Methotrexate, Doxorubicin, and Cisplatin (MAP) Plus Maintenance Pegylated Interferon Alfa-2b Versus MAP Alone in Patients With Resectable High-Grade Osteosarcoma and Good Histologic Response to Preoperative MAP: First Results of the EURAMOS-1 Good Response Randomized Controlled Trial

نویسندگان

  • Stefan S. Bielack
  • Sigbjørn Smeland
  • Jeremy S. Whelan
  • Neyssa Marina
  • Gordana Jovic
  • Jane M. Hook
  • Mark D. Krailo
  • Mark Gebhardt
  • Zsuzsanna Pápai
  • James Meyer
  • Helen Nadel
  • R. Lor Randall
  • Claudia Deffenbaugh
  • Rajaram Nagarajan
  • Bernadette Brennan
  • G. Douglas Letson
  • Lisa A. Teot
  • Allen Goorin
  • Daniel Baumhoer
  • Leo Kager
  • Mathias Werner
  • Ching C. Lau
  • Kirsten Sundby Hall
  • Hans Gelderblom
  • Paul Meyers
  • Richard Gorlick
  • Reinhard Windhager
  • Knut Helmke
  • Mikael Eriksson
  • Peter M. Hoogerbrugge
  • Paula Schomberg
  • Per-Ulf Tunn
  • Thomas Kühne
  • Heribert Jürgens
  • Henk van den Berg
  • Tom Böhling
  • Susan Picton
  • Marleen Renard
  • Peter Reichardt
  • Joachim Gerss
  • Trude Butterfass-Bahloul
  • Carol Morris
  • Pancras C.W. Hogendoorn
  • Beatrice Seddon
  • Gabriele Calaminus
  • Maria Michelagnoli
  • Catharina Dhooge
  • Matthew R. Sydes
  • Mark Bernstein
چکیده

PURPOSE EURAMOS-1, an international randomized controlled trial, investigated maintenance therapy with pegylated interferon alfa-2b (IFN-α-2b) in patients whose osteosarcoma showed good histologic response (good response) to induction chemotherapy. PATIENTS AND METHODS At diagnosis, patients age ≤ 40 years with resectable high-grade osteosarcoma were registered. Eligibility after surgery for good response random assignment included ≥ two cycles of preoperative MAP (methotrexate, doxorubicin, and cisplatin), macroscopically complete surgery of primary tumor, < 10% viable tumor, and no disease progression. These patients were randomly assigned to four additional cycles MAP with or without IFN-α-2b (0.5 to 1.0 μg/kg per week subcutaneously, after chemotherapy until 2 years postregistration). Outcome measures were event-free survival (EFS; primary) and overall survival and toxicity (secondary). RESULTS Good response was reported in 1,041 of 2,260 registered patients; 716 consented to random assignment (MAP, n = 359; MAP plus IFN-α-2b, n = 357), with baseline characteristics balanced by arm. A total of 271 of 357 started IFN-α-2b; 105 stopped early, and 38 continued to receive treatment at data freeze. Refusal and toxicity were the main reasons for never starting IFN-α-2b and for stopping prematurely, respectively. Median IFN-α-2b duration, if started, was 67 weeks. A total of 133 of 268 patients who started IFN-α-2b and provided toxicity information reported grade ≥ 3 toxicity during IFN-α-2b treatment. With median follow-up of 44 months, 3-year EFS for all 716 randomly assigned patients was 76% (95% CI, 72% to 79%); 174 EFS events were reported (MAP, n = 93; MAP plus IFN-α-2b, n = 81). Hazard ratio was 0.83 (95% CI, 0.61 to 1.12; P = .214) from an adjusted Cox model. CONCLUSION At the preplanned analysis time, MAP plus IFN-α-2b was not statistically different from MAP alone. A considerable proportion of patients never started IFN-α-2b or stopped prematurely. Long-term follow-up for events and survival continues.

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عنوان ژورنال:

دوره 33  شماره 

صفحات  -

تاریخ انتشار 2015