RESEARCH ARTICLE. Min Kyung Hyun 1, Jin Seub Hwang 1, Jin Hee Kim 1, Ji Eun Choi 1, Sung Young Jung 1, Jong-Myon Bae 1,2 * Abstract.

Similar documents
Survival and Intracranial Control of Patients With 5 or More Brain Metastases Treated With Gamma Knife Stereotactic Radiosurgery

Laboratory data from the 1970s first showed that malignant melanoma

We have previously reported good clinical results

: Ajou University College of Medicine, Suwon, Korea; Ajou University College of Medicine, Graduate

Management of single brain metastasis: a practice guideline

Brain metastases are common brain malignant neoplasms

A Population-Based Study on the Uptake and Utilization of Stereotactic Radiosurgery (SRS) for Brain Metastasis in Nova Scotia

Stereotactic Radiosurgery for Brain Metastasis: Changing Treatment Paradigms. Overall Clinical Significance 8/3/13

Optimal Management of Isolated HER2+ve Brain Metastases

Outcome of Surgical Resection of Symptomatic Cerebral Lesions in Non-Small Cell Lung Cancer Patients with Multiple Brain Metastases

Jefferson Digital Commons. Thomas Jefferson University. Mark E Linskey Department of Neurosurgery, University of California-Irvine Medical Center

Neurological Change after Gamma Knife Radiosurgery for Brain Metastases Involving the Motor Cortex

Standardized Thyroid Cancer Mortality in Korea between 1985 and 2010

ORIGINAL ARTICLE. Annals of Oncology 28: , 2017 doi: /annonc/mdx332 Published online 27 June 2017

Prognostic indices in stereotactic radiotherapy of brain metastases of non-small cell lung cancer

Outcomes in patients with brain metastasis from esophageal carcinoma

SUCCESSFUL TREATMENT OF METASTATIC BRAIN TUMOR BY CYBERKNIFE: A CASE REPORT

Title: What is the role of pre-operative PET/PET-CT in the management of patients with

Mehmet Ufuk ABACIOĞLU Neolife Medical Center, İstanbul, Turkey

Radiotherapy for Brain Metastases

STEREOTACTIC RADIOSURGERY FOR LIMITED BRAIN METASTASES IN IRANIAN BREAST CANCER PATIENTS

Clinical Commissioning Policy: Stereotactic Radiosurgery / Radiotherapy For Cerebral Metastases. December Reference : NHSCB/D5/1

Sergio Bracarda MD. Head, Medical Oncology Department of Oncology AUSL-8 Istituto Toscano Tumori (ITT) San Donato Hospital Arezzo, Italy

RESEARCH HUMAN CLINICAL STUDIES

PROSPERO International prospective register of systematic reviews

Treatment outcomes and prognostic factors of gallbladder cancer patients after postoperative radiation therapy

BMI and Breast Cancer in Korean Women: A Meta-Analysis

AUTHOR S PERSONAL COPY

Nonsmall Cell Lung Cancer Presenting with Synchronous Solitary Brain Metastasis

Metastatic epidural spinal cord compression (MESCC)

Outcomes after Reirradiation for Brain Metastases

Systematic reviews and meta-analyses of observational studies (MOOSE): Checklist.

Palliative radiotherapy near the end of life for brain metastases from lung cancer: a populationbased

Current status of hepatic surgery in Korea

!"#$%&'()*+,-./01 !"#$ N! !"#$%&'()*+,- !"#$%&'()*+,-)*./01!"#$% &'()*+,-./#0!"#$#%

Comparative Analysis of Efficacy and Safety of Multisession Radiosurgery to Single Dose Radiosurgery for Metastatic Brain Tumors

Gamma Knife Surgery for Brain Metastasis from Renal Cell Carcinoma : Relationship Between Radiological Characteristics and Initial Tumor Response

Local control of brain metastases by stereotactic radiosurgery in relation to dose to the tumor margin

Brain metastases arise in 10% 40% of patients

Liang-Hua Ma, Guang Li *, Hong-Wei Zhang, Zhi-Yu Wang, Jun Dang, Shuo Zhang and Lei Yao

Treatment of Brain Metastases

Insulin Secretory Capacity and Insulin Resistance in Korean Type 2 Diabetes Mellitus Patients

Evidence Based Medicine for Gamma Knife Radiosurgery. Metastatic Disease GAMMA KNIFE SURGERY

Stereotactic radiosurgery for the treatment of melanoma and renal cell carcinoma brain metastases

Patients with Single Brain Metastasis from Non-Small Cell Lung Cancer Equally Benefit from Stereotactic Radiosurgery and Surgery: A Systematic Review

Tr a d i t i o n a l ly, WBRT has been the standard approach

VINCENT KHOO. 8 th EIKCS Symposium: May 2013

Quality of life (QoL) in metastatic breast cancer patients with. maintenance paclitaxel plus gemcitabine (PG) chemotherapy:

Hong Kong Hospital Authority Convention 2018

Selecting the Optimal Treatment for Brain Metastases

Update on management of metastatic brain disease. Peter Hoskin Mount Vernon Cancer Centre Northwood UK

Changes in the seroprevalence of IgG anti-hepatitis A virus between 2001 and 2013: experience at a single center in Korea

Prognostic Factors for Survival in Patients Treated With Stereotactic Radiosurgery for Recurrent Brain Metastases After Prior Whole Brain Radiotherapy

Diagnostic Analysis of Patients with Essential Hypertension Using Association Rule Mining

Journal of Breast Cancer

The detection rate of early gastric cancer has been increasing owing to advances in

ARROCase Brain Metastases

Research Article Have Changes in Systemic Treatment Improved Survival in Patients with Breast Cancer Metastatic to the Brain?

