"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead
Original article
peer-reviewed

Radiosurgery to the Postoperative Tumor Bed for Metastatic Carcinoma Versus Whole Brain Radiation After Surgery



Abstract

Background

The treatment paradigm from postoperative whole brain radiation therapy (WBRT) to post-operative stereotactic radiosurgery (SRS) to the tumor bed has shifted with little data to evaluate whether each treatment modality confers equivalent tumor control and survival outcomes.

Methods

Patients with surgical resection of single brain metastases from January 2010 to December 2014 were treated postoperatively with either WBRT or SRS. Retrospective patient data was compared for local control, distant brain recurrence, overall survival, and radiation complications.

Results

Forty-six received WBRT, and 37 received tumor bed SRS. Twelve of 35 (34%) SRS patients experienced local recurrence compared to 17 of 31 (55%) WBRT patients (p = 0.09). The median survival was 440 days (14.7 months) for SRS and 202 days (6.7 months) for WBRT (p = 0.062, log-rank). SRS demonstrated improved survival benefit in the first six months (p = 0.0034; Wilcoxon). Radiation-related adverse changes after SRS (22%) were not statistically different from WBRT (8.7%) (p = 0.152). Age (p = 0.08), systemic cancer status (p = 0.30), Graded Prognostic Assessment (p = 0.28), number of brain metastases at diagnosis (p = 0.65), tumor volume at diagnosis (p = 0.13), new brain lesions (p = 0.74) and neurologic versus systemic cause of death (p = 0.11) did not differ between the groups.

Conclusions

Following surgical resection, tumor bed SRS can be used effectively in lieu of WBRT to treat brain metastases with comparable local control and distant control and without significantly more adverse events.

Introduction

Traditionally, brain metastases have been treated with surgical resection followed by whole brain radiation therapy (WBRT) to decrease the rates of local recurrence, distant brain recurrence and neurologic cause of death [1-2]. Since it treats the entire brain, WBRT is thought to control tumor progression by treating identifiable metastases and otherwise unidentifiable micrometastases. However, WBRT has become increasingly implicated with global cognitive impairment that persists after cessation of treatment [3-4], thereby expanding concerns regarding quality of life despite reducing tumor burden. Furthermore, WBRT may not increase overall survival time [5-6]. Consequently, shifts in the treatment paradigm for brain metastases from postoperative WBRT to postoperative stereotactic radiosurgery (SRS) to the tumor bed are occurring [7].

SRS delivers high-dose radiations to a discrete volume within the brain. Because SRS spares healthy brain parenchyma, it confers a theoretically favorable alternative to WBRT and is being increasingly utilized in the management of brain metastases. SRS confers less cognitive decline in patients relative to WBRT [5, 8-10] and improved quality of life [11]. A number of studies have examined the ability of SRS to the post-resection tumor bed to control metastatic brain disease after tumor resection [12-27]. All of these studies, however, look only at populations of patients treated with SRS and do not compare outcomes between postoperative WBRT and SRS. Questions remain as to whether tumor bed SRS imparts long-term survival advantages equivalent to those of WBRT [9].

Based on these gaps in the understanding of the potential benefits of SRS to the post-resection tumor bed, we sought to compare the outcomes of patients who received surgical resection followed by either WBRT or SRS for brain metastases. We hypothesized that the outcomes related to tumor control of tumor-bed SRS would be clinically equivalent to those of postoperative WBRT without an increase in complications.

Materials & Methods

Patient data

All patients who received either surgical resection followed by WBRT or SRS for a presumed metastatic brain tumor from January 1, 2010 to December 31, 2014 at the University Hospital were retrospectively identified from patient treatment databases of the senior author [National Science Library (NSL)]. Patients were excluded if they were from the Veterans' Administration system or state prisoners (due to different Institutional Review Board processes), if they had no documentable follow-up after radiation treatment, or if they died within three months of treatment.

Waiver of consent was granted by the University of Missouri Health Sciences Institutional Review Board (IRB #1210881). Electronic medical records were reviewed for variables collected at the time of diagnosis, including age, sex, status of systemic disease outside of the brain (no evidence, stable, or progressive), number of brain metastases, site of primary malignancy (lung, breast, melanoma, colorectal, other), and tumor volume. Graded Prognostic Assessment (GPA) [28] was also determined. The data collected following treatment included chemotherapy received (yes or no), development of adverse radiation changes, management of adverse radiation changes (observation, steroids, or surgery), same site recurrence, distant recurrence within the central nervous system (CNS), and cause of death (neurologic or systemic).

