Diagnosis and treatment of Kaposi's sarcoma: European consensus-based interdisciplinary guideline (EDF/EADO/EORTC)

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3077442 29 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Diagnosis and treatment of Kaposi's sarcoma: European consensus-based interdisciplinary guideline (EDF/EADO/EORTC)
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Kaposi's sarcoma (KS)is a multifocal neoplasm of lymphatic endothelium-derived cells infected with human herpesvirus 8. Four clinical subtypes are distinguished: the classic, the endemic, the epidemic subtype in HIV positive patients and the iatrogenic subtype. The diagnosis is primarily based on clinical features and confirmation by histology with immunohistochemistry. Cutaneous distribution and severity, mucosal, nodal and visceral involvement depend on the type of KS with in general indolent behaviour and chronic evolution in the classic subtype and the more severe forms in iatrogenic or epidemic subtypes. Management should aim at achieving disease control. For localised lesions, several local therapies have been developed without randomised trial comparisons. Radiotherapy, intralesional chemotherapies and electrochemotherapy have high response rates. Topical treatments—imiquimod or topical 9-cis-retinoid acid—can also be used. Systemic treatments are reserved for locally aggressive extensive and disseminated KS: the recommended first-line agents are pegylated liposomal doxorubicin (PLD)and paclitaxel. In CKS, PLD or low-dose interferon-alfa are the recommended first-line agents in younger patients. In AIDS-related KS, combination antiretroviral therapy is the first treatment option; specific systemic treatment is needed only in case of extensive disease and in the prevention and treatment of immune reconstitution inflammatory syndrome. In post-transplant KS, tapering down immunosuppressive therapy and switching to mammalian target of rapamycin (m-TOR)inhibitors are used. Follow-up schedules for patients with KS disease depend on aggressiveness of the disease. © 2019 Elsevier Ltd
Έτος δημοσίευσης:
2019
Συγγραφείς:
Lebbe, C.
Garbe, C.
Stratigos, A.J.
Harwood, C.
Peris, K.
Marmol, V.D.
Malvehy, J.
Zalaudek, I.
Hoeller, C.
Dummer, R.
Forsea, A.M.
Kandolf-Sekulovic, L.
Olah, J.
Arenberger, P.
Bylaite-Bucinskiene, M.
Vieira, R.
Middleton, M.
Levy, A.
Eggermont, A.M.
Battistella, M.
Spano, J.P.
Grob, J.J.
Pages, C.
the European Dermatology Forum (EDF), the European Association of Dermato-Oncology (EADO)and the European Organisation for Research
Treatment of Cancer (EORTC)
Περιοδικό:
EUROPEAN JOURNAL OF CANCER
Εκδότης:
Elsevier Ireland Ltd
Τόμος:
114
Σελίδες:
117-127
Λέξεις-κλειδιά:
9 cis retinoid acid; alpha interferon; alpha2a interferon; alpha2b interferon; bevacizumab; doxorubicin; imiquimod; immunomodulating agent; lenalidomide; mammalian target of rapamycin; mammalian target of rapamycin inhibitor; paclitaxel; pomalidomide; unclassified drug, antiretroviral therapy; Article; cancer incidence; cancer prevention; cancer prognosis; cancer radiotherapy; cancer staging; clinical feature; cryosurgery; diagnostic test; disease control; electrochemotherapy; epidemic; epidemiological data; follow up; histopathology; human; Human herpesvirus 8; Human immunodeficiency virus; immune reconstitution inflammatory syndrome; immunohistochemistry; immunosuppressive treatment; infection risk; Kaposi sarcoma; laser surgery; local therapy; managed care; meta analysis; mortality rate; organ transplantation; pathogenesis; polymerase chain reaction; practice guideline; priority journal; randomized controlled trial (topic); risk assessment; risk factor; serology; systematic review; systemic therapy; topical treatment; treatment response; clinical trial; consensus; Europe; female; Kaposi sarcoma; male; multicenter study; pathology, Consensus; Europe; Female; Humans; Male; Risk Factors; Sarcoma, Kaposi
Επίσημο URL (Εκδότης):
DOI:
10.1016/j.ejca.2018.12.036
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