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RecruitingNCT06452485RT-HYPEUpdated Jul 16, 2026

Postoperative Re-irradiaTion With and Without HYPERthermia, or Surgery Only: Toxicity, Quality of Life and Survival in Patients With Locoregional Recurrent Breast Cancer

An observational study in Locoregional Recurrence, Breast Cancer and Re-irradiation, sponsored by Amsterdam UMC, location VUmc. Recruiting at 1 site in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-16.

Sponsored by Amsterdam UMC, location VUmc · Observational

From the registry’s dates

  • Started Feb 2024; still recruiting 2 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
18 Years and older
Sex
All
01

Study summary

In the Netherlands, breast cancer patients with locoregional recurrence (LRR) and intermediate- and high-risk factors are treated with surgery with or without postoperative re-irradiation with or without hyperthermia. Retrospective studies showed that 3-year locoregional control after postoperative re-irradiation with hyperthermia was 68-83%, and severe toxicity in up to 40% of LRR patients. Unfortunately, no prospective (randomized) data are available on clinical outcomes. Consequently, variation exists in hyperthermia-treatment and re-irradiation schedules. Prospective real-world data on oncological outcomes, toxicity and quality of life is highly needed for shared decision-making between patients and professionals. These data will be used in the design of a future randomized trial in high-risk LRR patients.

Read the detailed description

The optimal management of LRR breast cancer is multidisciplinary, and based on various prognostic risk factors and previous treatments. The surgical treatment of local recurrences is salvage mastectomy after previous breast-conserving therapy, or local excision after previous mastectomy. Regional treatment of tumor-positive lymph nodes consists of axillary radiotherapy and/or lymph node dissection. Intermediate- and high-risk LRR patients have an indication for surgery +/- postoperative irradiation to improve locoregional control and disease-free survival. In previously irradiated high-risk LRR patients, postoperative re-irradiation is administered with or without hyperthermia in the Netherlands depending on the treating center and treating professional. In unresectable LRR, primary re-irradiation with hyperthermia is the evidence-based standard of care in high-risk LRR in the Netherlands. Hyperthermia is used to increase the therapeutic efficacy of re-irradiation. The introduction of preoperative systemic therapy in 2010 resulted in more resectable high-risk LRRs. This resulted in an increased number of resectable LRR and indications for postoperative re-irradiation instead of primary re-irradiation, including variation in the use of hyperthermia. There is no evidence-based standard of care regarding the combination of postoperative re-irradiation with or without hyperthermia in high-risk LRR patients. The major problem is that only retrospective data and no prospective (randomized) data is available on oncological outcomes (survival and recurrence) and toxicity following postoperative re-irradiation and hyperthermia. Consequently, there is a high need to assess oncological outcomes and toxicity of postoperative re-irradiation with or without hyperthermia in a randomized controlled trial (RCT). So far, an RCT has not been feasible due to the large variation in postoperative re-irradiation and hyperthermia, and preferences regarding hyperthermia-treatment by professionals. In the RT-HYPE study, the investigators evaluate oncological outcomes, toxicity and quality of life in high-risk LRR patients, including the harmonization of hyperthermia-treatment. The results of the RT-HYPE study are needed for the optimization of the shared decision making (SDM) process on post-operative re-irradiation with or without hyperthermia, between professionals and patients. In addition, these results allow to set-up a future RCT comparing postoperative re-irradiation with and without hyperthermia treatment. During the inclusion of patients since February 2024, we have observed some variation in the treatment of high-risk LRRs between participating centers, which is a result of the SDM-process and variation in clinical practice. Consequently, in some patients postoperative re-irradiation +/- hyperthermia is omitted. Also, in patients with a local chest wall recurrence, surgery is sometimes omitted in case of an excellent response to NAST, limiting local treatment to re-irradiation (+/-hyperthermia) only. Consequently, both surgical and radiotherapy treatments vary in high risk LRR patients. In addition, recently published evidence in primary breast cancer showed that post-mastectomy and/or axillary radiotherapy is not needed in selected patients (SUPREMO, Kunkler et al. NEJM 2025, NSABP B-51/RTOG 1304 Mamounas et al. NEJM 2025). First, the randomized controlled SUPREMO trial evaluated the omission of post mastectomy radiotherapy (PMRT) in breast cancer patients with pT1 2N1, pT3N0, or pT2N0 with grade 3 +/- lymphovascular invasion, treated with mastectomy, axillary dissection and systemic therapy. The median follow-up was 9.6 years. Post-mastectomy radiotherapy did not increase 10-year overall survival (i.e. primary endpoint), which was 81.4% with PMRT and 81.9% without PMRT. Secondary outcomes including 10-yr local (1.1%+PMRT, 4.5% no PMRT) and locoregional recurrence rates (2.7%+PMRT, 4.5% no PMRT), disease-free survival (76.2%+PMRT, 75.5% no PMRT) and distant-metastasis free survival (78.2%+PMRT, 79.2% no PMRT) were comparable in both groups. Second, the randomized controlled NSABP B-51/RTOG 1304 trial evaluated postoperative axillary nodal irradiation (ax RT) in patients with clinical stage T1-3N1 and tumor negative axillary lymph nodes after neoadjuvant systemic therapy, (targeted) axillary dissection and local treatment (i.e. breast-conserving surgery and whole breast irradiation or mastectomy (and no PMRT)). After a median follow-up of 59.5 months, 5-year invasive breast cancer recurrence-free interval (i.e. primary endpoint) was 92.7 (+axillary RT) and 91.8% (no axillary RT). The secondary outcomes were similar in both groups, i.e. 5-yr locoregional recurrence-free (98.9% +ax RT, 98.4% no ax RT), distant recurrence-free survival (93.4%+ax RT), 93.4% no ax RT), disease-free survival (88.3% +ax RT, 88.5% no ax RT). Since the indication for postoperative re-irradiation in high-risk LRR is extrapolated from primary breast cancer, in the absence of evidence in the recurrent setting, it is likely that the group with high-risk LRR treated with surgery without postoperative re-irradiation +/- hyperthermia treatment, will increase. After discussion with the study team and radiation oncologists of participating centers in October 2025, we have decided to include two additional groups that reflect current clinical practice: 1. Patients with high-risk LRR (as described in Section Inclusion Criteria) who do not receive postoperative re-irradiation after salvage mastectomy. 2. Patients with a chest wall recurrence after previous mastectomy (as described in Section Inclusion Criteria) and a clinical/radiological complete response after NAST and treated with re-irradiation (+/- hyperthermia) for any microscopic disease without local excision.

