- Open Access
International validation of the EORTC QLQ-PRT20 module for assessment of quality of life symptoms relating to radiation proctitis: a phase IV study
Radiation Oncologyvolume 13, Article number: 162 (2018)
Although patients experience radiation proctitis post radiotherapy no internationally tested instruments exist to measure these symptoms. This Phase IV study tested the scale structure, reliability and validity and cross-cultural applicability of the EORTC proctitis module (QLQ-PRT23) in patients who were receiving pelvic radiotherapy.
Patients (n = 358) from six countries completed the EORTC QLQ-C30, QLQ-PRT23 and EORTC Quality of Life Group debriefing questions. Clinicians completed the EORTC Radiation Therapy Oncology Group scale. Questionnaires were completed at four time-points. The module’s scale structure was examined and validated using standard psychometric analysis techniques.
Three items were dropped from the module (QLQ-PRT23 → QLQ-PRT20). Factor analysis identified five factors in the module: bowel control; bloating and gas; emotional function/lifestyle; pain; and leakage. Inter-item correlations were within r = 0.3–0.7. Test-Retest reliability was high. All multi-item scales discriminated between patients showing symptoms and those without symptomology. The module discriminated symptoms from the clinician completed scoring and for age, gender and comorbidities.
The EORTC QLQ-PRT20 is designed to be used in addition to the EORTC QLQ-C30 to measure quality of life in patients who receive pelvic radiotherapy. The EORTC QLQ-PRT20 is quick to complete, acceptable to patients, has good content validity and high reliability.
Australian and New Zealand Clinical Trials Registry (ANZCTR) ACTRN12609000972224.
‘Radiation proctitis’ or ‘pelvic radiation disease’ is an unpleasant recurrent symptom that occurs following pelvic radiotherapy. Patients present with: anorectal pain, rectal bleeding and/or blood clots, bowel urgency, frequent diarrhoea, profuse mucous discharge, faecal and/or mucous incontinence [1,2,3,4]. Symptoms can have profound social and psychological consequences for patients and their families [5, 6].
The reported incidence of radiation proctitis ranges between 2 and 20% [2, 7]. However, the true incidence is likely to have been underestimated as clinician evaluation of symptoms utilise toxicity scales which focus on rectal bleeding and do not include assessment of urgency of defaecation and/or mucous/faecal incontinence. The move to conformal radiation techniques and intensity modulated radiotherapy has helped to reduce toxicity [8,9,10]. Conversely, there has been a trend towards dose escalation studies , external beam radiotherapy plus high dose rate brachytherapy  and an increase in the range of indications for pelvic radiation . Prospective trials are needed to establish the true incidence of the condition, the effect it has on patients’ quality of life (QoL) and the best forms of treatment.
QoL instruments provide a reliable and valid method of assessing the impact of treatment on patients’ lives and evaluating topical, medical, nutritional and surgical options . A recent systematic review provides a summary of the most frequently used QoL questionnaires for prostate cancer . The EORTC Quality of Life Group (QLG) modules developed for cervical (CX24) and prostate (PR25) cancer are also useful for identifying disease-specific issues, but do not adequately address problems associated with radiation proctitis. The one questionnaire directly assessing QoL in patients with radiation proctitis fails to address all the proctitis related issues and has not been validated internationally . The EORTC QLG therefore developed and tested a module specifically for radiation proctitis that could be administered with the EORTC QLQ-C30 (EORTC core questionnaire for quality of life) . We have published Phase I-III testing of the EORTC proctitis module in Australia  and Phase III pretesting of the module internationally .
The primary objective of this Phase IV study was to test the scale structure, reliability, validity and cross-cultural applicability of the proctitis module in patients who were receiving pelvic radiotherapy.
This prospective multi-centre study followed the EORTC QLG guidelines for module development . QoL data was collected alongside socio-demographic and clinical background data (including comorbidities). A trial protocol was developed and reviewed by the EORTC QLG prior to commencing the study. Ethics approval was gained from Curtin University and participating sites. The trial was also registered on the Australian and New Zealand Clinical Trials Registry (ANZCTR) ACTRN12609000972224.
Patients were recruited from Australia, Italy, Norway, Canada (French speaking), France and Germany. This enabled testing of the module in English, Norwegian, Italian, German and French. The module was translated for each language in collaboration with the translation team at the EORTC Quality of Life Department .
Patients were eligible if they were receiving a radical course of pelvic irradiation (> 45 Gray) and were able to converse freely in the language that the questionnaire was written. Patients were ineligible if they had previously received radiotherapy or the radiation dose prescribed was less than 45 Gray.
