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DOI: 10.5935/2526-8732.20200046
Patient reported outcome measure applicability in clinical oncology
Aplicabilidade das medidas de resultados relatados pelo paciente na oncologia clínica
ABSTRACT
Patient Reported Outcomes (PROs) are a report that comes from patients on a specific subject, describing how they feel about a condition or therapy. The term includes a range of constructions and methodology and can cover concepts such as symptoms to physical assessment, well-being and social involvement. The process can be described as a measure of patient reported outcome (Patient Reported Outcome Measure - PROM). In oncology, PROMs help healthcare professionals and systems to reduce the impact of treatment on patient's quality of life. In recent years, several studies have shown improvement in the evaluated outcomes. In our country, there is still little information on this subject, especially when it comes to cancer patients. Hence, we think that it is of utmost importance to review the particularities of this tool, in order to stimulate further discussion of the subject in our country.
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RESUMO
Os resultados relatados pelo paciente (RRPs) são relatórios provenientes de pacientes sobre um assunto específico, descrevendo como eles se sentem a respeito de uma condição ou terapia. O termo inclui uma gama de construções e metodologia, e pode abranger conceitos como sintomas para avaliação física, bem-estar e envolvimento social. O processo pode ser descrito como uma medida de resultado relatado pelo paciente (Patient Reported Outcome Measure - PROMs). Em oncologia, os RRPs ajudam os profissionais e sistemas de saúde a reduzir o impacto do tratamento na qualidade de vida do paciente. Nos últimos anos, diversos estudos demonstraram melhora nos resultados avaliados. Em nosso país, ainda são poucas as informações sobre o assunto, principalmente quando se trata de pacientes com câncer. Assim, pensamos ser da maior importância rever as particularidades desta ferramenta, a fim de estimular uma maior discussão sobre o assunto em nosso país.
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INTRODUCTION
Advances in oncology have recently promoted higher cure rates in some cases as well as significantly improved the survival of patients with metastatic disease. However, many of the new treatments are accompanied by non-negligible toxicities. Patients receiving cancer treatment have a variety of associated side effects such as fatigue, nausea and vomiting, alopecia, and pain.[ [1] ] In clinical practice, it is necessary to seek a balance between the benefits of prolonged survival or delayed progression with the possible negative effects of treatment on quality of life.[ [2] ]
In cancer treatment trials, the standard source of adverse symptom data is clinician reporting by use of items from the National Cancer Institute's (NCI) Common Terminology Criteria for Adverse Events (CTCAE),[ [3] ] and these outcomes are analysed only under clinician's impressions.
Despite the existence of validated questionnaires using information reported by patients to assess quality of life, these are processed within a methodology to provide a metric as a way of scoring.[ [4] ] Currently, there is a new emphasis on “survival” in which self- management and quality of life assessment have key roles to play.[ [5] ]
In this context, Patient Reported Outcome (PROs) are reports that come directly from patients on a specific subject without interpretation, describing how they feel about a condition or therapy.[ [6] ] The report includes a wide range of terms and methodology, covering concepts that can range from symptoms to physical assessment, well-being, and social involvement. The process can be described as a measure of patient reported outcome (Patient Reported Outcome - PROM).[ [4] ]
PROMs are tools used to capture a patient's perspective of their own treatments and care.[ [7] ] PROMs can be generic (measuring aspects of health status and quality of life common to most patients), disease-specific (e.g., cancer) or condition-specific (applicable to a service sector such as rehabilitation or mental health services or to a population segment such as the elderly).
In the specific case of oncology, PROMs can help doctors and health systems to reduce the impact of treatment on patients' quality of life thus contributing to better outcomes. In the last decade, several studies in different areas of oncology have included PROMs as part of the outcome's assessment.
In Brazil, there is still little information about PROMs, especially in the oncology area. The aim of this article is to review the usage history of this tool, its implications, benefits, and perspectives in cancer treatment. To demonstrate the importance of this approach and reinforce its use as an outcome in cancer treatment, we reviewed the literature and discussed the results and challenges for its use in an expanded way.
