[Metastasectomy in renal cell cancer after neoadjuvant therapy with multi-tyrosine kinase inhibitors]

P Firek1, S Richter, J Jaekel

  • 1EURO-Prostatazentrum Aachen, Klinik und Poliklinik für Urologie und Kinderurologie, Universitätsklinikum der RWTH Aachen, Pauwelsstrraße 30, 52074 Aachen, Deutschland. peter.firek@bonifatius-lingen.de

Der Urologe. Ausg. A
|November 25, 2011
PubMed
Abstract

Insights

Metastasectomy after multi-tyrosine kinase inhibitor (MTKI) therapy for metastatic renal cell carcinoma (mRCC) can achieve complete remission. Surgical resection of active cancer tissue in patients with resectable metastases offers a favorable prognosis.

Area of Science:

  • Oncology
  • Surgical Oncology
  • Medical Oncology

Context:

  • Metastatic renal cell carcinoma (mRCC) presents significant therapeutic challenges.
  • Complete remission in mRCC is rare, with uncertainty regarding residual tumor viability after treatment.
  • Neoadjuvant therapy with multi-tyrosine kinase inhibitors (MTKI) is an emerging strategy.

Purpose:

  • To evaluate the outcomes of metastasectomy in patients with mRCC following neoadjuvant MTKI therapy.
  • To assess the feasibility and complication rates of surgical resection in this patient cohort.
  • To determine the presence and viability of residual tumor post-neoadjuvant treatment.

Summary:

  • Eleven patients with mRCC underwent metastasectomy after at least 3 months of stable partial remission with MTKI therapy (sunitinib, bevacizumab/interferon, or temsirolimus).
  • All metastases were completely resected, with 82% showing histologically active, Ki-67 positive cancer tissue.
  • Major surgical interventions were required in some cases; perioperative complications were minimal, but recurrence occurred in 6 patients within 19 months.

Impact:

  • Metastasectomy in experienced centers is associated with low complication rates for mRCC.
  • Surgical resection of isolated, resectable mRCC metastases can lead to complete remission and a favorable prognosis.
  • The presence of biologically active tumor tissue supports the indication for surgical intervention.