 후 분할 정위방사선치료를 시행한 20명을 대상으로 후향적 분석을 하였다. 종양의 장경은 $2~6.5\;cm$ (평균: 3.8 cm)였다. 분할 정위방사선치료는 1회 조사량으로 5와 10 Gy였고 선량은 계획용 표적체적(planning target volume)에 맞추어 처방하였으며 회전중심점 선량의 $85\~90\%$등선량 곡선에 치료를 하였다. 주 $3\~5$회 치료하여 2주 동안 총 50 Gy를 조사하였다(중앙선량: 50 Gy). 추적관찰기간은 $3\~55$개월(중간 추적관찰기간: 23개월)이었다. 결과 : 전체 치료 반응률은 $60\%$이었으며 완전 반응 4명($20\%$), 부분 반응 8명($40\%$), 안정성 병변이 8명($40\%$)이었다. 전체 환자의 1년 및 2년 생존율은 각각 $70\%$, $43.1\%$이었으며 중앙 생존기간은 20개월이었다. 1년 및 2년 무병 생존율은 각각 $65\%$, $32.5\%$이었으며 중앙 무병생존기간은 19개월이었다. 치료 부작용으로 소화장애가 16명($60\%$), 오심/구토가 8명($40\%$), 간 기능 저하가 6명($30\%$)에서 발생하였으나 부작용에 의한 사망은 없었다. 결론 : 원발성 간암의 분할 정위방사선치료는 비교적 안전하고 효과적인 방법이었다. 따라서 단일 병변이면서 비교적 종양의 크기가 작은 간암에서 내과적으로 수술이 불가능하거나 수술을 거부하는 환자에서 국소 치료방법으로 고려할 수 있을 것으로 사료된다.

• Journal of Korean Neurosurgical Society
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• 제29권8호
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• pp.1024-1029
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• 2000

Objectives : With recent improvements in neuroimaging and the development of third and fourth-generation radiosurgical dose-planning soft ware, came a renewed interest in using radiosurgery for the treatment of movement disorders. Radiosurgery involves no opening of the cranium and no incisions, eliminating both the risk of hemorrhage from passing an electrode to the depths of meningitis from operative infection. It is for these reasons stereotactic radiosurgical treatment of movement disorders has value in a small subgroup of patients. The authors report four cases of Parkinson's disease and one case of dystonia that were treated by Gamma knife. Methods : Radiosurgical nucleus ventralis intermedius thalamotomy using the gamma knife unit was performed to make lesion in two Parkinson's disease patients. A radiation dose of 120Gy was delivered to nucleus using a single 4-mm collimator plug pattern following classic anatomical landmarks. Patients were followed for a median of 10.5 months(range 9-12 months). An independent neurological evaluation of tremor, based on the change in the United Parkinson's Disease Rating Scale tremor score(UPDRS), was correlated with a subjective evaluation. Gamma knife ventrolateral(V.O.P) thalamotomy was performed in one case of dystonia. A central dose of 150Gy was delivered and the patient was followed for 18 months. Gamma knife globus pallidus interna pallidotomy was performed in two Parkinson's disease patients. A radiation dose of 130Gy(range 120-140Gy) was delivered. Patients were followed for a median of 13 months(range 9-14 months). Result : Ventrolateral thalamotomy in dystonia produced regained left hand usage in order to be able to use the telephone. Ventralis intermedius thalamotomy produced an excellent improvement of the tremor in one case, mild improvement of the tremor in the other case of Parkinson's disease. A globus pallidus internalis(GPi) pallidotomy produced improvement of rigidity and dyskinesia : one other showed no change. There were no neurological complications. Conclusion : Gamma Knife thalamotomy considered a safe and effective technique for the treatment of tremor in Parkinson's disease. Although the results from Longer follow-up is not available yet, the short-term results seem to be encouraging.