INTRODUCTION. Tae Yong Park, Young Chul Na, Won Hee Lee, Ji Hee Kim, Won Seok Chang, Hyun Ho Jung, Jong Hee Chang, Jin Woo Chang, Young Gou Park

두경부영역의악성림프종 태경 1 이형석 1 서인석 1 이용섭 1 조석현 1 최정혜 2 안명주 2. Hodgkin s and Non-Hodgkin s Lymphoma of Head and Neck

Gamma Knife Radiosurgery A tool for treating intracranial conditions. CNSA Annual Congress 2016 Radiation Oncology Pre-congress Workshop

PROSPERO International prospective register of systematic reviews

Surveillance report Published: 17 March 2016 nice.org.uk

Management of Single Brain Metastases Practice Guideline Report #9-1

Only Estrogen receptor positive is not enough to predict the prognosis of breast cancer

Are there the specific prognostic factors for triplenegative subtype of early breast cancers (pt1-2n0m0)?

Epidermal growth factor receptor mutation and pattern of brain metastasis in patients with nonsmall cell lung cancer

JAMA. 2006;295:

The clinical utilization of radiation therapy in Korea between 2009 and 2013

Collection of Recorded Radiotherapy Seminars

Tania Kaprealian, M.D. Assistant Professor UCLA Department of Radiation Oncology August 22, 2015

Br a i n metastases occur in 20 40% of all patients. The results of resection after stereotactic radiosurgery for brain metastases.

See the corresponding editorial in this issue, pp J Neurosurg 114: , 2011

The Role of Radiation Therapy in the Treatment of Brain Metastases. Matthew Cavey, M.D.

The Epidemiology of Diabetes in Korea

Cancerous esophageal stenosis before treatment was significantly correlated to poor prognosis of patients with esophageal cancer: a meta-analysis

Original Article Value of Adding Boost to Whole Brain Radiotherapy after Surgical Resection of Limited Brain Metastases

A new score predicting the survival of patients with spinal cord compression from myeloma

Treatment of Right Colonic Diverticulitis: The Role of Nonoperative Treatment

Workshop: Cochrane Rehabilitation 05th May Trusted evidence. Informed decisions. Better health.

2. The effectiveness of combined androgen blockade versus monotherapy.

Recent Trend in the Incidence of Premalignant and Malignant Skin Lesions in Korea between 1991 and 2006

Imaging-cytology correlation of thyroid nodules with initially benign cytology

Alectinib Versus Crizotinib for Previously Untreated Alk-positive Advanced Non-small Cell Lung Cancer : A Meta-Analysis

Pre-operative stereotactic radiosurgery treatment is preferred to post-operative treatment for smaller solitary brain metastases

Experience of Korea Acute Myocardial Infarction Registry (KAMIR)

Cerebral metastases occur in 20% 40% of cancer

SUPPLEMENTAL MATERIAL

Additional radiation boost to whole brain radiation therapy may improve the survival of patients with brain metastases in small cell lung cancer

Endocrine Surgery. Characteristics of the Germline MEN1 Mutations in Korea: A Literature Review ORIGINAL ARTICLE. The Korean Journal of INTRODUCTION

Incidence and Multiplicities of Adenomatous Polyps in TNM Stage I Colorectal Cancer in Korea

PROSPERO International prospective register of systematic reviews

CME. Special Article. Received 27 October 2011; revised 9 December 2011; accepted 15 December Practical Radiation Oncology (2012) 2,

Clinical Study Does Time between Imaging Diagnosis and Initiation of Radiotherapy Impact Survival after Whole-Brain Radiotherapy for Brain Metastases?

The effect of resection of the primary tumour for stage IV colorectal cancer on patient survival: a systematic review and meta-analysis

Prescription dose and fractionation predict improved survival after stereotactic radiotherapy for brainstem metastases

Br a i n metastases are the tumors most frequently. Safety and efficacy of Gamma Knife surgery for brain metastases in eloquent locations

Nationwide Cancer Incidence in Korea,

Meta-analyses: analyses:

Treatment outcomes and survival based on drug resistance patterns in multidrug-resistant

Transcription:

