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Stereotactic Ablative Radiotherapy for OligoMetastatic Breast Cancer (TAORMINA)

Primary Purpose

Breast Cancer Stage IV, Oligometastatic Disease

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
SABR
Sponsored by
Vastra Gotaland Region
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer Stage IV

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Histologically or cytological confirmed recurrent OMBC.
  2. Age ≥18 years old.
  3. OMBC defined as 1-5 metastases in a maximum of two organs confirmed by PET-CT.
  4. Patients already on 1st line systemic treatment can be enrolled if repeated tumour evaluations show stable disease.
  5. Patients with de novo stage IV OMBC must have a controlled primary tumour regardless of primary surgery or primary systemic treatment.
  6. Patients with local recurrence and OMBC must have a controlled local recurrence.
  7. ECOG/WHO 0-2.
  8. Life expectancy > 6 months.
  9. Known ER, PgR and HER2 status of either primary tumour or metastasis (preferred).
  10. If measurable lesions, each ≤ 5 cm.
  11. Symptomatic bone metastases are allowed if ablative therapy can be delivered (femoral metastasis not allowed).
  12. Adequate organ function for the planned treatment according to local guide-lines.
  13. 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.
  14. For patients with abdominal metastases: adequate renal function with a calculated creatinine clearance of > 60mL/min.
  15. 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.
  16. Negative pregnancy test within 14 days prior to start of treatment*.
  17. If childbearing potential, willing to use an effective form of contraception*.
  18. 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.
  19. Signed informed consent and willingness to follow the trial procedures.

Exclusion Criteria:

  1. > 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).
  2. Oligometastases in brain.
  3. Malignant pleural effusion or ascites.
  4. 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.
  5. Unable to undergo imaging by either CT scan or MRI.
  6. 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.
  7. Pregnancy or breast-feeding.
  8. Concurrent malignancy requiring therapy (excluding non-invasive carcinoma or carcinoma in situ).

Sites / Locations

  • Sahlgrenska University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Experimental SABR arm

Control systemic therapy arm

Arm Description

Standard first line systemic therapy + SABR.

Standard first line systemic therapy.

Outcomes

Primary Outcome Measures

Progression-free survival (PFS)
Time from the date of randomisation to the date of disease-progression at any site or death from any cause.

Secondary Outcome Measures

Overall survival (OS)
Time from the date of randomisation to the date of death from any cause.
Local Control Rate (LCR)
Time from the date of randomisation to the date of progress in previously treated metastases
Safety analysis - acute toxicity
Reported according to CTCAE v.5.0
Safety analysis - late toxicity
Reported according to CTCAE v.5.0
Health-related quality of life Cancer-30
European Organisation for Research and Treatment of Cancer-Quality of Life Questionnaires Cancer-30 (EORTC-QLQ C30)
Health-related quality of life Breast-23
European Organisation for Research and Treatment of Cancer-Quality of Life Questionnaire Breast-23 (EORTC-QLQ B23)

Full Information

First Posted
April 11, 2022
Last Updated
October 18, 2022
Sponsor
Vastra Gotaland Region
Collaborators
Sahlgrenska University Hospital, Sweden, Azienda Ospedaliero-Universitaria Careggi, Region Örebro County, Skane University Hospital, Uppsala University Hospital, Karolinska University Hospital, University Hospital, Umeå, Sundsvall Hospital, Karlstad Central Hospital, Gävle Hospital, Centrallasarettet Västerås, Oslo University Hospital, St. Olavs Hospital, Haukeland University Hospital, University of Stavanger, University Hospital of North Norway
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1. Study Identification