• Journal of Dental Anesthesia and Pain Medicine
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• 제22권5호
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• pp.357-367
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• 2022

Background: Low-dose dexmedetomidine may be a suitable alternative to opioids for pediatric ambulatory procedures under general anesthesia (GA). However, the recovery profile remains unclear. Herein, we aimed to evaluate the effects of low-dose dexmedetomidine on the recovery profile of children. Methods: Seventy-two children undergoing ambulatory oral rehabilitation under GA were randomly and equally distributed into two groups (D and F). Group D received an infusion of dexmedetomidine 0.25 ㎍/kg for 4 min for induction, followed by maintenance of 0.4 ㎍/kg/h. Group F received an infusion of fentanyl 1 ㎍/kg over 4 min for induction, followed by maintenance at 1 ㎍/kg/h. The primary outcome was the extubation time. The secondary outcomes were awakening time, end-tidal sevoflurane (ET-Sevo) requirement, change in hemodynamic parameters, Richmond Agitation-Sedation Scale (RASS), Children's Hospital of Eastern Ontario pain scale (CHEOPS) score, length of PACU stay, and incidence of adverse events. Results: Statistically significant differences were observed in the recovery profile between the groups: the median time for extubation was 3.65 (3.44-6.2) vs. 6.25 (4.21-7) minutes in groups D vs. F (P=0.001), respectively, while the corresponding awakening times were 19 (18.75-21) and 22.5 (22-24) minutes, respectively (P < 0.001). The mean ET-Sevo was low in group D (1.1 vs. 1.2; P < 0.001). The heart rate was significantly low across all time points in group D, without resulting in bradycardia. The median RASS and CHEOPS scores were also significantly lower in group D. No significant differences were observed in the mean arterial pressure, incidence of adverse events, or length of PACU stay. Conclusion: Low-dose dexmedetomidine was more effective than fentanyl as an opioid substitute at providing a better recovery profile in pediatric ambulatory oral rehabilitation under GA. Dexmedetomidine also significantly reduced sevoflurane consumption without causing adverse events or prolonging hospital stay.

• Radiation Oncology Journal
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• 제27권1호
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• pp.29-34
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• 2009

목적: 초기성문암에서 근치적 방사선치료는 성대를 보전하면서 완치할 수 있다. 저자들은 초기 성문암에서 방사선 치료 후 재발양상, 장기생존율 및 음성보존율을 알아보고자 하였다. 대상 및 방법: 1988년 2월부터 2003년 12월까지 계명대학교 방사선종양학과에서 초기(1, 2기) 성문부의 편평상피암으로 진단되어 방사선치료를 받은 환자 70명을 대상으로 하였다. 환자의 연령분포는 39세에서 79세로 중앙값 63세이며 병리학적으로 모두 편평상피암이었다. 병기로는 1기가 58명, 2기가 12명이었으며 남자가 67명으로 대부분을 차지하였다. 방사선치료선량은 하루 $1.8{\sim}2.2$ Gy 분할선량으로 총방사선량은 $54{\sim}70.2$ Gy로 병기 1기에는 중앙값 60 Gy, 2기에는 중앙값 66 Gy를 조사하였다. 추적관찰기간은 13개월에서 180개월로 중앙값이 77.5개월이었다. 생존율은 Kaplan Meier법을 사용하였으며 Log Rank법을 이용하여 분석하였다. 두 군 간의 비교는 Chi-square법을 이용하였다. 결과: 전체 환자에서 방사선치료 후 국소제어는 69명(98.5%)에서 되었으며 5년 생존율은 93.9%, 5년 무병생존율이 84.1%이었고 구제수술 후 5년 무병생존율은 92.8%로 1기는 93.1%, 2기는 91.7%이었다. 13명(18.5%)에서 국소재발을 하였으며 이 중 9명은 구제수술로 치료되었으며 4명은 재발을 진단받고 추적관찰이 되지 않았다. 방사선 치료 후 국소재발까지의 평균기간은 24개월($3{\sim}69$개월)이었다. 성문암으로 사망한 사람은 2명으로 폐, 뼈, 간의 전신전이로 각각 33, 71개월 후 사망하였고 9명은 성문암의 재발이나 전이 없이 다른 질환으로 평균 73개월 후 사망하였다. 방사선치료 후 심각한 만성 부작용은 없었다. 전체적으로 62명(88.5%)에서 음성을 보존할 수 있었다. 결론: 초기 성문암에서 방사선치료는 효과적인 치료법이며 우수한 장기생존율과 음성보존율을 얻을 수 있으므로 우선적으로 고려되어야 할 치료법이다.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제28권5호
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• pp.470-476
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• 2006

