J Cancer 2017; 8(9):1525-1529. doi:10.7150/jca.18600

Research Paper

Short Survival Time after Palliative whole Brain Radiotherapy: Can We Predict Potential Overtreatment by Use of a Nomogram?

Carsten Nieder1, 2, Jan Norum2, 3, Mandy Hintz4, Anca L. Grosu4, 5 Corresponding address

1. Department of Oncology and Palliative Medicine, Nordland Hospital, 8092 Bodø, Norway;
2. Department of Clinical Medicine, Faculty of Health Sciences, University of Tromsø, 9037 Tromsø, Norway;
3. Northern Norway Regional Health Authority trust, 8038 Bodø, Norway;
4. Department of Radiation Oncology, University Hospital Freiburg, 79106 Freiburg, Germany;
5. German Cancer Consortium (DKTK), Freiburg, and German Cancer Research Centre (DKFZ), D-69121 Heidelberg, Germany.

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How to cite this article:
Nieder C, Norum J, Hintz M, Grosu AL. Short Survival Time after Palliative whole Brain Radiotherapy: Can We Predict Potential Overtreatment by Use of a Nomogram?. J Cancer 2017; 8(9):1525-1529. doi:10.7150/jca.18600. Available from http://www.jcancer.org/v08p1525.htm

Abstract

Background: Many patients with brain metastases undergoing whole brain radiotherapy (WBRT) have very limited survival. The purpose of this study was to validate a nomogram derived from a large American database and to examine its ability to better predict short survival (cut-off 2 months) than previous models.

Material and Methods: This retrospective study included 254 European patients treated with primary WBRT. In addition, an exploratory analysis of patients managed with best supportive care (BSC) was performed too.

Results: Median survival after WBRT was 3.0 months. The median nomogram point sum was 122 (range 31-212). The nomogram-predicted median survival for a patient with 122 points is 3.3 months. Despite the nomogram's ability to stratify the patients into different prognostic groups, the survival curves of patients with intermediate point sum in the range of 90-139 points were largely superimposable. The poorest prognostic group with ≥180 points had a median and maximum survival of 1.8 and 4.6 months, respectively. Among these 18 patients (7%) 9 survived for less than and 9 for more than 2 months. Comparable survival outcomes were observed after BSC in a smaller group of 8 patients with ≥180 points.

Conclusions: Because of several differences between the original and validation findings, the nomogram should be examined in additional large databases. Its ability to predict poor survival is promising and possibly comparable to our previously published models. The final goal of developing a validated model that allows poor prognosis patients to safely forego WBRT without compromising survival or quality of life requires further research efforts.

Keywords: brain metastases, prognostic factors, nomogram, radiotherapy.

Introduction

Development of better local and systemic treatment approaches has resulted in individually tailored management of patients with parenchymal brain metastases from solid extracranial primary tumors [1]. High local control rates and preservation of neurocognitive function can be achieved with stereotactic radiotherapy and surgical resection [2]. These recent developments have led to a decrease in the prescription of primary whole brain radiotherapy (WBRT). Fewer and fewer patients with favorable prognostic features are now being treated with upfront WBRT as the sole local management approach [3]. However, it is a matter of debate whether or not WBRT should be offered to patients with adverse prognostic factors [4]. Their survival is often limited to few weeks, and therefore best supportive care (BSC) might also be an option. The challenge is, however, to predict who is in this subgroup. Previous attempts to use prognostic scores, such as the recursive partitioning analysis (RPA) [5] or graded prognostic assessment (GPA) [6], to select patients appropriate for BSC were not successful [7, 8]. Even within the poor prognosis group of the RPA or diagnosis-specific (DS) GPA survival was heterogeneous. Thus, clinicians are afraid to withhold local therapy to patients who may experience prolonged survival when local measures lead to, at least temporary, control of the brain metastases. A disadvantage of this practice is overtreatment of patients with short survival, resulting in the fact that they often spend a large part of the remaining life span on active treatment [9] instead of spending time with their beloved ones.

