Dersleri yüzünden oldukça stresli bir ruh haline sikiş hikayeleri bürünüp özel matematik dersinden önce rahatlayabilmek için amatör pornolar kendisini yatak odasına kapatan genç adam telefonundan porno resimleri açtığı porno filmini keyifle seyir ederek yatağını mobil porno okşar ruh dinlendirici olduğunu iddia ettikleri özel sex resim bir masaj salonunda çalışan genç masör hem sağlık hem de huzur sikiş için gelip masaj yaptıracak olan kadını gördüğünde porn nutku tutulur tüm gün boyu seksi lezbiyenleri sikiş dikizleyerek onları en savunmasız anlarında fotoğraflayan azılı erkek lavaboya geçerek fotoğraflara bakıp koca yarağını keyifle okşamaya başlar
Reach Us +44-330-822-4832

GET THE APP

Journal of Palliative Care & Medicine - Palliative Radiotherapy at the End of Life
ISSN: 2165-7386

Journal of Palliative Care & Medicine
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
  • Research Article   
  • J Palliat Care Med 355, Vol 9(2)
  • DOI: 10.4172/2165-7386.1000355

Palliative Radiotherapy at the End of Life

Susan Y Wu1, Lisa Singer2, Lauren Boreta1, Michael A Garcia1, Shannon E Fogh1 and Steve E Braunstein1*
1Department of Radiation Oncology, University of California, San Francisco, United States
2Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, United States
*Corresponding Author: Steve E Braunstein, Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, United States, Tel: +415-502-6926 , Email: Steve.Braunstein@ucsf.edu

Received: 25-Aug-2018 / Accepted Date: 08-Mar-2019 / Published Date: 15-Mar-2019 DOI: 10.4172/2165-7386.1000355

Abstract

Purpose: A significant proportion of patients with advanced cancer undergo palliative radiotherapy (RT) within their last 30 days of life. This study characterizes palliative RT at our institution and aims to identify patients who may experience limited benefit from RT due to imminent mortality.

Materials and methods: 518 patients treated with external beam RT to a site of metastatic disease between 2012-2016 were included. Mann-Whitney U and chi-squared tests were used to identify factors associated with RT within 30 days of death (D30RT).

Results: Median age at RT was 63 years (IQR 54-71). Median time from RT to death was 74 days (IQR 33-174). 125 patients (24%) died within 30 days of RT. D30RT was associated with older age at RT (64 vs. 62 years, p=0.04), shorter interval since diagnosis (14 vs. 31 months, p<0.001), liver metastasis (p=0.02), lower KPS (50 vs. 70, p<0.001), lower BMI (22 vs. 24, p=0.001), and inpatient status at consult (56% vs. 26%, p<0.001). Patients who died within 30 days of RT were less likely to have hospice involved in their care (44% vs. 71%, p=0.001). D30RT was associated with higher Chow and TEACHH scores at consult (p<0.001 for both).

Conclusions: 24% of patients received palliative RT within 30 days of death. Additional tools are necessary to help physicians identify patients who would benefit from short treatment courses or alternative interventions to maximize quality at the end of life.

Keywords: Radiation therapy; Palliative care; Predictive tools

Introduction

More than half of patients treated with radiotherapy (RT) are treated with palliative intent. RT has well-established utility for pain palliation from bone metastases, may be used to improve neurological function or prevent further neurological compromise in patients with brain or spinal cord metastases, and can be used to alleviate symptoms due to obstruction by tumor.

While the response rate to RT in the treatment of bone metastases is high, at approximately 60%, the time frame for symptomatic improvement is typically measured in weeks [1-4]. Palliative RT for brain metastases may result in stable or improved neurologic symptoms in about half of patients, however is also associated with side effects and may not improve overall survival [5-7]. Patients undergoing RT at the end of life may not experience symptomatic benefit and may spend a significant proportion of their remaining life expectancy receiving treatment [8]. Time spent on treatment at the end of life may not align with patients’ end of life goals, particularly in the United States where single fraction RT is less commonly utilized. Medicare data suggests that in the United States, almost 8% of patients dying of cancer will receive RT in their last month of life, and almost 20% of these patients will be treated in 10 or more fractions [9,10].

