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Journal of Neuro-Oncology

, Volume 96, Issue 1, pp 103–114 | Cite as

The role of steroids in the management of brain metastases: a systematic review and evidence-based clinical practice guideline

  • Timothy C. Ryken
  • Michael McDermott
  • Paula D. Robinson
  • Mario Ammirati
  • David W. Andrews
  • Anthony L. Asher
  • Stuart H. Burri
  • Charles S. Cobbs
  • Laurie E. Gaspar
  • Douglas Kondziolka
  • Mark E. Linskey
  • Jay S. Loeffler
  • Minesh P. Mehta
  • Tom Mikkelsen
  • Jeffrey J. Olson
  • Nina A. Paleologos
  • Roy A. Patchell
  • Steven N. KalkanisEmail author
Open Access
Invited Manuscript

Abstract

Question

Do steroids improve neurologic symptoms in patients with metastatic brain tumors compared to no treatment? If steroids are given, what dose should be used? Comparisons include: (1) steroid therapy versus none. (2) comparison of different doses of steroid therapy.

Target population

These recommendations apply to adults diagnosed with brain metastases.

Recommendations

Steroid therapy versus no steroid therapy

Asymptomatic brain metastases patients without mass effect

Insufficient evidence exists to make a treatment recommendation for this clinical scenario.

Brain metastases patients with mild symptoms related to mass effect

Level 3 Corticosteroids are recommended to provide temporary symptomatic relief of symptoms related to increased intracranial pressure and edema secondary to brain metastases. It is recommended for patients who are symptomatic from metastatic disease to the brain that a starting dose of 4–8 mg/day of dexamethasone be considered.

Brain metastases patients with moderate to severe symptoms related to mass effect

Level 3 Corticosteroids are recommended to provide temporary symptomatic relief of symptoms related to increased intracranial pressure and edema secondary to brain metastases. If patients exhibit severe symptoms consistent with increased intracranial pressure, it is recommended that higher doses such as 16 mg/day or more be considered.

Choice of Steroid

Level 3 If corticosteroids are given, dexamethasone is the best drug choice given the available evidence.

Duration of Corticosteroid Administration

Level 3 Corticosteroids, if given, should be tapered slowly over a 2 week time period, or longer in symptomatic patients, based upon an individualized treatment regimen and a full understanding of the long-term sequelae of corticosteroid therapy.

Given the very limited number of studies (two) which met the eligibility criteria for the systematic review, these are the only recommendations that can be offered based on this methodology. Please see “Discussion” and “Summary” section for additional details.

Keywords

Brain metastases Steroids Neurologic symptoms Steroid dosage Systematic review Practice guideline 

Rationale

Glucocorticoids have typically been used to assist in controlling cerebral edema in the early supportive care of the patient with newly diagnosed metastatic brain disease. Dexamethasone is generally considered the steroid of choice because of its minimal mineralocorticoid effect and long half-life, although any other corticosteroid can be effective if given in equipotent doses. Steroids have been used alone for palliation of symptoms and in combination with radiotherapy as an initial course of therapy. A review of the available literature indicates that the majority of these patients have been managed with starting doses of 4–8 mg/day and it has been stated that up to 75% of patients with brain metastases show marked neurological improvement within 24–72 h after beginning dexamethasone [1]. However, side effects from chronic dexamethasone administration, including myopathy, are frequent and contribute to disability. Asymptomatic or minimally symptomatic patients may benefit little from the routine administration of steroid therapy and be exposed to these toxicities. Although successful clinical experience would lead to the conclusion that the role of steroids is firmly established in the management of brain metastases, even a cursory review of the literature will demonstrate significant variability in recommendations and a general lack of well-controlled studies addressing this specific issue.

This systematic review addresses the role of corticosteroids in the treatment of metastatic brain disease with the following overall objectives:
  1. 1.
    To systematically review the evidence available for the following treatment comparisons for patients diagnosed with brain metastases specifically addressing the following questions:
    • Do steroids improve neurologic symptoms in patients with metastatic brain tumors compared to no treatment?

    • If steroids are given, what dose should be used?

     
  2. 2.

    To make recommendations based on this evidence for the role of corticosteroids in the management of these patients.

     

Methods

Search strategy

The following electronic databases were searched from 1990 to September 2008: MEDLINE®, Embase®, Cochrane Database of Systematic Reviews, Cochrane Controlled Trials Registry, and Cochrane Database of Abstracts of Reviews of Effects. A broad search strategy using a combination of subheadings and text words was employed. The search strategy is documented in the methodology paper for this guideline series by Robinson et al. [2]. Reference lists of included studies were also reviewed.

Eligibility criteria

  • Published in English with a publication date of 1990 forward.

  • Patients with brain metastases.

  • Fully-published peer-reviewed primary comparative studies (all comparative study designs for primary data collection included; e.g., RCT, non-randomized trials, cohort studies or case-control studies).

  • Study comparisons include one or more of the following:

  • steroid therapy versus none.