RESEARCH ARTICLE Survival Outcomes after Whole Brain Radiation Therapy and/or Stereotactic Radiosurgery for Cancer Patients with Metastatic Brain Tumors in Korea: A Systematic Review Min Kyung Hyun 1, Jin Seub Hwang 1, Jin Hee Kim 1, Ji Eun Choi 1, Sung Young Jung 1, Jong-Myon Bae 1,2 * Abstract Aim: To compare survival outcomes after whole brain radiation therapy (WBRT), stereotactic radiosurgery (SRS), and WBRT plus SRS combination therapy in Korea, by performing a quantitative systematic review. Materials and Methods: We searched 10 electronic databases for reports on Korean patients treated with WBRT or SRS for brain metastases published prior to July 2010. Independent reviewers screened all articles and extracted the data. When a Kaplan-Meier survival curve was available, median survival time and standard errors were calculated. Summary estimates for the outcomes in each study were calculated using the inverse variance random-effects method. Results: Among a total of 2,761 studies, 20 studies with Korean patients (n=1,053) were identified. A combination of 12 studies (n=566) with WBRT outcomes showed a median survival time of 6.0 months (95%CI: 5.9-6.2), an overall survival rate of 5.6% (95%CI: 1-24), and a 6-month survival rate of 46.5% (95%CI: 37.2-56.1). For nine studies (n=412) on SRS, the median survival was 7.9 months (95%CI: 5.1-10.8), and the 6-month survival rate was 63.1% (95%CI: 49.8-74.8). In six studies (n=75) using WBRT plus SRS, the median survival was 10.7 months (95%CI: 4.7-16.6), and the overall and 6-month survival rates were 16.8% (95%CI: 6.2-38.2) and 85.7% (95%CI: 28.3-96.9), respectively. Conclusions: WBRT plus SRS showed better 1-year survival outcome than of WBRT alone for Korean patients with metastatic brain tumors. However, the results of this analysis have to be interpreted cautiously, because the risk factors of patients were not adjusted in the included studies. Keywords: Neoplasm metastasis - brain - radiotherapy - radiosurgery - Korean patients Asian Pac J Cancer Prev, 14 (12), 7401-7407 Introduction The diagnosis and treatment of brain tumors have improved recently, yet the number of patients with metastatic brain tumors continues to increase (Fox et al., 2011; Lichtor, 2013). Metastatic brain tumors occur in probably 25-35% of all cancer patients (Cairncross et al., 1980), although the exact number is not known. With the development of several new treatment methods, more cases are being actively treated. Therapeutic options now include radiation therapy, surgery, chemotherapy, and combinations of these approaches. Radiation therapy may be administered as whole-brain radiotherapy (WBRT), stereotactic radiosurgery (SRS), or WBRT plus SRS. Since 1985, when SRS was introduced in Korea (NECA, 2011), the number of WBRT procedures for metastatic brain tumors has decreased, while the number of SRS procedures has increased in Korea. Nevertheless, radiation therapy continues to be controversial, as does the optimum treatment for patients with metastatic brain tumors (Gwak, 2009). The prognosis for a patient with a metastatic brain tumor is very poor, and thus the goals of treatment are to improve the quality of life and extend survival time. Several randomized clinical trials (RCTs) have been conducted, and median survival periods have been reported based on the type of radiation therapy (Kondziolka et al., 1999; Andrews et al., 2004; Aoyama et al., 2006; Chang et al., 2009). The reported median survival times are 5.7 (Andrews, Scott et al., 2004) and 7.3 (Kondziolka et al., 1999) months after WBRT, 15.2 (Chang et al., 2009) and 8.0 (Aoyama, Shirato et al., 2006) months after SRS, and 5.7 (Chang, Wefel et al., 2009) and 7.5 (Aoyama et al., 2006) months after WBRT plus SRS. However, there is still controversy over the optimal treatment of metastatic brain tumor and there is no evidence of survival outcomes according to radiation therapy in Korean patients. Thus, 1 National Evidence-based Healthcare Collaborating Agency, 2 Jeju National University School of Medicine, Jeju, Korea *For correspondence: jmbae@jejunu.ac.kr Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 7401

