Long-term Safety of Sunitinib in Metastatic Renal Cell Carcinoma

Eur Urol. 2016 Feb;69(2):345-51. doi: 10.1016/j.eururo.2015.07.006. Epub 2015 Jul 26.

Abstract

Background: Metastatic renal cell carcinoma (mRCC) patients receiving first-line sunitinib typically survive >2 yr, with chronic treatment sometimes extending to ≥6 yr.

Objective: To analyze long-term safety with sunitinib in mRCC patients.

Design, setting, and participants: Data were pooled from 5739 patients in nine trials, comprising seven phase II studies, a phase III study, and an expanded-access trial in various treatment settings (e.g., cytokine refractory or treatment-naïve).

Outcome measurements and statistical analysis: Interval and cumulative time-period analyses evaluated the incidence of treatment-related adverse events (TRAEs) for up to 6 yr, in the overall population and in those with long-term (≥2 yr) sunitinib treatment.

Results and limitations: Among long-term patients (n=807), most TRAEs occurred initially in the first year and then decreased in frequency; TRAEs following this pattern included decreased appetite, diarrhea, dysgeusia, dyspepsia, fatigue, hypertension, mucosal inflammation, nausea, and stomatitis. However, hypothyroidism increased by interval analysis from 6% at 0-<6 mo to 42% at 5-<6 yr and by cumulative analysis from 14% at 0-<1 yr to 36% over 6 yr. Grade 3/4 TRAEs in long-term patients peaked during the first year and then steadily decreased. The overall population displayed only minor differences from long-term patients, with no clinically significant differences between grade ≥3 TRAE profiles (<5% difference in incidence rates at all intervals). Limitations included retrospective design, assessment variability, lack of pharmacokinetic data, and absence of baseline characteristics for long-term patients.

Conclusions: Prolonged sunitinib was not associated with new types or increased severity of TRAEs. Except hypothyroidism, toxicity was not cumulative.

Patient summary: More than 800 mRCC patients received sunitinib for between 2 and 6 yr without experiencing new or more severe treatment-related toxicity. Clinicians may be able to prescribe chronic sunitinib treatment for as long as patients continue to derive clinical benefit, without untoward additional risk.

Keywords: Long-term safety; Renal cell carcinoma; Sunitinib; Toxicity; Treatment-related adverse events.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anorexia / chemically induced
  • Antineoplastic Agents / adverse effects*
  • Carcinoma, Renal Cell / drug therapy*
  • Carcinoma, Renal Cell / secondary*
  • Clinical Trials, Phase II as Topic
  • Clinical Trials, Phase III as Topic
  • Diarrhea / chemically induced
  • Dysgeusia / chemically induced
  • Dyspepsia / chemically induced
  • Fatigue / chemically induced
  • Female
  • Humans
  • Hypertension / chemically induced
  • Hypothyroidism / chemically induced
  • Indoles / adverse effects*
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / pathology*
  • Male
  • Mucositis / chemically induced
  • Nausea / chemically induced
  • Pyrroles / adverse effects*
  • Stomatitis / chemically induced
  • Sunitinib
  • Time Factors

Substances

  • Antineoplastic Agents
  • Indoles
  • Pyrroles
  • Sunitinib