The purpose of this study is to characterize use of palliative RT in patients with advanced cancer at a single institution and identify factors associated with RT within 30 days of death (D30RT).

Methods

Patient information

We performed a retrospective review to identify patients who received external beam RT to a site of metastatic disease at the University of California, San Francisco between 2012-2016. Patients treated with stereotactic radiosurgery (SRS) for limited brain metastases were excluded from this analysis as this represents a highly select group of patients; at our institution, each case is reviewed at a weekly multidisciplinary SRS tumor board and the treatment decision takes into account factors such as patient performance status, control of extracranial disease, and potential systemic therapy options. As our patient list was generated using ICD codes for secondary malignant neoplasms (196-198, C78, and C79) listed in our electronic medical record system (MOSAIQ; Elekta; Stockholm, Sweden), we also excluded patients receiving potentially palliative RT to their primary tumor.

Patient characteristics such as age, gender, primary diagnosis, prior chemotherapy or other systemic treatment, performance status at consult, use of hospice services, and radiation dose/fractionation were abstracted from the medical record. In addition to clinical variables used to calculate the TEACHH and Chow scores described below, we also recorded BMI, as weight loss has been shown to be a poor prognostic sign in patients with cancer, and inpatient status at the time of consult [10,11]. Vital status and date of death were confirmed with our institutional tumor registry. This retrospective review was approved by the institutional review board.

Prognostic scores

The TEACCH and Chow models have been described previously [12,13]. The Chow model of risk factors grouping is simple to use and categorizes patients based on 3 risk factors: non-breast primary, nonbone metastases, and KPS ≤ 60. Group I includes patients with 0-1 risk factors, Group II with 2 risk factors, and group 3 with all three risk factors [14]. The TEACHH model assigns points based on the following risk factors: non-breast or prostate primary, age > 60, ECOG performance status 2-4, liver metastases, hospitalization within 3 months of palliative RT consult, and 2 or more prior palliative chemotherapy courses [12]. Patients with 0-1 risk factors are categorized in group A, 2-4 risk factors in group B, and 5-6 risk factors in group C.

Statistics

The Shapiro-Wilk test was used to evaluate normality of continuous variables. Mann-Whitney U and Chi-squared tests were used to compare patients who received RT within 30 days of death (D30RT) and those who did not. D30RT was calculated from the start of RT. Multivariate analysis was used to identify factors associated with D30RT. A two-sided p<0.05 was considered significant. Statistics were performed using IBM SPSS, version 24 (SPSS; Chicago, IL).

Results

518 patients were included in this analysis. The median age at initial diagnosis was 60 years (interquartile range (IQR) 50-68 years) (Table 1).

Variable Median (IQR) or % (n, of 518)
Age at diagnosis 60 (50-68)
Percent female 46% (238)
Race
White 66% (340)
East Asian 14% (74)
African American 8.7% (45)
Southeast Asian 3.7%  (19)
Asian NOS 3.7%  (19)
Other (includes American Indian, Pacific Islander) 4.1% (21)
Percent Hispanic 9.1% (47)
Survival time since diagnosis (months) 28 (11-53)
Primary diagnosis
Lung 26% (137)
Breast 19% (97)
Prostate 9.7% (50)
Renal cell 5.8% (30)
Colorectal 5.8% (30)
Hepatocellular 3.8% (20)
Head and Neck 3.5% (18)
Skin 3.3% (17)
Other* 23% (119)
Metastatic at diagnosis 49% (254)
Site of metastases
Brain 47% (244)
Lung 55% (284)
Liver 40% (208)
Bone only 17% (90)
BMI last course 24(21-27)
KPS last consult 60 (50-80)
KPS >70 45% (231/511)
Hospitalization within 3 months of RT consult 58% (289/500)
TEACHH score** %(n, of 450) Median survival, months (IQR)
0-1 6.2% (32/450) 6 (2.8-11)
4-Feb 68% (352/450) 2.2 (1.0-5.0)
6-May 13% (66/450) 1.3 (0.5-2.3)
CHOW model**
I 18% (92/510) 4.7 (2-11)
II 44% (227/510) 2.5 (1.0-5.6)
III 37% (191/510) 1.6 (0.7-2.7)
Hospice involved
Yes 47% (245)
No 28% (147)
Unknown 24% (126)
Place of death
Inpatient, acute care 23%  (120)
Home 29% (151)
Inpatient hospice, non-acute care 10% (52)
SNF (not hospice) 1.5% (8)
Unknown 36% (187)

Table 1: Patient characteristics.