  • comparison of different doses of steroid therapy.

  • Number of study participants with brain metastases ≥5 per study arm for at least two of the study arms.

  • Baseline information on study participants is provided by treatment group in studies evaluating interventions exclusively in patients with brain metastases. For studies with mixed populations (i.e., includes participants with conditions other than brain metastases), baseline information is provided for the intervention sub-groups of participants with brain metastases.

Study selection and quality assessment

Two independent reviewers evaluated citations using a priori criteria for relevance and documented decisions in standardized forms. Cases of disagreement were resolved by a third reviewer. The same methodology was used for full text screening of potentially relevant papers. Studies which met the eligibility criteria were data extracted by one reviewer and the extracted information was checked by a second reviewer. The PEDro scale was used to rate the quality of randomized trials [3, 4]. The quality of comparative studies using non-randomized designs was evaluated using eight items selected and modified from existing scales as outlined in Appendix B of the Methodology chapter in this brain metastases guideline series [2].

Evidence classification and recommendation levels

Both the quality of the evidence and the strength of the recommendations were graded according to the criteria endorsed by the American Association of Neurological Surgeons (AANS) and the Congress of Neurological Surgeons (CNS). These criteria are provided in the methodology paper of this guideline series.

Guideline development process

The AANS/CNS convened a multi-disciplinary panel of clinical experts to develop a series of practice guidelines on the management of brain metastases based on a systematic review of the literature conducted in collaboration with methodologists at the McMaster University Evidence-based Practice Center.

Scientific foundation

Despite the widespread use of steroids in the management of brain metastases, only two publications met the stated eligibility criteria [5, 6]. Figure 1 outlines the flow of studies through the review process. These two studies are outlined in the attached evidentiary table. In order to expand the information base for the “Discussion” section of this chapter, additional searches were undertaken by reviewing the bibliographies of these two papers and additional review of the published literature addressing the treatment of metastatic brain disease for references to steroid administration. These articles are summarized in the “Discussion”.
Fig. 1

Flow of studies to final number of eligible studies

Studies meeting search criteria

The only two papers that met the search criteria are summarized below [5, 6]. The details are also summarized in the accompanying evidentiary table (Table 1). In expanding the literature review to seek out additional supporting information for the "Discussion" portion of this document, we did not encounter any additional high quality studies specifically addressing the role of steroids in brain metastases. This was in agreement with several previous authors who upon review of the topic have encountered a lack of detailed, controlled accounts of steroid use in the studies under review, including the large randomized controlled trials that often form the basis of treatment decisions and recommendations [1, 7, 8, 9].
Table 1

Summary of studies meeting the systematic review eligibility criteria

First author (year): Vecht et al. (1994), [5]

Study characteristics

Study outcomes

Study quality

Study design RCT (two trials reported)

Inclusion criteria for both RCTs

KPS < 80, histologically confirmed diagnosis of solid cancer outside nervous system, together with single or multiple BM diagnosed by CT

Exclusion criteria for both RCTs

Age > 75 years; KPS = 90 or 100; prior RT to brain; likelihood of early treatment with neurosurgery; glucocorticoid administration in the previous 3 months; BM secondary to lymphoreticular malignancy; diabetes mellitus or disability due to causes other than BM

Interventions

First RCT

 G1: dexamethasone 8 mg/day p.o. × 7 day (then tapered to discontinue)

 G2: dexamethasone 16 mg/day p.o. × 7 day (then tapered to discontinue)

Second RCT

 After G1 versus G2 not significantly different at day 7

 G3: Dexamethasone 4 mg/day p.o. × 28 day (then tapered to discontinue)

 G4: Dexamethasone 16 mg/day p.o. × 28 day (then tapered to discontinue)

Notes: all pts scheduled for RT to started at some point after Day 7

(RT dose/schedule not reported); all pts received ranitidine 150 mg bid

Median follow-up: not reported

# male:

G1: 14/20; G2: 14/22; G3: 12/24; G4: 7/23

Median age (range): median not reported; mean age ± SD:

G1: 61 ± 7.6 years

G2: 61 ± 11.5 years

G3: 60 ± 9.9 years

G4: 56 ± 10.9 years

Predominant tumor types:

G1: lung 11/20, breast 4/20, gastrointestinal 4/20, other 1/20

G2: lung 10/22, breast 6/22, kidney 3/22, gastrointestinal 1/22

G3: lung 10/24, breast 7/24, kidney 3/24, gastrointestinal 1/24

G4: lung 12/23, breast 5/23, gastrointestinal 2/23, kidney 2/23

# of brain metastases:

Not reported

Extra-cranial disease:

Note reported

Baseline functional performance:

Mean KPS ± SD (range)

 G1: 58.5 ± 11.8 (40–80)

 G2: 61.4 ± 9.4 (50–80)

 G3: 65.0 ± 10.6 (40–80)

 G4: 57.8 ± 14.1(30–80)