Once the data was collected and collated, SRS patients were compared to WBRT patients for the outcome measures of local control, new brain metastases, overall survival, and adverse radiation changes.

Radiation treatment

Patients were chosen for SRS or WBRT at the discretion of the treating radiation oncologist and neurosurgeon in a non-randomized fashion. 

All SRS patients were treated with SRS using the Varian Trilogy TX linear accelerator system (Varian, Palo Alto, CA) at the Ellis Fischel Cancer Center, part of the University of Missouri Health System. Each patient underwent neuronavigational magnetic resonance imaging (MRI). In addition, the patient was immobilized with an Aquaplast Mask (Civco, Coralville, IA) which was attached to the couch. When appropriate, the patient was administered intravenous (IV) contrast dye, and axial images were obtained throughout the head for the planning computed tomography (CT) scan. Initially a bite block was constructed as a part of the immobilization apparatus, but this was discontinued in 2013 in favor of using Vision RT (London, UK). The planning CT scan was fused to the planning magnetic resonance image (MRI). The gross tumor volume (GTV) was contoured to the leading edge of the enhancement on gadolinium-enhanced T1-weighted axial MRI images at the site of the previously defined tumor for which the surgery was performed. The treatment plan was then optimized by dosimetry and physics using Varian Eclipse (Varian, Palo Alto, CA). Each plan used seven or eight static fields with a mini-multileaf collimator with 2.5 mm leaves. The prescription tumor volume (PTV) included a 2 mm expansion of the GTV as is usually done with frameless SRS [12-14, 16, 18, 25-27]. The dose to the margin was 1500 centigray (cGy) prescribed to the 80% isodose line for single fraction SRS. If the spherical diameter equivalent of the GTV exceeded 3 cm, then fractionated radiosurgery was performed in which the dose to the margin was 2100 cGy prescribed in three fractions to the 80% isodose line. Dose constraints to critical structures for single fraction SRS included the following: eyes - 800 cGy, optic nerves - 800 cGy, optic chiasm - 800 cGy, and brainstem - 1000 cGy.

The treatment plans were reviewed by the radiation oncologist and the neurosurgeon. Prior to each treatment, quality assurance was performed by physics on the multi-leaves, isocenter and cone beam. Immediately prior to each treatment, a cone beam CT was performed and compared to the reference CT and adjustments if any were made. A six degrees of freedom couch (Civco, Coralville, IA) was added when the Vision RT system was installed, which allowed for rotational adjustments of the couch at the time of treatment. Using the Vision RT system, the patient’s position during treatment delivery was monitored.

For whole brain radiation therapy, treatments were performed at Ellis Fischel Cancer Center or a nearby local community hospital. All patients were immobilized using the Aquaplast Mask. CT images were obtained for simulation. Typically, treatments were delivered using lateral or anterior oblique fields using photons. The doses were 3000 cGy delivered in 10 or 12 fractions.

Definitions

The status of systemic disease was defined on the basis of computed tomography/positron emission tomography (CT/PET) of the body or CT of the chest/abdomen/pelvis. Cause of death was defined as neurologic if the patient suffered progressive neurological deficits or symptoms indicative of elevated intracranial pressure with stable systemic disease; otherwise, the cause of death was defined as systemic (e.g. the patient died from infection, widespread tumor burden, cardiac events, or unknown). Time to treatment was measured between the date of surgery and the date of the first SRS or WBRT treatment. Same site recurrence was defined as the appearance of new enhancement or tumor growth in or immediately around the previously resected tumor bed on follow-up MRI, and distant recurrence was defined as evidence of tumor recurrence elsewhere within the brain. Adverse radiation events were defined as increased cerebral edema and enhancement after treatment with brain PET/CT indicative of a hypometabolic lesion with improvement on subsequent follow-up without surgical intervention or with pathological confirmation of radiation necrosis.

