Beyond biology: the impact of marital status on survival of patients with adrenocortical carcinoma

Zachary Klaassen 1, Lael Reinstatler 1, Martha K. Terris 1, Willie Underwood III 2, Kelvin A. Moses 1

1 Department of Surgery, Section of Urology, Medical College of Georgia, Georgia Regents University, Augusta, GA, USA; 2 Department of Urology, Roswell Park Cancer Institute, Buffalo, NY, USA

ABSTRACT

Purpose: To analyze the association of marital status and survival of patients with ACC using a population-based database.

Material and Methods: Patients with ACC were abstracted from the Surveillance Epide- miology and End Results (SEER) database from 1988-2010 (n=1271). Variables included marital status (married vs single/divorced/widowed (SDW)), gender, age, race, tumor (T) and node (N) classification, receipt of surgery, and SEER stage. Statistical analysis was performed using Cox proportional hazard models to generate hazard ratios and 95% confidence intervals.

Results: There were 728 (57.3%) females and median age was 56 years (IQR 44-66). Patients who were alive were more frequently married (65.6% vs 61.6%, p=0.008), fe- male (61.1% vs 58.0%, p=0.001), younger (median 51 vs 57 years, p=0.0001), submitted to adrenalectomy (88.6% vs 63.8%, p<0.0001), and more favorable SEER stage (loca- lized-64.9% vs 29.9%; regional-25.1% vs 30.1%; distant 4.8% vs 31.5%, p<0.0001) compared to patients dead of disease (DOD). On multivariable analysis, factors signi- ficantly associated with all-cause mortality were SDW status (HR 1.28, 95% CI 1.09- 1.51), age, non-operative management, and N+ disease. Risk factors for disease-spe- cific mortality included SDW status (HR 1.30, 95% CI 1.07-1.56), age, non-operative management, T-classification, and N+ disease.

Conclusions: Marital status is significantly associated with survival in patients with ACC. Our results suggest that the decreased survival seen among SDW individuals highlights an area for further research and needed intervention to reduce disparity.

ARTICLE INFO

Key words:

Adrenocortical Carcinoma; Marital Status; Social Class; Survival; Disease

Int Braz J Urol. 2015; 41: 1108-15

Submitted for publication: July 20, 2014

Accepted after revision: June 10, 2015

INTRODUCTION

Adrenocortical carcinoma (ACC) is a rare malignancy with a reported incidence of 0.5-2 per million, a recurrence rate of 60-80%, and 5-year overall survival of 20-47% (1, 2). Despite advan- ces in imaging and treatment regimens over the past 20 years, survival outcomes in patients with ACC continue to remain poor. Therefore, clinicians must seek additional factors to optimize outcomes in this select group of patients.

The effect of marital status on disease spe- cific survival (DSS) in patients with cancer has been reported across several malignancies, al- though the reason for a survival benefit provided by marriage has not been completely elucidated (3-9). In a recent study analyzing the impact of marital status on the 10 leading causes of cancer- -related death in the US, Aizer et al. found that single-divorced-widowed (SDW) patients were at greater risk of presentation with metastatic dise- ase, under treatment and cancer specific mortali-

ty (3). These results suggest that SDW patients with malignancy represent an at-risk population that may benefit from structured support and intervention.

Apart from the known risk factors that im- pact survival such as TNM classification, we sou- ght to identify other significant factors specific to survival outcomes. Given the poor survival asso- ciated with ACC and paucity of literature reporting the effect of socioeconomic variables on survival in these patients, the objective of this study was to assess the impact of marital status on overall survival (OS) and DSS in patients with ACC. Fur- thermore, we sought to identify other non-clinical or pathologic factors that may be associated with greater risk of mortality. Our hypothesis was that SDW patients and patients with poorer socioeco- nomic status (SES) would have worse OS and DSS compared to married patients and those with more favorable SES.

MATERIALS AND METHODS

Study Population: The study cohort con- sisted of patients from all 18 registries compri- sing the Surveillance, Epidemiology and End Re- sults (SEER) database from 1988-2010. The SEER database reports cancer specific outcomes from specific geographic areas representing 28% of the US population (10). Patients ≥18 years of age with ACC were identified in the SEER database utilizing the primary site codes C74.0 and C74.9, and Inter- national Classification of Diseases for Oncology, 9th edition (ICD-9) code 1940 for a study cohort of 1271 patients. Patients were divided into three groups (alive, dead of disease (DOD) and dead of other causes (DOC)).

