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Recruiting NCT05377047

Stereotactic Ablative Radiotherapy for OligoMetastatic Breast Cancer

No phase Interventional Breast Cancer Stage IV Oligometastatic Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: SABR.
Who it may be relevant to
Registry conditions: Breast Cancer Stage IV, Oligometastatic Disease. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Sweden
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Treatment of Oligometastatic Breast Cancer - a Randomised Phase 3 Trial Comparing Stereotactic Ablative Radiotherapy and Systemic Treatment With Systemic Treatment Alone as 1st Line Treatment

Overview

TAORMINA is an international, multicentre, randomised phase 3 trial for patients with oligometastatic breast cancer (OMBC) that will be allocated to combined stereotactic ablative radiotherapy (SABR) + systemic therapy (investigational arm) versus systemic therapy alone (control arm) as 1st line therapy.

Detailed description

TAORMINA is an international, multicentre, randomised phase 3 trial for patients with oligometastatic breast cancer (OMBC) that will be allocated to combined stereotactic ablative radiotherapy (SABR) + systemic therapy (investigational arm) versus systemic therapy alone (control arm) as 1st line therapy.

Patients with 1-5 metastases in 1-2 organs (confirmed by PET-CT) with any breast cancer subtype can be enrolled. All metastases must be available for SABR.

The primary aim is to investigate if the addition of SABR to the oligometastatic sites in addition to the standard first-line treatment can improve progression-free survival (PFS).

Secondary aims are to compare overall survival (OS), response rate and time to development of new lesions, acute and late toxicity. quality of life, time to start of chemotherapy (luminal patients).

Exploratory analyses:

Circulating tumour DNA as an early sign of disease progression. Immun panel for determination of the effect of SABR on patients´ immune response.

To investigate the survival for each BC subtype (Luminal, HER2+ and TNBC). To investigate survival in patients with de novo OMBC and recurrent OMBC respectively.

Stratifications are based on subtype (luminal, HER2-positive vs TNBC) and type of OMBC (de novo vs. recurrent) without formal sample size calculation for the stratification factor (exploratory analysis).

Patients with de novo metastatic OMBC that is planned for neoadjuvant treatment are recommended to complete treatment followed by standard surgery and radiotherapy or SABR towards the primary tumour lesion(s).

Interventions

  • Radiation SABR
    Stereotactic Ablative Radiotherapy is delivered to all metastatic lesions.

Primary outcome measures

  • Progression-free survival (PFS) [Time frame: 3 years after the last patient inclusion]
Secondary outcome measures (6)
  • Overall survival (OS) [Time frame: 3 years after the last patient inclusion]
  • Local Control Rate (LCR) [Time frame: 3 years after the last patient inclusion]
  • Safety analysis - acute toxicity [Time frame: From the first dose of SABR to 3 months after the last dose of SABR]
  • Safety analysis - late toxicity [Time frame: From the first dose of SABR to 3 years after the last dose of SABR]
  • Health-related quality of life Cancer-30 [Time frame: At base-line and after 3, 6, 9, 12, 18, 24 and 36 months after registration.]
  • Health-related quality of life Breast-23 [Time frame: At base-line and after 3, 6, 9, 12, 18, 24 and 36 months after registration.]

Eligibility criteria

Inclusion criteria

  • Histologically or cytological confirmed recurrent OMBC.
  • Age ≥18 years old.
  • OMBC defined as 1-5 metastases in a maximum of two organs confirmed by PET-CT.
  • Patients already on 1st line systemic treatment can be enrolled if repeated tumour evaluations show stable disease.
  • Patients with de novo stage IV OMBC must have a controlled primary tumour regardless of primary surgery or primary systemic treatment.
  • Patients with local recurrence and OMBC must have a controlled local recurrence.
  • ECOG/WHO 0-2.
  • Life expectancy > 6 months.
  • Known ER, PgR and HER2 status of either primary tumour or metastasis (preferred).
  • If measurable lesions, each ≤ 5 cm.
  • Symptomatic bone metastases are allowed if ablative therapy can be delivered (femoral metastasis not allowed).
  • Adequate organ function for the planned treatment according to local guide-lines.
  • For patients with liver metastasis:
  • No cirrhosis or hepatitis
  • Hepatic function:
  • Total bilirubin level < 3.0 x institutional ULN
  • ALT, AST, GGT, and alkaline phosphatase levels < 3.0 x institutional ULN
  • Albumin > 2.5 mg/dL
  • Metastasis not adjutant to stomach or small bowel.
  • For patients with abdominal metastases: adequate renal function with a calculated creatinine clearance of > 60mL/min.
  • Toxicities from previous adjuvant therapies (excluding alopecia) must have recovered to grade 1 (defined by CTCAE 5.0). Stable grade 2 peripheral neuropathy are considered individually by the investigator.
  • Negative pregnancy test within 14 days prior to start of treatment\*.
  • If childbearing potential, willing to use an effective form of contraception\*.
  • No other malignancy during the last 5 years except for radically treated basal or squamous cell carcinoma of the skin or CIS of the cervix.
  • Signed informed consent and willingness to follow the trial procedures.