Min Kyung Hyun et al we conducted a systematic literature review and metaanalysis to estimate survival outcomes in Korean patients with metastatic brain tumors after WBRT, SRS, and WBRT plus SRS. Materials and Methods Literature search We developed the protocol for a systematic literature review by considering population, intervention, comparison, and outcome (PICO) search methods,, data extraction techniques, quality assessment, and metaanalysis. Searches of the literature published up to 29 June 2010 were performed in Ovid-Medline (1950-2010 week 25), Ovid-Embase (1950-2010 week 25), the Cochrane library (1950-2010 week 25), KoreaMed (http://www. koreamed.org), KISS (http://kiss.kstudy.com), KMBASE (http://kmbase.medric.or.kr), ndsl (http://www.ndsl.kr), KiSTi (http://society.kisti.re.kr), KOSTRO (http://www. kostro.or.kr), and JKNS (http://jkns.or.kr), using various combinations of MeSH headings and keywords such as neoplasm metastasis, radiotherapy, radiosurgery, gamma knife, cyberknife, linac, whole brain radiotherapy, whole brain irradiation, stereotactic radiosurgery, and Korea without restricting languages. Moreover, the references of all of the identified eligible articles were manually searched for additional relevant citations. Study selection, data extraction, and quality assessment Articles selected for the systematic review met all of the inclusion criteria: i) patients: all Korean patients with brain metastasis; ii) interventions: WBRT, SRS, or WBRT plus SRS combination therapy; iii) outcomes: median survival time, overall, 6-month, and 1-year survival rates; iv) timing: studies conducted since 1985, when SRS was introduced in Korea; and v) type of studies: all study designs except case reports. Study selection, data extraction, and evaluation were performed independently by four reviewers (JEC, JHK, MKH, SYJ). The information entered on the data extraction form, designed specifically for this study, included study design, follow-up period, inclusion/exclusion criteria, sample size, gender and age of subjects, primary cancer, single/solitary/multiple tumors, recurrence, Karnofsky Performance Status (KPS), Eastern Clinical Oncology Group (ECOG) score, corresponding authors affiliation, baseline characteristics, treatment protocol, and outcome variables. When more than one intervention (i.e., WBRT, SRS, WBRT plus SRS) was reported in a study, we extracted the data for each intervention. Four reviewers (JEC, JHK, MKH, SYJ) evaluated the quality of each study using the Critical Guide to Case Series Reports(Carey and Boden, 2003), which contains eight items. Each study was graded on the basis of whether an item was present (+), absent (-), or unclear (?). Disagreements were decided by consensus, reached through discussion and negotiations. When consensus could not be reached, an outside party became involved, and the decisions were always based on the majority opinion. 7402 Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 Data collection process and meta-analysis We performed a meta-analysis to synthesize the outcomes for each intervention. If overall, 6-month, or 1-year survival rates were not given in the text of the paper, but the data were presented in a bar chart or Kaplan- Meier curve, the survival rates were calculated from the graphic data. In case series, we calculated the survival rates directly when possible. Standard errors of the median survival times are needed for meta-analysis; however, these were generally not provided in the articles. Therefore, we estimated the standard errors from the raw data or Kaplan-Meier curves, using a statistical equation (SPSS, 2007). In particular, for studies that presented a Kaplan-Meier curve, the median survival time and standard error calculations were performed according to a published method (Tierney et al., 2007). Two authors independently calculated the values and compared their results. In the case of a disagreement, both authors recalculated the results to reach an outcome. We used a standard inverse variance meta-analysis to combine the outcomes of each study and obtain average effects and 95% confidence intervals (CI). We also report estimates from fixed and random effect models using an inverse-variance approach. To assess heterogeneity across studies, we visually examined forest plots and used the Cochrane Q-statistic and l2 statistic. Publication bias was assessed using funnel plots, the Begg and Mazumdar rank correlation (the Begg test), and Egger s linear regression asymmetry test of the intercept (the Egger test). When publication bias was suspected, we used the Duval and Tweedie nonparametric trim-and-fill method to obtain symmetry in the funnel plot and to determine the influence of hypothetical studies on the pooled estimate. We conducted the metaanalyses using Comprehensive Meta-analysis 2.0 (Biostat, Englewood, NJ). Results Search results Figure 1 illustrates the process of selecting articles for inclusion in the systematic review and meta-analysis. Among 2,761 studies (346 from international databases and 2,415 from domestic Korean databases), 432 were duplicates; 2,310 were excluded; and one additional study was identified by searching references. Finally 20 studies (n=1,053) were identified. Five of the 20 studies reported the outcomes of two types of interventions, and one study reported on WBRT, SRS, and WBRT plus SRS (see Table 4). Thus, the meta-analysis included 12 studies (n=566) on WBRT, nine studies (n=412) on SRS, and six studies (n=75) on WBRT plus SRS. A summary of the included studies is presented in the Appendix. Fifteen (75%) of the studies were published since 2000, and the corresponding authors affiliation was neurosurgery in 45% of these. All of the SRS-related studies were published since 2003, and the corresponding author s affiliation was neurosurgery in most of these. Meta-analysis We performed a meta-analysis by intervention and

outcomes. The results of the meta-analysis of radiation therapy for each outcome in brain metastasis patients are summarized in Table 1. Table 2 shows the results of tests for publication bias. Whole brain radiation therapy Median survival period after WBRT was estimated as 6.0 months (95%CI: 5.9-6.1) by combining four studies (n=104). Overall survival after WBRT was estimated as 5.5% (95%CI: 1.1-23.7) by combining two studies (n=32); 6-month survival was estimated as 46.5% (95%CI: 37.2-56.1) by combining nine studies (n=365); and 1-year survival was estimated as 27.95% (95%CI: 19.8-37.8) by combining nine studies (n=360; Figure 2). The median survival months and overall survival showed no evidence of statistical heterogeneity among the studies (overall survival: I2=0, p=0.343; median survival month: I2=0, p=0.084). However, the 6-month and 1-year survival rates exhibited some evidence of statistical heterogeneity among the studies (6-month survival: 2761 articles identified through database searching I2=57.7, p=0.015; 1-year survival: I2=60.8, p=0.009), and thus we employed a random effect model to test for significance. Stereotactic radiosurgery Median survival after SRS was estimated as 7.9 months (95%CI: 7.9-8.1) by combining eight studies (n=171). The 6-month survival rate was estimated as 63.1% (95%CI: 49.8-74.8) by combining five studies (n=325), and 1-year survival was estimated as 34.3% (95%CI: 23.2-47.6) by combining four studies (n=339; Figure 3). In all outcomes, there was evidence of statistical heterogeneity among the studies (median survival month: I 2 =99.84, p<0.001; 6-month survival: I 2 =68.4, p=0.013; 1-year survival: I 2 =68.5, p=0.023). Thus, we used a random effect model. As publication bias was suspected in the SRS 6-month survival (Table 2), we conducted a trim-and-fill analysis, which yielded a 6-month survival estimate of 54.9% A) 7 of additional articles id entified through hand se arch 432 of articles after duplicates removed 6 of full text articles excl uded, with reasons * Reasons 1 of non-p 1 of non-i 2 of non-s 1 of non-o 1 of non-t 1 of studies included in qualitative synthesis 2329 of articles screened 152 of full text articles assess ed for eligibility 19 of articles included in quan titaive synthesis 20 of articles included in quan titaive synthesis (meta-analysis) WBRT 12 SRS 9 WBRT plus SRS 6 Figure 1. Study Flow Diagram 2177 of articles exclude d 133 of full text articles e xcluded, with reasons * Reasons 39 of non-population 15 of non-intervention 31 of non-study design 41 of non-outcome 7 of non-timing Figure 3. Outcomes after Stereotactic Radiosurgery. A) Median survival; B) 6-month survival; and C) 1-year survival B) C) A) C) B) D) Figure 2. Outcomes after Whole Brain Radiation Therapy. A) Median survival; B) Overall survival; C) 6-month survival; and D) 1-year survival Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 7403

