Importance of Technique, Target Selection, Contouring, Dose Prescription, and Dose-Planning in External Beam Radiation Therapy for Cervical Cancer: Evolution of Practice From EMBRACE-I to II

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  • Thomas Berger
  • Yvette Seppenwoolde, Medical University of Vienna
  • ,
  • Richard Pötter, Medical University of Vienna
  • ,
  • Marianne Sanggaard Assenholt
  • Jacob C. Lindegaard
  • Remi A. Nout, Department of Human Genetics, Leiden University Medical Center (LUMC).
  • ,
  • Astrid de Leeuw, University Medical Center Utrecht, Utrecht
  • ,
  • Ina Jürgenliemk-Schulz, University Medical Center Utrecht, Utrecht
  • ,
  • Li Tee Tan, Addenbrooke's Hospital
  • ,
  • Dietmar Georg, Medical University of Vienna
  • ,
  • Christian Kirisits, Medical University of Vienna
  • ,
  • Isabelle Dumas, Gustave Roussy
  • ,
  • Nicole Nesvacil, Medical University of Vienna
  • ,
  • Jamema Swamidas, Tata Memorial Hospital
  • ,
  • Robert Hudej, Institute of Oncology
  • ,
  • Gerry Lowe, Mount Vernon Cancer Centre
  • ,
  • Taran Paulsen Hellebust, University of Oslo, Oslo University Hospital, Oslo, Universitetet i Oslo
  • ,
  • Geetha Menon, University of Alberta
  • ,
  • Lars Fokdal
  • Kari Tanderup
  • EMBRACE Collaborative Group

Purpose: To describe the evolution of external beam radiation therapy (EBRT) from EMBRACE-I (general guidelines for EBRT) to the initial phase of the EMBRACE-II study (detailed protocol for EBRT). Methods and Materials: EMBRACE-I enrolled 1416 locally advanced cervical cancer patients treated with chemoradiation including image-guided adaptive brachytherapy during 2008 to 2015. From March 2016 until March 2018, 153 patients were enrolled in the ongoing EMBRACE-II study, which involves a comprehensive detailed strategy and accreditation procedure for EBRT target contouring, treatment planning, and image guidance. EBRT planning target volumes (PTVs), treated volumes (V43 Gy), and conformity index (CI; V43 Gy/PTV) were evaluated in both studies and compared. Results: For EMBRACE-I, conformal radiation therapy (60% of patients) or intensity-modulated radiation therapy (IMRT) and volumetric arc therapy (VMAT; 40%) was applied with 45 to 50 Gy over 25 to 30 fractions to the elective clinical target volume (CTV). For pelvic CTVs (82%), median PTV and V43 Gy volumes were 1549 and 2390 mL, respectively, and CI was 1.54. For pelvic plus paraortic nodal (PAN) CTVs (15%), median PTV and V43 Gy volumes were 1921 and 2895 mL, and CI was 1.51. For pelvic CTVs treated with 45 to 46 Gy, the use of conformal radiation therapy was associated with a median V43 Gy volume that was 546 mL larger than with IMRT/VMAT. For pelvic CTVs treated with IMRT, the use of a dose prescription ≥48 Gy was associated with a median V43 Gy volumes that was 428 mL larger than with a dose prescription of 45 to 46 Gy. For EMBRACE-II, all patients were treated with: IMRT/VMAT, daily IGRT, 45 Gy over 25 fractions for the elective CTV, and simultaneously integrated boost for pathologic lymph nodes. For pelvic CTVs (61%), median PTV and V43 Gy volumes were 1388 and 1418 mL, and CI was 1.02. For pelvic plus PAN CTVs (32%), median PTV and V43 Gy volumes were 1720 and 1765 mL, and CI was 1.03. From EMBRACE-I to initial II, median V43 Gy was decreased by 972 mL (41%) and 1130 mL (39%), and median CI decreased from 1.54 to 1.02 and 1.51 to 1.03 for pelvic and pelvic plus PAN irradiation, respectively. Conclusions: Application of IMRT/VMAT, IGRT, and a 45-Gy dose provides the potential of higher conformality inducing significant reduction of treated volume. Adherence to a detailed protocol including comprehensive accreditation, as in EMBRACE-II, reduces considerably V43 Gy and V50 Gy and improves conformality and interinstitutional consistency.

OriginalsprogEngelsk
TidsskriftInternational Journal of Radiation Oncology Biology Physics
Vol/bind104
Nummer4
Sider (fra-til)885-894
Antal sider10
ISSN0360-3016
DOI
StatusUdgivet - 2019

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