In the last decades, advances have been made for a better analysis of the quality of life of patients during health treatment. In this period, there is a greater involvement of patients in decision-making, aiming at a better quality of life for them.[ [11] ] PROMs are tools that give support to this analysis, and their study has grown in different areas of health. Nowadays, the countries with the most trials and the greatest implementation of PROMs in clinical practice are England, the Netherlands, Sweden, and the United States.[ [7] ]
In 1975, prior to the studies related to PROMs, Sweden started using the “quality of life records”, which were records with information about symptoms presented by patients noted by health professionals at the time. PROMs started to be introduced in England in the 2000s.[ [7] [11] ] In 2008, one of the first analyses took place with the evaluation of the satisfaction of patients undergoing mastectomy and breast reconstruction. In the following year, different studies investigated patients who underwent hip surgery, herniorrhaphy and varicose vein, showing benefits with the use of PROMs. After these studies, the use of this tool became mandatory in such elective surgeries in different centers in England.[ [11] ] The evaluation of PROMs in the cardiology field started in 2013, and one of its first studies have analysed the quality of life after myocardial revascularization.[ [11] [12] ]
In recent years new studies have appeared in Oncology. In 2017, a review from the Memorial Sloan Kettering Cancer Center demonstrated benefits with the use of PROMs as regarding quality of life and overall survival in patients undergoing cancer treatment.[ [14] ]
In 2019, the use of PROMs showed that women with breast cancer who underwent adjuvant radiotherapy had an impaired body image.[ [15] ] On the other hand, despite its advances, studies in certain areas are still lacking. As an example, a systematic review of 2019 evaluated studies related to quality of life in patients with ovarian cancer, however none of them used PROMs as a tool.[ [13] ]
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METHODS
Research on scientific articles was carried out on the PubMed platform (pubmed.ncbi.nlm.nih.gov) with the following terms: PROMS - Patient Reported Outcome, cancer and quality of life, from March to April of 2020. All the 18 studies identified in the search were included and are listed in[Table 1] . The present work is a narrative of the reviewed studies, regardless of the methodology applied in each study.
ARTICLE |
BODY LOCATION |
PROM ASSESSMENT METHOD |
CONCLUSION |
---|---|---|---|
Kundu et al. (2019)[26] |
PROSTATE |
PROMIS application for symptom assessment (anxiety, depression, pain, fatigue) during hormone therapy |
The use of online tools may assist in reducing the adverse effects of hormone therapy in men with prostate cancer. |
Lane et al. (2016)[27] |
PROSTATE |
Questionnaires already validated EPIC; ICIQ-UI; ICSmalaSF; HADS; EQ-5D-3L |
PROMS of cancer patients were like that of patients without cancer. |
Hoque et al. (2019)[28] |
PROSTATE |
The expanded prostate cancer index composite responded by |
Email is an interesting tool for collecting PROM information. |
Cuypers et al. (2018)[29] |
PROSTATE |
Patients participated in online treatment decisions with forms and counselling |
Patients who have not used online counselling need further guidance for decision making. |
Yue et al. (2018)[30] |
LUNG NON-SMALL CELLS |
Questionnaire: MD Anderson symptom inventory lung cancer module |
The use of PROMS allowed cancer patients to be identified with a greater risk of developing symptoms related to radiotherapy. |
Lenderking et al. (2019)[31] |
LUNG NON-SMALL CELLS |
Questionnaire: QLQ-C30 and GHS /QOL |
The outcomes reported by patients were associated with the response to treatment with brigatinib. |
Felip et al. (2018)[32] |
SQUAMOUS LUNG |
Questionnaire: QLQ-C30 and GHS/QOL |
Afatinib showed better quality of life than erlotinib. |
Lee et al. (2018)[33] |
LUNG NON-SMALL CELLS |
Questionnaire: EORTC QLQLC13; EORTC QLC- C30 |
Patients who used osimertinib had better quality of life as described by PROMS. |
Wu et al. (2018)[34] |
EGFR MUTATED LUNG |
Questionnaire: EORTC QLQLC13; EORTC QLC- C30 |
Afatinib presented a better symptom profile as described by PROMS. |
Sebastian et al. (2018)[35] |
LUNG NON-SMALL CELLS |
Questionnaire: PRO-CTCAE analyses |