Barnholtz-Sloan et al. [10] developed a nomogram for individualized estimation of overall survival from the Radiation Therapy Oncology Group's (RTOG) randomized trials [10]. The overall median survival in this large study with more than 2000 patients was 136 days (4.5 months). Table 1 shows the baseline characteristics that contributed to the nomogram. They were a mixture of the prognostic factors that also were part of the RPA, GPA and DS-GPA. In this model, the use of the nomogram results in a total point sum that corresponds to a certain predicted median, 6-month and 12-month survival probability. The purpose of the present study was to validate the nomogram in a European patient population and to examine its ability to predict short time survival better than the models previously tested by our group. We used identical methods and definitions as in our previous studies, e.g. for short survival (max. 2 months) [7].

 Table 1 

Baseline characteristics included in the nomogram (Barnholtz-Sloan et al. 2012 [8])

ParameterAlso included in the RPA and DS-GPA
Primary tumor site and histologynoyes
Status of primary disease (controlled/uncontrolled)yesno
Metastatic spread (brain alone/other sides)yesyes
Ageyesyes
Karnofsky performance statusyesyes
Number of brain lesions (single/multiple)noyes

RPA: recursive partitioning analysis

DS-GPA: diagnosis-specific graded prognostic assessment

Material and Methods

Patients and treatment

This retrospective intention-to-treat study included 254 consecutive patients with brain metastases from common primary tumors included in the DS-GPA model (breast, lung, kidney, gastrointestinal cancer and malignant melanoma) who received palliative WBRT as primary treatment. Total doses in the range of 20-40 Gy were prescribed. The number of fractions ranged from 5-20. Patients who failed to complete all fractions of WBRT were also included. Since the main endpoint was short time survival, patients treated with upfront resection or stereotactic radiotherapy were not included, as those were supposed to have a superior prognosis. Most institutions reserve aggressive local management for patients considered to have better prognosis. The patients were treated between 2006 and 2015 and identified from a previously described prospectively maintained database [11], which included data from the radiotherapy centers in Bodø and Freiburg. Second line surgery or stereotactic radiotherapy for failure after WBRT was not an exclusion criterion. Systemic treatment was given according to local standards at the discretion of the medical oncologists. Prognosis was calculated according to the RPA, DS-GPA and nomogram as described in the original publications [5, 6, 10].

Statistical methods

Actuarial survival from the first day of radiotherapy was calculated employing the Kaplan-Meier method, and different groups were compared using the log-rank test (SPSS 22, IBM Corp., Armonk, NY, USA). Nine patients were alive at last follow-up (May 15, 2016). The median follow-up was 22 months (range 4-84). Date of death was known in all other patients.

Results

Patient characteristics

The median age was 64 years (range 24-93). The median Karnofsky performance status (KPS) was 70 (range 30-100). Ninety-nine patients (39%) had less than four brain metastases. A controlled primary tumor was present in 164 patients (65%). However 220 had extracranial metastases (87%). Eighty-eight patients (35%) had non-small cell lung and 61 (24%) breast cancer. Further patient characteristics are shown in Table 2. According to the RPA score, 10 patients (4%) had a favorable, 150 (59%) an intermediate, and 94 (37%) an unfavorable prognosis. According to the 4-tiered DS-GPA model, 9 patients (3%) were in the best, 34 (13%) in the second best, 64 (25%) in the second worst, and 146 (57%) in the worst prognostic group. The median DS-GPA point sum was 1.0.