02

Conditions studied

  • Locoregional Recurrence
  • Breast Cancer
  • Re-irradiation
  • Hyperthermia

Keywords

  • locoregional recurrence, breast cancer, treatment, re-irradiation, hyperthermia, patient-reported outcomes, quality of life, toxicity
03

In context

Breast Neoplasms

14,825 studies on the registry are indexed under Breast Neoplasms; 3,319 are open to participants now.

This study's planned enrollment of 500 is above the median of 184 across 3,235 observational studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Amsterdam UMC, location VUmc is the lead sponsor of 305 studies on the registry; 84 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Eligible patients with local and/or regional recurrence (LRR), i.e true recurrence or second primary tumor:

  1. After previous breast-conserving therapy and LRR with high-risk characteristics* treated with salvage mastectomy after previous mastectomy or salvage mastectomy and postoperative re-irradiation

    +/- hyperthermia treatment. In both groups (neo)-adjuvant treatment

  2. After previous mastectomy with a chest wall recurrence treated with local excision with or without NAST and postoperative re irradiation (+/-hyperthermia). If these patients have a complete clinical/radiological response after NAST and no surgery (i.e. local excision) is performed, treatment with re-irradiation (with/without hyperthermia) is indicated. Treatment with regional re-irradiation in case of a regional recurrence after (targeted) axillary dissection is allowed.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • ≥ 18 years old
  • WHO performance scale ≤ 2
  • Diagnosed with local +/- regional recurrence (LRR) (i.e. true recurrence or second primary) with high-risk tumor characteristics* and previously treated with postoperative local +/- regional irradiation for primary breast cancer/previous recurrence with an indication for salvage mastectomy with/without postoperative re-irradiation (+/-hyperthermia)** if re-irradiation: including overlap of re-irradiated volume with previous irradiated volume
  • Diagnosed with a chest wall recurrence and treated with local excision with/without NAST and postoperative re irradiation with/without hyperthermia. In patients with a clinical/radiological complete response after systemic treatment, NO surgery and re irradiation (+/- hyperthermia) (since surgery is not possible in this group)
  • (Neo-)adjuvant systemic (NAST) treatment is allowed
  • Use of PET(FES/FDG)-CT for staging of nodal and disseminated disease
  • Oligometastases in lymph nodes in the mediastinum, neck, contralateral axillary/supraclavicular region (up to a maximal number of five) is allowed
  • Proficient in Dutch at a level allowing to understand the questionnaires and patient information sheet