Reported symptoms were mild to moderate in the group using osimertinib. |
Bordoni et al. (2018)[36] |
LUNG NON-SMALL CELLS |
Questionnaire: HRQoL |
Afatinib presented a better symptom profile as described by PROMS. |
Brow et al. (2018)[37] |
COLON |
Questionnaire: Short form 36QoL outcomes included the short form (SF)-36 GBFQ; FS |
Aerobic exercise has improved many HRQoL. |
Price and Bednarski et al. (2017)[38] |
COLON |
Trimodal combination: minimally invasive cx, ERP and Telerecovery |
|
Blaby et al. (2014)[39] |
BLADDER |
Questionnaire: Develop EORTC for bladder cancer |
|
Staehler et al. (2018)[40] |
KIDNEY |
Questionnaire: EORTC QLQ-C30) |
Patients using sunitinib had greater symptoms and worsened quality of life but were not clinically significant. |
Abernethy et al. (2009)[41] |
BREAST |
Questionnaire: FACT-G; FACT-B; MDASI; FACIT-F; FACIT-Self-Efficacy Scale; PCM, an 86-item survey for common cancer- and treatment-related symptoms; Satisfaction and acceptability survey |
33.3% of clinicians disclosed that their clinical decisions were influenced by symptom alerts; clinicians' email responses to symptom alerts were to maintain treatment course (46%), to assess the patient at the following clinic appointment (33%), or to prescribe a new symptom treatment (8%). |
Anderson et al. (2015)[42] |
BREAST |
Questionnaire: IVR-related pain and symptom List; MDASI; BQ-II; PMI PROMs |
16 of 50 (32%) of patients, at the first visit, felt encouraged to address symptoms with clinicians that they otherwise would not have discussed, which increased to 48% (16 of 33 patients) by the fourth visit. |
Bock et al. (2012)[43] |
BREAST |
Questionnaire: Unspecified PROM (symptoms and health history) |
More than half of symptoms mentioned by both patients and clinicians were addressed, regardless of number of symptoms. |
Improved outcomes
The number of new drugs approved for cancer treatment has increased exponentially in recent years. However, in many cases these treatments have received approval from regulatory agencies based on substitute outcomes (such as tumour reduction and/or progression-free survival), postponing the assessment of overall survival and quality of life after drug use is released.[ [16] ]
A data analysis study carried out between 2008 and 2012 showed that 67% of the drugs approved by the FDA (Food and Drug Administration) for cancer treatment did not demonstrate gains in overall survival or quality of life. Only 14% of the drugs approved demonstrated improvement in overall late survival when compared to previous treatments after an average of 4.4 years on the market.[ [17] ]
In Europe, a study carried out between 2009 and 2013 of drug approvals by the EMA (European Medicines Agency) presented similar data, with 57% of approvals with no impact on overall survival or quality of life, only 15% of the drugs presented a significant result in overall survival after an average of 5.5 years of commercialization.[ [18] ]
The clinical evaluation of the patient is crucial to start a new cancer therapy, with the performance scale (PS) of Karnofsky and the Eastern Cooperative Oncology Group (ECOG) being the most used. However, there is great variability between doctors, nurses, caregivers, and especially patients in this assessment. Health professionals tend to frequently overestimate the patient's PS when compared to their own perceptions of the PS.[ [19] ] Therefore, data from previous studies have shown that up to 50% of terminal cancer patients receive some form of cancer treatment in their last 30 days of life.[ [20] [21] ]
In this scenario, PROMs can have an impact on behavior change since in treatments with marginal benefits the patient's perception can be decisive for the start of a new treatment. Reducing treatments that have a significant impact on quality of life without leading to a clinically significant outcome improvement.
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Diseases assessed by PROMs
There are different impacts on quality of life among different types of cancer treatments. Symptoms and effects of treatment may vary according to the type of treatment such as surgery, radiotherapy, chemotherapy, immunotherapy, etc. Another determining factor is the location and type of cancer. Several studies have developed methods for PROM assessment according to the location of the tumour due to the different effects of treatments.