Primary outcome

Change in KPS on day 7 from day 0

First RCT

Mean (SD) absolute change in KPS at day 7:

G1: 8.0 ± 10.1; G2: 7.3 ± 14.2 (P = NS)

% pts with improved KPS on day 7:

G1: 60%; G2: 54%

Mean (SD) absolute change in KPS at day 28:

G1: 6.7 ± 18.4; G2: 13.8 ± 14.5 (P = NS)

% pts with improved KPS on day 28:

G1: 53%; G2: 81%

Second RCT

Mean (SD) absolute change in KPS at day 7:

G3: 6.7 ± 11.3; G4: 9.1 ± 12.4 (P = NS)

% pts with improved KPS on day 7:

G3: 67%; G4: 70%

Mean change in KPS (SD) at day 28

G3: 7.1 ± 18.2; G4: 5.6 ± 18.5 (P = NS)

% pts improved:

G3: 62%; G4: 50%

Adverse events: reported combined results

Toxic effects more frequent in G2 + G4 (16 mg) (P < 0.03)

Incidence of cushingoid facies or ankle edema increased with duration of treatment (P = 0.02 at day 7 and P = 0.03 at day 28) and with higher doses of dexamethasone

At day 28: reported combined results from both RCTs

Raised glucose:

G1: 25%; G2/G4: 21%; G3: 18%

Raised blood pressure:

G1: 12%; G2/G4: 26%; G3: 45%

Infectious disease:

G1: 6%; G2/G4: 9%; G3: 9%

Gastrointestinal complaints:

G1: 6%; G2/G4: 24%; G3: 18%

Mental changes:

G1: 19%; G2/G4: 21%; G3: 14%

Ankle edema:

G1: 13%; G3: 14%; G2/G4: 26%

Cushingoid facies:

G1: 69%; G3: 32%; G2/G4: 65%

Proximal weakness:

G1: 38%; G3: 14%; G2/G4: 38%

AANS/CNS evidence classification: Class 1

Due to the relatively small size, heterogeneity in study design and lack of clarity in the statistical presentation and analysis there are concerns about over generalizing the results and conclusions of this trial.

First author (year): Wolfson et al. (1994), [6]

Study design: prospective randomized phase II trial [stratified by response to high-dose dexamethasone]

Inclusion criteria

Measurable BM on CT; histologically confirmed primary malignancy; granulocyte counts >1,000/mm3 and serum glucose <300 mg%

Exclusion criteria

Primary malignancies including lymphomas, germ cell tumors, primary CNS tumors, SCLC, multiple primaries, and unknown primaries; resected BMs; illnesses such as active peptic ulcer disease, uncontrolled diabetes mellitus (serum glucose ≥ 300 mg%), adrenal insufficiency or being seropositive for HIV

prior cranial RT; administration of steroid therapy more than 24 h prior to study entry

Interventions

G1: dexamethasone 24 mg i.v. every 6 h for 48 h prior to WBRT; then dexamethasone 4 mg p.o. every 6 h for 2 weeks during WBRT

G2: dexamethasone 24 mg i.v. every 6 h for 48 h prior to WBRT

Doses

G1: WBRT: 30 Gy at 3 Gy/fraction

G2: WBRT: 30 Gy at 3 Gy/fraction

Note: all pts given H-2 blockers during steroid administration and oral phenytoin for seizure prophylaxis

Median follow-up: not reported

# male

G1: 2/7; G2: 3/5

Median age (range): not reported by treatment group

Overall median age: 58 years

Tumor type

G1: NSCLC 5/7, breast 2/7

G2: NSCLC 3/5, breast 1/5, bladder 1/5

# of brain metastases

G1: 1 BM 2/7, 2 BM 4/7, >2 BM 1/7

G2: 1 BM 2/5, 2 BM 1/5, >2 BM 2/5

Extra-cranial disease: Extra-cranial metastases:

G1: 5/7; G2: 3/5

Baseline functional performance

Not reported

Primary outcome

Overall survival

Survival

Overall median survival: 4 months (no between group statistical analyses due to limited pt numbers)

Functional performance

Change in general performance status:

G1: improved 2/7, deteriorated 1/7, no change 4/7

G2: improved 0/5, deteriorated 1/5, no change 4/5

Change in neurological function class:

G1: improved 1/7, deteriorated 1/7, no change 5/7

G2: improved 0/5, deteriorated 1/5, no change 4/5

Cause of death

Non-specific and not reported by treatment group

Adverse events/other

Transient hyperglycemia: 1/12

AANS/CNS evidence classification: class 1

Despite this qualifying as class I the small size and lack of any statistical analysis render this article useless for any recommendations.