Exclusion criteria

  • > 1 line of systemic treatment for OMBC due to previous progressing disease (previous treatment of isolated local recurrences with a 2nd adjuvant treatment not included).
  • Oligometastases in brain.
  • Malignant pleural effusion or ascites.
  • Metastasis growth that involves > 3 vertebra and adjacent spinal cord, spine instability or neurological deficit resulting from compression, 25% spinal canal compromise or progressive neurological deficit.
  • Unable to undergo imaging by either CT scan or MRI.
  • Evidence of any other medical conditions (such as psychiatric illness, infectious diseases, neurological conditions, physical examination or laboratory findings) that may interfere with the planned treatment or affect patient compliance.
  • Pregnancy or breast-feeding.
  • Concurrent malignancy requiring therapy (excluding non-invasive carcinoma or carcinoma in situ).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Sweden · 1 center
  • Sahlgrenska University Hospital — Gothenburg

Publications

  • Milano MT, Zhang H, Metcalfe SK, Muhs AG, Okunieff P. Oligometastatic breast cancer treated with curative-intent stereotactic body radiation therapy. Breast Cancer Res Treat. 2009 Jun;115(3):601-8. doi: 10.1007/s10549-008-0157-4. Epub 2008 Aug 22. PMID 18719992
  • Milano MT, Katz AW, Zhang H, Okunieff P. Oligometastases treated with stereotactic body radiotherapy: long-term follow-up of prospective study. Int J Radiat Oncol Biol Phys. 2012 Jul 1;83(3):878-86. doi: 10.1016/j.ijrobp.2011.08.036. Epub 2011 Dec 13. PMID 22172903
  • Scorsetti M, Franceschini D, De Rose F, Comito T, Villa E, Iftode C, Navarria P, D'Agostino GR, Masci G, Torrisi R, Testori A, Tinterri C, Santoro A. Stereotactic body radiation therapy: A promising chance for oligometastatic breast cancer. Breast. 2016 Apr;26:11-7. doi: 10.1016/j.breast.2015.12.002. Epub 2016 Jan 3. PMID 27017237
  • Milano MT, Katz AW, Zhang H, Huggins CF, Aujla KS, Okunieff P. Oligometastatic breast cancer treated with hypofractionated stereotactic radiotherapy: Some patients survive longer than a decade. Radiother Oncol. 2019 Feb;131:45-51. doi: 10.1016/j.radonc.2018.11.022. Epub 2018 Dec 28. PMID 30773186
  • Trovo M, Furlan C, Polesel J, Fiorica F, Arcangeli S, Giaj-Levra N, Alongi F, Del Conte A, Militello L, Muraro E, Martorelli D, Spazzapan S, Berretta M. Radical radiation therapy for oligometastatic breast cancer: Results of a prospective phase II trial. Radiother Oncol. 2018 Jan;126(1):177-180. doi: 10.1016/j.radonc.2017.08.032. Epub 2017 Sep 21. PMID 28943046
  • David S, Tan J, Savas P, Bressel M, Kelly D, Foroudi F, Loi S, Siva S. Stereotactic ablative body radiotherapy (SABR) for bone only oligometastatic breast cancer: A prospective clinical trial. Breast. 2020 Feb;49:55-62. doi: 10.1016/j.breast.2019.10.016. Epub 2019 Nov 6. PMID 31734589
  • Li MP, Kelly D, Tan J, Siva S, Kron T, David S. Single-fraction stereotactic ablative body radiotherapy for sternal metastases in oligometastatic breast cancer: Technique and single institution experience. J Med Imaging Radiat Oncol. 2020 Aug;64(4):580-585. doi: 10.1111/1754-9485.13075. Epub 2020 Jun 25. PMID 32588550
  • Palma DA, Olson R, Harrow S, Gaede S, Louie AV, Haasbeek C, Mulroy L, Lock M, Rodrigues GB, Yaremko BP, Schellenberg D, Ahmad B, Senthi S, Swaminath A, Kopek N, Liu M, Moore K, Currie S, Schlijper R, Bauman GS, Laba J, Qu XM, Warner A, Senan S. Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Tria PMID 32484754

Identifiers

NCT: NCT05377047 · SABO 21-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