Statistical analysis

Summary statistics were used to assess patients’ characteristics. Means and standard deviations or medians were compared for numerical characteristics, such as age and number of metastases. Frequency distributions were compared for categorical characteristics such as sex, status of systemic disease, neurologic cause of death, chemotherapy treatment, and cancer primary. Two-sample t-tests were conducted to compare numerical characteristics between groups. Chi-square or Fisher's Exact tests were used to compare categorical characteristics between groups.

The Wilcoxon rank-sum test was used to test differences in tumor volume between groups. A log-normal survival model was used to assess the relationship between survival time and tumor volume or number of metastases. Wilcoxon rank-sum tests were used to assess the relationship between tumor volume and dichotomous outcomes, such as same site recurrence, distant recurrence, and radiation changes. The Mann-Whitney U-test was performed to assess the relationship between graded prognostic assessment and treatment type selected.

Overall survival (OS) was computed using the Kaplan-Meier method, and survival distributions were compared using a multivariate regression model adjusting for the following patient characteristics: age, sex, and status of systemic disease. A log-normal survival model was ultimately selected for this comparison.

The following binary outcomes were compared using the Chi-square test: same site recurrence, distant recurrence, and radiation changes. Odds ratios and 95% confidence intervals were reported. Due to concern that individuals who died within three months of surgical resection would skew results because of their presumed more severe disease, these patients were excluded from analysis of binary outcomes as previously stated. All 13 patients were treated with WBRT.

Data was analyzed using statistical software SAS 9.4 (SAS Institute Inc. Cary, NC, USA). A p-value of less than 0.05 was considered statistically significant.

Results

Patient demographics

Following surgery, 37 patients received SRS to the resection bed and 46 patients received WBRT. Age (p = 0.08), systemic cancer status (p = 0.30), number of brain metastases at diagnosis (p = 0.65), tumor volume at diagnosis (p = 0.13), chemotherapy regimen (p = 0.18), development of new brain lesions (p = 0.74), and neurologic versus systemic cause of death (p = 0.11) did not differ between the groups. GPA was not different between the groups (p=0.28). In both the groups, the most common primary was non-small cell lung cancer (NSCLC), followed by breast cancer and melanoma (Table 1). The tumor type also did not differ between the groups (p = 0.26).

  Surgery + SRS (n = 37) Surgery + WBRT (n = 46) p-Value
Age (mean ± SD) 63 ± 12 59 ± 8.5 0.080
Female 46% 57% 0.34
Number of metastases (median) 1.00 1.00 (n=41)b 0.65
Tumor volume (cm3) (mean + SD) 14.8 ± 8.5 19.5 ± 13.6 0.13
Time to treatment 20.5 ± 18.3 26.5 ± 10.5  
Status of systemic disease     0.34
         No evidence 11% 24%  
         Stable 22% 17%  
        Progressive 68% 59%  
Neurological cause of death 43% 66% 0.11
Grade Prognostic Assessment 2.5 ± 0.67 2.3 ± 0.70 0.28
Chemotherapy received 91% 80% 0.18
Cancer primary     0.26
          NSCLC 51% 52%  
          SCLC 0% 7%  
          Breast 14% 15%  
         Melanoma 16% 7%  
        Colorectal 11% 4%  

Of the patients in the SRS group, 34 (91.9%) had gross total resection and two (8.1%) had subtotal resection. The extent of resection did not differ (p = 0.47) for the WBRT group, with 44 (95.7%) with gross total resection and two (4.3%) with subtotal resection. SRS was performed 26.5 days (mean) after surgery. WBRT was started 20.5 days (mean) after surgery, these results were not different between groups (p = 0.092).

Overall survival

Median survival was 202 days (CI: 116, 295) for WBRT, and 440 days (CI: 218, 662) for SRS (Figure 1). Both log-rank and Wilcoxon tests were used to compare survival curves. Using the log-rank test, giving equal weight to all time points, overall survival was not statistically different between groups (p = 0.063). However, the Wilcoxon test, weighing early time points more heavily showed improved survival benefit for SRS over WBRT within the first six months (p = 0.0034). Four of 37 (10.8%) SRS patients died within the first six months compared to 15 of 46 (32.6%) WBRT patients.

Multivariate regression was performed using a log-normal model for survival time. Age (p = 0.83), male sex (p = 0.40), and status of systemic disease (p = 0.15) did not differ between groups and were selected as covariates based on their empirical, epidemiological association with poorer prognostic outcomes. The survival benefit conferred by SRS over WBRT remained statistically significant (p = 0.00034).