Radiation oncologists identified patients eligible for the study. Written informed consent was obtained. Participants were recruited from March 2010 and data collection ceased May 2014.
Data was collected at the following time-points:
At least 2 weeks prior to radiotherapy treatment (when they saw their radiation oncologist) (T1);
During first week of treatment (T2);
End of treatment (T3);
At the three to 6 months scheduled follow-up appointment, after treatment completion (T4).
Patients completed the first round questionnaires when they saw their radiation oncologist prior to commencing treatment. On subsequent occasions the questionnaires were either provided when they were attending for treatment or posted to them.
Patients completed a demographics questionnaire, the EORTC QLQ-C30  and the proctitis module (QLQ-PRT23). They also responded to these debriefing questions:
How long did it take you to complete the questionnaire?
Did anyone help you to complete the questionnaire?
Were there questions that you found confusing or difficult to answer?
Were there questions that you found upsetting?
The treating radiation oncologists completed the EORTC Radiation Therapy Oncology Group (RTOG) classification system at each time-point .
The primary endpoint was to evaluate the scale structure of the QLQ-PRT23. Using the EORTC QLG guidelines for sample size calculation the accepted ‘rule of thumb’ is that 15 responses per item are needed . As the Phase III module had 21 items, and allowing for a 10% dropout rate, we needed a sample of 350 participants.
The original study design was based on the 2002 EORTC QLG guidelines for module development . The statistical analysis plan was updated to reflect the 2011 EORTC QLG guidelines for module development(Version 4) . All analyses were conducted using SPSS version 23 with alpha levels set to p < .05.
The initial stage of the development of the EORTC proctitis module identified seven areas of interest for providing QoL information specific to radiation proctitis: incontinence, pain, bleeding, social function, role and performance, fatigue and emotional function. Of these, fatigue was dropped after consultation with health professionals and patients (Phase 1b). While the question items in subsequent versions of the proctitis module (PRT21, PRT23) were based on the remaining six areas, this paper presents the first formal analysis of the scale structure of this module.
Because radiation proctitis occurs as a possible side effect of pelvic radiotherapy the exploration of the scale structure of the module was performed on T3 (post treatment completion) data.
Exploratory Factor Analysis (EFA) was used to investigate the structure of QLQ-PRT23 questions 31–51 . Questions 52–54 were not included in the item and scale structure review analysis because they were single-item scales and collected specific clinical information relevant to patient comfort and future treatment.
The results of the EFA were refined through consultation with the research team. Multi-trait scaling analysis was used to test the construct validity (convergent and discriminant validity) of the proposed multi-item scales. Within the module, convergent validity was considered adequate when an item was highly correlated to its own proposed scale corrected for overlap, operationally defined as r ≥ 0.4 . Discriminant validity was supported when an item demonstrated lower correlations with other proposed scales compared to its own proposed scale. Possible scaling errors were flagged when an item correlated more highly to some other scale compared to its own proposed scale . Scaling failures were identified when this difference was greater than two standard errors .
The homogeneity, usefulness and level of fit of items within the proposed scale were examined. The internal reliability for the scales was assessed using Cronbach’s alpha coefficient with an r ≥ 0.70 considered adequate27.
Intra-class correlations coefficients (ICC) of the proposed scales between T1 (2 weeks before treatment) and T2 (first week of treatment) data sets and their test re-test reliabilities were examined. Significant differences in patient responses were not expected at these time-points . ICC’s of > 0.7 were considered acceptable and ICC’s > 0.9 were excellent .
Convergent validity of the QLQ-PRT20 was examined via correlations with conceptually similar rating scales from the QLQ-C30. Based on the item names, previous literature and team discussion prior to analysis the following scales were expected to correlate highly (r ≥ 0.4) at T3: QLQ-PRT20 Emotional Function/Lifestyle scale and the QLQ-C30 Global Health Status and Emotional and Social scales; QLQ-PRT20 Pain scale and the QLQ-C30 Pain scale.
Two methods were used to assess discriminant validity: Known Groups Analysis based on age , location/type of tumour, and presence of co-morbidities , and Responsiveness to Change at T2 (first week of treatment) and T3 (Post treatment).
In total, 358 patients participated: 181 from Australia; 86 from Italy; 47 from Norway; 34 from Canada (French speaking); four from France; and six from Germany. Patient demographics and clinical characteristics by country are summarized in Table 1. Further details about the treatment patients received for each diagnosis are provided in Additional file 1 and patient comorbidities are shown in Additional file 2. The attrition rate was 10%.