Abbreviations: BM brain metastases, CNS central nervous system, G1 Group 1, G2 Group 2, G3 Group 3, G4 Group 4, KPS Karnofsky performance score, NSCLC non-small cell lung cancer, NR not reported, Pts patients, RCT randomized control trial, RT radiotherapy, SCLC small cell lung cancer, SD standard deviation, WBRT whole-brain radiation therapy

The first of the two studies to meet the search criteria described a randomized study of 4, 8 and 16 mg/day dosing of dexamethasone and found no advantage to higher dosing in patients who were not felt to be in impending danger of cerebral herniation [5]. Vecht et al., published their findings from two consecutively executed double-blind randomized trials in patients with brain metastases and Karnofsky performance scores (KPS) of 80 or less which were designed to evaluate the minimum effective dose of oral dexamethasone. Initially a dexamethasone dosage of 8 mg/day (Group 1) was compared to 16 mg/day (Group 2), followed by a comparison of 4 mg/day (Group 3) versus 16 mg/day (Group 4). The outcomes of interest were alteration in KPS and the frequency of side effects at days 0, 7, 28, and 56.

In the initial study, although both groups showed an improvement, there was no significant difference in KPS improvement comparing the 8-mg group versus the 16-mg group at day 7 (mean 8.0 ± 10.1 versus 7.3 ± 14.2). At the 28 day point, there was a larger but still non-significant rate of improvement thought to be biased by earlier steroid tapering in the lower group.

In the second trial, again both groups showed improvement. However, no significant difference between the 4- and 16-mg group (comparing 6.7 ± 11.3 points at day 7 and 7.1 ± 18.2 points at day 28, versus 9.1 ± 12.4 and 5.6 ± 18.5 points, respectively) could be detected. Side effects (Cushingoid changes and extremity edema) occurred more frequently in the 16 mg/day versus the 4 mg/day group at Day 28 (Combined frequency 91% versus 46%, P < 0.03).

The authors conclude that for the majority of patients, the lower doses of 4 and 8 mg dexamethasone per day have an equivalent effect on improving neurologic performance when compared to a dose of 16 mg/day at 1 and 4 weeks of treatment, in moderately symptomatic patients without signs of impending herniation. A non-significant trend toward improvement at 28 days was noted with the higher dosage. The authors postulated that the early taper in the lower dosage group led to an increase in recurrence of symptoms that may have increased this apparent effect. The dosing recommendation from this study resulted in a set 4 mg/day dosage with a dose taper for 28 days in patients with no symptoms of mass effect used for the second study.

Side effects appeared to be dose-dependent, occurring more frequently in patients using 16 mg/day. Therefore, the authors concluded that steroid related toxicity was increased with the higher daily dosage. Although the study is double blind and randomized, the relatively small size, inconsistencies in the design and lack of clarity in the presentation of the data and analysis are concerns. Nonetheless, this work appears to be the most detailed and informative available to assist with formulating treatment recommendations. The data, while extremely limited, support a set of treatment recommendations which follow a general trend toward higher steroid dosages in symptomatic patients exhibiting greater mass effect symptoms of increased intracranial pressure, as opposed to lower doses of steroids for asymptomatic patients.

Wolfson et al. [6] prospectively studied 12 patients with histologically confirmed malignancies and radiographically documented brain metastases and attempted to evaluate the indications for glucocorticoids. Patients were scored for general performance status and neurologic function class. All subjects received 24 mg of intravenous dexamethasone every 6 h for 48 h and after an assessment, were randomized to receive either 4 mg of oral dexamethasone every 6 h (Group 1) or no steroids (Group 2) during radiotherapy (30 Gy in ten fractions). Prior to randomization, five (33%) had a positive response and eight (67%) had no response to the high dose level. Seven patients were randomized to continue receiving steroids at the reduced level and five received none during radiotherapy. The change in general performance status for Group 1 was: Improved 2/7 (29%), deteriorated 1/7 (15%), no change 4/7 (57%). For Group 2, the change in performance status was: Improved 0/5 (0%), deteriorated 1/5 (20%) and no change 4/5 (20%). The change in neurological function for Group 1 was: Improved 1/7 (14%), deteriorated 1/7 (14%), no change 5/7 (72%); change in neurological function for Group 2 was: Improved 0/5 (0%), deteriorated 1/5 (20%), no change 4/5 (80%). No statistical analysis was performed due to the small sample size. The authors conclude that the specific role of steroids in treating patients with metastatic carcinoma to the brain remains uncertain and should be evaluated in a cooperative prospective trial. Due to the small size and lack of any statistical analysis, it is impossible to reach any conclusion based on this study; therefore, no recommendations will be made based on this small trial.

Discussion

Role of steroids in metastatic brain disease

Given the extremely limited number of studies which satisfied the conditions of our search criteria, an additional discussion of published literature on the subject of corticosteroids in metastatic brain disease is provided to offer a larger context for this topic. While the following studies were not part of the body of evidence considered in formulating treatment recommendations in our evidence-based guidelines, they do highlight areas of interest where clinical trials are still required to answer important steroid-related questions.

