Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05334459
Other study ID # ISTMET-BHWGI2022-1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2022
Est. completion date March 31, 2028

Study information

Verified date April 2022
Source Ankara Oncology Research and Training Hospital
Contact Lutfi Dogan, Prof
Phone +905057134549
Email lutfidogan1@yahoo.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Locoregional (LRT) of the primary tumor in de-novo metastatic breast cancer (dnMBC) is no longer only a surgical challenge, but more the final decision of a multidisciplinary tumor board including medical oncologists, radiation oncologists and surgical oncologists. It is no longer only a question of locoregional control but rather a wider issue of improving overall survival (OS), due to the possible biological link between primary tumor and metastases. A multimodal approach, including LRT with curative intent should be considered for selected dnMBC patients, especially for the subset of bone-only metastatic ones.


Description:

Five to eight percent of breast cancer (BC) patients present with distant metastasis at diagnosis which is known as 'de novo' metastatic breast cancer (dnMBC). These patients represent up to 25% of all MBC patients and tend to have more favorable prognosis than those who relapse during follow-up. Recent data showed that approximately 40% of dnMBC patients undergo locoregional treatment (LRT). Most of the retrospective series over the past two decades showed that LRT not only controls locoregional progression, but also contributes to overall survival (OS), moreover meta-analyses suggest that surgical resection of the primary tumor may improve OS with a hazard ratio (HR) of around 0.60. MF07-01 study, one of the first clinical randomized trials, showed that the patients with diagnosis of dnMBC undergoing LRT followed by systemic therapy had an additional 14% OS benefit by the end of the 10-year follow-up when compared with patients who received only systemic therapy. Patient-related factors (i.e. age, comorbidities), metastatic burden (i.e. site and number of metastases) and more prominently tumor biology are major factors for therapeutic decisions in dnMBC. Metastatic sites differ according to the intrinsic BC subtypes. Bone and lymph nodes are more common sites for metastasis in hormone receptor (ER, PR) positive BC patients whereas visceral and brain metastasis is more common in Her2 positive & triple negative BC. Tailored therapy, such as targeted therapy & immunotherapy is based on IHC profile, genetic & molecular features in intrinsic subtypes (i.e. luminal A-like, luminal B-like Her2 negative, luminal B-like Her2 positive, Her2 positive nonluminal & basal-like breast cancer). Tailored therapy contributes to survival outcomes. Aromatase inhibitors (AI: anastrozole, letrozole, exemestane) with cyclin dependent kinase 4/6 inhibitors (CDKi: ribociclib, palbociclib, abemaciclib) are standard of care as first line setting in postmenopausal metastatic Her2 negative luminal-like breast cancer (mHN-LBC) patients. In the last decade, first line AI/CDKi combination has been shown to increase progression free survival (PFS) and objective response rates (ORR). Recently, updated OS outcomes with a median follow-up of more than 6.5 years has been presented at ESMO congress in September 2021. It has been reported that first line ribociclib and letrozole combination has been shown to have significant OS advantage over letrozole in mHN- 2 LBC. So, AI/CDKi combination as first line systemic treatment in postmenopausal mHN-LBC significantly decreases both progression and mortality rates. In Turkey, ribociclib and palbociclib are available options as CDKi. Therefore, AI/CDKi (ribociclib/palbociclib) combination is also preferred as first line setting for postmenopausal mHN-LBC in our country. Hormone receptor (ER, PR) and Her2 positivity might differ for primary & metastatic sites in BC, especially in relapsed patients. Discordance (i.e 'positivity conversion to negativity' or 'negativity conversion to positivity') rates are reported as 10-30% for ER, 20-50% for PR and 10-15% for Her2 in relapsed MBC, but data is limited for dnMBC. It has been reported that total discordance rate as 27% for ER / PR and/or Her2 between primary tumor and metastatic sites in MBC. It was 14.26% for ER/PR & 7.8% for Her2 status, respectively. They evaluated 16703 MBC patients in a large scale real-life multicenter French ESME cohort. In this cohort, 2169 patients had biopsy from both primary tumor and metastatic site within 6 months of MBC diagnosis, only 10% (n:1677) had optimal biopsy material for ER/PR & Her2 discordance evaluation. Taking into account these high discordance rates, synchronous biopsy from primary tumor and metastatic sites should be preferred in prospective clinical trial designs in dnMBC. However, it might not be so easy and pragmatic in daily practice. Moreover, radiotherapy (RT) techniques have considerably improved, allowing for the radiation dose to conform more precisely to the three-dimensional shape of the tumor, thus enabling much higher radiation doses and better tumor control with less toxicity. Observational studies showed that bone was the most common site of metastasis (around 45% of patients) and up to 30% of patients were diagnosed with bone-only metastases. For oligometastatic disease, some retrospective and prospective series demonstrated that local treatment of all metastases, when feasible, was significantly associated with prolonged survival. Patients with oligometastatic bone-only MBC treated with stereotactic radiotherapy had better clinical outcomes than those who had metastasis at other sites. It has been reported that local breast surgery was associated with better survival outcomes for the patients with only one metastatic site involvement (i.e. bone, liver or lung), but not for brain-only metastasis when they stratified the patients according to the distant metastatic sites. Our study group (BOMET trial) demonstrated that LRT prolonged survival and decreased locoregional recurrence in a prospectively maintained registry study with a median follow-up of 3 years, previously. Timing of primary breast surgery either at diagnosis or after systemic treatment provided a survival benefit similar to systemic therapy alone in bone-only dnMBC patients. Two ongoing prospective phase III trials (NCT02089100, NCT02364557) are evaluating the role of metastases local ablation (Stereotactic Body Radiation therapy (SBRT) or surgery) with curative intent in oligometastatic breast cancer. In conclusion, LRT of the primary tumor in dnMBC is no longer only a surgical challenge, but more the final decision of a multidisciplinary tumor board including medical oncologists, radiation oncologists and surgical oncologists. It is no longer only a question of locoregional control but rather a wider issue of improving OS, due to the possible biological link between primary tumor and metastases. A multimodal approach, including LRT with curative intent should be considered for selected dnMBC patients, especially for the subset of bone-only metastatic ones.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date March 31, 2028
Est. primary completion date March 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Primary breast tumor amenable for complete surgical resection, patients in good physical condition for receiving protocol driven locoregional and systemic treatments and receiving radiotherapy. Exclusion Criteria: - Primary tumor not amenable for complete resection; primary tumor with extended infection, bleeding, or necrosis; patients with poor physical condition which prevents the patient from receiving protocol driven locoregional and systemic treatment; synchronous primary cancer at the contralateral breast; clinically involved contralateral axillary nodes; patients not suitable for adequate follow-up, and failure to give informed consent. Pregnancy and lactation.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
radiotherapy
Oligometastatic disease (defined here as 5 or fewer sites of metastatic disease involving 3 or fewer organ systems) Primary tumor biopsy, Metastatic site biopsy (Bone, liver, etc) (if there is, based on institutional practice) o ER / PR /Her2 /Ki67 study) Collection of CTC. Radiotherapy (RT) to the primary breast tumor (Hypo fractionated) All patients will receive the standard of care treatment with CDK4/6 inhibitor + AI for 6 months (at least 26 weeks). o Denosumab, Biphosphonate for bone metastasis RT to metastatic side (if visible). Continue Systemic therapy 12 months, patients will have LRT surgery (BCS/mastectomy + LN evaluation; SLNB+ALND) + RT (based on the institutional practice). Collect CTC and ER/PR/Her 2 in the final specimen ST will be continued until progression and/or unmanageable toxicity. Radiologic evaluation every 3-6-month based on institutional practice.

