Contemporary best practice in the management of urothelial carcinomas of the renal pelvis and ureter.
Maristella BianconiAlessia CimadamoreLuca FaloppiMario ScartozziMatteo SantoniAntonio Lopez-BeltranLiang ChengMarina ScarpelliRodolfo MontironiPublished in: Therapeutic advances in urology (2019)
Upper tract urothelial carcinoma (UTUC) accounts for 5% of urothelial carcinomas (UCs), the estimated annual incidence being 1-2 cases per 100,000 inhabitants. Similarly to bladder UC, divergent differentiations and histologic variants confer an adverse risk factor in comparison with pure UTUC. Molecular and genomic characterization studies on UTUC have shown changes occurring at differing frequencies from bladder cancer, with unique molecular and clinical subtypes, potentially with different responses to treatment. Systemic chemotherapy is the standard approach for patients with inoperable locally advanced or metastatic UCs. Although initial response rates are high, the median survival with combination chemotherapy is about 15 months. In first-line chemotherapy several cisplatin-based regimens have been proposed. For patients with advanced UC who progress to first-line treatment, the only product licensed in Europe is vinflunine, a third-generation, semisynthetic, vinca alkaloid. Better response rates (15-60%), with higher toxicity rates and no overall survival (OS) benefit, are generally achieved in multidrug combinations, which often include taxanes and gemcitabine. The US FDA has recently approved five agents targeting the programmed death-1 and programmed death ligand-1 pathway as a second-line therapy in patients with locally advanced or metastatic UC with disease progression during or following platinum-containing chemotherapy. Potential therapeutic targets are present in 69% of tumours analyzed. Specific molecular alterations include those involved in the RTK/Ras/PI(3)K, cell-cycle regulation and chromatin-remodeling pathways, many of them have either targeted therapies approved or under investigation. Angiogenic agents, anti-epidermal growth factor receptor therapy, phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) pathway inhibitors and immunotherapeutic drugs are being successfully investigated.
Keyphrases
- locally advanced
- squamous cell carcinoma
- rectal cancer
- neoadjuvant chemotherapy
- cell cycle
- epidermal growth factor receptor
- phase ii study
- radiation therapy
- high grade
- urinary tract
- risk factors
- cell proliferation
- small cell lung cancer
- tyrosine kinase
- healthcare
- transcription factor
- copy number
- primary care
- emergency department
- dna methylation
- dna damage
- advanced non small cell lung cancer
- single molecule
- oxidative stress
- drug delivery
- bone marrow
- protein kinase
- drug administration
- human health
- drug resistant
- cancer therapy
- quality improvement
- lymph node