 Table 2 

Primary tumor type and nomogram point sum

PrimarynMedian sum (range)Median survival in months
Breast cancer6183 (31-131)4.0
NSCLC, adenocarcinoma62119 (47-192)3.5
NSCLC, squamous cell carcinoma14179.5 (135-201)2.4
NSCLC, large cell carcinoma12135.5 (73-206)2.1
SCLC27147.5 (54-200)3.2
Malignant melanoma35140 (74-202)3.0
Gastrointestinal tumor*26146.5 (79-212)2.0
Kidney cancer17139 (102-165)2.6

NSCLC: non-small cell lung cancer, SCLC: small cell lung cancer

*mainly colorectal and esophageal cancer

RPA and DS-GPA

Both scores predicted survival. According to the three-tiered RPA, median survival was 5.6, 3.8 and 1.9 months (p<0.0001, log-rank test pooled over all strata). In class III 6-month and 12-month survival rates were 12 and 4%, respectively. According to the four-tiered DS-GPA, median survival was 16.4, 4.5, 3.5 and 2.5 months (p<0.0001, log-rank test pooled over all strata). In class IV 6-month and 12-month survival rates were 17 and 8%, respectively.

Nomogram and survival

The median nomogram point sum was 122 (range 31-212, 25th percentile 94, 75th percentile 151). The median survival was 3.0 months (95% confidence interval 2.6-3.4 months). The nomogram-predicted median survival for a patient with 122 points is 100 days (3.3 months). Table 3 shows survival outcomes for different prognostic groups with median survival ranging from 1.8 to 14.8 months for the extreme strata, defined as a point sum of <70 points and ≥180 points, respectively (p<0.0001, log-rank test pooled over all strata). Despite this ability to stratify the patients into different prognostic groups, the survival curves of patients with intermediate point sum, especially in the range of 90-139 points, were superimposable, as already suggested by the data shown in Table 3. Figure 1 shows the comparison of our own and RTOG database-derived survival outcomes. For many of the strata, minimal differences were observed. The poorest prognostic group with ≥180 points had a median and maximum survival of 1.8 and 4.6 months, respectively. Among these 18 patients (7%), 9 survived for less than and 9 for more than 2 months. We observed survival of less than 2 months in one patient with point sum <70 (1/21, 5%), three patients with point sum 70-79 (3/16, 19%), and four patients with point sum 80-89 (4/17, 24%).

 Table 3 

Survival outcomes stratified by nomogram point sum (p<0.0001, log-rank test pooled over all strata)

Point sumnMedian survival in months6-month survival probability12-month survival probability
<702114.871%52%
70-79163.138%19%
80-89173.541%12%
90-99234.024%9%
100-109243.125%8%
110-119213.624%13%
120-129232.622%17%
130-139203.030%25%
140-149232.422%13%
150-159252.024%4%
160-169132.515%0%
170-179102.80%0%
≥180181.80%0%

Best supportive care (BSC)

Our brain metastasis database contained 51 patients managed with BSC who had complete information to calculate the nomogram point sum. Eight of these (16%) had a point sum ≥180. Median and maximum survival were 1.6 and 4.2 months, respectively. Four of them survived for more than 2 months.

Discussion

We performed a retrospective validation study of the nomogram developed by Barnholtz-Sloan et al. [10] in a European patient population and examined the nomogram's ability to predict short time survival better than previous models tested by our group [7, 8]. The study population consisted mainly of patients with intermediate or poor prognosis who were judged not to be appropriate candidates for aggressive local therapies, such as surgery or stereotactic radiotherapy. In the RTOG database, a small minority of resected or radiosurgically treated patients were included, e.g., participants in RTOG trial 95-08, while the vast majority was treated with primary palliative WBRT [10]. In addition, 57% of our patients belonged to the worst prognostic DS-GPA group, compared to 11% in the original study. This discrepancy likely explains why the median survival in our study was only 3.0 months, while the RTOG patients survived for a median of 4.5 months. The prognostic impact of both RPA and DS-GPA could be confirmed in our study.

 Figure 1 

Median survival of patients with different point sums in the RTOG and own database

J Cancer Image (Click on the image to enlarge.)