Unique Protocol Identification Number
NCT05377047
Brief Title
Stereotactic Ablative Radiotherapy for OligoMetastatic Breast Cancer
Acronym
TAORMINA
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
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 19, 2022 (Actual)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
December 31, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vastra Gotaland Region
Collaborators
Sahlgrenska University Hospital, Sweden, Azienda Ospedaliero-Universitaria Careggi, Region Örebro County, Skane University Hospital, Uppsala University Hospital, Karolinska University Hospital, University Hospital, Umeå, Sundsvall Hospital, Karlstad Central Hospital, Gävle Hospital, Centrallasarettet Västerås, Oslo University Hospital, St. Olavs Hospital, Haukeland University Hospital, University of Stavanger, University Hospital of North Norway

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Stage IV, Oligometastatic Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomisation 2:1 (systemic treatment + SABR vs systemic treatment)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
345 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental SABR arm
Arm Type
Experimental
Arm Description
Standard first line systemic therapy + SABR.
Arm Title
Control systemic therapy arm
Arm Type
No Intervention
Arm Description
Standard first line systemic therapy.
Intervention Type
Radiation
Intervention Name(s)
SABR
Intervention Description
Stereotactic Ablative Radiotherapy is delivered to all metastatic lesions.
Primary Outcome Measure Information:
Title
Progression-free survival (PFS)
Description
Time from the date of randomisation to the date of disease-progression at any site or death from any cause.
Time Frame
3 years after the last patient inclusion
Secondary Outcome Measure Information:
Title
Overall survival (OS)
Description
Time from the date of randomisation to the date of death from any cause.
Time Frame
3 years after the last patient inclusion
Title
Local Control Rate (LCR)
Description
Time from the date of randomisation to the date of progress in previously treated metastases
Time Frame
3 years after the last patient inclusion
Title
Safety analysis - acute toxicity
Description
Reported according to CTCAE v.5.0
Time Frame
From the first dose of SABR to 3 months after the last dose of SABR
Title
Safety analysis - late toxicity
Description
Reported according to CTCAE v.5.0
Time Frame
From the first dose of SABR to 3 years after the last dose of SABR
Title
Health-related quality of life Cancer-30
Description
European Organisation for Research and Treatment of Cancer-Quality of Life Questionnaires Cancer-30 (EORTC-QLQ C30)
Time Frame
At base-line and after 3, 6, 9, 12, 18, 24 and 36 months after registration.
Title
Health-related quality of life Breast-23
Description
European Organisation for Research and Treatment of Cancer-Quality of Life Questionnaire Breast-23 (EORTC-QLQ B23)
Time Frame
At base-line and after 3, 6, 9, 12, 18, 24 and 36 months after registration.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Katarzyna Kulbacka-Ortiz, CTO
Phone
+46721470685
Email
katarzyna.kulbacka-ortiz@vgregion.se
First Name & Middle Initial & Last Name or Official Title & Degree
Annika Baan
Phone
+46700906097
Email
annika.baan@vgregion.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barbro K Linderholm, MD, PhD
Organizational Affiliation
Sahlgrenska University Hospital, Gothenburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sahlgrenska University Hospital
City
Gothenburg
State/Province
Västra Götalandsregionen
ZIP/Postal Code
41345
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Barbro Kristina Linderholm, P.I.
Phone
0313427941
Email
barbro.linderholm@oncology.gu.se

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18719992
Citation
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.
Results Reference
result
PubMed Identifier
22172903
Citation
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.
Results Reference
result
PubMed Identifier
27017237
Citation
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.
Results Reference
result
PubMed Identifier
30773186
Citation
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.
Results Reference
result
PubMed Identifier
28943046
Citation
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.
Results Reference
result
PubMed Identifier
31734589
Citation
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.
Results Reference
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PubMed Identifier
32588550
Citation
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.
Results Reference
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PubMed Identifier
32484754
Citation
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 Trial. J Clin Oncol. 2020 Sep 1;38(25):2830-2838. doi: 10.1200/JCO.20.00818. Epub 2020 Jun 2.
Results Reference
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Stereotactic Ablative Radiotherapy for OligoMetastatic Breast Cancer

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