A review of the outcomes in the Radiation Therapy Oncology Group (RTOG) studies examining various radiotherapeutic regimens for patients with metastatic brain disease demonstrated a dramatic early improvement in patients treated concurrently with steroids during the early phases of the trials [10]. However, as the authors note, the administration of steroids was not well controlled in these studies and was not a primary point of interest so, although these observations contributed to the overall clinical impression that steroids were of benefit in the adjuvant treatment of brain metastases, it is difficult to extrapolate treatment recommendations from these studies. In Borgelt et al., this is shown by the fact that symptomatic patients receiving steroids had a significant improvement in neurological function as opposed to those who did not receive steroids. None of these studies suggested that the use of steroids halted time to progression.

Gaspar et al. [7] published an American College of Radiology (ACR) Committee on Appropriateness Criteria consensus report following an expert panel review on the pre-irradiation evaluation and management of brain metastases. The authors cite six articles to support the generation of their expert opinions [5, 6, 10, 11, 12, 13]. They initially note that although clinical experience has established the effectiveness of corticosteroids in reducing symptoms and radiographic peritumoral edema, controversy remains on the specific indications and dosage used. They point out that the earliest studies to support steroid use prior to radiotherapy used radiation dosing schemes that are presently atypical and that there was evidence that steroids were only indicated when there was a concern about raised intracranial pressure [10, 11, 12]. In one study, 27% of patients who received 10 Gy of single fraction whole brain radiotherapy (WBRT) experienced signs of increased intracranial pressure [12]. They also note evidence from one trial indicating that patients who were moderately symptomatic who received steroid therapy during radiation experienced a more rapid improvement in their clinical symptoms, although there was no impact on progression-free or overall survival. This review went onto outline several papers addressing the acute and chronic side effects and the studies that address dosing and toxicity [5, 6, 13].

This consensus review summarizes the authors’ views on steroid use for metastatic brain disease by indicating that the patient who shows evidence of elevated intracranial pressure, but who does not require immediate surgical attention for either hydrocephalus or impending herniation, should receive 4–6 mg/day of dexamethasone in divided doses and that the routine use of corticosteroids in patients without neurological symptoms is not necessary.

Effect of steroids on radiographic edema

In 1982, Hatam et al. [14] prospectively studied the effect of dexamethasone therapy on peritumoral edema based on computed tomography (CT) describing specifically three cases of metastatic intracranial disease in which a linear decrease in edema volume was observed, reducing the measured volume of edema to one-fourth of the initial volume after 2 weeks of treatment starting with 4 mg four times daily and tapered to 1 mg/day. The exact time course for the metastatic patients was not reported separately but the authors did report a substantial clinical improvement in these patients they felt was associated with the use of dexamethasone.

Andersen et al. [11] published a subsequent report in 1994 that quantified the effect of steroid therapy over time on peritumoral brain edema in vivo using a magnetic imaging based technique. Magnetic resonance based assessments of peritumoral edema were undertaken on 23 brain tumor patients including 13 with brain metastases at baseline and at Days 1, 3 and 7 after starting steroid therapy. Intravenous dexamethasone was used at dose of 0.26–0.64 mg/kg (for a 70 kg patient this range is 20–45 mg/day). After 7 days of steroid treatment the total edema area was reduced by 10.3% in the metastatic patients, with an average reduction in mean volume of 4.6% after 24 h of treatment and 13.5% after 7 days. This effect was observed for up to 63 days and it was demonstrated that after 40–63 days (6–9 weeks) of steroid therapy the peritumoral water content was close to the upper normal range for white matter. The authors concluded that steroids significantly reduce the volume of peritumoral edema in patients with metastatic brain disease even after a few days of treatment. They postulate a mechanism of steroid-induced reduction in edema below the level of absorption and commented that they thought they may have obtained the same effects with a dose-reduction to minimize potential side effects.

Minamikawa et al. [15] studied the effect of glucocorticoid treatment (methylprednisolone, dose not specified) on the apparent diffusion coefficient (ADC) imaging in a series of 13 patient including four with metastatic brain disease. Although it is not possible to examine the effects on the metastatic patients separately, the authors suggested that ADC imaging was a more sensitive technique than conventional MRI imaging for studying the effects of steroids on peritumoral edema, even in the absence of detectable MRI changes.

Dosing and toxicity

Hempen et al. [13] retrospectively reviewed 138 consecutive patients to evaluate the impact of dosage and duration of dexamethasone administration during radiation therapy for patients with both primary and metastatic brain tumors (n = 91). The dosage of dexamethasone was gradually reduced from an initial median dose of 7–12 mg/day to a median of 1–6 mg/day with an average duration of 7 weeks for the metastatic group. The authors reported a period of initial clinical improvement with relatively few side effects. Specifically, 33% of patients reported improvement in symptoms with steroid use prior to radiotherapy, 44% during radiotherapy and 11% following radiotherapy. However, as dexamethasone was continued, this trend reversed and less symptom relief was observed with increasing toxicity. Life-threatening complications were rare. Side effects attributed to steroid use included: hyperglycemia (47%), peripheral edema (11%), psychiatric disorder (10%), candidiasis (7%), Cushing’s syndrome (4%), muscular weakness (4%) and pulmonary embolus (2%). Of a cohort of 13 clinically asymptomatic patients who received no dexamethasone during radiotherapy, 12 (92%) showed no sign of worsening neurological problems. The patient with worsened symptoms had brain stem involvement. The authors conclude that dexamethasone effectively minimizes neurological symptoms and radiation therapy related side effects in patients with both primary and secondary brain tumors. The toxicity of dexamethasone was noted to increase over time and therefore a patient-specific dosing pattern and taper was recommended. The authors suggested that a prospective study specifically addressing the relative balance of symptom relief versus toxicity would be of benefit and that there is little evidence to support the use of steroids in the asymptomatic patient.