The median age at final RT course was 63 years (IQR 54-71 years). The median survival time from diagnosis to final RT course was 28 months (IQR 11-53 months). Sixty-six percent of patients (340/518) were Caucasian, while 14% (74/518) were East Asian and 8.7% (45/518) African American. Forty-nine percent of patients (254/518) had metastatic disease at diagnosis. Forty-five percent of patients (231/511) had a KPS>70 at the time of final RT consult; KPS was not recorded at the time of consultation in 8 patients. Fifty eight percent of patients (289/500) were hospitalized within 3 months of RT consult.

The most common primary malignancies were lung (26%, 137/518), breast (19%, 97/518) and prostate (9.7%, 50/518). The most common treatment sites were bone (57%, 293/518) and brain (28%, 146/518) (Table 2).

Characteristics Median (IQR) or % (n, of 518)
Palliative course # 1 (1-2)
Age at RT 63 (54-71)
Prescribed fractions 5 (4-10)
1 17% (89)
4-Feb  9.6% (50)
5 32% (167)
9-Jun 3.5% (18)
10 34% (177)
>10 3.3% (17)
Treatment site
Bone 57% (293)
Brain 28% (146)
Lung 2.9% (15)
Node 1.7% (9)
Other* 11% (55)
Incomplete RT course 12% (63)

Time from start of last RT course to death (days)

74 (33-174)

Table 2: Summary of RT.

The median number of palliative chemotherapy regimens prior to RT was 1, though the range was quite large (0-13 regimens) (IQR 0-3 regimens).

The median time from the start of last RT course to death was 74 days (IQR 33-174 days). 125 patients (24%) died within 30 days of RT. D30RT was associated with older median age at initial diagnosis (63 vs. 59 years, p=0.002) and at the time of final RT course (64 vs. 62 years, p=0.04), shorter interval since diagnosis (14 vs. 31 months, p<0.001), liver but not brain or lung metastasis (p = 0.02, 0.43, and 0.06 respectively), lower median KPS at consultation (50 vs. 70, p<0.001), lower median BMI (22 vs. 24, p=0.001), and inpatient status at consult (56% vs. 26%, p<0.001)(Table 3).

Parameters D30RT (median (IQR) or % (proportion)**) D>30RT  (median (IQR) or % (proportion)**)) Chi-squared or p-value
Age at diagnosis 63 (52-70) 59 (47-67) 0.002
Age at RT 64 (55-73) 62 (52-70) 0.04
Gender, % female 42% (52/125) 47% (184/393) 0.35
% Hispanic 5.8% (7/119) 11%  (40/381) 0.15
Survival time (months, diagnosis to RT) 14 (5-38) 31 (14-59) <0.001
KPS at RT consult 50 (20-70) 70 (50-80) <0.001
KPS>70 27% (33/124) 51% (198/387) <0.001
BMI at RT consult 22 (IQR 20-25) 24 (21-27) 0.001
Primary diagnosis breast/prostate 18% (22/125) 32% (124/393) 0.003
Treatment site
Bone 53% (66/125) 77% (227/393) 0.35
Brain 34% (43/125) 26% (103/393) 0.09
Lung 4% (5/125) 3% (10/393)  
Other* 9%(11/125) 13% (53/393)  
Hospitalization within 3 months of consult 78% (97/125) 51% (192/375) < 0.001
Metastatic at diagnosis 50% (62/125) 50% (191/388) 0.94
Sites of metastases
Non-bone 90% (112/125) 80% (315/392) 0.02
Brain 51% (63/124) 47% (181/387) 0.43
Lung 62% (78/125) 53% (206/390) 0.06
Liver 50% (62/125) 38% (146/386) 0.02
Palliative RT course 1 (1-2) 1 (1-2) 0.15
Prescribed fractions 5 (3-10) 5 (4-10) 0.14
TEACHH score 3 (2-4) 4 (3-4) <0.001
TEACHH Group
A 1.6% (2/124) 9% (30/326) <0.001
B 74% (92/124) 80%(260/326)
C 24%(30/124) 11%(36/326)
Chow Group
I 3% (5/124) 23% (87/386) <0.001
II 41% (51/124) 46% (176/386)
III 55% (68/124) 32% (123/386)
Inpatient consult 56% (70/125) 26% (103/393) <0.001
Hospice involved 44% (54/122)  71% (191/270) <0.001