Qualitative survey responses were received at each time-point. At T1 responses were received from 281 participants. The response rates for follow-up questionnaires were similar (80%). Table 2 summarises response patterns for the follow-up questionnaires. Overall, 62% of participants who completed the qualitative follow up questions at T1 indicated they completed the questionnaires within 10 min, 23.5% took 11–15 min and 11.4% took 16–20 min. Similar rates were reported across the other times points.
Thirteen percent found at least one question confusing at T1, but most of these were related to bowel issues. Few issues were reported with the bowel related questions during or post treatment. Overall, the majority of participants did not have problems understanding the questions. Of those respondents who provided written comments: most provided additional clarifications and/or elaborated on co-morbidity issues.
Completion of QLQ questionnaires
The numbers of patients returning completed QLQ questionnaires (QLQ-C30 and QLQ-PRT23) was approximately 98% at T1. For the QLQ-PRT23 missing item rates were approximately 1%. Question 51 (Q51) “How unhappy would you feel if you lived the rest of your life with your bowel habit as it is now?” recorded the highest missing data (3.7% at T1). Participants may not have answered this question at T1 because they had not commenced radiotherapy. The question with the highest and most consistent rate of missing entries was Q53 “Highest number of times you had to open your bowels in any 24 hour period” with rates between 3 and 4% across T1-T4.
Investigation of possible cultural factors influencing the completion of the QLQ-PRT23 focused on the four main language groups rather than patient’s country of treatment: English, Italian, Norwegian and French (see Table 1).
Comparing these language groups, 78% of women recruited were from the Italian cohort. The Italian cohort were 2.8 times less likely (odds ratio) to have a comorbid disorder than members of the other language groups while the French cohort were 2.95 times more likely; χ2(3) = 18.73, p < .001. The Italian cohort were also significantly younger (5 years) than the other language groups; F(3,348) = 8.03, p < .001.
The response patterns for the T3 QLQ-PRT23 was found to be similar across the language groups although the Italian and Norwegian cohorts had higher symptom reporting on some items compared to the French and English-speaking cohorts: Specifically, items with higher symptom reporting for the Norwegian cohort were Q32, 42, 43 and high scores for the Italian cohort were Q40 and 48.
Item and scale structure review
Item and scale structure were assessed using the T3 QLQ-PRT23 responses. The QLQ-PRT23 consisted of 23 items with one optional question. The final three questions (Q52–54) were not included in the item and scale structure review as they concerned specific clinical information.
After review, items Q41 (presence of dark blood in stools), Q45 (Have you had to wear a pad because of your bowel problems?) and Q47 (Have your daily activities been limited by your bowel problems?) were dropped due to low prevalence, poor fit and/or multicollinearity.
The final module analysed was 20 items with an optional additional question and will now be identified as EORTC QLQ-PRT20.
Numerous factor structures were explored starting with the original six areas of interest which showed relatively poor fit. A five-factor structure best accounted for the data and after team discussions the structure shown in Table 3 was chosen as the most clinically parsimonious. Five factors descriptors were assigned: Bowel Control; Bloating and Gas; Emotional Function/Lifestyle; Pain and Leakage.
Multi-trait scaling analysis supported the EFA with one exception (Q46), which was moved out of the Bowel Control scale to the Emotional function/Lifestyle to correct for an indicated scaling failure. The results of the final multi-trait scaling analysis are in Table 4.
Overall, the reliability of the scales were acceptable with Cronbach α’s exceeding 0.70 for Bowel Control, Bloating and Gas, and Emotional Function/Lifestyle scales (Table 4) . The remaining scale; Leakage, was close to this level (0.693).
Test-retest reliability and validity analyses were performed on the linear transforms (outcomes 0–100) for the proposed scales similar to that outlined in the EORTC scoring manual . Pre-treatment test–retest reliability (T1 and T2) results are presented in Table 5. The ICCs for each of the multi-item scales were rated as fair (> 0.6) to acceptable (> 0.7).
The QLQ-PRT20 scales correlated well with the predicted scales from the QLQ-C30 (Table 6). Notably, the QLQ-PRT20 Emotional Functioning/Lifestyle scale demonstrated relatively high correlations with all the selected scales of the QLQ-C30, and the QLQ-C30 Pain Symptom scale showed similarly high correlations with all the QLQ-PRT20 multi-item scales with the exception of Leakage.
