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A randomised study of tailored toxicity-based dosage of fluorouracil-epirubicin-cyclophosphamide chemotherapy for early breast cancer (SBG 2000-1)

Lindman, Henrik (författare)
Uppsala universitet,Experimentell och klinisk onkologi,Uppsala University Hospital
Andersson, M. (författare)
Copenhagen University Hospital,Rigshosp, Dept Oncol, Copenhagen, Denmark
Ahlgren, J. (författare)
Gävle Hospital,Gavle Cent Hosp, Dept Oncol, Gavle, Sweden;Orebro Univ Hosp, Dept Oncol, Orebro, Sweden,Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark,Aarhus University Hospital
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Balslev, E. (författare)
Herlev Hospital,Herlev Hosp, Dept Oncol, Herlev, Denmark,Rigshosp, Dept Oncol, Copenhagen, Denmark,Copenhagen University Hospital
Sverrisdottir, A. (författare)
Stockholm South General Hospital,Soder Sjukhuset, Dept Oncol, Stockholm, Sweden;Landspitali, Dept Oncol, Reykjavik, Iceland
Holmberg, S. B. (författare)
Sahlgrenska University Hospital,Dept Surg, Molndal, Sweden
Bengtsson, N. O. (författare)
Umeå University,Umea Univ Hosp, Dept Oncol, Umea, Sweden
Jacobsen, E. H. (författare)
Vejle Hospital,Vejle Hosp, Dept Oncol, Vejle, Denmark,Vasteras Hosp, Dept Oncol, Vasteras, Sweden;Aalborg Univ Hosp, Dept Oncol, Aalborg, Denmark,Västmanland Hospital
Jensen, A. B. (författare)
Karolinska Institutet,Karolinska University Hospital
Hansen, J. (författare)
Västmanland Hospital
Tuxen, M. K. (författare)
Herlev Hospital,Herlev Hosp, Dept Oncol, Herlev, Denmark
Malmberg, L. (författare)
Karlstad Hospital,Karlstad Hosp, Dept Oncol, Karlstad, Sweden;Boras Hosp, Dept Oncol, Boras, Sweden
Villman, K. (författare)
Örebro University Hospital,Orebro Univ Hosp, Dept Oncol, Orebro, Sweden
Anderson, H. (författare)
Lund University,Lunds universitet,Medicinsk onkologi,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Medical oncology,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund Univ, Dept Clin Sci, Div Canc Epidemiol, Lund, Sweden
Ejlertsen, B. (författare)
Copenhagen University Hospital
Bergh, J. (författare)
Karolinska Institutet,Karolinska University Hospital
Blomqvist, C. (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi,Orebro Univ Hosp, Dept Oncol, Orebro, Sweden,Uppsala University Hospital
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Elsevier BV, 2018
2018
Engelska 8 s.
Ingår i: European Journal of Cancer. - : Elsevier BV. - 0959-8049 .- 1879-0852. ; 94, s. 79-86
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Study aim: Retrospective studies have demonstrated a worse outcome in breast cancer patients not developing leukopenia during adjuvant chemotherapy. The SBG 2000-1 is the first randomised trial designed to compare individually dosed chemotherapy without G-CSF support based on grade of toxicity to standard-dosed chemotherapy based on body surface area (BSA). Methods: Patients with early breast cancer were included and received the first cycle of standard FEC (fluorouracil 600 mg/m2, epirubicin 60 mg/m2, cyclophosphamide 600 mg/m2). Patients with nadir leukopenia grade 0–2 after first cycle were randomised between either 6 additional courses of tailored FEC with increased doses (E 75–90 mg/m2, C 900–1200 mg/m2) or fixed treatment with 6 standard FEC. Patients with grade 3–4 leukopenia were registered and treated with 6 standard FEC. Primary end-point was distant disease-free survival (DDFS). Results: The study enrolled 1535 patients, of which 1052 patients were randomised to tailored FEC (N = 524) or standard FEC (N = 528), whereas 401 patients with leukopenia grade 3–4 continued standard FEC and formed the registered cohort. Dose escalation did not statistically significantly improve 10-year DDFS (79% and 77%, HR 0.87, CI 0.67–1.14, P = 0.32) or OS (82% and 78%, respectively, HR 0.89, CI 0.57–1.16, P = 0.38). Corresponding estimates for the registered group of patients were DDFS 79% and OS 82%, respectively. Conclusions: The SBG 2000-1 study failed to show a statistically significant improvement of escalated and tailored-dosed chemotherapy compared with standard BSA-based chemotherapy in patients with low haematological toxicity, although all efficacy parameters showed a numerical advantage for tailored treatment.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Adjuvant
Breast cancer
Chemotherapy
Dosage
Dose tailoring
Leukopenia
Adjuvant

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art (ämneskategori)
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