Table 3: Characteristics of patients and treatment in those who died within 30-days of RT (D30RT) and those who did not (D>30RT).

D30RT was associated with higher Chow and TEACHH scores at the time of consult (p<0.001 for both). D30RT was associated with a greater likelihood of not completing the prescribed RT course compared to those who lived longer than 30 days following start of RT (42% vs. 6%, p<0.001). Despite poor outcomes, patients who died within 30 days of RT were less likely to have hospice involved in their care (44% vs. 71%, p=0.001).

Overall, 12% of patients (63/518) did not complete their final RT course. Patients who did not complete radiation were more likely to be inpatients at the time of RT consultation (19% vs. 9%, p=0.001) or have been hospitalized within 3 months of RT (16% vs. 8%, p=0.005). Patients who did not complete treatment were more likely to have a KPS<70 than those who completed treatment (84% vs. 51%, p<0.001). Patients with a BMI<25th percentile were less likely to complete RT than those with a BMI≥25th percentile (62% vs. 76%, p=0.02). Patients who did not complete RT were prescribed more fractions than those who completed RT (median 8 vs. 5 fractions, p=0.001) and were more likely to be treated for brain than bone metastases (21% vs. 11%, p<0.001). The rate of D30RT was not significantly higher in patients treated for brain metastases than bone metastases (42% vs. 29%, p=0.13). Patients who did not complete RT had a shorter period from last RT to death compared to those who did complete treatment (median 18 vs. 73 days, p<0.001). Patients unable to complete their last RT course were more likely to be in TEACHH group C (24% vs. 11%, p<0.001) and Chow group III (55% vs. 32%, p<0.001).

Increased hospice enrollment was associated with a longer interval since diagnosis (28 months vs. 21 months, p=0.04). Hospice was less likely to be involved when inpatients were evaluated for RT compared to outpatients (31% vs. 42%, p=0.02). There was no association between age at diagnosis, age at RT, TEACHH or Chow score, or KPS and hospice involvement. Patients enrolled in hospice were less likely to die in a hospital setting (6.2%) but rather at home (67%) or in a non-acute care inpatient setting (27%, inpatient hospice unit or skilled nursing facility) compared to those not enrolled in hospice (81% in a hospital, 13% at home, 6% non-acute care inpatient) (p<0.001).

Discussion

Almost one-quarter of patients receiving palliative RT in this series were treated within their last 30 days of life, slightly higher than reported elsewhere, though Ellsworth et al. did find that in a cohort of patients receiving RT for bone metastases, 26% were treated within 30 days of death [8,10,14]. Gripp et al. demonstrated that 15% of patients referred for palliative RT died within 30 days of admission, however this number may be lower than what we observed due to poorer performance status in their cohort (KPS<50 in >90% of patients compared to 25% of patients in our study), in whom RT may have been deferred [8].

Forty-two percent of patients who received RT within 30 days of death in this cohort did not complete their planned RT course, consistent with the literature [15]. Identification of patients who may not benefit from treatment requires physicians to prognosticate, a task that is difficult and often overly optimistic [16,17]. Several tools have been developed to assist in estimating life expectancy. The palliative prognostic index uses palliative performance status, which is strongly correlated with and can be used interchangeably with KPS, oral intake, and clinical symptoms such as dyspnea, delirium, and edema to estimate life expectancy in patients receiving palliative care [18,19], and performs comparably to similar scores that also take into account white blood cell count, lymphocyte percentage, or delirium in cancer patients [20]. A nomogram has also been created that includes time since diagnosis, performance status, albumin, LDH, and lymphocyte count to predict 15, 30, and 60-day survival [21].