Description of Covariates: Demographic variables of interest included marital status (mar- ried vs single/divorced/widowed (SDW)), gen- der, age at diagnosis, race (African American vs Caucasian vs Hispanic vs other), SEER registry, and median census county data for educational attainment (<9th grade vs Ba- chelor degree), poverty level, % foreign born, % unemployed, and household income. Clinical and pathologic variables included receipt of surgery (adrenalectomy vs none vs other), laterality (left vs right vs bilateral), American Joint Committee

on Cancer (AJCC) 7th edition tumor (T) and node (N) classification, metastasis (yes/no), SEER stage (localized vs regional vs distant vs unstaged), and median OS (SEER survival data-censoring date September 10, 2013).

Statistical analysis

Descriptive statistics for demographic and clinicopathological variable comparisons was per- formed using t-test and Chi square test. Survival estimates were calculated using the Kaplan-Meier method for OS and DSS by marital status, gen- der, age at diagnosis, race, T-classification, and N-classification. Cox proportional hazard analysis was performed to generated hazard ratios for risk factors of mortality. The model was constructed and analyses were performed using backward se- lection, removing all insignificant variables until the best-fit model was achieved. In this model, T- -classification and N-classification were adjusted for, while SEER stage was not adjusted for in order to refrain from including confounding variables. Statistical analyses were performed using SAS 9.3 (SAS Institute, Cary, NC). All tests were two-sided and with a statistical significance set at p<0.05.

RESULTS

Population Demographics

There were 728 females (57.3%) and 543 males (42.7%) with a median age of 56 years (IQR 44-66). There were 422 patients who were alive (33.2%), 685 patients (53.9%) DOD and 164 patients (12.9%) DOC (Table-1). A signifi- cantly higher percentage of alive patients were married (65.6% vs 61.6% vs 51.8%; p=0.008), female (61.1% vs 58.0% vs 44.5%; p=0.001) and younger at diagnosis (median 51 years vs 57 years vs 65 years; p<0.001) compared to those DOD and DOC, respectively. There was no signi- ficant difference for educational status, poverty/ income, foreign born status, and unemployment between the groups.

Clinicopathologic Analysis

Patients who were alive had a higher fre- quency of adrenalectomy (88.6% vs 63.8% VS

Table 1 - Demographics of 1271 patients with adrenocortical carcinoma.
VariableAliveDead of DiseaseDead other Causesp-value
Patients, n (%)422 (33.2)685 (53.9)164 (12.9)
Marital Status, n (%)0.008
Married277 (65.6)422 (61.6)85 (51.8)
SDW134 (31.8)241 (35.2)74 (45.1)
Unknown11 (2.6)22 (3.2)5 (3.1)
Gender, n (%)0.001
Male164 (38.9)288 (42.0)91 (55.5)
Female258 (61.1)397 (58.0)73 (44.5)
Median age, years (IQR)51 (42, 61)57 (44, 66)65 (56, 74)<0.001
Race, n= (%)0.44
Caucasian320 (75.8)533 (77.8)121 (73.8)
Hispanic40 (9.5)64 (9.4)19 (11.5)
AAM27 (6.4)42 (6.1)16 (9.8)
Other35 (8.3)46 (6.7)8 (4.9)
Median <9th Grade Education, % (IQR)5.7 (3.9, 8.9)5.9 (3.7, 9.9)5.9 (3.8, 8.9)0.88
Median <High School Education, % (IQR)13.9 (10.0, 20.1)14 (9.9, 20.3)13.5 (11.3, 18.9)0.78
Median >Bachelor Degree, % (IQR)29.2 (21.6, 35.6)29.2 (23.2, 39.6)30.1 (23.3, 38.4)0.05
Median <Poverty, % (IQR)13.4 (10.5, 16.3)12.3 (10.2, 16.3)12.2 (9.9, 16.3)0.56
Median Foreign Born, % (IQR)15.4 (6.9, 28.8)17.8 (7.7,30.5)16.3 (9.4, 29.4)0.38
Median Unemployed, % (IQR)9.1 (7.9, 9.8)9.2 (7.5, 9.8)9.2 (7.7, 9.8)0.85
Median Household Income, % (IQR)56,550 (48,340,57,580 (51,770, 70,570)58,820 (54,090, 70,570)0.08
67,010)

