Utilization of Patient-Reported Outcomes to Guide Symptom Management during Stereotactic Body Radiation Therapy for Clinically Localized Prostate Cancer

Introduction Utilization of patient-reported outcomes (PROs) to guide symptom management during radiation therapy is increasing. This study focuses on the use of the Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP) as a tool to assess urinary and bowel bother during stereotactic body radiation therapy (SBRT) and its utility in guiding medical management. Methods Between September 2015 and January 2017, 107 patients with clinically localized prostate cancer were treated with 35–36.25 Gy via SBRT in five fractions. PROs were assessed using EPIC-CP 1 h prior to the first fraction and after each subsequent fraction. Symptom management medications were prescribed based on the physician clinical judgment or if patients reported a moderate to big problem. Clinical significance was assessed using a minimally important difference of 1/2 SD from baseline score. Results A median baseline EPIC-CP urinary symptom score of 1.5 significantly increased to 3.7 on the day of the final treatment (p < 0.0001). Prior to treatment, 9.3% of men felt that their overall urinary function was a moderate to big problem that increased to 28% by the end of the fifth treatment. A median baseline EPIC-CP bowel symptom score of 0.3 significantly increased to 1.4 on the day of the final treatment (p < 0.0001). Prior to treatment, 1.9% of men felt that their overall bowel function was a moderate to big problem that increased to 3.7% by the end of the fifth treatment. The percentage of patients requiring an increased dose of alpha-antagonist increased to 47% by the end of treatment, and an additional 28% of patients required a short steroid taper to manage moderate to big urinary problems. Similarly, the percentage of patients requiring antidiarrheals reached 12% by the fifth treatment. Conclusion During the course of SBRT, an increasing percentage of patients experienced clinically significant symptoms many of which required medical management. Monitoring patient symptoms during treatment allowed for prompt detection and management of acute urinary and bowel symptoms. The usage of symptom management medications was high in this study compared to historical controls and may be due to increased physician awareness of moderate to big patient problems.


BACKGRoUNd
The utilization of stereotactic body radiation therapy (SBRT) for the treatment of clinically localized prostate cancer is increasing (1). SBRT precisely delivers high doses of radiation to the prostate while minimizing radiation exposure to the bladder and rectum. With SBRT, biochemical disease-free survival is high, while late morbidity has been comparable to conventionally fractionated radiation therapy (2,3). Currently, there are limited data suggesting that any particular treatment for prostate cancer has superior outcomes compared to the others (4,5). As a result, the patient's choice of intervention is generally guided by their preference for a given treatment's side effect profile. Prostate SBRT may have a higher rate of grade 2 acute toxicities than conventionally fractionated radiation therapy (6,7). However, they may be of shorter duration, and many patients may still choose SBRT due to its convenience (8) and lower PSA nadirs (9). Thus, prostate SBRT utilization is likely to continue to gain popularity emphasizing the importance of developing clinical strategies to identify urinary and bowel symptoms early and individualize management to improve each patient's quality of life (QOL) during treatment. Utilization of patient-reported outcomes (PROs) to guide acute symptom management during radiation therapy is increasing (10). One such example is the Expanded Prostate Cancer Index Composite-26 (EPIC-26), which is the standard questionnaire employed to assess treatment-related morbidity on prostate cancer clinical trials (11)(12)(13). However, its 26 questions may be too burdensome for repetitive measures over a short-time period. Excessive respondent burden has shown to reduce questionnaire response rates and data accuracy (14). The Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP) is a single-page version of the EPIC-26 that was developed for general clinical use (15,16). It is a psychometrically validated questionnaire that allows for multiple assessments over a short period of time while minimizing patient burden (15). It contains 16 questions that assess several health-related QOL domains including the urinary and bowel domains.
Limited data are available on PROs during SBRT. Urinary and bowel symptoms commonly present during the 2-week course of SBRT. Further knowledge in this area would improve patient expectations prior to treatment. The objective of this study was to prospectively collect and report the urinary and bowel QOL outcomes during SBRT in patients with clinically localized prostate cancer. In addition, we demonstrate the feasibility of incorporating the EPIC-CP into daily clinical practice during a course of radiation therapy and its utilization in symptom management.

