Early Breast Cancer Clinical Trial
Official title:
The DBCG Proton Trial. Adjuvant Breast Proton Radiation Therapy for Early Breast Cancer Patients: The Skagen Trial 2, a Clinically Controlled Randomised Phase III Trial
The majority of early breast cancer patients are treated with adjuvant radiation therapy (RT) as part of their multimodal therapy. The aim of the RT is to lower the risk of local, regional and distant failure and improve survival. Modern RT is been provided with photon therapy. Now, more proton therapy facilities are opened, including in Denmark. Proton RT may have the potential to cause lower dose to heart and lung during breast RT. This trial will randomise patients between standard photon RT versus experimental proton RT. The primary endpoint is 10 year risk of heart disease.
Adjuvant breast cancer radiation therapy (RT) is standard for all patients operated with
breast conservation and for patients diagnosed with large tumours and/or node-positive
disease. Around 65% of all breast cancer patients treated with RT have whole breast RT
without nodal RT, whilst the remaining 35% are treated with loco-regional RT (target is
breast / chest wall and regional nodal volumes). RT leads to fewer local and regional
recurrences, a decrease in breast cancer death and improves overall survival. Since 2014,
when the DBCG IMN study showed overall survival gain from internal mammary node (IMN) RT, IMN
RT has been standard for all high-risk patients in Denmark. IMN RT causes a significant
increase in dose to the heart and lung, thus heart and lung sparing RT techniques based on
deep inspiration breath hold (DIBH), volumetric arc therapy and tomotherapy are increasingly
used to lower dose to heart and lung whilst maintaining dose to breast and nodal targets.
These advanced techniques are used in all DBCG departments routinely. Despite using advanced
RT techniques, some patients still receive high RT dose to heart and lung.
Proton therapy (PT) has not been widely used nor investigated for adjuvant breast cancer RT,
because there are only few proton centres. However, due to the properties of PT it is
possible to achieve optimal dose coverage of relevant targets and at the same time ensure low
dose to organs at risk compared with photon RT. In an energy-dependent manner, PT will
deposit the majority of its dose in tissue depths defined by the Bragg peak. In practice,
this translates into i) the ability to deliver the peak energy to target volumes of irregular
3-dimensional shape using pencil-beam scanning technology, ii) a sharp dose fall-off
following deposition of energy in the target and iii) reduction of the integral dose to the
patient. Within millimeters, the exit dose drops off from 90% to 10%, resulting in the
virtual absence of an exit dose. The effectiveness, safety and feasibility of PT has been
reported in few small cohort studies with limited follow up, and there is a lack of
clinically controlled randomised trials documenting benefit from PT, evaluated either as
higher tumour control and/or as fewer morbidities.
This trial tests standard photon RT versus experimental proton RT for selected early breast
cancer patients.
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