Local brain recurrence/control

Same site recurrence at the tumor bed developed in 34% of SRS patients and 55% of WBRT patients over the course of the study, but this difference was not statistically significant (p = 0.093). Local control rate at the tumor bed for SRS was 91.4% at six months, 65.2% at 12 months, and 40% at two years. WBRT local control rates at the tumor bed did not differ significantly, with 75.9%, 64.3% and 16.6% for the same time periods for surviving patients.

Distant brain recurrence/control

Distant brain recurrence (elsewhere from the surgical bed) occurred in 44% of SRS patients and 40% of WBRT patients (p = 0.74) over the course of the study. Distant control with SRS was similar to local control, with 82.9% at six months, 65.2% at 12 months, and 40% at 24 months. Distant control for WBRT patients was 75.9% at six months, 57.1% at 12 months and 50% at 24 months, not statistically different from SRS distant control. Ten SRS patients (26.1%) had salvage WBRT for local or distant recurrence and seven (15.2%) had salvage SRS. Two WBRT patients (4.3%) had salvage surgery and two (4.3%) had salvage SRS.

Radiation changes

Radiation-related adverse changes were not statistically more common with SRS (eight of 37; 21.6%) than with WBRT (four of 46; 8.7%) (p = 0.152) (Table 2)). Of the eight SRS patients who developed radiation-related changes, diagnosis was based on CT/PET in seven and surgery in one. Three were treated with observation alone, four were treated with corticosteroids alone, and one was treated with both surgery and corticosteroids. 

  Surgery + SRS n = 37 Surgery + WBRT n = 46 OR(95% CI) p-Value
Same site recurrence 34% 55% 0.43(0.15-1.16) 0.09
Distant recurrence 44% 40% 1.18(0.44-3.21) 0.74
Radiation changes 28% 10% 3.39(0.81-14.01) 0.081

Discussion

This study demonstrates that following surgical resection, SRS to the tumor bed has comparable treatment benefit to that of WBRT for patients with brain metastases. Local control, distant central nervous system control, and overall survival were similar. Furthermore, SRS appears to be associated with an early survival advantage. Local radiation-related changes were not significantly increased with SRS.

Our study differs from most other investigations of SRS to the post-resection tumor bed in that we directly compare our postoperative SRS patients to a group of patients treated with postoperative WBRT from the same institution over the same time period. In doing so, we hoped to minimize historical biases. However, we cannot fully account for our own selection bias of patients chosen for SRS or WBRT after their surgical resection. Addressing the issue of selection bias is important, particularly in view of our observation of an early survival advantage for the SRS patients. Unfortunately, the electronic medical record documentation does not adequately provide a rationale for the treatment plan chosen. Factors frequently identified with improved survival, such as age, GPA, and systemic cancer status also did not differ between groups [29-30]. Tumor volume and number of tumors treated were also identified as important prognostic factors [29] which were not significantly different as well. Thus, we cannot determine any patient selection bias for SRS in this retrospective study. Likewise, the reason for the observed early survival advantage is not definable. Even so, the observations that less WBRT patients received salvage therapy and more WBRT patients died within three months of surgery and were excluded from analysis suggests that WBRT patients likely had some degree of more severe disease contributing to selection bias. 

Our results are comparable to those reported in other studies which have examined rates of local control, distant control, survival, and adverse events after SRS to the post-resection tumor bed. The results of these studies are summarized in Table 3 for comparison. The margin dose in our study was similar to the lower end of the spectrum used in the other studies, which make the good results for SRS more compelling. Adverse radiation change in our study appears to be somewhat more frequent with 21.7% of patients having some changes on MRI. Most likely, this result relates to how radiation change was defined. Furthermore, of the eight patients with radiation-related changes in our study, seven (87.5%) were managed with observation or a course of glucocorticosteroids. Only five of 37 (13.9%) required treatment, with only one (2.7%) needing surgical intervention for pathologically confirmed radiation necrosis, a result consistent with reports from other series. Even though the rate of radiation change was not statistically different between SRS and WBRT in this study, a larger series of patients may have demonstrated differences in this regard, so caution is necessary in interpretation.