Min Kyung Hyun et al Table 1. Meta-analysis of Radiation Therapy for Each Outcome in Patients with Brain Metastases Intervention Outcome No. of No. of Model Point 95%CI I 2, % Heterogeneity Studies Patients estimate p value WBRT Median survival, months 4 104 I-V, F-M 6.022 5.897-6.147 <0.001 0.842 Overall survival 2 32 I-V, F-M 0.055 0.011-0.237 0 6-month survival 9 365 I-V, R-M 0.465 0.372-0.561 57.702 1-year survival 9 360 I-V, R-M 0.279 0.198-0.378 60.827 SRS Median survival, months 8 171 I-V, R-M 7.93 5.091-10.769 99.849 0 6-month survival 5 325 I-V, R-M 0.631 0.498-0.748 68.433 1-year survival 4 339 I-V, R-M 0.343 0.232-0.476 68.501 0.023 WBRT+SRS Median survival, months 4 35100.0I-V, R-M 10.669 4.721-16.617 97.066 0 Overall survival 4 27 I-V, F-M 0.168 0.062-0.382 <0.001 0.484 6.3 6-month survival 2 48 I-V, R-M 0.857 10.1 0.283-0.989 20.3 83.826 0.013 1-year survival 2 48 I-V, R-M 0.718 0.429-0.896 70.51 0.066 *Abbreviations: WBRT, whole brain radiation therapy; SRS, stereotactic radiosurgery; 75.0WBRT+SRS, WBRT plus SRS combination therapy; Pts, Patients, I V, inversevariance method; F-M, fixed model; R-M, random model; CI, confidence interval Table 2. Tests for Publication Bias 56.3 46.8 Intervention Outcome Egger Test Begg Test p value p value WBRT Median survival, months 0.857 1 6-month survival 0.076 0.917 1-year survival 0.068 0.466 SRS Median survival, months 0.998 0.764 6-month survival 0.032 0.086 1-year survival 0.865 0.734 WBRT+SRS Median survival, months 0.595 0.734 Overall survival 0.844 0.734 *Abbreviations: WBRT, whole brain radiation therapy; SRS, stereotactic radiosurgery; WBRT+SRS, WBRT plus SRS combination therapy Table 3. Comparison of Median Survival (months) of Korean Pateints Compared with Other Countries Study Study WBRT SRS WBRT design plus SRS This study 6 7.9 10.7 Kondziolk et al. (1999) RCT 7.5 11 Sneed et al. (1999) RC 11.3 11.1 Chidel et al. (2000) RC 10.5 6.4 Hoffman et al. (2001) RC 13.9 14.5 Sneed et al. (2002) RC 7.2 8.6 Noel et al. (2003) RC 7 14 Andrews et al. (2004)* RCT 5.7 6.5 Combs et al. (2004) RC 9 6 Datta et al. (2004) RC 6 6 Aoyama et al. (2006) RCT 8 7.5 Rades et al. (2007) RC 7 13 Chang et al. (2009) RCT 15.2 5.7 Lee et al. (2008) RC 6 29 *Mean survival (months); **Abbreviations: WBRT, whole brain radiation therapy; SRS, stereotactic radiosurgery; WBRT+SRS, WBRT plus SRS combination therapy; RCT, randomized clinical trial; cohort, RC, retrospective cohort (95%CI: 39.1-69.8) when two studies were excluded. This estimate was not significantly different from the original estimate (63.1%). Whole brain radiation therapy plus stereotactic radiosurgery Median survival after WBRT plus SRS was estimated as 10.7 months (95%CI: 11.6-12.1) by combining four studies (n=35), and overall survival was estimated as 16.8% (95%CI: 6.2-38.2) by combining four studies (n=27). The 6-month and 1-year survival rates were 7404 50.0 Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 0 Newly diagnosed without treatment 38.0 Newly diagnosed with treatment 54.2 23.7 A) Figure 4. Outcomes after Whole Brain Radiation Therapy Plus Stereotactic Radiosurgery. A) Median survival; B) 6-month survival; C) 6-month survival; and D) 1-year survival B) C) D) estimated as 85.7% (95%CI: 23.8-98.9) and 71.8% (95%CI: 42.9-89.6), respectively, by combining two studies (n=48) for each. The wide confidence intervals in both cases are attributable to the inclusion of only two studies. There was no evidence of statistical heterogeneity in overall survival among the studies (I 2 =0, p=0.484). However, because there was evidence of statistical heterogeneity in the other outcomes (median survival month: I 2 =97.1, p<0.001; 6-month survival: I 2 =83.8, p=0.013; 1-year survival: I 2 =70.5, p=0.066), we used a random effect model. Persistence or recurrence Remission None 12.8 51.1 33.1 Chemotherapy