In 1999, Lagerwaard et al. [8] published an extensive retrospective review of 1,292 patients with metastatic brain disease referred to a single institution to identify prognostic (risk) factors. The majority of patients were treated with WBRT (n = 1,079, 84%); 118 (9%) were treated with steroids only and 95 (7%) with surgery and radiotherapy. Data obtained included: age, sex, performance status, number and distribution of brain metastases, site of primary tumor, histology, interval between primary tumor and brain metastases, systemic tumor activity, serum lactate dehydrogenase, response to steroid treatment, and treatment modality. Dexamethasone was used in a dose range of 4–16 mg/day (mean dosage 14.6 mg/day), which was “tapered slowly and discontinued in the weeks following therapy” (specific details not stated).

Response to steroid therapy was judged retrospectively, from review of the medical records, as good (marked improvement), moderate (some improvement) or little (little or no improvement). Both univariate and multivariate analyses were performed. The overall median survival was 3.4 months, with 6 month, 1, and 2 year survival percentages of 36, 12, and 4%, respectively. Median survival was 1.3 months in patients treated with steroids only, 3.6 months in patients treated with radiotherapy, and 8.9 months in patients treated with surgical resection followed by radiotherapy (all comparisons P < 0.0001).

Multivariate analysis confirmed the previously reported observation that the impact of treatment modality on survival in patients with brain metastases was the most significant single factor in predicting survival. However, response to steroid treatment, performance status, systemic tumor activity and serum lactate dehydrogenase levels were also all independent prognostic factors on survival, second only to treatment modality in level of significance. Site of primary tumor, age, and number of brain metastases were also identified as prognostic factors.

The authors concluded that the strongest prognostic (risk) factors were choice of treatment modality, response to steroids, performance status, and evidence of systemic disease and they proposed using these classifiers in identifying favorable and unfavorable subgroups of patients with brain metastases for future studies.

Millar et al. [9] attempted to assess the impact of steroid therapy in the management of brain metastases by undertaking a systematic review of published randomized trials on WBRT for multiple cerebral metastases. In this extensive review published in 2004, the authors identified 21 full manuscripts of published randomized controlled trials involving WBRT in the treatment of multiple brain metastases from 1971 to 2003. They attempted to extract details on the use and type of steroid, timing of steroids relative to radiotherapy, response assessment and contribution of steroids to overall outcome. They reported that 18 of the 21 trials reviewed documented steroid use. Overall survival was an outcome assessed in all studies. Thirteen studies assessed neurological response and ten assessed a radiographic endpoint. Ten of the studies (48%) suggested a positive effect of steroid use on the outcome assessed. Only one study—in the palliative setting—provided a fixed steroid dose.

The authors concluded that the reporting of steroid use in previously published randomized trials assessing treatment for patients with brain metastases is “non-uniform and not sufficiently detailed” making it difficult to assess the treatment effect. They call for a more standard approach to steroid dose in future studies or at a minimum better reporting of dosages used to better determine symptom response and durability of response. They also note that side effects of steroid use and the ability to taper off steroids after treatment intervention are additional outcomes of interest in the planning of future studies.

Weissman et al. [16] published their experience with a treatment regimen designed to reduce steroid toxicity in 20 patients with newly diagnosed brain metastases. All patients received dexamethasone starting at 8 mg twice daily for 4 days then 4 mg twice daily for 4 days followed by 2 mg twice daily until the last day of radiation therapy. Radiation dose and schedules ranged from 20 Gy in five fractions to 58 Gy in 29 fractions. Fourteen patients (70%) received dexamethasone for a minimum of 24 h before their first radiation treatment and seven of those patients (50%) experienced improvement in neurologic symptoms and signs before radiotherapy. Fourteen patients (70%) completed the entire course of radiation and dexamethasone as planned. One patient required reinstitution of dexamethasone within 30 days of finishing radiation for neurological decline. The authors felt that the twice-daily dose was well tolerated. Steroid related toxicity included hyperglycemia (5%), candida esophagitis (5%), steroid pseudorheumatism (10%), peripheral edema (5%) and steroid withdrawal syndrome (5%).

