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dc.contributor.authorMorales González, Manuel José
dc.contributor.authorExpósito, María del Carmen
dc.contributor.otherMedicina Interna, Dermatología y Psiquiatría
dc.date.accessioned2024-11-10T21:05:53Z
dc.date.available2024-11-10T21:05:53Z
dc.date.issued1995
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/40030
dc.description.abstractPleural effusions are common in patients with cancer and cause a significant morbidity. The optimal treatment for the control of pleural effusions is not defined. In patients with drug-sensitive tumors (e.g. breast cancer, lymphomas, small-cell lung cancer) systemic chemotherapy is the treatment of choice. For patients with other solid tumors and in recurrences despite systemic chemotherapy, the optimal treatment consists of thoracostomy-tube drainage with the instillation of a sclerosing agent [3]. Several agents are used to achieve pleuorodesis: tetracycline, bleomycin, quinacrine, nitrogen mustard, doxorubicin, mitoxantrone and talc [7]. Mitoxantrone shows a steep dose/effect relationship for different human tumor cell lines in vitro, and is a drug well tolerated locally [2]. Whilst the usual dose of mitoxantrone for intrapleural therapy is 30 mg [6], we increased the dose to 40 mg.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesSupportive Care Cancer, 1995, 3
dc.rightsLicencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES
dc.titleIntrapleural mitoxantrone for the palliative treatment of malignant pleural effusions
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1007/BF00365856
dc.subject.keywordIntrapleural mitoxantrone
dc.subject.keywordpleural effusions


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