4 research outputs found
Measurement properties of instruments to assess pain in children and adolescents with cancer: a systematic review protocol
Background: Pain in children and adolescents with cancer has been identified as an area where many healthcare
professionals seek guidance. This protocol details a systematic review whose aim is to explore current knowledge
regarding measurement instruments to assess pain (and pain-related distress) in children and adolescents with cancer.
After completion of the review, the information will be used in the development of a clinical practice guideline.
Methods: We will search four electronic databases (MEDLINE via PubMed, CINAHL, PsycINFO and HaPI). Additional
relevant studies will be identified by reference checking and expert consultation. All citations will be screened
independently by two reviewers in a three-step approach: first selection based on title, second selection based on
abstract, third selection based on full-text. Studies in children and adolescents with cancer that aimed to evaluate the
clinimetric properties of an existing pain measurement instrument or to develop a new pain measurement instrument
and that include at least one relevant outcome (reliability, validity, responsiveness, interpretability, clinical utility) are
eligible for inclusion. For all steps of evidence selection, a detailed list with eligibility criteria will be determined a priori.
Data extraction and quality assessment of included studies (according to the COnsensus-based Standards for the
selection of health Measurement INstruments, COSMIN criteria) will be conducted independently by two authors.
Discussion: This systematic review will provide an overview of the current literature regarding measurement
instruments to assess pain in children and adolescents with cancer. This knowledge synthesis will be used to formulate
recommendations for clinical
Prediction of mucositis risk secondary to cancer therapy: a systematic review of current evidence and call to action
PURPOSE: Despite advances in personalizing the efficacy of cancer therapy, our ability to identify patients at risk of severe treatment side effects and provide individualized supportive care is limited. This is particularly the case for mucositis (oral and gastrointestinal), with no comprehensive risk evaluation strategies to identify high-risk patients. We, the Multinational Association for Supportive Care in Cancer/International Society for Oral Oncology (MASCC/ISOO) Mucositis Study Group, therefore aimed to systematically review current evidence on that factors that influence mucositis risk to provide a foundation upon which future risk prediction studies can be based. METHODS: We identified 11,018 papers from PubMed and Web of Science, with 197 records extracted for full review and 113 meeting final eligibility criteria. Data were then synthesized into tables to highlight the level of evidence for each risk predictor. RESULTS: The strongest level of evidence supported dosimetric parameters as key predictors of mucositis risk. Genetic variants in drug-metabolizing pathways, immune signaling, and cell injury/repair mechanisms were also identified to impact mucositis risk. Factors relating to the individual were variably linked to mucositis outcomes, although female sex and smoking status showed some association with mucositis risk. CONCLUSION: Mucositis risk reflects the complex interplay between the host, tumor microenvironment, and treatment specifications, yet the large majority of studies rely on hypothesis-driven, single-candidate approaches. For significant advances in the provision of personalized supportive care, coordinated research efforts with robust multiplexed approaches are strongly advised.H. R. Wardill, S. T. Sonis, N. M. A. Blijlevens, Y. Z. A. Van Sebille, M. A. Ciorba, E. A. H. Loeffen, K. K. F. Cheng, P. Bossi, L. Porcello, D. A. Castillo, S. Elad, J. M. Bowen, On behalf of The Mucositis Study Group of the Multinational Association of Supportive Care in Cancer, International Society of Oral Oncology (MASCC/ISOO