These tools, however, do not evaluate prognosis using cancer specific characteristics. The TEACHH score and Chow model are two prognostic tools that have been developed to predict life expectancy in patients with advanced cancer [12,13]. Both take into account KPS and primary diagnosis; the Chow model also incorporates non-bone metastases while the TEACHH score includes prior chemotherapy, recent hospitalizations, and specifically hepatic metastases.

The TEACHH score categorizes patients into three groups (A, B, and C) with distinct survival times from the start of RT (19.9 months, 5 months, and 1.7 months, respectively) [12]. The Chow “number of risk factors” model categorizes patients into three groups (I, II, and III) with median survival times of approximately 15, 6.5, and 2.5 months respectively [14]. In our cohort, median survival was shorter than estimated across all TEACHH and Chow groups (Table 1). This may reflect use of palliative RT earlier in the disease course among the TEACHH cohort, with a shorter time from diagnosis to RT consult (1.8 months, calculated as the sum of time from diagnosis to metastasis and from metastasis to RT consult), compared to 28 months in our cohort. Patients in our cohort were also more likely to have received prior palliative RT than patients in the TEACHH cohort (44% vs. 12.5%). Compared to the Chow training set, our cohort had a substantially lower percentage of patients with bone-only metastases (17% vs. 29%), which may translate into a more significant disease burden and thus poorer prognosis in our patients.

As only 45% of patients (30/66) in TEACHH group C and 36% of patients (68/191) in Chow group III died within 30 days of RT, the integrated prognostic tools currently available do not appear sufficiently specific to identify patients at risk for imminent death at the time of RT consultation.

In the United States, there is a tendency to prescribe more protracted treatment regimens in patients with longer anticipated survival [22]. Initial concern regarding durability of control following short course RT may have stemmed from higher re-treatment rates seen following single-fraction RT in RTOG 9714 [23], however the Dutch Bone Metastases Study showed that re-irradiation occurred at a higher rate among non-responders and at lower pain scores in the cohort that received single fraction RT compared to the cohort that received multi-fraction RT, despite similar overall response rates, time to, and duration of response [3]. This suggests that higher retreatment rates after single fraction RT may be due to physician views on the safety of retreatment.

A large body of evidence has demonstrated that single fraction RT courses are as effective as more protracted courses with regard to onset of symptomatic improvement, duration of relief, relative proportion of patients experiencing improvement, and subsequent quality of life in patients with bone metastases [1,24,25]. Similarly, overall survival and functional outcomes are similar between shorter and longer RT courses in the treatment of malignant cord compression, though local control may be improved with longer treatment courses [26]. Similarly, while more fractionated schedules may result in improved PFS in patients with brain metastases, several trials have demonstrated no improvement in survival or neurological status [27].

However, a survey of practicing members of the American Society of Radiation Oncology suggests the most common palliative fractionation pattern in the United States remains 30 Gy in 10 fractions; single-fraction treatment is more common among those practicing in Canada, Australia, and New Zealand [28]. In a survey of radiation oncologists practicing within the Veterans Healthcare Administration, physicians who had been in practice for more than 10 years were less likely to offer single fraction RT compared to those with fewer years in practice (63% vs. 90%, p=0.01) suggesting there may be shifts in practice patterns over time [29]. Of note, this survey also found that those who had ever worked in private practice were less likely to offer single fraction RT (64% vs. 88%, p=0.03), suggesting that practice patterns may be influenced by practice setting.

Patients receiving RT at the end of life are increasingly receiving more advanced treatment modalities, with a decrease in the proportion receiving 2D RT from 75% to 33% from 2000 to 2009 [30]. Use of 3D RT increased from 27% to 59%, and use of IMRT increased from 0% to 6.2% over the same period. As patients live longer with advanced cancer, and potentially receive more palliative RT courses, there may be indications for such techniques, including retreatment or treatment in close proximity to prior fields. However more advanced planning techniques require more planning and quality assurance time, which is already limited for patients with poor prognosis.