Locations

Country Name City State
Turkey Lutfi Dogan Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara Oncology Research and Training Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (8)

Lee SJ, Park S, Ahn HK, Yi JH, Cho EY, Sun JM, Lee JE, Nam SJ, Yang JH, Park YH, Ahn JS, Im YH. Implications of bone-only metastases in breast cancer: favorable preference with excellent outcomes of hormone receptor positive breast cancer. Cancer Res Treat. 2011 Jun;43(2):89-95. doi: 10.4143/crt.2011.43.2.89. Epub 2011 Jun 30. — View 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. — View Citation

Onderdonk BE, Gutiontov SI, Chmura SJ. The Evolution (and Future) of Stereotactic Body Radiotherapy in the Treatment of Oligometastatic Disease. Hematol Oncol Clin North Am. 2020 Feb;34(1):307-320. doi: 10.1016/j.hoc.2019.09.003. Epub 2019 Oct 28. Review. — View Citation

Sledge GW Jr, Toi M, Neven P, Sohn J, Inoue K, Pivot X, Burdaeva O, Okera M, Masuda N, Kaufman PA, Koh H, Grischke EM, Conte P, Lu Y, Barriga S, Hurt K, Frenzel M, Johnston S, Llombart-Cussac A. The Effect of Abemaciclib Plus Fulvestrant on Overall Survival in Hormone Receptor-Positive, ERBB2-Negative Breast Cancer That Progressed on Endocrine Therapy-MONARCH 2: A Randomized Clinical Trial. JAMA Oncol. 2020 Jan 1;6(1):116-124. doi: 10.1001/jamaoncol.2019.4782. — View Citation

Soran A, Dogan L, Isik A, Ozbas S, Trabulus DC, Demirci U, Karanlik H, Soyder A, Dag A, Bilici A, Dogan M, Koksal H, Sendur MAN, Gulcelik MA, Maralcan G, Cabioglu N, Yeniay L, Utkan Z, Simsek T, Karadurmus N, Daglar G, Yildiz B, Uras C, Tukenmez M, Yildirim A, Kutun S, Ozaslan C, Karaman N, Akcay MN, Toktas O, Sezgin E. The Effect of Primary Surgery in Patients with De Novo Stage IV Breast Cancer with Bone Metastasis Only (Protocol BOMET MF 14-01): A Multi-Center, Prospective Registry Study. Ann Surg Oncol. 2021 Sep;28(9):5048-5057. doi: 10.1245/s10434-021-09621-8. Epub 2021 Feb 2. — View Citation