SDW = single/divorced/widowed; IQR = interquartile range; AAM = African American; SEER = Surveillance Epidemiology and End Results

67.7%; p<0.0001) compared to patients DOD or DOC, respectively (Table-2). Furthermore, patients who were alive had more favorable T classifica- tion (p<0.0001), more favorable N classification (p<0.0001), less frequency of metastatic disease (1.7% vs 25.4% vs 17.1%; p<0.0001), and have more favorable SEER stage (p<0.0001) compared to patients DOD or DOC. Median survival was 9 months (IQR 3-24) for patients DOD and 10 mon- ths (IQR 1-51) for patients DOC (Figure-1A). DSS was statistically significantly associated with ma- rital status (Figure-1B, p=0.009), age at diagnosis

(decade) (Figure-1D, p<0.0001), T-classification (Figure-1E, p<0.0001), and N-classification (Fi- gure-1F, p<0.0001), but was not associated with gender (Figure-1C, p=0.18).

Risk Factors for Mortality

On multivariable analysis, significant factors associated with increased risk of all-cau- se mortality were SDW status (HR 1.28, 95% CI 1.09-1.51), older age (HR 1.43, 95% CI 1.31-1.55), % <9th grade education (HR 1.06, 95% CI 1.00- 1.13), non-operative management (HR 3.18, 95%

Table 2 - Clinical and pathologic variables of 1271 patients with adrenocortical carcinoma.
VariableAliveDead of DiseaseDead other Causesp-value
Surgical Approach, n (%)<0.0001
Adrenalectomy374 (88.6)437 (63.8)111 (67.7)
None36 (8.5)212 (30.9)41 (25.0)
Other11 (2.6)30 (4.4)9 (5.5)
Laterality, n (%)0.08
Left222 (52.6)347 (50.7)96 (58.5)
Right190 (45.0)300 (43.8)61 (37.2)
Bilateral1 (0.3)8 (1.1)1 (0.6)
T Classification, n (%)<0.0001
TX39 (9.3)82 (12.0)30 (18.3)
T01 (0.2)00
T132 (7.6)10 (1.5)14 (8.5)
T2228 (54.0)192 (28.0)57 (34.8)
T368 (16.1)91 (13.3)18 (11.0)
T447 (11.1)136 (19.8)31 (18.9)
N Classification, n (%)<0.0001
NX79 (18.7)244 (35.6)58 (35.4)
N0332 (78.7)356 (52.0)89 (54.2)
N111 (2.6)85 (12.4)17 (10.4)
Metastasis, n (%)7 (1.7)174 (25.4)14 (8.5)<0.0001
SEER Stage, n (%)<0.0001
Localized274 (64.9)205 (29.9)77 (46.9)
Regional106 (25.1)206 (30.1)40 (24.4)
Distant20 (4.8)216 (31.5)28 (17.1)
Unstaged22 (5.2)58 (8.5)19 (11.6)
Median Survival, months (IQR)53 (17, 112)9 (3, 24)10 (1, 51)<0.0001

SEER = Surveillance Epidemiology and End Results; IQR = interquartile range

CI 2.57-3.95), T-classification (TX vs T1-HR 1.78, 95% CI 1.12-2.82; T3 vs T1-HR 2.28, 95% CI 1.45- 3.60; T4 vs T1-HR 2.58, 95% CI 1.66-4.03), and N+ disease (HR 2.27, 95% CI 1.74-2.97). SDW sta- tus was also a significant risk factor for disease- -specific mortality (HR 1.30, 95% CI 1.07-1.56), as did older age (HR 1.46, 95% CI 1.32-1.61), non- -operative management (HR 3.56, 95% CI 2.80- 4.52), T-classification (TX vs T1-HR 2.58, 95% CI 1.30-5.13; T2 vs T1-HR 2.19, 95% CI 1.14-4.22; T3 vs T1-HR 3.66, 95% CI 1.87-7.14; T4 vs T1- HR 3.97, 95% CI 2.05-7.69), and N+ disease (HR

2.37, 95% CI 1.76-3.19). Gender was included in the model and additionally in the Kaplan-Meier analysis and there was no significant difference in outcomes on multivariate analysis.