Patient selection
The Medstar Georgetown University Hospital Internal Review Board (IRB) approved this single-institution prospective QOL study (IRB 12-1175). Patients eligible for study inclusion had prostate cancer treated with SBRT over 2 weeks. All patients provided informed consent prior to treatment. Patient and treatment characteristics such as age, race, prostate volume, pretreatment PSA, T stage, Gleason score, risk groups, hormone treatment, and dose were acquired from the medical records. Risk groups were defined using the D' Amico criteria.

sBRt treatment Planning and delivery
Stereotactic body radiation therapy treatment planning and delivery were performed as previously described (6,7). Gold fiducials were placed into the prostate using ultrasound guidance. Fused thin cut CT images and high-resolution MR images were used for treatment planning. The clinical target volume (CTV) included the prostate and proximal seminal vesicles. The planning target volume (PTV) included a 3-mm (inferior, superior, and posterior) or 5-mm (anterolateral) expansion around the CTV. A prescription dose of 35-36. 25 Gy was delivered to the PTV in five fractions of 7-7.25 Gy over 2 weeks. The bladder, prostatic urethra, membranous urethra, and rectum were contoured and evaluated with dose-volume histogram analysis during treatment planning as previously described (7). Target position was confirmed multiple times during each treatment with a minimum of three properly placed fiducials (17). Prophylactic alpha-adrenergic antagonists were initiated 5 days prior to SBRT and continued throughout the treatment course. Patients were instructed to start a low-residual diet 5 days prior to SBRT simulation and remain on it until 1 week after the completion of treatment. Enemas were performed prior to simulation and each treatment. Symptom management medications were prescribed based on physician clinical judgment (SPC) or if patients reported a moderate to big problem. In general, patients with bothersome urinary symptoms were managed with alpha-adrenergic antagonist dose increases. Patients with refractory urinary symptoms were treated with a short steroid taper (4 mg dexamethasone for 7 days followed by 2 mg dexamethasone for 7 days). Patients with bothersome bowel symptoms were managed with anti-diarrheal medication (loperamide).

Follow-up and statistical Analysis
On-treatment PRO assessment time points were prospectively collected 1 h prior to the first SBRT fraction and after each subsequent treatment using the EPIC-CP as part of the on-treatment visit (OTV). The EPIC-CP is a validated tool that measures urinary and bowel bother (15). Furthermore, EPIC-CP scores at initial consultation (baseline) and 1 week post-SBRT were obtained from the EPIC-26 questionnaire that is filled out at these time points in our clinic (6,7). The score for each EPIC-CP question was calculated from the corresponding question in the EPIC-26 as previously described (18). To statistically compare changes between time points, the levels of responses were assigned a score, and the significance of the mean changes in the scores was assessed by paired t-test. Each domain contained three questions that were assigned numerical scores of 0-4. The domain scores were the summation of the three question scores (0-12) with higher numbers corresponding to increased bother. The responses to individual questions were grouped into three clinically relevant categories (no problem, very small to small problem, and moderate to big problem). Wilcoxon signed-rank test and chi-square analysis were used to assess differences in QOL scores in comparison to baseline. Paired t-test was used to assess the significance of the change in scores. Clinical significance was assessed using minimally important difference (MID) in EPIC-CP score, which is defined as a difference of one half SD from baseline score (19).