In 2006, the results of a series of systematic reviews with the stated purpose “to establish evidence-based guidelines and identify controversies regarding the management of patients with brain metastases” was published by Soffietti et al. [1]. This was conducted by a multi-disciplinary task force of the European Federation of Neurological Societies and includes a review of data obtained from the Cochrane Library, bibliographic databases, overview papers and previous guidelines from scientific societies and organizations. Under the section on supportive care and steroids only one original article is cited and reviewed, and that is the publication by Vecht [5], which also met the eligibility criteria for this guideline paper and is discussed extensively in the scientific foundation section. This paper was used to support the recommendation that, in most cases, initial dexamethasone doses should not exceed 4–8 mg/day. However, in patients with more severe symptoms related to increased intracranial pressure doses of 16 mg/day or higher should be considered (Level of Evidence B) [17]. The remainder of the recommendations were based on uniform consensus of the task force (referred to as a “Good Practice Point”) and are summarized below. Dexamethasone was noted as the corticosteroid of choice and twice daily dosing was thought to be sufficient (Good Practice Point). Tapering of steroid dosing within 1 week of starting therapy and discontinuation within 2 weeks if possible was encouraged (Good Practice Point). Finally, patients who do not have signs or symptoms of increased intracranial pressure do not have to be treated with steroids (Good Practice Point).

Given the very limited number of studies that met the inclusion criteria for the systematic literature review on the role of steroids in metastatic brain disease, we are unable to propose specific guidelines on many of the issues of central interest to the treating physician.

In summarizing the Discussion section above we are able to offer the following observations: first, Overall the literature favors the position that corticosteroids are of benefit in providing temporary symptomatic relief of CNS symptoms related to increased intracranial pressure and edema secondary to brain metastases [1, 7, 8, 9, 10, 13]. Secondly, dexamethasone is the steroid most often used, with the rationale that it has limited mineralocorticoid effects. Other steroids have been used with similar reported clinical responses. Dosing has been recommended to be sufficient at twice daily although more frequent dosing has been suggested with increasing concern for raised intracranial pressure and impending herniation [1, 7, 8, 11, 14]. Finally, based primarily on the asymptomatic patients in the study by Hempen et al., it is the opinion offered in the available studies that asymptomatic patients do not require steroids [1, 7, 13]. Numerous authors cite concerns for the toxicity of steroid therapy and due to the lack of a uniform recommendation on dosing and the apparent complexity of the response in individual patients it has been recommended that dose reduction be considered within 1 week of initiation of treatment. The dose reduction appears to often require alteration in individual patients due to the diversity of response [1, 7, 9, 13, 16].

An interesting observation in the review of the literature on this subject is the number of authors who appear to assume that steroids are a mainstay of treatment for the patient with metastatic brain disease despite the relative lack of detailed information available to guide specific therapy. In general, the evidence for specific dosages and regimens of steroids are poorly detailed. On the other hand, there is very little information provided in the literature that suggests that steroids are of no benefit in this patient population with the exception of the asymptomatic patient.

Given the general consensus in the literature that steroids are of benefit in selected patients with metastatic brain disease and the frequent observation that dosing needs to be specifically tailored to the individual, it appears unlikely that in depth studies specifically addressing this issue will be forthcoming. However, the need for additional recommendations for dosing and duration of therapy may result in an increased awareness of this concern and potentially an alteration of clinical trials designed to address comparisons.

Summary and conclusions

In terms of articles meeting the search criteria described in the methods section above, the study by Vecht et al. [5] stands alone in providing the most convincing data on the role for steroids in patients with brain metastases and for the choice of dosing. Based on their observations of improvement in all groups treated with steroids, a level 3 recommendation can be made as follows:

Steroid therapy versus no therapy

Corticosteroids are recommended to provide temporary symptomatic relief of CNS symptoms related to increased intracranial pressure and edema secondary to brain metastases. (Level 3 recommendation). Dexamethasone is the corticosteroid of choice, mainly because of its limited mineralocorticoid effects, and should be tapered slowly over several weeks to avoid rebound symptoms.

The Vecht et al. [5] article provides evidence that the administration of steroids provides relief of symptoms in patients with symptomatic brain metastatic disease; however, recognizing that there is no control group (a “no treatment group”) only the lowest grade of recommendation can be made.

Vecht et al. [5] also conclude that a starting dose of 4–8 mg/day be considered, unless patients exhibit severe symptoms consistent with increased intracranial pressure. They further recommended that those patients at high risk for severe consequences from raised intracranial pressure be considered for more aggressive dosing on the order of doses of 16 mg/day or higher. This study is relied upon heavily in the systematic review and consensus reports summarized in the "Discussion" section above [1, 7, 9]. However, the number of patients involved is relatively small and the study lacks a validation group; thus, despite the randomized design and ranking yielding a higher class of evidence, the recommendation itself is downgraded to reflect these concerns. Based on this study design and results, the following recommendation can be made.

