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Ultrahypofractionated Versus Normofractionated Sequential Boost After Whole-breast Radiation Therapy in Patients Treated With Breast-conserving Surgery for Breast Cancer (ULTIMO)

28 de julho de 2026 atualizado por: Cancer Research Antwerp

The ULTIMO trial is a monocentric, prospective, randomised controlled, open-label, phase III interventional clinical trial, with a non-inferiority design, in patients with breast cancer undergoing breast conservative treatment (BCT). After giving informed consent and verifying eligibility, data collection starts and patients will be randomized in one of the following treatment arms:

  • Standard treatment arm: Breast Conserving Surgery (BCS) takes place, followed by the SoC hypofractionated Whole Breast Radiation Therapy (WBRT) and SoC normofractioned sequential boost (normSEB) of 10Gy over 5 fractions.
  • Experimental treatment arm: Breast Conserving Surgery (BCS) takes place, followed by the SoC hypofractionated WBRT and experimental ultrahypofractionated sequential boost (ultSEB) of 6Gy in a single fraction.

The primary objective of the ULTIMO study is to assess whether the ultSEB RT boost protocol is non-inferior to the current SoC normSEB RT boost protocol. This assessment will be based on the cosmetic outcome of the breasts, while also taking into account quality of life (QoL), the frequency and intensity of (S)AEs of interest (breast pain and fibrosis), and oncological survival.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

132

Estágio

  • Fase 3

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Antwerpen
      • Antwerp, Antwerpen, Bélgica, 2610
        • Ziekenhuis aan de Stroom

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Breast cancer patients referred for WBRT + boost to the lumpectomy cavity
  • Patients ≥18y
  • Karnofsky Performance Score >70%, or ECOG <2
  • Life expectancy of more than 5 years
  • Invasive tumour free resection margins, defined as R0 resection on the pathology report
  • Written informed consent

Exclusion Criteria:

  • Previous contralateral breast cancer
  • Previous RT of the same breast or thorax.
  • Metastatic disease (M1)

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Standard treatment arm (SoC; Normofractionated boost RT)

In the control arm, the boost of the radiation therapy will be delivered according to the standard of care fractionation and dosage scheme. This consists of 5 fractions of 2Gy each, adding up to a total dose of 10Gy.

All other treatments are not considered to be study-specific and are performed according to the standard of care treatment for breast cancer.

Standard of care fractionation and dosage scheme of the sequential radiation therapy boost. This consists of 5 fractions of 2Gy each, adding up to a total dose of 10Gy.
Outros nomes:
  • normSEB
Experimental: Experimental treatment arm (Hypofractionated boost RT)

In the experimental arm, the boost of the radiation therapy is delivered in a ultrahypofractionated scheme. This consists of a single fraction of 6Gy.

All other treatments are not considered to be study-specific and are performed according to the standard of care treatment for breast cancer.

The radiation therapy sequential boost is delivered in a ultrahypofractionated scheme. This consists of a single fraction of 6Gy.
Outros nomes:
  • ultSEB

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Cosmetic non-inferiority - BCCT.core scoring
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

BCCT.core is a software package for evaluating photographs of breasts after BCS. The 'Global cosmetic result' from the two frontal photos (arms up, and arms down) will be averaged and then used as the individual value of this measure. The results are scored on a 4-point Likert scale, coded as 0-3.

Analysis metric:

The change from baseline at 1 and 3YFU will be used. Negative values will be transformed to '1' to signal an inferiority event, positive or values of zero will be transformed to '0' to signal non-inferiority.

For comparisons and estimands, please refer to the SAP.

Method of aggregation:

The results will be reported as a contingency table reporting both frequencies and proportions of non-inferior and inferior results in each treatment arm.

Time point(s):

A baseline assessment is performed during the screening visit, followed by repeated measurements during the 1 and 3YFU (primary endpoint) visits.

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Cosmetic outcome - Expert panel, AIS-TAS
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The AIS is a tool for scoring breast cosmesis based on standardized photos. It comprises of 5 items, each comprising of a 5 point Likert-scale, coded as 1 to 5. The score is given based on the group of photos taken at a single time point. The scores of all items are summed to produce the TAS, which consequently ranges from 5 to 25. The AIS is used in an expert panel setting, where all scores, from each assessor are averaged per item.

A higher scores represents a more favourable cosmetic outcome.

Analysis metric:

AIS-TAS absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit, followed by repeated measurements during the 1 and 3YFU (primary endpoint) visits.

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Cosmetic outcome - Expert panel, AIS-Symmetry
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The AIS is a tool for scoring breast cosmesis based on standardized photographs. It comprises of 5 items, each comprising of a 5 point Likert-scale, coded as 1 to 5. The score is given based on the group of photos taken at a single time point. The AIS is used in an expert panel setting, where all scores, from each assessor are averaged per item.

A higher scores represents a more favourable cosmetic outcome.

Analysis metric:

AIS-Symmetry score absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit, followed by repeated measurements during the 1 and 3YFU (primary endpoint) visits.