When used appropriately, palliative RT in patients with advanced cancer may relieve symptoms and preserve quality of life. Despite the cost of RT, palliative radiotherapy at the end of life may not translate to increased costs of care in patients appropriately referred to hospice [9].

Together this data suggests we may not be optimally caring for patients at the end of life and that there are many questions that still need to be explored in order to optimize timing and dose of palliative radiation therapy for these patients. Development of prognostic models may allow better patient selection in this context, however the current tools available are not specific for patients at risk for death within 30 days of treatment. Earlier integration of palliative care or hospice services may allow patients and physicians to optimally direct treatment at the end of life.

As all patients in this study received palliative RT to a site of metastatic disease, which is generally not available on hospice, our cohort is likely enriched with patients interested in pursing more aggressive treatment options; thus the rate of hospice involvement in our cohort is not representative of practice patterns at our institution or more broadly generalizable. Unfortunately access to palliative RT while on hospice is quite limited, with 1%-3% of patients serviced by hospice agencies receiving RT [31,32]. Pilot programs have been developed to increase access to RT on hospice, however billing for services remains a significant hurdle to implementation, and patient volume described in the literature is limited [33]. Furthermore, maintaining such programs may be resource intensive due to high rates of personnel turnover [34]. Given the median cost for single fraction RT is approximately $1800 (23) and Medicare hospice payment rates may reach $976 for those requiring continuous home care (for the 2018 fiscal year , compared to $193 for routine home care), it may be possible to find a way to make palliative RT economically feasible [33].

This study is limited in that data was obtained retrospectively and may be incomplete, particularly for patients who were seen prior to the transition to electronic medical records or who received care at other institutions. In particular, data regarding prior chemotherapy was quite limited; while we typically had records documenting the regimen, we often lacked the total number of cycles received. Documentation of the specific indication for palliative RT was inconsistent and highly heterogeneous, which made further analysis difficult. Furthermore, due to the retrospective nature of the data, our information regarding symptomatic improvement and quality of life in patients undergoing palliative radiation at the end of life is limited, however warrants further investigation. One study has suggested that in patients receiving palliative RT within 30 days of death, only 26% may experience some measure of palliation of their symptoms [17].

Our findings are also limited in that patients treated at our institution may have more advanced disease than patients seen in the community, especially those enrolled in Phase I trials or seen in the inpatient setting. Additionally, a significant proportion of patients not enrolled in hospice were being followed by palliative care services. We were unable to more thoroughly assess patterns of palliative care referrals or quantify use of palliative care services in this cohort due to changes in referral codes over time. However it is likely that end-of-life and goals-of-care discussions were occurring more often than it would seem solely based on the rate of hospice enrollment.

Conclusion

A substantial proportion of patients with advanced cancer undergo palliative RT within 30 days of death. Radiotherapy at the end of life must align with patient-directed goals of care, and offer maximal palliation without interfering with other palliative or hospice practices aimed at maintaining quality of remaining life. Further work is needed to design an integrated prognostic tool that can be used to identify patients at high risk for imminent mortality.

