Radiotherapy & Oncology
Volume 96, Issue 2 , Pages 192-198, August 2010

Boosting the tumor bed from deep-seated tumors in early-stage breast cancer: A planning study between electron, photon, and proton beams

  • José I. Toscas

      Affiliations

    • Instituto Oncológico Teknon, Barcelona, Spain
    • Corresponding Author InformationCorresponding author. Address: Instituto Oncológico Teknon, C/Vilana 12, 08022 Barcelona, Spain.
  • ,
  • Dolors Linero

      Affiliations

    • Instituto Oncológico Teknon, Barcelona, Spain
  • ,
  • Isabel Rubio

      Affiliations

    • Instituto Oncológico Teknon, Barcelona, Spain
  • ,
  • Alberto Hidalgo

      Affiliations

    • Servei de Radiodiagnòstic, Clínica Teknon, Barcelona, Spain
  • ,
  • Raquel Arnalte

      Affiliations

    • Instituto Oncológico Teknon, Barcelona, Spain
  • ,
  • Lluís Escudé

      Affiliations

    • Instituto Oncológico Teknon, Barcelona, Spain
  • ,
  • Luca Cozzi

      Affiliations

    • Medical Physics, Oncology Institute of Southern Switzerland, CH, Switzerland
  • ,
  • Antonella Fogliata

      Affiliations

    • Medical Physics, Oncology Institute of Southern Switzerland, CH, Switzerland
  • ,
  • Raymond Miralbell

      Affiliations

    • Instituto Oncológico Teknon, Barcelona, Spain
    • Service de Radio-Oncologie, Hopitaux Universitaires de Genève, CH, Switzerland

Received 14 January 2010; received in revised form 14 May 2010; accepted 14 May 2010. published online 10 June 2010.

Abstract 

Purpose

To assess the potential dosimetric advantages and drawbacks of photon beams (modulated or not), electron beams (EB), and protons as a boost for the tumor bed in deep-seated early-stage breast cancer.

Material and methods

Planning CTs of 14 women with deep-seated tumors (i.e., ⩾4cm depth) were selected. The clinical target volume (CTV) was defined as the area of architectural distortion surrounded by surgical clips. The planning treatment volume (PTV) was the CTV plus 1cm margin. A dose of 16Gy in 2Gy fractions was prescribed. Organs at risk (OARs) were heart, lungs, breasts, and a 5-mm thick skin segment on the breast surface. Dose–volume metrics were defined to quantify the quality of concurrent treatment plans assessing target coverage and sparing of OAR. The following treatment techniques were assessed: photon beams with either static 3D-conformal, dynamic arc (DCA), static gantry intensity-modulated beams (IMRT), or RapidArc (RA); a single conformal EB; and intensity-modulated proton beams (IMPT). The goal for this planning effort was to cover 100% of the CTV with ⩾95% of the prescribed dose and to minimize the volume inside the CTV receiving >107% of the dose.

Results

All techniques but DCA and EB achieved the planning objective for the CTV with an inhomogeneity ranging from 2% to 11%. RA showed the best conformity, EB the worst. Contra-lateral breast and lung were spared by all techniques with mean doses <0.5Gy (zero for protons). The ipsi-lateral lung received a mean dose <10% of that prescribed with photon beams and <2% with IMPT, increasing to 17% with EB. The heart, in left-sided breast tumors, received also the highest dose with EB. The skin was best protected with RA with a mean dose of 5.4Gy and V15Gy=2.4%.

Conclusions

Boosting the tumor bed in early-stage breast cancer with optimized photon or proton beams may be preferred to EB especially for deep-seated targets. The marked OAR (i.e., ipsi-lateral breast, lung, heart, and skin surface) dose-sparing effect may allow for a potential long-term toxicity risk reduction and better cosmesis. DCA or RA may also be considered alternative treatment options for patients eligible for accelerated partial breast irradiation trials.

Keywords: Breast cancer, Conservative treatment, Boost technique, IMRT, RapidArc, Protons

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0167-8140(10)00311-7

doi:10.1016/j.radonc.2010.05.007

Radiotherapy & Oncology
Volume 96, Issue 2 , Pages 192-198, August 2010