Table 4. Summary Table of Included Studies Study Enrollment Affiliation of Intervention (n) Outcome (Y/N) period corresponding WBRT SRS WBRT+SRS Overall 6-month 1-year Median author survival survival survival survival (M) Hong SE (1994) 1991~1993 Radiation Oncology 24 Y Y Baik JS (1997) 1992.1~1995.12 Neurology 165 19 Y Jang SS (1998) 1994.1~1997.4 Therapeutic Oncology 33 Y Y Lee SN (1999) 1987.1~1998.1 Internal Medicine 30 Y Y Y Yoo H (1999) 1987~1994 Neurosurgery 25 Y Y Cho MJ (2000) 1997.8~1998.12 Therapeutic Oncology 11 Y Kim DY (2000) 1995.10~1998.2 Therapeutic Oncology 100.0 19 Y Y Y Kim CS (2002) 1985.1~1998.3 Neurosurgery 15 6.3 Y Y 10.1 Kim HJ (2003) 1996.10~2002.2 Therapeutic Oncology 29 20.3 Y Y Kim IK (2003) 1993.1~2002.9 Surgery 10 Y Y Ko YS (2003) 1998.1~2003.1 Neurosurgery 75.0 44 Y Y Y Park BJ (2003) 1996.1~2000.12 Neurosurgery 15 10 Y Y Lee JD (2004) 1986.3~2003.5 Surgery 100.0 2 3 56.3 2 46.8 Y Y Kwon KY (2007) 2002.1~2005.10 Neurosurgery 204 Y Y 50.0 6.3 10.1 20.3 54.2 Yang SY (2008) 1998.1~2005.12 Neurosurgery 15 Y Y Y Gu HW (2009) 2000.11~2008.4 Neurosurgery 106 Y Y Y Gwak HK (2009) 2001.1~2008.1 Radiation Oncology 75.0 160 Y Kim CJ (2009) 2004.1~2006.12 Radiation Oncology 39 29 Y Park SH (2009) 2005.1~2006.12 Neurosurgery 19 14 56.3 46.8 Y Y Y 38.0 Han JH (2010) 1991~2007 Neurosurgery 7 4 Y Y 50.0 54.2 23.7 *Abbreviations: WBRT, whole brain radiation therapy; SRS, stereotactic radiosurgery; WBRT+SRS, WBRT plus SRS combination therapy Discussion 0Kaplan-Meier curves, according to a published method (Tierney et al., 2007). To evaluate the accuracy of the This study is the first reported quantitative systematic analyses, two authors independently processed the same 38.0 review of survival outcomes after radiation therapy in data and compared findings, which were recalculated 23.7 Korean patients with metastatic brain tumors. After as necessary. Through this process, a large amount of WBRT, 1-year survival rate was 5.6%, and after WBRT 0information was gathered from many studies and was used plus SRS, 1-year survival was 71.8%. Without overlapping to determine current survival outcomes in Korean patients. of the CI, WBRT plus SRS showed better 1-year survival Our study has several limitations. First, the survival outcome than of WBRT alone for Korean patients with outcomes of the different types of radiation therapy difficult metastatic brain tumors. However, the results of this to compare at the same level, because we performed a analysis have to be interpreted cautiously, because the risk one-arm meta-analysis. But, we can be found statistical factors of patients are not adjusted in the included studies. difference based on intersection of CI, and WBRT plus Table 3 shows the median survival times after radiation SRS showed better 1-year survival rate than of WBRT therapy in patients with brain metastases reported in alone. Second, quality of life is very important outcomes studies contained in a recently published systematic review for metastatic brain tumor patients. But we analyzed only (Linskey et al., 2010; Patil et al., 2010). The ranges of the survival outcome of each intervention and did not the median survival times reported in all of the studies consider quality adjusted life year, because we did not find were 5.7-7.5, 7.0-29.0, and 5.7-14.5 months after WBRT, a relevant study that reported outcomes. Third, metastatic SRS, and WBRT+SRS, respectively. The median survival brain tumors are very heterogeneous disease with varied ranges reported for the retrospective cohorts were 6.0 risk factors (i.e. the primary tumor site, the number 7.0, 7.0-29.0, and 6.0-14.5 months, after WBRT, SRS, of metastasis, history of previous treatment, patients and WBRT+SRS, respectively. In our study, the pooled functional status, etc). But, we couldn t analyzed based on estimates for each treatment were within these ranges. In risk factors, because we did not find a reported outcome other words, the median survival of radiation therapy in stratified by varied risk factors, after whole brain radiation Korean patients with metastatic brain tumors was within therapy and/or stereotactic radiosurgery for cancer patients the ranges reported from other countries. with metastatic brain tumors. Fourth, the included studies Fifteen (75%) of the studies were published since were all observational studies, and there was evidence 2000, and the affiliation of the corresponding author was of statistical heterogeneity in some outcomes. Although neurosurgery in 45% of these (Table 4). Additionally, we performed subgroup and sensitivity analyses, we all SRS reports were published since 2003, and the were unable to resolve the heterogeneity. Patients with 100.0 corresponding author s affiliation was neurosurgery in metastatic brain tumors differ in terms of the severity of most of these (Table 4). the primary cancer, the site of metastasis, the number of We extracted available data from all reported brain metastases, and general health condition. Therefore, 75.0 observational cohort studies, even though there was no their treatment is not uniform. Furthermore, medical teams formal RCT. In some studies, survival outcomes were rightly use every possible treatment method to increase presented only in graphic form, and great effort was made to calculate survival rates from the graphs, bar charts, and Newly diagnosed without Newly diagnosed treatment without treatment Newly diagnosed with Newly treatment diagnosed with treatment life expectancy for these patients, making a well-designed RCT impossible for metastatic brain tumor patients. The 50.0 Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 7405 Persistence or recurrence Persistence or recurrence Remission Remission None None 1 5 1 5 3 3 6. 56 31

