@article {7969,
	title = {Systemic chemotherapy in inoperable or metastatic bladder cancer},
	journal = {Annals of Oncology},
	volume = {17},
	year = {2006},
	note = {Cited By :30Export Date: 21 February 2017},
	month = {2006},
	pages = {553 - 561},
	abstract = {Urothelial cancer is a common malignancy. The management of patients with recurrent disease after cystectomy or initially metastatic or unresectable disease represents a therapeutic challenge. Systemic chemotherapy prolongs survival but long-term survival remains infrequent. During recent years there has been improvement due to the use of novel chemotherapeutic agents, mainly gemcitabine and the taxanes. The long-considered-standard MVAC has been challenged by combinations showing more favourable toxicity profiles and equal (gemcitabine-cisplatin) or even improved (dose-dense, G-CSF-supported MVAC) efficacy. Specific interest has also been generated in specific groups of patients (elderly patients, patients with renal function impairment or comorbidities), who are not fit for the standard cisplatin-based chemotherapy but can derive significant benefit from carboplatin- or taxane-based treatment. Retrospective analyses have enabled the identification of groups of patients with different prognoses, who possibly require different therapeutic approaches. Modern chemotherapy offers a chance of long-term survival in patients without visceral metastases, possibly in combination with definitive local treatment. Finally, the progress of targeted therapies in other neoplasms seems to be reflected in advanced bladder cancer by recent studies indicating that biological agents can be combined with modern chemotherapy. The true role of such therapies is currently being evaluated. {\textcopyright} 2006 Oxford University Press.},
	keywords = {Bladder cancer, Chemotherapy, Gemcitabine, Mvac, Taxanes},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645343556\&doi=10.1093\%2fannonc\%2fmdj079\&partnerID=40\&md5=98c1489f5f60be419c21aad43fe3efbc},
	author = {Bamias, A. and Tiliakos, I. and Karali, M.-D. and Dimopoulos, M.A.}
}