Low-dose rate brachytherapy(LDR) has been effective modality for treatment of oral cancer. But the disadvantage of LDR is radioexposure of medical staff. To overcome this problem, high dose rate(HDR) brachytherapy has been developed. Our study evaluates the outcomes of patients with tongue cancer as treated by HDR brachytherapy. Between 2002 and 2005, eight patients with carcinoma of the tongue were treated with HDR brachytherapy. Five patients had AJCC stage I or II disease and the remaining three patients had AJCC stage III or IV. The male-to-female ratio was 2:6 and the mean age was 60.1 years (range: 21-80 years).The median follow-up time was 23.8 months (range: 7-55 months). There was no local failure until now. Three patients showed some complications. Two patients showed soft tissue necrosis. There was no bone sequela in all cases. Our experience in treating tongue cancer with HDR brachytherapy is encouraging, because it gave a satisfactory local control. Prospective studies are necessary to delineate the optimum indication for this treatment modality and long-term outcome.

• Clinical and Experimental Vaccine Research
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• 제12권1호
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• pp.60-69
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• 2023

Purpose: Although the fast development of safe and effective messenger RNA (mRNA) vaccines against severe acute respiratory syndrome coronavirus 2 has been a success, waning humoral immunity has led to the recommendation of booster immunization. However, knowledge of the humoral immune response to different booster strategies and the association with adverse reactions is limited. Materials and Methods: We investigated adverse reactions and anti-spike protein immunoglobulin G (IgG) concentrations among health care workers who received primary immunization with mRNA-1273 and booster immunization with mRNA-1273 or BNT162b2. Results: Adverse reactions were reported by 85.1% after the first dose, 94.7% after the second dose, 87.5% after a third dose of BNT162b2, and 86.0% after a third dose of mRNA-1273. They lasted for a median of 1.8, 2.0, 2.5, and 1.8 days, respectively; 6.4%, 43.6%, and 21.0% of the participants were unable to work after the first, second, and third vaccination, respectively, which should be considered when scheduling vaccinations among essential workers. Booster immunization induced a 13.75-fold (interquartile range, 9.30-24.47) increase of anti-spike protein IgG concentrations with significantly higher concentrations after homologous compared to heterologous vaccination. We found an association between fever, chills, and arthralgia after the second vaccination and anti-spike protein IgG concentrations indicating a linkage between adverse reactions, inflammation, and humoral immune response. Conclusion: Further investigations should focus on the possible advantages of homologous and heterologous booster vaccinations and their capability of stimulating memory B-cells. Additionally, understanding inflammatory processes induced by mRNA vaccines might help to improve reactogenicity while maintaining immunogenicity and efficacy.

• Radiation Oncology Journal
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• 제32권1호
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• pp.14-22
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• 2014

Purpose: To evaluate the safety and efficacy of transcatheter arterial chemoembolization (TACE) followed by radiotherapy (RT) in treatment-na$\ddot{i}$ve patients with locally advanced hepatocellular carcinoma (HCC). Materials and Methods: Eligibility criteria were as follows: newly diagnosed with HCC, the Barcelona Clinic Liver Cancer stage C, Child-Pugh class A or B, and no prior treatment for HCC. Patients with extrahepatic spread were excluded. A total of 59 patients were retrospectively enrolled. All patients were treated with TACE followed by RT. The time interval between TACE and RT was 2 weeks as per protocol. A median RT dose was 47.25 $Gy_{10}$ as the biologically effective dose using the ${\alpha}/{\beta}$ = 10 (range, 39 to 65.25 $Gy_{10}$). Results: At 1 month, complete response was obtained in 3 patients (5%), partial response in 27 patients (46%), stable disease in 13 patients (22%), and progressive disease in 16 patients (27%). The actuarial one- and two-year OS rates were 60.1% and 47.2%, respectively. The median OS was 17 months (95% confidence interval, 5.6 to 28.4 months). The median time to progression was 4 months (range, 1 to 35 months). Grade 3 or greater liver enzyme elevation occurred in only two patients (3%) after RT. Grade 3 gastroduodenal toxicity developed in two patients (3%). Conclusion: The combination treatment of TACE followed by RT with two-week interval was safe and it showed favorable outcomes in treatment-na$\ddot{i}$ve patients with locally advanced HCC. A prospective randomized trial is needed to validate these results.