DISCUSSION

This population-based study analyzing factors associated with mortality in patients with ACC demonstrates that SDW patients have signi- ficantly worse all cause and cancer specific mor- tality compared to married patients. Furthermore,

Figure 1 - Kaplan-Meier survival estimates for (A) overall survival; (B) disease-specific survival by marital status (p=0.009); (C) disease-specific survival by T-classification (p<0.0001), and (D) disease-specific survival by N-classification (p<0.0001).

A

B

1.0

+

Censored

1.0

+ Censored

0.8

0.8

Survival Probability

Survival Probability

0.6

0.6

0.4

0.4

0.2

0.2

0.0

0.0

p = 0.009

0

50

100

150

200

250

0

50

100

150

200

250

Survival months

Number at risk

Survival months

1271

1176

322

158

74

24

Number at risk

MaritalStatus

Married

Single Divorced Widowed

Married

699

669

200

102

49

16

SDW

375

340

76

34

15

7

C

D

1.0

+ Censored

1.0

+ Censored

0.8

0.8

Survival Probability

0.6

Survival Probability

0.6

0.4

0.4

0.2

0.2

0.0

p < 0.0001

0

50

100

150

200

250

0.0

p < 0.0001

Survival months

0

50

100

150

200

250

Survival months

Number at risk

N-Stage

NO

N1

NX

NO

688

655

197

88

38

15

N1

96

89

7

3

0

0

Nx

323

293

77

49

27

8

Number at riskT ClassificationT1T2T3T4TX
T1424117932
T2420411155793613
T31591513317115
T4183172331660
TX121106331682

age was also associated with mortality in addition to poor staging characteristics. Although male pa- tients had worse outcomes on univariate analysis, gender did not retain significance as a risk factor on multivariable analysis. In contrast to many stu- dies in other malignancies, there was no signifi- cance found for ethnicity or socioeconomic status on outcomes. The importance of this study is that it is the first to show the effect of marital status on mortality outcomes in patients with ACC.

The survival benefit associated with ma- rital status has been described in other urologic malignancies, including bladder, prostate, penile and testis cancer (4-9). Gore and colleagues de- monstrated a clear survival benefit among mar- ried patients undergoing radical cystectomy iden- tified within the SEER database from 1973-2000 compared to SDW patients (6). This positive effect was an independently significant factor even when controlling for pathological factors, gender

Table 3 -Cox proportional analysis of risk factors for mortality in 1271 patients with adrenocortical carcinoma.
Overall Mortality HR (95% CI)p-valueCancer Specific Mortality HR (95% CI)p-value
Marital StatusMarriedRefRef
SDW1.28 (1.09-1.51)0.0031.30 (1.07-1.56)0.007
GenderFemaleRefRef
Male1.17 (1.00-1.38)0.0491.02 (0.85-1.22)0.84
Age#Per decade1.43 (1.31-1.55)<0.00011.46 (1.32-1.61)<0.0001
RaceWhiteRefRef
African-American1.29 (0.95-1.77)0.111.17 (0.80-1.72)0.42
Hispanic1.22 (0.92-1.61)0.181.12 (0.80-1.56)0.50
Other1.07 (0.76-1.50)0.710.97 (0.66-1.42)0.85
%<9th Grade EducationPer 1% change1.06 (1.00-1.13)0.0391.07 (0.99-1.14)0.055
%< High School EducationPer 1% change0.96 (0.93-0.99)0.0420.96 (0.92-0.99)0.038
LateralityLeftRefRef
Right0.89 (0.76-1.04)0.150.87 (0.73-1.05)0.15
Bilateral0.96 (0.42-2.19)0.920.99 (0.43-2.31)0.99
SurgeryAdrenalectomyRefRef
None3.18 (2.57-3.95)<0.00013.56 (2.80-4.52)<0.0001
Other1.11 (0.73-1.70)0.621.17 (0.70-1.98)0.55
T ClassificationT1RefRef
TX1.78 (1.12-2.82)0.0142.58 (1.30-5.13)0.007
T21.44 (0.93-2.22)0.102.19 (1.14-4.22)0.018
T32.28 (1.45-3.60)0.00043.66 (1.87-7.14)0.0001
T42.58 (1.66-4.03)<0.00013.97 (2.05-7.69)<0.0001
N ClassificationN0RefRef
NX0.92 (0.76-1.11)0.370.96 (0.77-1.20)0.73
N12.27 (1.74-2.97)<0.00012.37 (1.76-3.19)<0.0001

