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Effective local control of advanced soft tissue sarcoma with neoadjuvant chemoradiotherapy and surgery: A single institutional experience.
Stubbe, F; Agaimy, A; Ott, O; Lettmaier, S; Vassos, N; Croner, R; Hohenberger, W; Fietkau, R; Semrau, S.
Afiliação
  • Stubbe F; Department of Radiation Oncology, University of Erlangen-Nurnberg, Universitätsstraße 27, 91054 Erlangen, Germany.
  • Agaimy A; Pathology Institute, University of Erlangen-Nurnberg, Krankenhausstraße 8-10, 91054 Erlangen, Germany.
  • Ott O; Department of Radiation Oncology, University of Erlangen-Nurnberg, Universitätsstraße 27, 91054 Erlangen, Germany.
  • Lettmaier S; Department of Radiation Oncology, University of Erlangen-Nurnberg, Universitätsstraße 27, 91054 Erlangen, Germany.
  • Vassos N; Department of Surgery, University of Erlangen-Nurnberg, Krankenhausstraße 12, 91054 Erlangen, Germany.
  • Croner R; Department of Surgery, University of Erlangen-Nurnberg, Krankenhausstraße 12, 91054 Erlangen, Germany.
  • Hohenberger W; Department of Surgery, University of Erlangen-Nurnberg, Krankenhausstraße 12, 91054 Erlangen, Germany.
  • Fietkau R; Department of Radiation Oncology, University of Erlangen-Nurnberg, Universitätsstraße 27, 91054 Erlangen, Germany.
  • Semrau S; Department of Radiation Oncology, University of Erlangen-Nurnberg, Universitätsstraße 27, 91054 Erlangen, Germany. Electronic address: sabine.semrau@uk-erlangen.de.
Cancer Radiother ; 20(1): 6-13, 2016 Feb.
Article em En | MEDLINE | ID: mdl-26700874
ABSTRACT

PURPOSE:

There is a sound theoretical basis but little clinical evidence substantiating the benefits of concurrent chemoradiotherapy with two-drug chemotherapy for locally advanced soft tissue sarcomas. Our five-year data on the feasibility and effectiveness of neoadjuvant chemoradiotherapy with systemically effective doses of adriamycin and ifosfamide combined is presented here. PATIENTS AND

METHODS:

Between 2000 and 2011, 53 patients with UICC (2010) stage I (n=1, 1.9%), II (n=12, 22.7%) or III (n=40, 75.5%) nonmetastatic soft tissue sarcoma received neoadjuvant chemoradiotherapy with ifosfamide (1.5 g/m(2)/day, d1-5, q28) and doxorubicin (50mg/m(2)/day, d3, q28) plus concurrent radiotherapy with a target dose of 50-64 Gy (median 60 Gy). The treatment of 34 patients (64.2%) was combined with hyperthermia.

RESULTS:

At five years, the local control rate was 89.9% (± 5.7%), distant metastasis-free survival 66.6% (± 7.6%), and survival 83.3% (± 6%). The R0 resection rate was 81.1%. Radiotherapy was completed as planned in all patients and chemotherapy in 42/53 (70.2%). Grades III (n=21, 29.6%) and IV (n=18, 34%) leukopenia was the main acute adverse event. All acute and chronic non-hematologic toxicities were moderate.

CONCLUSION:

Neoadjuvant chemoradiotherapy for soft tissue sarcoma is associated with good feasibility, manageable acute and late toxicities, and high local efficacy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Neoplasias de Tecidos Moles Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Neoplasias de Tecidos Moles Idioma: En Ano de publicação: 2016 Tipo de documento: Article