AUTHOR # of patients SRS delivery platform Margin dose (Gy) Survival Local control Distant control Adverse radiation effects Salvage WBRT
Brennan, et al. [12] 40 LINAC frame-based 15 – 22 14.7 78%§ 56%§ 17.5% 65.2%
Broemme, et al. [13] 44 LINAC frameless 17 – 18 15.9 87%; 63.5%§ 91% ; 77%§ 39% 2.3% 38%
Choi, et al. [14] 120 CyberKnife frameless 20 (median) 10 – 30 17 97% - 84%§ 65%; 54%§; 38% 3 – 8%  
Choi, et al. [15] 24 GammaKnife frame based 15 (median) 43.1%§; 23.7%& 82%; 71%§      
Do, et al. [16] 30 IMRT frame-based 15 – 18 51%§ 82%§ 37% total 69%§ 6.6% (spectroscopy) 47%
Hartford, et al. [17] 47 LINAC frame-based 10 (median) 8 – 20 52.5%§ 31.7% 85%§ 66.9% 44%§; 25%   49%
Iorio-Morin, et al. [6] 110 GammaKnife frame-based 18 11 84%; 73%§; 64% 58%   19% (edema) 32% (enhancement) 28%
Jagannathan, et al. [18] 47 GammaKnife frame-based 19 (mean) 12 94% (14 FU) 38% (5.6 FU) 11% (steroids)  
Jensen, et al. [19] 102 GammaKnife frame-based 17 (median) 10.8 46.8%§ 80.8% 35.4% 3% (surgery) 39%
Kalani, et al. [20] 68 GammaKnife frame-based 15 30.2 64.3%    
Karlovits, et al. [21]   LINAC 15 (median) 15.0   56% (16 months)   30.7%
Kelly, et al. [22] 18 LINAC frameless 18 (median) 15 – 18 89% 89% (12.7 FU) 65% (12.7 FU) 0%  
Luther, et al. [23] 120 GammaKnife frame-based 16 (median) 96% 87%§; 74% 85.8% 50% 3% 39.2%
Rwigema, et al. [24] 77 Cyberknife frameless 18 (median) 14.5; 91%; 62.5%§; 43.6% 76.1%76.1%§;74.3%   2.6% 26%
Soltys, et al. [25] 72 CyberKnife frameless 18 (median) 15 – 30 15.1 77%#; 57%§ 88%; 79%§ 70%; 47%§ 9.2% (steroids) 3.9% (surgery) 19%
Steinmann, et al. [26] 33 frameless fractionated 36 – 40   20.2 64%§ 30.4 71%§ 12.4 57%§ 0% 45.4%
Wang, et al. [27] 37 CyberKnife frameless fractionated 24   80% 80% 5.4%  
PRESENT STUDY 37 LINAC frameless 15 (median) 14.6 89.2% 91.4%; 65.2%§; 40% 82.9%‡; 65.2%§; 40%‖ 21.7% 10.8% (steroids) 2.7% (surgery)   26.1%

 

The potential value of an SRS treatment plan to the postoperative tumor bed cannot be understated. For patients with metastatic cancer of the brain surviving for longer periods of time after treating their brain disease, long-term quality of life and adverse sequelae associated with treatment are important considerations. Patients frequently express their fears regarding the potential negative effects of whole brain radiation, and studies have shown that long-term survivors of WBRT may incur cognitive and mobility impairments, both of which reduce quality of life. SRS has been shown to be superior to WBRT in terms of reducing cognitive impairment in patients with metastatic cancer to the brain [5, 8-10]. This study provides additional support for equivalence of clinical disease control. Additional work will be necessary to fully ascertain quality of life impacts.

This study has a few limitations. Like all retrospective studies, a number of unaccounted-for confounding factors could be present. The population size is small, which can mask true differences in outcome(s) between treatment groups. The rationale for decision to treat based on physician preference review of patients’ medical records does not readily lend insight into why SRS was selected over WBRT for many of the patients. A selection bias is likely present, and the patients in the SRS and WBRT groups were not matched. Neurocognitive and mobility functions were not formally assessed as outcome measures, thereby missing an opportunity for determination of a superior treatment. Nevertheless, despite these limitations, the study supports clinical equipoise of SRS to the postoperative tumor bed compared to WBRT after surgery.