References

  1. Chow E, Zeng L, Salvo N, Dennis K, Tsao M, et al. (2012) Update on the systematic review of palliative radiotherapy trials for bone metastases. Clin Oncol (R Coll Radiol) 24: 112-124.
  2.  McDonald R, Ding K, Brundage M, Meyer  RM, Nabid A, et al. (2017) Effect of radiotherapy on painful bone metastases: A secondary analysis of the NCIC clinical trials group symptom control trial SC.23. JAMA Oncol 3: 953-959.
  3.  van der Linden YM, Lok JJ, Steenland E, Martijn H, van Houwelingen H, et al. (2004) Single fraction radiotherapy is efficacious: A further analysis of the dutch bone metastasis study controlling for the influence of retreatment. Int J Radiat Oncol Biol Phys 59: 528-537.
  4. Dennis K, Wong K, Zhang L, Culleton S, Nguyen J, et al. (2011) Palliative radiotherapy for bone metastases in the last 3 months of life: Worthwhile or Futile? Clin Oncol 23: 709-715.
  5. Bezjak A, Adam J, Barton R, Panzarella T, Laperriere N, et al. (2002) Symptom response after palliative radiotherapy for patients with brain metastases. Eur J Cance 38: 487-496.
  6. Chow E, Davis L, Holden L, Tsao M, Danjoux C (2005) Prospective assessment of patient-rated symptoms following whole brain radiotherapy for brain metastases. J Pain Symptom Manage 30: 18-23.
  7. Mulvenna  P, Nankivell M, Barton R, Faivre-Finn C, Wilson P, et al. (2016) Articles Dexamethasone and supportive care with or without whole brain radiotherapy in treating patients with non-small cell lung cancer with brain metastases unsuitable for resection or stereotactic radiotherapy (QUARTZ): results from a phase 3, non-inferiority, randomised trial. The Lancet 388: 2004-2014.
  8. Gripp S, Mjartan S, Boelke E, Willers R (2010) Palliative radiotherapy tailored to life expectancy in end-stage cancer patients: reality or myth?. Cancer 116: 3251-3256.
  9. Guadagnolo BA, Liao K-P, Elting L, Giordano S, Buchholz  TA, et al. (2013) Use of Radiation Therapy in the Last 30 Days of Life Among a Large Population-Based Cohort of Elderly Patients in the United States. J Clin Oncol 31: 80-87.
  10. Ellsworth SG, Alcorn SR, Hales RK (2014) Patterns of care among patients receiving radiation therapy for bone metastases at a large academic institution. Int  J  Radiat Oncol  Biol Phys  89: 1100-1105.
  11. Dewys WD, Begg C, Lavin PT, Band PR, Bennett JM, et al. (1980) Prognostic effect of weight loss prior to chemotherapy in cancer patients. The American Journ of Med 69: 491-497.
  12. Krishnan MS, Epstein-Peterson Z, Chen Y-H, Tseng YD, Wright AA, et al. Predicting life expectancy in patients with metastatic cancer receiving palliative radiotherapy: The TEACHH model. Cancer 120: 134-141.
  13. Chow E, Abdolell M, Panzarella T, Harris K, Bezjak  A, et al. (2008) Predictive Model for Survival in Patients With Advanced Cancer. J Clin Oncol 26: 5863-5869.
  14. Tiwana MS, Barnes M, Kiraly A, Olson RA (2016) Utilization of palliative radiotherapy for bone metastases near end of life in a population-based cohort. BMC Palliat Care 15: 2.
  15. Toole M, Lutz S, Johnstone PAS (2012) Radiation oncology quality: Aggressiveness of cancer care near the end of life. J Am Coll Radiol 9: 199-202.
  16. Gripp S, Moeller S, Bölke E, Schmitt G, Matuschek C, et al. (2007) Survival prediction in terminally ill cancer patients by clinical estimates, laboratory tests, and self-rated anxiety and depression. J Clin Oncol 25: 3313-3320.
  17. Chow E, Davis L, Panzarella T, Hayter  C, Szumacher  E, et al. (2005) Accuracy of survival prediction by palliative radiation oncologists. Int  J  Radiat  Oncol Biol Phys 61: 870-873.
  18. Morita T, Tsunoda J, Inoue S, Chihara S (2016) Improved accuracy of physicians' survival prediction for terminally ill cancer patients using the Palliative Prognostic Index. Palliat Med 15: 419-424.