HR = hazard ratio; SEER = Surveillance, Epidemiology and End Results #Decades: 18-59, 60-69, 70-79, 80+

and race. Sammon et al. analyzed 14,859 patients undergoing radical cystectomy (RC) between 1988 and 2006 and found that never-married males had a higher rate of non-organ confined disea- se at RC, a trend not observed in never-married females (4). SDW men and women also displayed a higher rate of all-cause mortality and disease specific mortality. In an analysis of the SEER da- tabase from 1988-2006, Abdollah et al. identified 163,697 men undergoing radical prostatectomy (RP) with organ confined prostate cancer (7). They

found that men who were SDW had more advan- ced stage at RP and higher cause-specific and all- -cause mortality compared to married men. The same group assessed the effect of marital status on OS and cancer-specific mortality for patients with squamous cell carcinoma of the penis (8). Between 1988 and 2006, they identified 1,844 patients with squamous cell carcinoma of the penis and found that unmarried men had a 1.5-fold higher risk for locally advanced disease at surgery and 1.3-fold higher risk of overall mortality. Interestingly, un-

married men did not have an increased of cause- -specific mortality in this cohort.

The benefit of marriage in patients with cancer likely represents a stable social cons- truct, although the reasoning is subjective and the effect is likely multifactorial. For example, being married may reflect better access to he- althcare compared to unmarried patients. Ho- wever, better access to healthcare cannot be the total explanation because poor socioeco- nomic status still adversely affects outcomes in countries that have universal healthcare (3, 11). Psychosocial factors associated with being mar- ried may be influential as well. Married patients may be encouraged by their spouses to seek me- dical attention for worrisome symptoms, seek definitive treatment for conditions, and adhere to prescribed treatment regimens with the en- couragement of a supportive spouse (3, 12, 13). The effect of this bond is speculative, however it may be inferred that this relationship may improve adherence to treatment regimens and rigorous follow-up required of cancer patients. The diagnosis of cancer may illicit distress and subsequently depression. By having a supporti- ve partner, married patients have the ability to share the emotional burden of a cancer diagno- sis with their spouse (14). Ultimately, patients without a support system associated with mar- riage may be at risk for poor outcomes and may require additional effort in order to maximize excellent clinical outcomes.

Although the overall and cancer specific mortality rates for patients with ACC is dismal even in married patients, the role of clinicians and multidisciplinary teams is to recognize these disparities in outcomes for the SDW patient and provide avenues to improve survival for these patients to the level of the married patient. Fur- thermore, interventions to improve outcomes for the SDW patient may prove to be cost-effective in the overall healthcare structure and delive- rability of care. Previous studies outside of the urologic community have assessed the impact of promoting support mechanisms in oncology pa- tients (15, 16). In a study from the Massachusetts General Hospital, investigators randomly assig- ned 107 patients with metastatic non-small-cell

lung cancer to receive either early palliative care in conjunction with standard oncologic care or standard oncologic care alone (15). The authors found that patients receiving early palliative care had improved quality of life and mood, required less aggressive end-of-life care and ultimately had longer median survival (11.6 months vs. 8.9 months, p=0.02) compared to the control group. Aoun et al. randomized 26 palliative care patients living alone to having additional care-aid hours in their home and found that these patients had improved quality of life, preservation of self-dignity, ease of bur- den of everyday living, and reduced loneliness and isolation (16). Although similar studies have not been performed in married vs. SDW patients, particularly for the dismal prognosis associated with ACC, implementing comparable measures to the SDW population should be an area of further research endeavors.

There are some limitations that must be considered when interpreting the data. First, as with any retrospective analysis of a large adminis- trative database, SEER does not provide sufficient granularity to predict causal factors specifically re- lated to marital status and survival such as length of marriage, marital satisfaction, unmarried co-ha- bitational relationships, or long-term homosexual relationships. Secondly, the SEER database does not include details that may impact marital sta- tus such as the quality of the relationship, length of marriage, or health of the spouse. Furthermore, patients who are SDW may have a support system equivalent to that often associated with marriage (eg. extended family, coworkers, and friends). Fi- nally, the SEER database does not contain infor- mation related to patient comorbidities, which may be an unaccounted confounding factor in the cau- sal association between SDW patients and inferior survival outcomes, nor does it contain information regarding receipt of chemotherapy, which would be important to know for patients with high stage disease or recurrence. The major strength of this study is that it is the first to identify the impact of marital status on survival in ACC. These results suggest that a properly designed and implemented intervention for SDW patients may have a modest impact on this and other malignancies.