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#
DISCUSSION
The rapid expansion in the number of available PROMs made it difficult to select the most appropriate instrument for a defined objective.[ [8] ] This was exacerbated by the prolific development of digital tools and applications, many of which are well-intentioned, but lack rigorous development methods to assess item selection, validity, reliability, responsiveness, and interpretation.[ [9] ]
The methods of evaluating the outcome measures reported by patients are generated after a rigorous testing and review process to be validated.[ [22] ] Most of the scales developed are in the English language and were used in patients with mastery of that language.[ [23] ] Most of the studies that evaluated outcomes reported by patients in Brazilian articles about cancer used international questionnaires without valid translation. It is of utmost importance that questionnaires are adapted to the culture and language of the country where they are applied to remain reliable.[ [24] [25] ]
The small volume of articles found in this period and the great variability in methodology limit the quality of a possible systematic review. In this sense, we choose to carry out a narrative review, showing all the literature found, in order to encourage a discussion about the need for standardization of these studies.
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CONCLUSION
Cancer treatment involves different aspects, not only those related to objective outcomes such as free time for progression and overall survival, but also the possibility of providing a better quality of life for patients undergoing treatment. The use of PROMs meets this objective, and recent studies as mentioned in this review, have shown the benefits of using this tool in cancer patients. However, studies and standards are still lacking so that PROMs can have a wider coverage in different treatment centers. The approach of these aspects by the scientific community is extremely relevant so that we can standardize the evaluations and extract the best results from the application of PROMs.
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Conflicts of interest
The authors declare no conflict of interest relevant to this manuscript.
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- Basch E, Deal AM, Dueck AC, Scher HI, Kris MG, Hudis C. et al Overall survival results of a trial assessing patientreported outcomes for symptom monitoring during routine cancer treatment. JAMA 2017; Jul; 318 (02) 197-198
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Corresponding author:
Publication History
Received: 11 September 2020
Accepted: 05 October 2020
Article published online:
18 January 2021
© 2022. 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 work is properly cited.
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Alessandra Menezes Morelle, Fernando Castilho Venero, Rommel Fabricio Pereira da Silva, Rafael Dal Ponte Ferreira, Pedro Tofani Santanna. Patient reported outcome measure applicability in clinical oncology. Brazilian Journal of Oncology 2021; 17: e-20200046.
DOI: 10.5935/2526-8732.20200046
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REFERENCES
- Cella D, Peterman A, Passik S, Jacobsen P, Breitbart W.. Progress toward guidelines for the management of fatigue. Oncology 1998; Nov; 12 (11A) 369-377
- Kirkbride P, Tannock IF.. Trials in palliative treatment--have the goal posts been moved?. Lancet Oncol 2008; Feb; 9 (03) 186-187
- Diane MF, Savarese MD.. Common terminology criteria for adverse events [Internet]. Waltham. MA: UpToDate Inc; 2017. Nov cited ANO Mês dia Available from: https://www.uptodate.com/contents/common-terminology-criteriafor-adverse-events
- Wilson R.. Patient led PROMs must take centre stage in cancer research. Res Involv Engagem 2018; 4 (01) 7
- Richards MJ, Corner J, Maher J.. The National Cancer Survivorship Initiative: new and emerging evidence on the ongoing needs of cancer survivors. Br J Cancer 2011; Nov; 105 (Suppl 1): S1-S4
- Patrick DL, Burke LB, Powers JH, Scott JA, Rock EP, Dawisha S. et al Patient-reported outcomes to support medical product labeling claims: FDA perspective. Value Health 2007; Nov/Dec; 10 (Suppl 2): S125-S37
