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International Journal of Clinical Oncology

, Volume 24, Issue 4, pp 411–419 | Cite as

The combination of bevacizumab/temsirolimus after first-line anti-VEGF therapy in advanced renal-cell carcinoma: a clinical and biomarker study

  • Aristotelis BamiasEmail author
  • Vasilios Karavasilis
  • Nikolaos GavalasEmail author
  • Kimon Tzannis
  • Epaminontas Samantas
  • Gerasimos Aravantinos
  • Angelos Koutras
  • Ioannis Gkerzelis
  • Euthymios Kostouros
  • Konstantinos Koutsoukos
  • Flora Zagouri
  • George Fountzilas
  • Meletios-Athanasios Dimopoulos
Original Article
  • 197 Downloads

Abstract

Background

Vascular endothelial growth factor (VEGF) targeting represents the standard first-line therapy for metastatic renal-cell carcinoma (mRCC), while blocking the mammalian target of rapamycin (mTOR) is effective in relapsed disease. Since continuing blockade of VEGF may be of value, we studied the combination of bevacizumab with temsirolimus in mRCC patients relapsing after first-line treatment.

Methods

A prospective, phase II study of the combination of bevacizumab (10 mg/kg, every 2 weeks) with temsirolimus (25 mg weekly) in patients with mRCC who failed first-line anti-VEGF treatment. 6-month progression-free survival (PFS) rate was the primary end point. The association of VEGFa, VEGFR2, fibroblast growth factor (FGF) b, platelet-derived growth factor receptor (PDGFR) a and PDGFRb with prognostic factors and outcomes were also studied.

Results

39 patients were enrolled. First-line therapy included: sunitinib (n = 16), bevacizumab/interferon (n = 12), pazopanib (n = 10), sorafenib (n = 1). After a median follow-up of 37 months, 6-month PFS rate was 50.9% [95% confidence interval (CI) 33.8–65.7], median time to progression 6.8 months (95% CI 5.5–9.2) and median overall survival (OS) 18.2 months (95% CI 12.9–27.2). Objective response rate was 27%. The most common AEs were metabolic (33%), renal (8%) and gastrointestinal (GI) (7%). The most common grade 3–5 AEs were GI (18%), infections (14%) and metabolic (25%). Toxicity was the most frequent cause of treatment discontinuation (40%). FGFb levels were associated with OS.

Conclusions

In concert with recent data, our study confirms the efficacy of anti-VEGF/anti-mTOR combination in mRCC relapsing after anti-VEGF therapy. Toxicity was considerable leading to high rate of treatment discontinuations.

Trial registration

ClinicalTrials.gov: NCT01264341

Keywords

Renal cancer Metastatic Second-line, temsirolimus Bevacizumab FGF 

Notes

Acknowledgements

The correlative biomarker studies were supported by the Hellenic Genito-Urinary Cancer Group (HGUCG). The clinical study was supported by an internal HeCOG research grant and by research grants from F. Hoffmann-La Roche and Pfizer.

Compliance with ethical standards

Conflict of interest

Aristotelis Bamias: Honoraria, Advisory Boards, Research funding: Novartis, Pfizer, Roche, Astra-Zeneca, BMS, Bayer. Vasilios Karavasilis Advisory Board: Amgen, Pfizer, Novartis, BI, Lilly, Roche, Astellas, Genesis-Pharma and Janssen. Gerasimos Aravantinos Advisory Board: Novartis, BMS, Roche Hellas, Astra Zeneca, Sanofi, Amgen, Genesis Pharma, Merck, Pfizer. Angelos Koutras: Advisory Board: Roche. George Fountzilas. Advisory Board: Pfizer, Sanofi and Roche. Honoraria from Astra-Zeneca. Meletios-Athanassios Dimopoulos: Honoraria, Advisory Board: Janssen, Celgene, Amgen and Takeda.

Supplementary material

10147_2018_1361_MOESM1_ESM.docx (17 kb)
Supplementary material 1 (DOCX 16 KB)

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Copyright information

© Japan Society of Clinical Oncology 2018

Authors and Affiliations

  • Aristotelis Bamias
    • 1
    Email author
  • Vasilios Karavasilis
    • 2
  • Nikolaos Gavalas
    • 1
    Email author
  • Kimon Tzannis
    • 1
  • Epaminontas Samantas
    • 3
  • Gerasimos Aravantinos
    • 4
  • Angelos Koutras
    • 5
  • Ioannis Gkerzelis
    • 6
  • Euthymios Kostouros
    • 1
  • Konstantinos Koutsoukos
    • 1
  • Flora Zagouri
    • 1
  • George Fountzilas
    • 7
    • 8
  • Meletios-Athanasios Dimopoulos
    • 1
  1. 1.Department of Clinical Therapeutics, Alexandra HospitalNational and Kapodistrian University of AthensAthensGreece
  2. 2.Department of Medical Oncology, Papageorgiou Hospital, School of Health Sciences, Faculty of MedicineAristotle University of ThessalonikiThessaloníkiGreece
  3. 3.Third Department of Medical OncologyAgii Anargiri Cancer HospitalAthensGreece
  4. 4.Department of Medical OncologyAgii Anargiri Cancer HospitalAthensGreece
  5. 5.Division of Oncology, Department of Medicine, University HospitalUniversity of Patras Medical SchoolPatrasGreece
  6. 6.Department of UrologyGeneral Hospital Konstantopouleio Agia OlgaAthensGreece
  7. 7.Laboratory of Molecular OncologyHellenic Foundation for Cancer Research/Aristotle University of ThessalonikiThessaloníkiGreece
  8. 8.Aristotle University of ThessalonikiThessaloníkiGreece

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