ResULts
One-hundred seven patients with clinically localized prostate cancer were treated on a prospectively conducted IRB-approved institutional protocol between September 2015 and January 2017. The median patient age was 71 years (53-86 years) (  Figure 1). Baseline EPIC-CP summary domain scores and mean changes from baseline to week 1 post-SBRT are shown in Table 3.
A median baseline EPIC-CP urinary symptom score of 1.9 significantly increased to 3.3 1 week after the completion of treatment (p < 0.0001) (Table 3; Figure 2). Changes in EPIC-CP urinary symptom score were clinically significant by third treatment, exceeding the MID of 1.0. Prior to treatment, 11.2% of men felt that their overall urinary function was a moderate to big problem that increased to 37.9% by 1 week after the completion of treatment ( Table 4). The proportion of patients experiencing clinically meaningful specific urinary symptoms (moderate to big problem) also increased: dysuria from 0 (baseline) to 15.8%   (1 week post-SBRT); urine retention from 6.5 (baseline) to 11.6% (1 week post-SBRT); and urinary frequency from 11.2 (baseline) to 30.5% (1 week post-SBRT) ( Table 4). The percentage of patients requiring an increased dose of alpha-antagonist increased to 47% by the fifth treatment, and an additional 28% of patients required a short steroid taper to manage moderate to big urinary problems (Table 2; Figure 1). Clinically significant bowel symptoms were less common prior to and during SBRT treatment than urinary symptoms. A median baseline EPIC-CP bowel symptom score of 0.8 significantly increased to 3.4 1 week after the completion of treatment (p < 0.0001) (Table 3; Figure 3). Changes in EPIC-CP bowel symptom score were clinically significant by 1 week after the completion of treatment, exceeding the MID of 0.8. At baseline, 3.7% of men felt that their overall bowel function was a moderate to big problem that increased to 21.1% 1 week after the completion of treatment ( Table 4). The proportion of patients experiencing clinically meaningful specific bowel symptoms (moderate to big problem) also increased: bowel urgency/rectal pain from 1.9% (baseline) to 23.2% (1 week post-SBRT) and bowel frequency from 1.9% (baseline) to 14.7% (1 week post-SBRT) ( Table 4). The percentage of patients requiring antidiarrheals reached 12% by the fifth treatment (Table 2; Figure 1). dIsCUssIoN Acute side effects are an important consideration when prostate cancer patients are deciding on their treatment. SBRT is an extremely hypofractionated form of radiation therapy that may have more severe acute side effects than conventionally fractionated radiation therapy (6,7). A better understanding of the acute side effect profile of prostate SBRT would facilitate better patient education. Understanding the risk of potential acute side effects prior to beginning treatment and appropriately managing them when they occur may also prevent treatment regret (8). Thus, this study assessed patient-reported urinary and bowel symptoms during SBRT.
In this study, we assessed urinary and bowel symptoms on every day of treatment using the EPIC-CP. The EPIC-CP is a one-page questionnaire that was completed by the patient with the aid of the study coordinator (Malika Danner). Due to the low response burden, we were able to obtain a high response rate (100%) on every day of treatment. In the opinion of the radiation oncologist (SC), the questionnaire was helpful in guiding management decisions and did not greatly increase the length of the OTV.
Treatment interruptions during radiotherapy due to acute urinary and bowel symptoms may negatively affect cancer control (20). During the 2-week course of SBRT treatment, 46% of patients developed moderate to big problems with urinary and/or bowel function. This appears greater than the number of patients who experienced clinically significant symptoms during conventionally fractionated radiation therapy (21)(22)(23). Although the incidence of acute grade 2 toxicity appears high in this study, no patient's treatment was prolonged due to treatment related symptoms. This is possibly due to our timely medical management of moderate to big problems.
The usage of symptom management medications was high in this study as compared to historical controls (24). In this study, approximately 50% of patients required acute medical management for clinically significant urinary symptoms. This is higher than the 35% of patient whom we first reported who required medical management of urinary symptoms in the first month following prostate SBRT (24). Likewise, in this study, 12% of patients required acute medical management for clinically significant bowel symptoms. Once again, this is higher than the 5% of men who required medical management of bowel symptoms in our prior research (24). In the opinions of the authors, this increased rate of medication prescription may be due to increased physician awareness of moderate to big patient problems secondary to the use of frequent questionnaire administration.
This study has several limitations. Although the EPIC-CP has been validated to assess QOL outcomes in prostate cancer patients treated with radiation therapy (15), it has not specifically been validated to show changes in urinary and bowel symptoms on an every-other-day basis (25). EPIC-CP questionnaires were not administered at baseline and 1 week posttreatment. Thus, to obtain EPIC-CP scores at these time points for comparison, the answers to the corresponding EPIC-26 question were utilized to generate an EPIC-CP score at baseline and 1-week post-SBRT. In addition, the EPIC-CP does not have a question regarding rectal bleeding (18). However, rectal bleeding is an uncommon acute bowel symptom following SBRT (<5%) (6) and would likely be captured in the overall bowel problem question. Most importantly, we had difficulty comparing our results with those of conventionally fractionated radiation therapy due to the utilization of alternative questionnaires with different definitions of clinically significant symptoms. The recent definition of a standard set of patient-centered outcomes for men with localized prostate cancer may decrease this problem in future studies (11).

CoNCLUsIoN
During the course of SBRT, an increasing percentage of patients experienced clinically significant symptoms many of which required medical management. Monitoring patient symptoms during treatment allowed for prompt detection and management of acute urinary and bowel symptoms. The usage of symptom management medications was high in this study compared to historical controls and may be due to increased physician awareness of moderate to big patient problems.

ethICs stAteMeNt
The Medstar Georgetown University Hospital Institutional Review Board (IRB) approved this single-institution prospective quality of life study (IRB 12-1175).

AUthoR CoNtRIBUtIoNs
MD and M-yH are lead authors who participated in data collection, manuscript drafting, table/figure creation, and manuscript revision. MA and TY aided in data collection. SL is the dosimetrist who contributed dosimetric data and figures. BC and