The QLQ-PRT20 scales were assessed on their ability to discriminate patient groups based on their age, cancer type (prostate, cervix or rectal), presence of co-morbidities, and RTOG scores (Table 7). All QLQ-PRT20 scales discriminated between patients showing acute symptoms of radiation proctitis and those without symptomology based on the T3 RTOG ratings (RTOG 0–no symptoms vs. RTOG 1 + acute symptoms; p ≤ .02, r’s = 0.16–0.37). Scores for Emotional Function/Lifestyle (p = 0.011, r = 0.17) and Leakage (p = 0.043, r = 0.14) further discriminated between mild or moderate symptoms. Examining the point estimates and 95% CI’s of the QLQ-PRT20 scales based on the absence or presence of RP symptoms (based on the RTOG scores) suggest that scores above 20 for the Bowel Control, Bloating and Gas, and Emotional Function and Lifestyle scales are indicative of significant concern (Additional file 3). For the Pain and Leakage scales, scores above 15 appear to be of significant concern.
Cancer type/location discriminated between acute and no symptomology for three of the scales; Bloating and Gas, Emotional Function/Lifestyle and Pain. Emotional Function/Lifestyle was the best discriminating scale with both cancers of the rectum and cervix showing significantly higher social/emotional disturbance ratings than the prostate group (p < .001, r = 0.28rectal and r = 0.25cervix). The Bloating and Gas scale, reported higher ratings for the cervix compared to the prostate group (p = .004, r = 0.19). The Pain scale showed a trend for higher rating in cervix group compared to the prostate group (p = .074, r = 0.13).
Younger (≤=63 years) respondents reported higher levels of impact/symptoms for both the Emotional Functioning/Lifestyle and Bloating and Gas scales when compared to older (> 74 years) respondents (r = 0.24 and r = 0.22 respectively).
Responsiveness to change
The QLQ-PRT20 scales all demonstrated a strong ability to detect post treatment change in the patients from T2 (first week of treatment) to T3 (end of treatment): MeanΔ’s 7.5–12, all p < .001).
This study examined the reliability, validity and psychometric properties of the EORTC QLQ-PRT23 in an international sample of 358 patients receiving pelvic radiotherapy. Individual items and the internal structure of the scale were reviewed. The revised version, the QLQ-PRT20 comprises five dimensions: Bowel Control; Bloating and Gas; Emotional Function/Lifestyle; Pain; and Leakage. Three additional items are included to gain specific clinical information relevant to patient comfort and future treatment.
The proposed scales structure of the PRT20 have good internal reliability and face validity. Overall, the internal psychometric properties are strong. Eighty-six percent of participants completed the questionnaire within 15 minutes and participants did not find the questionnaire problematic/distressing.
The QLQ-PRT20 scales correlated well with the predicted scales from the QLQ-C30, suggesting good convergent validity. The QLQ-PRT20 Emotional Function/Lifestyle scale correlated well with all scales of the QLQ-30 which is appropriate as they are measuring similar things. Furthermore, the QLQ-C30 Pain Symptom scale and Global Health Status of the QLQ-C30 showed moderate-high correlations with all the QLQ-PRT20 multi-item scales apart from the Leakage scale. The fact that leakage did not correlate well with any of the QLQ-C30 items may be because the scales are measuring different lifestyle components and leakage is not likely to be a complaint unless patients are receiving pelvic treatment. The items within the leakage scale focus on unintentional release (leakage) of wind, mucous or liquid stools which are pertinent to proctitis. The leakage scale was kept separate to bowel control and bloating and gas because the questions focus on different symptoms and psychometric analyses suggested a better fit as an individual scale. The Emotional and Social Functioning on the QLQ-C30 also did not correlate well with bowel control and bloating and gas on the QLQ-PRT20; however, this is to be expected because the scales are measuring different lifestyle components.
The Emotional Function/Lifestyle scale discriminated for tumour type/location, age and presence of comorbidities. The Bloating and Gas scale discriminated between tumour type/location and age groups. This suggests that pain and leakage symptoms were similar regardless of age, tumour location and comorbidities, bowel issues did not vary based on age or comorbidities and bloating and gas symptoms were the same regardless of comorbidities.
The QLQ-PRT20 discriminated consistently between patients showing acute symptoms of radiation proctitis and those without symptomology based on the treating physician RTOG ratings. Scores on the QLQ-PRT20 Emotional Function/Lifestyle and Leakage scales further discriminated between those based on the degree of their symptomology (mild or moderate symptoms). The QLQ-PRT20 is suitable for measuring patient QoL because it provides more detail than using a clinician completed RTOG score, particularly when acknowledging weaknesses of clinician completed scales such as RTOG have been identified . The QLQ-PRT20 also demonstrated a good ability to detect change in symptomology over time showing it to be appropriate for use in monitoring acute symptoms following pelvic radiotherapy.