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Cosmetic outcome - Physician scoring
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The physician scoring scale (questionnaire, cfr. protocol) will be used to assess cosmetic outcome. The normalised average score of all items will be summed and used as outcome measure. This will be calculated as the score of an item divided by the amount of answering options minus 1 (k-1), averaged over all items. Some questions have the option 'not evaluable', if this answer is selected, then that item is not used in deriving the average score.

A higher scores represents a more favourable cosmetic outcome.

Analysis metric:

Absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Cosmetic outcome - Patient reported (PROM)
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The cosmetic evaluation questionnaire by Sneeuw at al. will be used to assess cosmetic outcome, as reported by the participant. The normalised average score of all items will be summed and used as outcome measure. This will be calculated as the score of an item divided by the amount of answering options minus 1 (k-1), averaged over all items.

A higher scores represents a more favourable cosmetic outcome.

Analysis metric:

Absolute values (calculated score) will be used for analysis.

Method of aggregation:

The mean, median, variance and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Quality of life - EORTC QLQ C30 v3 - Global health status/QoL
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The QoL (QLQ-C30) outcome variable is operationalised through the QLQ-C30 questionnaire. The answers are transformed into 3 separate scores, which can all range from 0 to 100. These scores are: Global health status/QoL, Functional scales, Symptom scales. Where a higher score on the first 2 scales indicate a better health state and QoL, while on the symptom scale a higher score indicates a higher level of disturbance by symptoms.

Analysis metric:

The QLQ-C30 Global health status absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Quality of life - EORTC QLQ C30 v3 -Functional scales
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The QoL (QLQ-C30) outcome variable is operationalised through the QLQ-C30 questionnaire. The answers are transformed into 3 separate scores, which can all range from 0 to 100. These scores are: Global health status/QoL, Functional scales, Symptom scales. Where a higher score on the first 2 scales indicate a better health state and QoL, while on the symptom scale a higher score indicates a higher level of disturbance by symptoms.

Analysis metric:

The QLQ-C30 Functional scales score absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Quality of life - EORTC QLQ C30 v3 -Symptom scales
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The QoL (QLQ-C30) outcome variable is operationalised through the QLQ-C30 questionnaire. The answers are transformed into 3 separate scores, which can all range from 0 to 100. These scores are: Global health status/QoL, Functional scales, Symptom scales. Where a higher score on the first 2 scales indicate a better health state and QoL, while on the symptom scale a higher score indicates a higher level of disturbance by symptoms.

Analysis metric:

The QLQ-C30 Symptom scales score absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Quality of life - EORTC QLQ BR23 v1 - Functional scales
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The QoL (QLQ-BR23) outcome variable is operationalised through the QLQ-BR23 questionnaire. The answers are transformed into 2 separate scores, which can both range from 0 to 100. These scores are: Functional scales; Symptom scales. Where a higher score on the functional scale indicate a better health state and QoL, while on the symptom scale a higher score indicates a higher level of disturbance by symptoms.

Analysis metric:

The QLQ-BR23 Functional scales score absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Quality of life - EORTC QLQ BR23 v1 - Symptom scales
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

The QoL (QLQ-BR23) outcome variable is operationalised through the QLQ-BR23 questionnaire. The answers are transformed into 2 separate scores, which can both range from 0 to 100. These scores are: Functional scales; Symptom scales. Where a higher score on the functional scale indicate a better health state and QoL, while on the symptom scale a higher score indicates a higher level of disturbance by symptoms.

Analysis metric:

The QLQ-BR23 Symptom scales score absolute values will be used for analysis.

Method of aggregation:

The mean, median, SD and IQR will be reported. For comparisons and estimands, please refer to the SAP.

Time point(s):

A baseline assessment is performed during the screening visit. It is then assessed again at 1 year, and 3 years of follow-up after the last study treatment (LST).

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Fibrosis
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

During the 1Y and 3Y Follow-Up study visits the overall and tumour bed fibrosis will be scored according to the 'National Cancer Institute Common Terminology Criteria for Adverse Events' (NCI-CTCAE) v5.0 AE reporting system. This scoring will be performed by either the principal- or sub-investigators.

Analysis metric:

Tabulation of absence vs. presence and severity of fibrosis will be used for analysis.

Method of aggregation:

The proportion of participants experiencing no 'Fibrosis' vs. any 'Fibrosis' will be used. As well as the frequency of all grades, including 0 (absence).

For comparisons and estimands, please refer to the SAP.

Time point(s):

Fibrosis will be assessed and recorded during the 1YFU and 3YFU study visits.

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Breast pain
Prazo: From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.

Operationalisation:

During the 1Y and 3Y Follow-Up study visits the occurrence of 'Breast pain' will be scored according to the 'National Cancer Institute Common Terminology Criteria for Adverse Events' (NCI-CTCAE) v5.0 AE reporting system. This scoring will be performed by either the principal- or sub-investigators.