Conclusions

Tumor bed SRS can be used to treat brain metastases effectively after surgical resection without significant adverse radiation effects, on par with WBRT. Given the potential for adverse effects of WBRT on cognition and mobility, treatment paradigms should strongly consider SRS to the postoperative tumor bed as the initial step after surgical resection of brain metastases.


References

  1. Kalkanis SN, Kondziolka D, Gaspar LE, Burri SH, Asher AL, Cobbs CS, Ammirati M, Robinson PD, Andrews DW, Loeffler JS, McDermott M, Mehta MP, Mikkelsen T, Olson JJ, Paleologos NA, Patchell RA, Ryken TC, Linskey ME: The role of surgical resection in the management of newly diagnosed brain metastases: a systemic review and evidence-based clinical practice guideline. J Neurooncol. 2010, 96:33–43. 10.1007/s11060-009-0061-8
  2. Patchell RA, Tibbs PA, Regine WF, Dempsey RJ, Mohiuddin M, Kryscio RJ, Markesbery WR, Foon KA, Young B: Postoperative radiotherapy in the treatment of single metastases to the brain: a randomized trial. JAMA. 1998, 280:1485–1489.
  3. Greene-Schloesser D, Moore E, Robbins ME: Molecular pathways: radiation induced cognitive impairment. Clin Cancer Res . 2013, 19:2294–2300. 10.1158/1078-0432
  4. Saad S, Wang TJ: Neurocognitive deficits after radiation therapy for brain malignancies. Am J Clin Oncol. 2015, 38:634–640. 10.1097/COC.0000000000000158
  5. Chang EL, Wefel JS, Hess KR, Allen PK, Lang FF, Kornguth DG, Arbuckle RB, Swint JM, Shiu AS, Maor MH, Meyers CA: Neurocognition in patients with brain metastases treated with radiosurgery or radiosurgery plus whole-brain irradiation: a randomised control trial. Lancet Oncol. 2009, 10:1037–1044. 10.1016/S1470-2045(09)70263-3
  6. Iorio-Morin C, Masson-Cote L, Ezahr Y, Blanchard J, Ebacher A, Mathieu D: Early Gamma Knife stereotactic radiosurgery to the tumor bed of resected brain metastasis for improved local control. J Neurosurg. 2014, 121:69–74.
  7. Sarpong Y, Litofsky MB, Litofsky NS: A paradigm shift in the radiation treatment of brain metastases. J Tumor. 2014, 2:223-230.
  8. Cole AM, Scherwath A, Ernst G, Lanfermann H, Bremer M, Steinmann D: Self-reported cognitive outcomes in patients with brain metastases before and after radiation therapy. Int J Radiat Oncol Biol Phys. 2013, 87:705–712. 10.1016/j.ijrobp.2013.07.037
  9. Tsao M, Xu W, Sahgal A: A meta-analysis evaluating stereotactic radiosurgery, whole-brain radiotherapy, or both for patients presenting with a limited number of brain metastases. Cancer. 2012, 118:2486–2493. 10.1002/cncr.26515
  10. Raber J, Rola R, LeFevour A, Morhardt D, Curley J, Mizumatsu S, VandenBerg SR, Fike JR: Radiation-induced cognitive impairments are associated with changes in indicators of hippocampal neurogenesis. Radiat Res. 2004, 162:39–47.
  11. Soffietti R, Kocher M, Abacioglu, Villa S, Fauchon, Baumert BG, Fariselli L, Tzuk-Shina T, Kortman R-D, Carrie C, Ben Hassel M, Kouri M, Valeinis E, van der Berge D, Mueller R-P, Tridello G, Collette L, Bottomley A: European organization for research and treatment of cancer phase II trial of adjuvant whole-brain radiotherapy versus observation in patients with one to three brain metastases from solid tumors after surgical resection or radiosurgery: quality of life results. J Clin Oncol. 2013, 31:65–72. 10.1200/JCO.2011.41.0639
  12. Brennan C, Yang TJ, Hilden P, Zhang Z, Chan K, Yamada Y, Chan TA, Lymberis SC, Narayana A, Tabar V, Gutin PH, Ballangrud A, Lis E, Beal K: A phase 2 trial of stereotactic radiosurgery boost after surgical resection for brain metastases. Int J Radiat Oncol Biol Phys. 2014, 88:130–136. 10.1016/j.ijrobp.2013.09.051
  13. Broemme J, Abu-Isa J, Kottke R, Beck J, Wiest R, Malthaner M, Schmidhalter D, Raabe A, Aebersold DM, Pica A: Adjuvant therapy after resection of brain metastases. Frameless image-guided LINAC-based radiosurgery and stereotactic hypofractionated radiotherapy. Strahlenther Onkol. 2013, 9:765–770. 10.1007/s00066-013-0409-z
  14. Choi CYH, Chang SD, Gibbs IC, Adler JR, Harsh GR, Lieberson RE, Soltys SG: Stereotactic radiosurgery of the postoperative resection cavity for brain metastases: prospective evaluation of target margin on tumor control. Int J Radiat Oncol Biol Phys. 2012, 84:336–342. 10.1016/j.ijrobp.2011.12.009