Min Kyung Hyun et al observational studies used were based on patients in actual medical practice, and thus despite their limitations, these studies reflect real-world circumstances. In that sense, our study is meaningful. In conclusion, we determined the survival outcomes after WBRT, SRS, and WBRT plus SRS for Korean patients with metastatic brain tumors. The pooled estimates for each treatment were within the ranges reported in studies from other countries. And WBRT plus SRS showed better than of WBRT alone in 1-year survival outcome for Korean patients with metastatic brain tumors. However, the results of this analysis have to be interpreted cautiously, because the risk factors of patients are not adjusted in the included studies. Acknowledgements This study was funded by National Evidence-based Healthcare Collaborating Agency (NECA), project no. NA2010-011. References Andrews DW, Scott CB, Sperduto PW, et al (2004). Whole brain radiation therapy with or without stereotactic radiosurgery boost for patients with one to three brain metastases: phase III results of the RTOG 9508 randomised trial. Lancet, 363, 1665-72. Aoyama H, Shirato H, Tago M, et al (2006). Stereotactic radiosurgery plus whole-brain radiation therapy vs stereotactic radiosurgery alone for treatment of brain metastases: a randomized controlled trial. JAMA, 295, 2483-91. Baik JS, Choi IS, Roh JK, et al (1997). Metastatic brain tumors: clinical aspects and prognosis. J Korean Neurol Assoc, 15, 358-67. Cairncross JG, Kim JH, Posner JB, et al (1980). Radiation therapy for brain metastases. Ann Neurol, 7, 529-41. Carey TS, Boden SD (2003). A critical guide to case series reports. Spine, 28, 1631-4. Chang EL, Wefel JS, Hess KR, et al (2009). Neurocognition in patients with brain metastases treated with radiosurgery or radiosurgery plus whole-brain irradiation: a randomised controlled trial. Lancet Oncol, 10, 1037-44. Chidel MA, Suh JH, Reddy C.A, et al. (2000). Application of recursive partitioning analysis and evaluation of the use of whole brain radiation among patients treated with stereotactic radiosurgery for newly diagnosed brain metastases. Int J Radiat Oncol Biol Phys, 47, 993-9 Cho MJ, Kim KH, Jang JY (2000). Initial experience of fractionated dtereotactic radiotherapy for metastatic brain tumors. J Korean Cancer Assoc, 32, 374-81. Combs SE, D. Schulz-Ertner D, Thilmann, C, et al (2004). Treatment of cerebral metastases from breast cancer with stereotactic radiosurgery. Strahlenther Onkol, 180, 590-6. Datta R, Jawahar A, Ampil FL, et al (2004). Survival in relation to radiotherapeutic modality for brain metastasis: whole brain irradiation vs. gamma knife radiosurgery. Am J Clin Oncol, 27, 420-4. Fox BD, Cheung VJ, Patel AJ, et al (2011). Epidemiology of metastatic brain tumors. Neurosurg Clin N Am, 22, 1-6. Gu HW, Sohn MJ, Lee DJ, et al (2009). Clinical analysis of novalis stereotactic radiosurgery for brain metastases. J Korean Neurosurg Soc, 46, 245-51. Gwak HK, Kim WC, Kim HJ, et al (2009). Survival analysis 7406 Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 of patients with brain metastasis by weighting according to the primary tumor oncotype. J Korean Soc Ther Radiol Oncol, 27, 140-4. Han JH, Kim DG, Park JC, et al (2010). Little response of cerebral metastasis from hepatocellular carcinoma to any treatments. J Korean Neurosurg Soc, 47, 325-31. Hoffman R, Sneed PK, McDermott MW, et al (2001). Radiosurgery for brain metastases from primary lung carcinoma. Cancer J, 7, 121-31. Hong SE (1994). Accelerated fractionation in the treatment of brain metastasis from non-small cell carcinoma of the lung. J Korean Soc Ther Radiol, 12, 165-73. Jang SS, Park WY, Kim WD. Palliative Radiotherapy for Brain metastases. J Korean Soc Ther Radiol Oncol, 16, 177-84. Kim CJ, Baek MY, Park SK, et al (2009). Comparison of stereotactic radiosurgery and whole brain radiotherapy in patients with four or more brain metastases. J Korean Soc Ther Radiol, 27, 163-8. Kim CS, Kang SS, Jung S, et al (2002). Prognostic factors in patients with brain metastases. J Korean Neurosurg Soc, 31, 203-9. Kim DY, Ahn YC, Huh SJ, et al (2000). Stereotactic radiotherapy for the treatment of brain metastases. J Korean Cancer Assoc, 32, 148-55. Kim HJ, Hong SM, Kim SZ, et al (2003). Efficacy of whole brain radiotherapy combined with fractionated stereotactic radiotherapy in metastatic brain tumors, and prognostic factors. Radiat Med, 21, 155-60. Kim IK, Lee RA, Moon SM, et al (2003). Brain metastasis of colorectal cancer. J Korean Soc Coloproctol, 19, 165-9. Ko YS, Oh YK, Nam TK (2003). Results of palliative radiotherapy to the metastatic brain tumor. Med J Chosun Univ, 28, 50-8. Kondziolka D, Patel A, Lunsford LD, et al (1999). Stereotactic radiosurgery plus whole brain radiotherapy versus radiotherapy alone for patients with multiple brain metastases. Int J Radiat Oncol Biol Phys, 45, 427-34. Kwon KY, Kong DS, Lee JI, et al (2007). Outcome of repeated radiosurgery for recurrent metastatic brain tumors. Clin Neurol Neurosurg, 109, 132-7. Lee JD, Yoon JH, Chang HS, et al (2004). Brain metastases from well-differentiated thyroid carcinoma. Korean J Head Neck Oncol, 20, 7-12. Lee SN, Choo MS, Lee KJ, et al (1999). The role of radiotherapy in patients with brain metastasis. Radiation Oncol J, 17, 281-6. Lee YK, Park NH, Kim JW, et al (2008). Gamma-knife radiosurgery as an optimal treatment modality for brain metastases from epithelial ovarian cancer. Gynecol Oncol, 108, 505-59. Lichtor T (2013). Clinical management and evolving novel therapeutic strategies for patients with brain tumors. In Tech Chapter, 9, 193. Linskey ME, Andrews DW, Asher AL, et al (2010). The role of stereotactic radiosurgery in the management of patients with newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline. J Neurooncol, 96, 45-68. NECA (2011). Utilization Patterns and Comparative Effectiveness of Radiotherapy for Metastatic Brain Tumor (NA2010-011) Seoul, Korea: The National Evidence-based Healthcare Collaborating Agency (NECA). 33. Noel G, Medioni J, Valery CA, et al (2003). Three irradiation treatment options including radiosurgery for brain metastases from primary lung cancer. Lung Cancer, 41, 333-43. Park BJ, Kim YJ, Cho MK (2003). LINAC radiosurgery for metastatic brain tumors. J Korean Neurosurg Soc, 33,