Analysis metric:

Tabulation of absence vs. presence and severity of 'Breast pain' will be used for analysis.

Method of aggregation:

The proportion of participants experiencing no 'Breast pain' vs. any 'Breast pain' will be used. As well as the frequency of all grades, including 0 (absence).

For comparisons and estimands, please refer to the SAP.

Time point(s):

Fibrosis will be assessed and recorded during the 1YFU and 3YFU study visits.

From enrollment to the end of follow-up at 3 years of follow-up, counting from the last study visit.
Oncological survival and time-to-event data - Overall Survival (OS)
Prazo: Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.

Operationalisation:

The oncological survival and TTE data are operationalised as time-to-event intervals for the events of interest listed below.

The 'OS' TTE/survival outcome will be reported according to the 2015 DATECAN consensus, including time-to-event data for the following events of interest: 'Death from any cause'.

Analysis metric:

The TTE data is registered in days from randomisation (Rz). Censoring will be used for participants without events at the end of their follow up.

Method of aggregation:

KM-estimates, as well as proportions free from events at follow-up visit timepoints will be reported. The non-aggregated data will be used for survival analysis. For comparisons and estimands, please refer to the SAP.

Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.
Oncological survival and time-to-event data - Breast Cancer-Specific Survival (BCSS)
Prazo: Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.

Operationalisation:

The oncological survival and TTE data are operationalised as time-to-event intervals for the events of interest listed below.

The 'BCSS' TTE/survival outcome will be reported according to the 2015 DATECAN consensus, including time-to-event data for the following events of interest: 'Death from breast cancer'.

Analysis metric:

The TTE data is registered in days from randomisation (Rz). Censoring will be used for participants without events at the end of their follow up.

Method of aggregation:

KM-estimates, as well as proportions free from events at follow-up visit timepoints will be reported. The non-aggregated data will be used for survival analysis. For comparisons and estimands, please refer to the SAP.

Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.
Oncological survival and time-to-event data - Relapse-Free Survival (RFS)
Prazo: Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.

Operationalisation:

The oncological survival and TTE data are operationalised as time-to-event intervals for the events of interest listed below.

The 'RFS' TTE/survival outcome will be reported according to the 2015 DATECAN consensus, including time-to-event data for the following events of interest: 'Death from any cause', 'Invasive ipsilateral breast tumor recurrence', 'Local Invasive recurrence', 'Regional Invasive recurrence', 'occurrence of metastases', or 'Ipsilateral DCIS'.

Analysis metric:

The TTE data is registered in days from randomisation (Rz). Censoring will be used for participants without events at the end of their follow up.

Method of aggregation:

KM-estimates, as well as proportions free from events at follow-up visit timepoints will be reported. The non-aggregated data will be used for survival analysis. For comparisons and estimands, please refer to the SAP.

Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.
Oncological survival and time-to-event data - Locoregional Relapse-Free Survival (L-RFS)
Prazo: Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.

Operationalisation:

The oncological survival and TTE data are operationalised as time-to-event intervals for the events of interest listed below.

The 'L-RFS' TTE/survival outcome will be reported according to the 2015 DATECAN consensus, including time-to-event data for the following events of interest: 'Death from any cause', 'Invasive ipsilateral breast tumor recurrence', 'Local Invasive recurrence', 'Regional Invasive recurrence', or 'Ipsilateral DCIS'.

Analysis metric:

The TTE data is registered in days from randomisation (Rz). Censoring will be used for participants without events at the end of their follow up.

Method of aggregation:

KM-estimates, as well as proportions free from events at follow-up visit timepoints will be reported. The non-aggregated data will be used for survival analysis. For comparisons and estimands, please refer to the SAP.

Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.
Oncological survival and time-to-event data - Distant-Relapse Free Survival (D-RFS)
Prazo: Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.

Operationalisation:

The oncological survival and TTE data are operationalised as time-to-event intervals for the events of interest listed below.

The 'D-RFS' TTE/survival outcome will be reported according to the 2015 DATECAN consensus, including time-to-event data for the following events of interest: 'Death from any cause', or 'occurrence of metastases'.

Analysis metric:

The TTE data is registered in days from randomisation (Rz). Censoring will be used for participants without events at the end of their follow up.

Method of aggregation:

KM-estimates, as well as proportions free from events at follow-up visit timepoints will be reported. The non-aggregated data will be used for survival analysis. For comparisons and estimands, please refer to the SAP.

Oncological TTE data will be registered at 1 and 3 years of follow-up after the last study treatment (LST). However, the exact dates of diagnosis/death will be used.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Melanie Machiels, MD, PhD, Iridium Netwerk

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

29 de março de 2022

Conclusão Primária (Real)

28 de novembro de 2025

Conclusão do estudo (Real)

25 de março de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

6 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

12 de maio de 2026

Primeira postagem (Real)

15 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

There is no current plan to share IPD. If sharing IPD could help our scientific knowledge/understanding, it could be considered. Before IPD is shared, a motivated request, ethical commission approval and a signed DTA is needed.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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