  15. Choi JW, Yong-Seok Im, Kong DS, Seol HJ, Nam DH, Lee JI: Effectiveness of postoperative gamma knife radiosurgery to the tumor bed after resection of brain metastases. World Neurosurg. 2015, 84:1752–1757. 10.1016/j.wneu.2015.07.045
  16. Do L, Pezner R, Radany E, Liu A, Staud C, Badie B: Resection followed by stereotactic radiosurgery to resection cavity for intracranial metastases. Int J Radiat Oncol Biol Phys. 2009, 73:486–491. 10.1016/j.ijrobp.2008.04.070
  17. Hartford A., Paravata A, Spire W, Jarvis LA, Fadul CE, Phodes CH, Erkmen K, Friedman J, Gladstone DJ, Hug EB, Roberts DW, Simmons NE: Postoperative stereotactic radiosurgery without whole-brain radiation therapy for brain metastases: potential role of the preoperative tumor size. Int J Radiat Oncol Biol Phys. 2013, 85:650–655. 10.1016/j.ijrobp.2012.05.027
  18. Jagannathan J, Yen C-P, Ray DK, Schlesinger D, Oskouian RJ, Pouratian N, Shaffrey ME, Larner J, Sheehan JP: Gamma Knife radiosurgery to the surgical cavity following resection of brain metastases. J Neurosurg. 2009, 111:431–438.
  19. Jensen CA, Chan MD, McCoy TP, Bourland JD, DeGuzman AF, Ellis TL, Ekstrand KE, McMullen KP, Munley MT, Shaw EG, Urbanic JJ, Tatter SB: Cavity-directed radiosurgery as adjuvant therapy after resection of brain metastasis. J Neurosurg. 2011, 114:1585–1591. 10.3171/2010.11.JNS10939
  20. Kalani MY, Filippidis AS, Kalain MA, Sanai N, Brachman D, McBride HL, Shetter AG, Smith KA: Gamma Knife surgery combined with resection for treatment of single brain metastasis: preliminary results. J Neurosurg. 2011, 113:90–96.
  21. Karlovits BJ, Quigley MR, Karlovits SM, Miller L, Johnson M, Gayou O, Fuhrer: R. Steretactic radiosurgery boost to the resection bed for oligometastatic brain disease: challenging the tradition of adjuvant whole-brain radiotherapy. Neurosurg Focus. 2009, 27:6. 10.3171/2009.9.FOCUS09191
  22. Kelly PJ, Lin YB, Yu AY, Alexander BM, Hacker F, Marcus KJ, Weiss SE: Stereotactic irradiation of the postoperative resection cavity for brain metastasis: a frameless linear accelerator-based case series and review of the technique. Int J Radiat Oncol Biol Phys. 2012, 82:95–101. 10.1016/j.ijrobp.2010.10.043
  23. Luther N, Kondziolka D, Mousavi JA, Engh JA, Niranjan A, Flickinger JC, Lunsford LD: Predicting tumor control after resection bed radiosurgery of brain metastases. Neurosurgery. 2013, 73:1001–1006. 10.1227/NEU.0000000000000148
  24. Rwigema J-CM, Wegner RE, Mntz AH, Paravati AJ, Burton SA, Ozhasoglu C, Heron DE: Stereotactic radiosurgery to the resection cavity of brain metastases: a retrospective analysis and literature review. Stereotact Funct Neurosurg. 2011, 89:329–337. 10.1159/000330387
  25. Soltys SG, Adler JR, Lipani JD, Jackson PS, Choi CYH, Puataweepong P, White S, Gibbs IC, Chang SD: Stereotactic radiosurgery of the postoperative resection cavity for brain metastases. Int J Radiat Oncol Biol Phys. 2008, 70:187–193. 10.1016/j.ijrobp.2007.06.068
  26. Steinmann D, Maertens B, Janssen S, Werner M, Fruhauf J, Nakumura M, Christiansen H, Bremer M: Hypofractionated stereotactic radiotherapy (hfSRT) after tumour resection of a single brain metastasis: report of a single-center individualized treatment approach. J Cancer Res Clin Oncol. 2012, 138:1523–1529. 10.1007/s00432-012-1227-x
  27. Wang C-C, Floyd SR, Chang C-H, Warnke PC, Chio C-C, Kasper EM, Mahadevan ET, Chen CC: Cyberknife hypofractionated stereotactic radiosurgery (HSRS) of resection cavity after excision of large cerebral metastasis: efficacy and safety of an 700 cGy x 3 daily fractions regime. ‎J Neurooncol. 2012, 106:601-610. 10.1007/s11060-011-0697-z
  28. Sperduto PW, Berkey BB, Gaspar LE, Mehta M, Curran W: A new prognostic index and comparison to three other indices for patients with brain metastases: an analysis of 1960 patients in the RTOG database. Int J Radiat Oncol Biol Phys. 2008, 70:510–514. 10.1016/j.ijrobp.2007.06.074
  29. Leth T, von Oettingen G, Lassen-Ramshad YA, Lukacova S, Høyer M: Survival and prognostic factors in patients treated with stereotactic radiotherapy for brain metastases. Acta Oncol. 2015, 54:107–14. 10.3109/0284186X.2014.921724
  30. Rades D, Gerdan L, Segedin B, Nagy V, Khoa MT, Trang NT, Schild SE: Brain metastasis. Prognostic value of the number of involved extracranial organs. Strahlentherapie und Onkologie. 2013, 189:996–1000. 10.1007/s00066-013-0442-y
Original article
peer-reviewed