276-80. Park SH, Hwang SK, Kang DH, et al (2009). Gamma knife radiosurgery for multiple brain metastases from lung cancer. J Clin Neurosci, 16, 626-9. Patil CG, Pricola K, Garg SK, et al (2010). Whole brain radiation therapy (WBRT) alone versus WBRT and radiosurgery for the treatment of brain metastases. Cochrane Database Syst Rev, 6, 6121. Rades D, Pluemer A, Veninga T, et al (2007). Whole-brain radiotherapy versus stereotactic radiosurgery for patients in recursive partitioning analysis classes 1 and 2 with 1 to 3 brain metastases. Cancer, 110, 2285-92. Sneed PK, Lamborn KR, Forstner JM, et al (1999). Radiosurgery for brain metastases: is whole brain radiotherapy necessary?. Int J Radiat Oncol Biol Phys, 43, 549-58. 39. Sneed PK, Suh JH, Goetsch SJ, et al (2002). A multiinstitutional review of radiosurgery alone vs. radiosurgery with whole brain radiotherapy as the initial management of brain metastases. Int J Radiat Oncol Biol Phys, 53, 519-26. SPSS (2007). PASW Statistics 17.0 Algorithms. SPSS, Inc. Tierney JF, Stewart LA, Ghersi D, et al (2007). Practical methods for incorporating summary time-to-event data into metaanalysis. Trials, 8, 16. Yang SY, Kim DG, Lee SH, et al (2008). Pulmonary resection tin patients with nonsmall-cell lung cancer treated with gamma-knife radiosurgery for synchronous brain metastases. Cancer, 112, 1780-6. Yoo H, Rhee CH, Yoon SM, et al (1999). Clinical analysis of 178 metastatic brain tumors. J Korean Neurosurg Soc, 28, 1185-93.. Asian Pacific Journal of Cancer Prevention, Vol 14, 2013 7407