Comparison of different doses of steroid therapy

It is recommended for patients who are symptomatic from metastatic brain disease that a starting dose of 4–8 mg/day of dexamethasone be considered, unless patients exhibit severe symptoms consistent with increased intracranial pressure. In these patients it is recommended that higher doses such as 16 mg/day or more be considered. (Level 3 recommendation)

Key issues for further investigation

Given the number of patients who receive steroids as a portion of their care for treating the signs and symptoms of brain metastases, the medical literature contains relatively few detailed reports specifically addressing this issue. It may be that the early observation that there was little effect on overall survival has limited the subsequent level of interest in this issue. Review of the literature finds that the majority of authors on the subject feel that there is a symptomatic benefit from the use of systemic steroids in the management of these patients. It is not clear that there is an urgent need for randomized trials specifically addressing the issue of steroid dosing and toxicity. However, future studies could be planned to allow better control, recording and analysis of steroid dosing and response to allow a more robust analysis of the risk to benefit ratio of various dosing regimens. This would potentially optimize the benefits while limiting the side effects, which could lead to an improvement in overall outcome in addition to improving quality of life measures in the short term.

No ongoing or recently closed clinical trials on the use of steroids for the management of brain metastases were found that met the eligibility criteria.

Notes

Acknowledgments

We would like to acknowledge the contributions of the McMaster Evidence-based Practice Center (EPC), Dr. Parminder Raina, (Director). Dr. Lina Santaguida (Co-Associate Director, Senior Scientist) led the EPC staff, which was responsible for managing the systematic review process, searching for and retrieving, reviewing, data abstraction of all articles, preparation of the tables and the formatting and editing of the final manuscripts.

Disclaimer of liability

The information in these guidelines reflects the current state of knowledge at the time of completion. The presentations are designed to provide an accurate review of the subject matter covered. These guidelines are disseminated with the understanding that the recommendations by the authors and consultants who have collaborated in their development are not meant to replace the individualized care and treatment advice from a patient’s physician(s). If medical advice or assistance is required, the services of a competent physician should be sought. The proposals contained in these guidelines may not be suitable for use in all circumstances. The choice to implement any particular recommendation contained in these guidelines must be made by a managing physician in light of the situation in each particular patient and on the basis of existing resources.

Disclosures

All panel members provided full disclosure of conflicts of interest, if any, prior to establishing the recommendations contained within these guidelines.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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Copyright information

© The Author(s) 2009

Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://creativecommons.org/licenses/by-nc/2.0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

Authors and Affiliations

  • Timothy C. Ryken
    • 1
  • Michael McDermott
    • 2
  • Paula D. Robinson
    • 3
  • Mario Ammirati
    • 4
  • David W. Andrews
    • 5
  • Anthony L. Asher
    • 6
  • Stuart H. Burri
    • 7
  • Charles S. Cobbs
    • 8
  • Laurie E. Gaspar
    • 9
  • Douglas Kondziolka
    • 10
  • Mark E. Linskey
    • 11
  • Jay S. Loeffler
    • 12
  • Minesh P. Mehta
    • 13
  • Tom Mikkelsen
    • 14
  • Jeffrey J. Olson
    • 15
  • Nina A. Paleologos
    • 16
  • Roy A. Patchell
    • 17
  • Steven N. Kalkanis
    • 18
    Email author
  1. 1.Department of NeurosurgeryIowa Spine and Brain InstituteIowa CityUSA
  2. 2.Department of NeurosurgeryUniversity of California San FranciscoSan FranciscoUSA
  3. 3.McMaster University Evidence-Based Practice CentreHamiltonCanada
  4. 4.Department of NeurosurgeryOhio State University Medical CenterColumbusUSA
  5. 5.Department of NeurosurgeryThomas Jefferson UniversityPhiladelphiaUSA
  6. 6.Department of NeurosurgeryCarolina Neurosurgery and Spine AssociatesCharlotteUSA
  7. 7.Department of Radiation OncologyCarolinas Medical CenterCharlotteUSA
  8. 8.Department of NeurosciencesCalifornia Pacific Medical CenterSan FranciscoUSA
  9. 9.Department of Radiation OncologyUniversity of Colorado-DenverDenverUSA
  10. 10.Department of Neurological SurgeryUniversity of Pittsburgh Medical CenterPittsburghUSA
  11. 11.Department of NeurosurgeryUniversity of California-Irvine Medical CenterOrangeUSA
  12. 12.Department of Radiation OncologyMassachusetts General HospitalBostonUSA
  13. 13.Department of Human OncologyUniversity of Wisconsin School of Public Health and MedicineMadisonUSA
  14. 14.Department of NeurologyHenry Ford Health SystemDetroitUSA
  15. 15.Department of NeurosurgeryEmory University School of MedicineAtlantaUSA
  16. 16.Department of NeurologyNorthshore University Health SystemEvanstonUSA
  17. 17.Department of NeurologyBarrow Neurological InstitutePhoenixUSA
  18. 18.Department of NeurosurgeryHermelin Brain Tumor Center, Henry Ford Health SystemDetroitUSA

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