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Clinical outcome of patients who reduced sunitinib or pazopanib during first-line treatment for advanced kidney cancer

  • Roberto Iacovelli
  • , Maria Cossu Rocca
  • , Luca Galli
  • , Ugo De Giorgi
  • , Roberto Sabbatini
  • , Matteo Santoni
  • , Alessandra Mosca
  • , Giuseppe Fornarini
  • , Francesco Massari
  • , Cristina Masini
  • , Melissa Bersanelli
  • , Elisa Biasco
  • , Cristian Lolli
  • , Annalisa Guida
  • , Rossana Berardi
  • , Carlo Terrone
  • , Alessandro Pastorino
  • , Andrea Ardizzoni
  • , Carmine Pinto
  • , Sebastiano Buti
  • Franco Nolè, Giampaolo Tortora
  • IRCCS Istituto Europeo di Oncologia - Milano
  • University of Pisa
  • IRCCS Istituto scientifico romagnolo per lo studio e la cura dei tumori - Meldola (FC)
  • University of Modena and Reggio Emilia
  • Marche Polytechnic University
  • University of Eastern Piedmont
  • San Martino Hospital Genoa
  • Alma Mater Studiorum University of Bologna
  • Azienda Ospedaliera Santa Maria Nuova di Reggio Emilia
  • Azienda Ospedaliero - Universitaria di Parma

Research output: Contribution to journalArticle

Abstract

Objectives To investigate the different outcomes in patients with metastatic renal cell carcinoma (mRCC) who receive a reduced first-line dose of sunitinib or pazopanib compared to those who continue at the standard dose. Patients and methods All the patients treated in 11 oncological centers in Italy for mRCC who started first-line treatment with sunitinib or pazopanib at the standard dose. Descriptive statistical tests were used to highlight differences among groups. Survival was estimated by the Kaplan-Meier method and compared across the groups using log-rank tests, the Cox proportional hazards model adjusted for statistically significant variables was also done. Results A total of 591 patients were included in the study. Of these, 45.7% received a reduced dose of sunitinib or pazopanib after a median treatment time of 3.6 months at the standard dose. The median overall survival in the patients who continued to receive the standard dose was 24.0 months compared to 49.4 months for those who received a reduced dose (hazard ratio = 1.80; 95% CI: 1.42–2.29; P<0.001). Only 45% of the patients received second-line therapy: 42.5% had an mTOR and 54.1% a tyrosine kinase inhibitor. Second-line overall survival was 19.8 and 11.8 months, respectively, in the patients who received, or did not, a reduced dose during first-line therapy (P = 0.007). Conclusions Toxicity-related dose reduction is a common event in mRCC patients who have started first-line therapy with either sunitinib or pazopanib. This is positively related to the outcomes of both first- and second-line therapy.
Original languageEnglish
Pages (from-to)541-541
Number of pages1
JournalUrologic Oncology
Volume35
DOIs
Publication statusPublished - 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Aged
  • Antineoplastic Agents
  • Dose reduction
  • Female
  • First-line
  • Humans
  • Indoles
  • Kidney Neoplasms
  • Male
  • Middle Aged
  • Oncology
  • Pazopanib
  • Pyrimidines
  • Pyrroles
  • Second-line
  • Sulfonamides
  • Sunitinib
  • Survival
  • Toxicity
  • Treatment Outcome
  • Urology
  • mRCC

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