- Williams K, Sansoni J, Morris D, Grootmaat P, Thompson C.. Patient-reported outcome measures. Literature review. Sydney: Australian Commission on Safety and Quality in Health Care;; 2016
- Maharaj AD, Samoborec S, Evans SM, Zalcberg J, Neale RE, Goldstein D. et al Patient-reported outcome measures (PROMs) in pancreatic cancer: a systematic review. HPB (Oxford) 2019; Feb; 22 (02) 187-203
- Alrubaiy L, Hutchings HA, Williams JG.. Assessing patient reported outcome measures: a practical guide for gastroenterologists. United European Gastroenterol J 2014; Dec; 2 (06) 463-470
- Black N.. Patient reported outcome measures could help transform healthcare. BMJ 2013; 346: f167
- Calvert M, Kyte D, Price G, Valderas JM, Hjollund NH.. Maximising the impact of patient reported outcome assessment for patients and society. BMJ 2019; Jan; 364: k5267
- Rotenstein LS, Huckman RS, Wagle NW.. Making patients and doctors happier - the potential of patient-reported outcomes. N Engl J Med 2017; Oct; 377 (14) 1309-1312
- Kargo AS, Coulter A, Jensen PT, Steffensen KD.. Proactive use of PROMs in ovarian cancer survivors: a systematic review. J Ovarian Res 2019; 12: 63
- Basch E, Deal AM, Dueck AC, Scher HI, Kris MG, Hudis C. et al Overall survival results of a trial assessing patientreported outcomes for symptom monitoring during routine cancer treatment. JAMA 2017; Jul; 318 (02) 197-198
- Kindts I, Laenen A, Van Den Akker M, Weltens C.. PROMs following breast-conserving therapy for breast cancer: results from a prospective longitudinal monocentric study. Nature 2019; Nov; 27 (11) 4123-4132
- Prasad V.. Do cancer drugs improve survival or quality of life?. BMJ 2017; Oct; 359: j4528
- Kim C, Prasad V.. Cancer drugs approved on the basis of a surrogate end point and subsequent overall survival: an analysis of 5 years of US Food and Drug Administration approvals. JAMA Intern Med 2015; Dec; 175 (12) 1992-1994
- Davis C, Naci H, Gurpinar E, Poplavska E, Pinto A, Aggarwal A.. Availability of evidence on overall survival and quality of life benefits of cancer drugs approved by the European Medicines Agency: retrospective cohort study of drug approvals from 2009-2013. BMJ 2017; Oct; 359: j4530
- Sørensen JB, Klee M, Palshof T, Hansen HH.. Performance status assessment in cancer patients. An inter-observer variability study. Br J Cancer 1993; Apr; 67 (04) 773-775
- Braga S.. Why do our patients get chemotherapy until the end of life?. Ann Oncol 2011; Nov; 22 (11) 2345-2348
- National Confidential Enquiry into Patient Outcome and Death (NCEPOD). For better, for worse?. A review of the care of patients who died within 30 days of receiving systemic anti-cancer therapy. London: NCEPOD;; 2008
- Vodicka E, Kim K, Devine EB, Gnanasakthy A, Scoggins JF, Patrick DL.. Inclusion of patient-reported outcome measures in registered clinical trials: evidence from ClinicalTrials.gov (2007-2013). Contemp Clin Trials 2015; Jul; 43: 1-9
- Porter ME, Larsson S, Lee TH.. Standardizing patient outcomes measurement. N Engl J Med 2016; Feb; 374 (06) 504-506
- Mastropietro AP, Oliveira EA, Santos MA, Voltarelli JC.. Functional assessment of cancer therapy bone marrow transplantation: portuguese translation and validation. Rev Saúde Pública 2007; Apr; 41 (02) 260-268
- Macarulla T, Hendifar AE, Li CP, Reni M, Riess H, Tempero MA. et al Landscape of healthrelated quality of life in patients with early-stage pancreatic cancer receiving adjuvant or neoadjuvant chemotherapy a systematic literature review. Pancreas 2020; Mar; 49 (03) 393-407
- Fox RS, Moreno PI, Yanez B, Estabrook R, Thomas J, Bouchard LC. et al Integrating PROMIS® computerized adaptive tests into a web-based intervention for prostate cancer. Health Psychol 2019; May; 38 (05) 403-409
- Lane A, Metcalfe C, Young GJ, Peters Tj, Blazeby J, Avery KNL. et al Patient-reported outcomes in the ProtecT randomized trial of clinically localized prostate cancer treatments: study design, and baseline urinary, bowel and sexual function and quality of life. BJU Int 2016; Dec; 118 (06) 869-879
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