CONCLUSIONS

ACC is a disease with an overall poor prognosis due to aggressive biological behavior. SDW status is associated with poorer survival in patients with ACC, suggesting that the decreased survival seen among SDW individuals in other urologic malignancies may also be relevant for patients with ACC. Health care providers caring for unmarried patients with ACC should be aware of the poorer outcomes in these patients, highli- ghting an area for further research and imple- mentation of improved support systems to reduce this disparity and improve their survival to that of married patients.

ABBREVIATIONS

ACC = adrenocortical carcinoma

SDW = single/divorced/widowed

DSS = disease specific survival

SES = socioeconomic status

SEER = Surveillance, Epidemiology and End Re- sult DOD = dead of disease

DOC = dead of other causes

CONFLICT OF INTEREST

None declared.

REFERENCES

1. Fassnacht M, Allolio B. Clinical management of adrenocortical carcinoma. Best Pract Res Clin Endocrinol Metab. 2009;23:273-89.

2. Meyer A, Niemann U, Behrend M. Experience with the surgical treatment of adrenal cortical carcinoma. Eur J Surg Oncol. 2004;30:444-9.

3. Aizer AA, Chen MH, McCarthy EP, Mendu ML, Koo S, Wilhite TJ, et al. Marital status and survival in patients with cancer. J Clin Oncol. 2013;31:3869-76.

4. Sammon JD, Morgan M, Djahangirian O, Trinh QD, Sun M, Ghani KR, et al. Marital status: a gender-independent risk factor for poorer survival after radical cystectomy. BJU Int. 2012;110:1301-9.

5. Pruthi RS, Lentz AC, Sand M, Kouba E, Wallen EM. Impact of marital status in patients undergoing radical cystectomy for bladder cancer. World J Urol. 2009;27:573-6.

6. Gore JL, Kwan L, Saigal CS, Litwin MS. Marriage and mortality in bladder carcinoma. Cancer. 2005;104:1188-94.

7. Abdollah F, Sun M, Thuret R, Abdo A, Morgan M, Jeldres C, et al. The effect of marital status on stage and survival of prostate cancer patients treated with radical prostatectomy: a population-based study. Cancer Causes Control. 2011;22:1085-95.

8. Thuret R, Sun M, Budaus L, Abdollah F, Liberman D, Shariat SF,et al. A population-based analysis of the effect of marital status on overall and cancer-specific mortality in patients with squamous cell carcinoma of the penis. Cancer Causes Control. 2013;24:71-9.

9. Abern MR, Dude AM, Coogan CL. Marital status independently predicts testis cancer survival — an analysis of the SEER database. Urol Oncol. 2012;30:487-93.

10. Surveillance, Epidemiology and End Results (SEER) Surveillance Epidemiology and End Results, 2013. National Cancer Institute. http://seer.cancer.gov/ Accessed 15 April 2014.

11. Ayanian JZ, Kohler BA, Abe T, Epstein AM. The relation between health insurance coverage and clinical outcomes among women with breast cancer. N Engl J Med. 1993;329:326-31.

12. Aizer AA, Paly JJ, Zietman AL, Nguyen PL, Beard CJ, Rao SK, et al. Multidisciplinary care and pursuit of active surveillance in low-risk prostate cancer. J Clin Oncol. 2012;30:3071-6.

13. Cohen SD, Sharma T, Acquaviva K, Peterson RA, Patel SS, Kimmel PL. Social support and chronic kidney disease: an update. Adv Chronic Kidney Dis. 2007;14:335-44.

14. Goldzweig G, Andritsch E, Hubert A, Brenner B, Walach N, Perry S, et al. Psychological distress among male patients and male spouses: what do oncologists need to know? Ann Oncol. 2010;21:877-83.

15. Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, et al. Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med. 2010;363:733-42.

16. Aoun S, O’Connor M, Skett K, Deas K, Smith J. Do models of care designed for terminally ill ‘home alone’ people improve their end-of-life experience? A patient perspective. Health Soc Care Community. 2012;20:599-606.

Correspondence address: Kelvin A. Moses, MD, PhD Department of Urologic Surgery Vanderbilt University A-1302 Medical Center North Nashville, TN 37232, USA

Fax: +1 615 322-8990

E-mail: kelvin.a.moses@vanderbilt.edu