Therefore, we contend that the QLQ-PRT20 alongside the EORTC QLQ-C30 is a suitable patient reported outcome that can be used to complement physician completed scales such as the RTOG scale. It provides a detailed picture of actual symptoms patients are experiencing following pelvic radiotherapy as well as providing a measure of how well the patient is coping with symptoms. The QLQ-PRT20 is different to site-specific modules because it focuses on quality of life related to side effects rather than treatment site and is effective in detecting symptoms specifically related to bowel issues experienced because of radiotherapy. We recommend that this module be used in conjunction with the EORTC QLQ-C30 to monitor patients’ side effects for pelvic radiotherapy.
A strength of this study is that it followed the EORTC QLG guidelines for module development for designing the study  and statistical analysis . Limitations include recruitment of a larger proportion of prostate cancer patients and less female patients. The intention of the study was to get broad coverage across a range of representative diagnoses because the focus was on treatment-related QOL rather than diagnosis-specific. Although there were differences in the populations recruited between the countries (e.g. more females were recruited from Italy and more prostate cancer patients overall) the response patterns for the T3 QLQ-PRT23 (i.e., clinically relevant) were compared graphically and found to be generally similar overall across the language groups. A further limitation is that this study did not fully reflect the coverage of countries/languages recommended within the EORTC QLG guidelines. The module was tested in four languages with a large proportion of patients being recruited from Australia (187/358), which may have caused some biases in relation to language and culture. This was due to challenges in accessing and recruiting sites by the study team. Whilst this clearly limits the conclusions drawn on the cross-cultural applicability, the study did cover broader regions based on language (Australia (English); Norway, Canada/France and Italy) recommended with the exception of Eastern Europe. However, it could be argued that it is unlikely that the results would have been very different had more international participants been recruited. Testing of the QLQ-BIL21 similarly reported that they recruited a larger proportion of participants in one country . Further research is needed to establish cross-cultural applicability of this module in different languages. Despite these limitations, we have shown that this module is relevant to patients in four countries with different diagnoses who received pelvic radiotherapy and demonstrated the scale structure, validity, reliability, and ability of this instrument to discriminate between symptoms.
The EORTC QLQ-PRT20 alongside the EORTC QLQ-C30 module is quick and easy to complete, acceptable to patients, has good content validity and high reliability (including test-retest reliability). Furthermore, we have shown that it can discriminate symptoms from clinician completed scoring and for age, gender and comorbidities. Further studies are required to determine the incidence of proctitis for different tumour sites and treatment regimens.
Australian and New Zealand Clinical Trials Registry
module for cervical cancer
Exploratory Factor Analysis
- EORTC QLG:
EORTC Quality of Life Group
European Organisation for Research and Treatment of Cancer
Intra-class correlations coefficients () of the proposed scales between
module for prostate cancer
EORTC core questionnaire for quality of life
quality of life questionnaire for proctitis
quality of life
Radiation Therapy Oncology Group scale
Time 1 = two weeks before treatment
Time 2 = first week of treatment
Time 3 = post treatment
Time 4 = At the three to six months scheduled follow-up appointment, after treatment completion
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This project was funded by the EORTC Quality of Life Group. Celine Fournier and Melissa Berg assisted in the management of the project and data collation. Additional collaborators include: Dr. Myriam Bouchard, Dr. Anne-Sophie Lessard and Dr. Julie Villa. Associate Professor Halkett is currently supported by a Research Fellowship from the Cancer Council of WA. Dr. Wigley is funded by the Australian Government’s Collaborative Research Networks (CRN) program. We also thank the participants who participated in the study.
Copies of the final module are available, upon compeletion of a signed agreement at the EORTC Quality of Life Department at http://groups.eortc.be/qol
This project was funded by the EORTC Quality of Life Group. A/Prof Halkett is currently supported by a Cancer Council of WA Research Fellowship.
Availability of data and materials
Please contact the authors for data requests.
Ethics approval and consent to participate
Ethics approval was gained from Curtin University and participating sites. Participants were provided with an information sheet and informed consent was gained prior to participating in the study.
Consent for publication
The authors declare that they have no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Treatment received by participants. (DOCX 18 kb)
Number of patients with existing co-morbidities and type. (DOCX 13 kb)
Means and 95% confidence intervals, range of the proposed QLQ PRT20 Proposed Scale compared to the RTOG score ratings indicting no symptoms (score = 0) vs. acute symptoms (score = 1+). (DOCX 13 kb)