Limitations of this study include the number of patients, statistical power of subgroup analyses, and retrospective design. Whereas the number of patients was limited in our study database, they represent the total cohort of the two radiotherapy departments and consequently express the daily practice at these units. It is possible that the nomogram results would have matched the RTOG database findings even closer in a larger cohort of patients. However, we could confirm that the nomogram predicts especially favorable and unfavorable survival with high accuracy. A certain proportion of false positive and false negative findings is a known drawback of essentially all predictive tools available in the field of oncology [12-15]. For patients with a point sum in the order of 90-139 points, no clear survival differences emerged. It is therefore necessary to examine the nomogram in additional databases.

A secondary endpoint of our study was prediction of very short survival after WBRT. In the terminal phase of cancer progression, many patients might not survive long enough to experience the beneficial effects of radiotherapy [16]. Disadvantages to patients and family members, such as acute side effects, travel distance and out-of-pocket costs, must also be considered. Similarly, unnecessary use of specialized health care resources (e.g., radiotherapy) should be kept in mind as such resources may be allocated to other patients and waiting lists may consequently be further minimized. It would therefore be desirable to avoid fruitless WBRT in patients who may experience the same survival and quality of life with optimal BSC. We have previously reported that patients with a DS-GPA score of 0-1.5 points and age ≥75 years or KPS ≤50 or uncontrolled primary tumor with extracranial metastases to at least two organs might be appropriate candidates for BSC [7]. A follow-up study suggested that patients with a combination of three new adverse features (elevated serum lactate dehydrogenase plus low albumin plus extracranial metastases to at least two organs) might also be considered for BSC [17]. We hoped that the nomogram could be an even better tool, as it is easy to handle and accurate enough to predict short survival of 2 months or less. However, even among those 7% of patients with the highest point sums (≥180), 50% survived for 2-4.6 months. Our BSC database was too small to create a sufficiently large group of patients with ≥180 points managed without WBRT. However, it was interesting to note, from this exploratory analysis, that the small group of 8 patients had survival outcomes that resembled those of their WBRT counterparts very closely. Despite the promising potential of the nomogram, our previous recommendations for patient selection will remain unaltered until larger studies have confirmed that WBRT and BSC result in undistinguishable outcomes.

As already realized in the RPA studies [5], patients with poor KPS (RPA class 3) are a heterogeneous group. Despite short median survival, post-treatment functional improvement is possible and might even be associated with survival beyond 12 months. Lee et al. have also reported that RPA class 3 patients who presented with hemiparesis, cognitive deficit or apraxia could respond to palliative radiotherapy with the potential to benefit from progression-free survival of 12 months or more [18], a finding in line with the authors' personal experience. In a prospective randomized phase II study WBRT was associated with improvements in cognitive and emotional function but also with worsened nausea [19]. Complete and partial imaging response rate was 55%. In a different study, a total of 14 symptom scores and overall quality of life were collected prospectively in 217 patients for up to 3 months [20]. Appetite loss, weakness, and nausea significantly increased from baseline, while balance, headache, and anxiety significantly decreased from baseline. Clearly, quality of life is a complex endpoint, which is influenced by extracranial disease extent and also side effects of systemic therapy. This endpoint has not been evaluated in our study. In general, important goals for the treatment of brain metastases include alleviating neurological symptoms, preventing their progression and neurological deterioration, and thus enhancing quality of life. Treatment decisions should not be based on life expectancy alone.

Conclusions

Because of several differences between RTOG database and present results, the nomogram should be examined in additional large studies. Despite its general ability to predict long and short time survival, our previous models for poor prognosis patients appear preferable because they were derived from larger subgroups. The final goal of developing a validated model that allows patients with adverse prognostic features to safely forego WBRT without compromising survival, symptom control and quality of life requires further research efforts.

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding address Corresponding author: Carsten Nieder, MD, Department of Oncology and Palliative Medicine, Nordland Hospital, 8092 Bodø, Norway, Tel: +47 75 57 8449, FAX: +47 75 53 4975, e-mail: carsten.niederno


Received 2016-12-2
Accepted 2017-2-4
Published 2017-6-1