Soran A, Ozmen V, Ozbas S, Karanlik H, Muslumanoglu M, Igci A, Canturk NZ, Utkan Z, Evrensel T, Sezgin E; MF07-01 Study Group. Primary Surgery with Systemic Therapy in Patients with de Novo Stage IV Breast Cancer: 10-year Follow-up; Protocol MF07-01 Randomized Clinical Trial. J Am Coll Surg. 2021 Dec;233(6):742-751.e5. doi: 10.1016/j.jamcollsurg.2021.08.686. Epub 2021 Sep 13. — View 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. — View Citation

Wang K, Shi Y, Li ZY, Xiao YL, Li J, Zhang X, Li HY. Metastatic pattern discriminates survival benefit of primary surgery for de novo stage IV breast cancer: A real-world observational study. Eur J Surg Oncol. 2019 Aug;45(8):1364-1372. doi: 10.1016/j.ejso.2019.02.013. Epub 2019 Feb 19. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Survival Phase I study to evaluate feasibility (overall and diseas free survival) of this curative intent treatment approach to patients presenting with dnMBC with oligometastatic disease. 5 years follow-up
See also
  Status Clinical Trial Phase
Withdrawn NCT04872608 - A Study of Letrozole, Palbociclib, and Onapristone ER in People With Metastatic Breast Cancer Phase 1
Terminated NCT02202746 - A Study to Assess the Safety and Efficacy of the VEGFR-FGFR-PDGFR Inhibitor, Lucitanib, Given to Patients With Metastatic Breast Cancer Phase 2
Completed NCT02506556 - Phosphatidylinositol 3-kinase (PI3K) Alpha iNhibition In Advanced Breast Cancer Phase 2
Recruiting NCT05534438 - A Study on Adding Precisely Targeted Radiation Therapy (Stereotactic Body Radiation Therapy) to the Usual Treatment Approach (Drug Therapy) in People With Breast Cancer Phase 2
Recruiting NCT03368729 - Niraparib in Combination With Trastuzumab in Metastatic HER2+ Breast Cancer Phase 1/Phase 2
Completed NCT04103853 - Safety, Tolerability, and Pharmacokinetics of Proxalutamide Therapy in Women With Metastatic Breast Cancer Phase 1
Terminated NCT01847599 - Educational Intervention to Adherence of Patients Treated by Capecitabine +/- Lapatinib N/A
Active, not recruiting NCT03147287 - Palbociclib After CDK and Endocrine Therapy (PACE) Phase 2
Not yet recruiting NCT06062498 - Elacestrant vs Elacestrant Plus a CDK4/6 Inhibitor in Patients With ERpositive/HER2-negative Advanced or Metastatic Breast Cancer Phase 2
Recruiting NCT05383196 - Onvansertib + Paclitaxel In TNBC Phase 1/Phase 2
Recruiting NCT04095390 - A Phase Ⅱ Trial of Pyrotinib Combination With CDK4/6 Inhibitor SHR6390 in Patients Prior Trastuzumab-treated Advanced HER2-Positive Breast Cancer Phase 2
Active, not recruiting NCT04432454 - Evaluation of Lasofoxifene Combined With Abemaciclib in Advanced or Metastatic ER+/HER2- Breast Cancer With an ESR1 Mutation Phase 2
Recruiting NCT03323346 - Phase II Trial of Disulfiram With Copper in Metastatic Breast Cancer Phase 2
Recruiting NCT05744375 - Trastuzumab Deruxtecan in First-line HER2-positive Locally Advanced/MBC Patients Resistant to Trastuzumab+Pertuzumab Phase 2
Completed NCT02924883 - A Study to Evaluate the Efficacy and Safety of Trastuzumab Emtansine in Combination With Atezolizumab or Atezolizumab-Placebo in Participants With Human Epidermal Growth Factor-2 (HER2) Positive Locally Advanced or Metastatic Breast Cancer (BC) Who Received Prior Trastuzumab and Taxane Based Therapy Phase 2
Completed NCT01881230 - Evaluate Risk/Benefit of Nab Paclitaxel in Combination With Gemcitabine and Carboplatin Compared to Gemcitabine and Carboplatin in Triple Negative Metastatic Breast Cancer (or Metastatic Triple Negative Breast Cancer) Phase 2/Phase 3
Completed NCT01942135 - Palbociclib (PD-0332991) Combined With Fulvestrant In Hormone Receptor+ HER2-Negative Metastatic Breast Cancer After Endocrine Failure (PALOMA-3) Phase 3
Active, not recruiting NCT04448886 - Sacituzumab Govitecan +/- Pembrolizumab In HR+ / HER2 - MBC Phase 2
Completed NCT01401959 - Trial of Eribulin in Patients Who Do Not Achieve Pathologic Complete Response (pCR) Following Neoadjuvant Chemotherapy Phase 2
Terminated NCT04720664 - Oral SM-88 in Patients With Metastatic HR+/HER2- Breast Cancer Phase 2