  19. Subramaniam S, Thorns A, Ridout M, Thirukkumaran T, Osborne TR (2015) Accuracy of prognosis prediction by PPI in hospice inpatients with cancer: a multi-centre prospective study. BMJ Support Palliat Care 5: 399-404.
  20. Maltoni M, Scarpi E, Pittureri C, Martini F, Montanari L, et al. (2012) Prospective comparison of prognostic scores in palliative care cancer populations. The Oncol 17: 446-454.
  21. Feliu J, Jiménez-Gordo AM, Madero R, Rodríguez-Aizcorbe JR, Espinosa E, et al. (2011) Development and validation of a prognostic nomogram for terminally ill cancer patients. J Natl Cancer Inst 103: 1613-1620.
  22. Bekelman JE, Epstein AJ, Emanuel EJ (2013) Single- vs Multiple-Fraction Radiotherapy for Bone Metastases From Prostate Cancer. JAMA 310: 1501-1502.
  23. Hartsell WF, Scott CB, Bruner DW, Scarantino CW, Ivker RA, et al. (2005) Randomized Trial of Short- Versus Long-Course Radiotherapy for Palliation of Painful Bone Metastases. JNCI J Natl Cancer Inst 97: 798-804.
  24. Wu JS-Y, Wong R, Johnston M, Bezjak A, Whelan T, et al. (2003) Meta-analysis of dose-fractionation radiotherapy trials for the palliation of painful bone metastases. Int  J  Radiat  Oncol  Biol Phys 55: 594-605.
  25. Westhoff PG, Verdam MGE, Oort FJ, Jobsen JJ, van Vulpen M, et al. (2016) Course of Quality of Life After Radiation Therapy for Painful Bone Metastases: A Detailed Analysis From the Dutch Bone Metastasis Study. Int J  Radiat Oncol Biol  Phys 95: 1391-1398.
  26. Rades D, Lange M, Veninga T, Stalpers LJ, Bajrovic A, et al. (2011) Final results of a prospective study comparing the local control of short-course and long-course radiotherapy for metastatic spinal cord compression. Int  J Radiat Oncol Biol Phys 79: 524-530.
  27. Tsao MN, Rades D, Wirth A, Lo SS, Danielson BL, et al. (2012) Radiotherapeutic and surgical management for newly diagnosed brain metastasis(es): An American Society for Radiation Oncology evidence-based guideline. Prac Radiat Oncol 2: 210-225.
  28. Fairchild A, Barnes E, Ghosh S, Ben-Josef E, Roos D, et al. (2009) International patterns of practice in palliative radiotherapy for painful bone metastases: evidence-based practice? Int  J  Radiat  Oncol  Biol Phys 75: 1501-1510.
  29. Moghanaki D, Cheuk AV, Fosmire H, Anscher MS, Lutz ST, et al. (2014) Availability of single-fraction palliative radiotherapy for cancer patients receiving end-of-life care within the Veterans Healthcare Administration. J Palliat Med 17: 1221-1225.
  30. Guadagnolo BA, Liao K-P, Giordano SH, Elting LS, Buchholz TA, et al. (2014) Increasing use of advanced radiation therapy technologies in the last 30 days of life among patients dying as a result of cancer in the United States. J Oncol Pract 10: e269-276.
  31. Lutz S, Spence C, Chow E, Janjan N, Connor S (2004) Survey on use of palliative radiotherapy in hospice care. J Clin Oncol 22: 3581-3586.
  32. Schuster J, Han T, Anscher M, Moghanaki D (2014) Hospice providers awareness of the benefits and availability of single-fraction palliative radiotherapy. J Hosp Palliat Nurs 16: 67-72.
  33. Update to Hospice Payment Rates, Hospice Cap, Hospice Wage Index, and Hospice Pricer for FY 2018.
  34. Schuster JM, Smith TJ, Coyne PJ, Lutz S, Anscher MS, et al. (2014) Clinic offering affordable radiation therapy to increase access to care for patients enrolled in hospice. J Oncol Pract 10: e390-395.

Citation: Wu SY, Singer L, Boreta L, Garcia MA, Fogh SE, et al. (2019) Palliative Radiotherapy at the End of Life. J Palliat Care Med 9: 355. DOI: 10.4172/2165-7386.1000355

Copyright: © 2019 Wu SY, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Post Your Comment Citation
Share This Article
Article Usage
  • Total views: 1987
  • [From(publication date): 0-2019 - Jul 17, 2024]
  • Breakdown by view type
  • HTML page views: 1399
  • PDF downloads: 588
Top