Radiosurgery to the Postoperative Tumor Bed for Metastatic Carcinoma Versus Whole Brain Radiation After Surgery


Author Information

Kristen Scheitler-Ring

Division of Neurological Surgery, University of Missouri School of Medicine

Bin Ge

Office of Medical Research, University of Missouri School of Medicine

Greg Petroski

Office of Medical Research, University of Missouri School of Medicine

Gregory Biedermann

Division of Radiation Oncology, University of Missouri School of Medicine, Columbia, USA

N. Scott Litofsky MD Corresponding Author

Division of Neurological Surgery, University of Missouri School of Medicine, Columbia, Missouri, USA


Ethics Statement and Conflict of Interest Disclosures

Human subjects: Consent was obtained by all participants in this study. University of Missouri Health Sciences IRB issued approval IRB #1210881. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: This work was funded by The Bob Willis Medical Student Fellowship of the American Brain Tumor Association in 2015 to Kristen Scheitler-Ring, BS and a Medical Student Summer Research Fellowship from University of Missouri School of Medicine Office of Medical Research to Kristen Scheitler-Ring, BS. . Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Acknowledgements

This work was funded by The Bob Willis Medical Student Fellowship of the American Brain Tumor Association in 2015 to Kristen Scheitler-Ring, BS and a Medical Student Summer Research Fellowship from University of Missouri School of Medicine Office of Medical Research to Kristen Scheitler-Ring, BS. The work was presented in part at the American Association of Neurological Surgeons Annual Meeting, April 30 – May 4, 2016 in Chicago, Illinois. The authors also wish to acknowledge Dianne McConnell, DVM, PhD for her assistance with data analysis and William Kennedy, PhD for review and editing of the section on Radiation treatment.


Original article
peer-reviewed

Radiosurgery to the Postoperative Tumor Bed for Metastatic Carcinoma Versus Whole Brain Radiation After Surgery


Figures etc.

SIQ
6.0
RATED BY 3 READERS
CONTRIBUTE RATING

Scholary Impact Quotient™ (SIQ™) is our unique post-publication peer review rating process. Learn more here.