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dc.contributor.authorGridelli, Cesare
dc.contributor.authorArdizzoni, Andrea
dc.contributor.authorLe Chevalier, Thierry
dc.contributor.authorManegold, Christian
dc.contributor.authorPerrone, Francesco
dc.contributor.authorThatcher, Nick
dc.contributor.authorVan Zandwijk, N
dc.contributor.authorDi Maio, Massimo
dc.contributor.authorMartelli, O
dc.contributor.authorDe Marinis, F
dc.date.accessioned2009-08-18T14:55:52Z
dc.date.available2009-08-18T14:55:52Z
dc.date.issued2004-03
dc.identifier.citationTreatment of advanced non-small-cell lung cancer patients with ECOG performance status 2: results of an European Experts Panel. 2004, 15 (3):419-26 Ann. Oncol.en
dc.identifier.issn0923-7534
dc.identifier.pmid14998843
dc.identifier.doi10.1093/annonc/mdh087
dc.identifier.urihttp://hdl.handle.net/10541/77735
dc.description.abstractBACKGROUND: Platinum-based combination chemotherapy is currently recommended as the standard treatment for patients with advanced non-small-cell lung cancer (NSCLC), but its benefit seems limited to fit patients with a performance status (PS) of 0 or 1. For PS2 patients, there is no consensus on standard treatment. With the aims of reviewing the evidence supporting each of these therapeutic options, possibly reaching a consensus for treatment of PS2 patients affected by advanced NSCLC in clinical practice, and suggesting the priorities for clinical research in this field, an European Experts Panel took place in Avellino, Italy in April 2003. RESULTS: and conclusions On the basis of current evidence, chemotherapy treatment appears justified for patients with advanced NSCLC and PS2. Single-agent chemotherapy (gemcitabine, vinorelbine, taxanes) could be the preferred option, although carboplatin-based or low-dose cisplatin-based doublets may represent alternative options. Stronger evidence is expected from new clinical research specifically focused on PS2 patients. Single-agent chemotherapy should be the standard arm against which experimental treatments are tested in randomised trials dedicated to PS2 patients. High priority should be given to the evaluation of tolerability and efficacy of platinum-based combinations, and to the testing of new biological agents. Another research priority is the improvement of supportive care. Patients strongly need symptomatic improvement: end points such as symptom relief, clinical benefit and quality of life should have a central position in trials dedicated to PS2 NSCLC patients.
dc.language.isoenen
dc.subjectLung Canceren
dc.subjectCancer Stagingen
dc.subject.meshAntineoplastic Agents
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshClinical Trials as Topic
dc.subject.meshExpert Testimony
dc.subject.meshHumans
dc.subject.meshKarnofsky Performance Status
dc.subject.meshLung Neoplasms
dc.subject.meshNeoplasm Staging
dc.titleTreatment of advanced non-small-cell lung cancer patients with ECOG performance status 2: results of an European Experts Panel.en
dc.typeArticleen
dc.contributor.departmentDivision of Medical Oncology, SG Moscati Hospital, Avellino, Italy. cgridelli@libero.iten
dc.identifier.journalAnnals of Oncologyen
html.description.abstractBACKGROUND: Platinum-based combination chemotherapy is currently recommended as the standard treatment for patients with advanced non-small-cell lung cancer (NSCLC), but its benefit seems limited to fit patients with a performance status (PS) of 0 or 1. For PS2 patients, there is no consensus on standard treatment. With the aims of reviewing the evidence supporting each of these therapeutic options, possibly reaching a consensus for treatment of PS2 patients affected by advanced NSCLC in clinical practice, and suggesting the priorities for clinical research in this field, an European Experts Panel took place in Avellino, Italy in April 2003. RESULTS: and conclusions On the basis of current evidence, chemotherapy treatment appears justified for patients with advanced NSCLC and PS2. Single-agent chemotherapy (gemcitabine, vinorelbine, taxanes) could be the preferred option, although carboplatin-based or low-dose cisplatin-based doublets may represent alternative options. Stronger evidence is expected from new clinical research specifically focused on PS2 patients. Single-agent chemotherapy should be the standard arm against which experimental treatments are tested in randomised trials dedicated to PS2 patients. High priority should be given to the evaluation of tolerability and efficacy of platinum-based combinations, and to the testing of new biological agents. Another research priority is the improvement of supportive care. Patients strongly need symptomatic improvement: end points such as symptom relief, clinical benefit and quality of life should have a central position in trials dedicated to PS2 NSCLC patients.


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