关键词: Cytokines Growth factors Guidelines Oral mucositis Systematic review

Mesh : Antineoplastic Agents / adverse effects therapeutic use Cytokines / therapeutic use Granulocyte-Macrophage Colony-Stimulating Factor / therapeutic use Humans Intercellular Signaling Peptides and Proteins / therapeutic use Male Mucositis / drug therapy Neoplasms / drug therapy Practice Guidelines as Topic Recombinant Proteins / therapeutic use Stomatitis / drug therapy

来  源:   DOI:10.1007/s00520-019-05170-9   PDF(Sci-hub)

Abstract:
OBJECTIVE: To update the clinical practice guidelines for the use of growth factors and cytokines for the prevention and/or treatment of oral mucositis (OM).
METHODS: A systematic review was conducted by the Mucositis Study Group of the Multinational Association of Supportive Care in Cancer/International Society of Oral Oncology (MASCC/ISOO). The body of evidence for each intervention, in each cancer treatment setting, was assigned an evidence level. The findings were added to the database used to develop the 2014 MASCC/ISOO clinical practice guidelines. Based on the evidence level, the following guidelines were determined: recommendation, suggestion, and no guideline possible.
RESULTS: A total of 15 new papers were identified within the scope of this section and were merged with 51 papers that were reviewed in the previous guidelines update. Of these, 14, 5, 13, 2, and 1 were randomized controlled trials about KGF-1, G-CSF, GM-CSF, EGF, and erythropoietin, respectively. For the remaining agents there were no new RCTs. The previous recommendation for intravenous KGF-1 in patients undergoing autologous hematopoietic stem cell transplantation (HSCT) conditioned with high-dose chemotherapy and TBI-based regimens is confirmed. The previous suggestion against the use of topical GM-CSF for the prevention of OM in the setting of high-dose chemotherapy followed by autologous or allogeneic stem cell transplantation remains unchanged.
CONCLUSIONS: Of the growth factors and cytokines studied for the management of OM, the evidence supports a recommendation in favor of KGF-1 and a suggestion against GM-CSF in certain clinical settings.
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