    * Definition of high-risk tumor characteristics are:

  • (Focal) irradical resection
  • All clinical and pathological stages except for low-risk LRR: - rcT1-2N0 - r(y)pT1-2N0 ** according to local clinical practice and/or shared decision making process

Exclusion criteria

Exclusion criteria:

  • Diagnosed with primary breast sarcoma
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Postoperative re-irradiation with hyperthermia

    Postoperative re-irradiation with hyperthermia in patients with locoregional recurrent breast cancer

    Other: No interventions, patient-reported outcomes (PROMs) and toxicity will be collected in both groups.

  • Postoperative re-irradiation without hyperthermia

    Postoperative re-irradiation without hyperthermia in patients with locoregional recurrent breast cancer

    Other: No interventions, patient-reported outcomes (PROMs) and toxicity will be collected in both groups.

  • surgery only

    Patients who do not receive postoperative re-irradiation after salvage mastectomy.

Interventions

  • OtherNo interventions, patient-reported outcomes (PROMs) and toxicity will be collected in both groups.

    Patients will receive standard of care. Patients need to fill in questionnaires, these are additional interventions for the included subject. Questionnaires for patient-reported outcomes (PROMs) and toxicity will be filled in one week before treatment, one week before re-irradiation, one week and three months after re-irradiation, one, two and five years after surgery.

06

What researchers measure

Primary outcomes

  1. Patient-reported toxicity according to PRO-CTCAE in LRR patients

    Patient-reported toxicity according to PRO-CTCAE after a median follow-up of five years after diagnosis of (subsequent) LRR disease.

    Time frame: Five years

Secondary outcomes

  1. Quality of Life at 2 and 5 years after diagnosis of LRR disease

    EORTC-C30

    Time frame: at 2 and 5 years after diagnosis of LRR disease

  2. Quality of Life at 2 and 5 years after diagnosis of LRR disease

    EORTC -BR45

    Time frame: at 2 and 5 years after diagnosis of LRR disease

  3. LRR-free survival in LRR patients

    Time frame: at 2 and 5 years after diagnosis of LRR disease

  4. distant metastasis-free survival in LRR patients

    Time frame: at 2 and 5 years after diagnosis of LRR disease

  5. breast-cancer event-free survival in LRR patients

    Time frame: at 2 and 5 years after diagnosis of LRR disease

  6. overall survival in LRR patients

    Time frame: at 2 and 5 years after diagnosis of LRR disease

  7. Referral patterns in patients diagnosed with LRR

    Referral patterns (per institute, professional, patient-related factors including performance status, and travel distance).

    Time frame: 5 year

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Feb 2024 (actual). Primary completion is estimated for Feb 2027, 36 months after the start.

Of 1,191 non-industry observational studies under Breast Neoplasms, half reached primary completion within 58 months of starting (the median), counting those still running; a quarter within 25 and three quarters within 139. This study's planned 36 months is below that.

Counting every sponsor, half of 1,380 studies reached it within 55 months; a quarter within 25 and three quarters within 126.

How these figures are worked out, and which studies are left out of them.

Registered
May 3, 2024
First posted
Jun 11, 2024
StartActual
Feb 1, 2024
Primary completionEst.
Feb 2027
CompletionEst.
Oct 2027
Last update
Jul 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06452485
Collaborators
Borstkanker Onderzoek Groep, Comprehensive Cancer Centre The Netherlands, Dutch Cancer Society
Responsible party
Desiree H.J.G.D. van den Bongard, MD Ph (Dr, Amsterdam UMC, location VUmc) — Principal investigator
First posted
Jun 11, 2024
Start date
Feb 1, 2024
Primary completion
Feb 2027 (estimated)
Completion
Oct 2027 (estimated)
Last update
Jul 16, 2026

Study contacts

Lisca Wurfbain, MD
Contact
l.f.wurfbain@amsterdamumc.nl
+31 6-25414750
Desiree Van Den Bongard, Dr
Contact
h.j.vandenbongard@amsterdamumc.nl
+31 6-25414750
Desiree Van Den Bongard, Dr
principal investigator · Amsterdam UMC

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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