Early Stage Breast CancerNCT03102307
Registry Trial to Evaluate the Clinical Utilization of Targeted Axillary Dissection (TAD)
An observational study of Early Stage Breast Cancer, run by Kliniken Essen-Mitte at 3 sites in Germany.
Trial summary
A downstaging of axillary tumor-spread can be achieved in about 40% of the patients receiving neoadjuvant chemotherapy (NACT). The impact of NACT on loco-regional tumor control has not yet been sufficiently investigated. Moreover the pathologic nodal status after NACT is a strong prognostic marker. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Early Stage Breast Cancer
- What is being tested?
- Not suitable for TAD and Suitable for TAD
- Type of treatment
- Surgery or procedure
- How many people
- 548 participants
- Where
- 3 sitesGermany
- Study dates
- 1 Feb 2017to 1 Oct 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with newly diagnosed invasive breast cancer with clinically affected lymph nodes
Who may be able to join
- informed consent
- invasive mamma carcinoma verified by needle biopsy of the primary tumor
- nodal positive (cN+) verified by axillary ultrasound
- cT stage 1-4c, multifocality allowed
- no sign of distant metastasis (cM0)
Who cannot join
- prior history of breast cancer
- prior ipsilateral extensive surgery of breast or axilla
- inflammatory or extramammary breast cancer
- pregnancy
- inability to understand the studies purpose
- no written patient informed consent
Trial locations and contacts
3 sites in 1 country.
Germany3 sites
Kliniken Essen-Mitte
Essen, North Rhine-Westphalia, 45136
Klinikum Esslingen
Esslingen am Neckar, 73730
Evangelische Kliniken Gelsenkirchen
Gelsenkirchen, 45879
About this study
Official title: A Prospective, Multicenter, Registry Trial to Evaluate Utilization Frequency and Feasibility of Targeted Axillary Dissection (TAD) After Needle Biopsy and Clip Placement in Early Breast Cancer With Clinically Affected Lymph Nodes
A downstaging of axillary tumor-spread can be achieved in about 40% of the patients receiving neoadjuvant chemotherapy (NACT). The impact of NACT on loco-regional tumor control has not yet been sufficiently investigated. Moreover the pathologic nodal status after NACT is a strong prognostic marker. Therefore it is most desirable to identify the approximately 40% of patients with pathologic complete response of the axilla, that could be spared from a potentially non beneficial axillary lymph node dissection (ALND). Attempts to identify these patients via sentinel lymph node biopsy (SLNB) after NACT have failed to provide acceptable false negative rates (FNR). The new concept of targeted axillary dissection (TAD) following NACT has shown promising results. Still multiple information about the clinical adoption of this procedure into clinical practice are missing. The SenTa registry trial is designed to assess the clinical implementation of TAD into general practice.
Read the detailed description
For decades the pathologic nodal status in early breast cancer has been of paramount importance, when evaluating the need for further adjuvant therapies. Nowadays tumor characteristics as receptor status and gene expression essays are increasingly included in this decision process. An increasing number of breast cancer patients are treated with neoadjuvant chemotherapy (NACT). A downstaging of axillary tumor-spread can be achieved in about 40% of the patients receiving NACT. The contribution of NACT to loco-regional tumor control is not fully integrated into the surgical treatment plan. The introduction of sentinel lymph node biopsy (SLNB) and the results of the ACOSOG (American College of Surgeons Oncology Group) Z0011 trial led to a reduction in radicalness of axillary surgery in the adjuvant setting. The impact of NACT on loco-regional tumor control in the neoadjuvant setting has not yet been sufficiently investigated. Moreover the pathologic nodal status after NACT is a strong prognostic marker. Therefore it is most desirable to identify the approximately 40% of patients with pathologic complete response of the axilla and distinguish these patients from those with tumor residuals which might need additional postneoadjuvant treatment. So far attempts to identify these patients via SLNB after NACT have failed to provide acceptable false negative rates (FNR) as reported in the SENTINA (Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy) trial and ACOSOG Z1071 trial.
Attempts have bee made to further improve FNR of SLNB after NACT in patients with clinically affected lymph nodes at initial presentation. A new concept of surgical axillary staging after NACT is the targeted axillary dissection (TAD). First results have shown to reduce FNR far below the desired threshold of 10%. In this procedure clinically suspicious lymph nodes are evaluated by core needle biopsy (CNB) or fine needle aspiration (FNA) before NACT. A clip is placed into the most suspicious appearing lymph node (target lymph node TLN) directly after biopsy. In case of proven metastasis surgical staging of the axilla is postponed to after completion of NACT. The targeted resection of the clipped node after NACT (target lymph node biopsy TLNB) displays a FNR of 2 - 4.2% according to first results published by Caudle et al. in 2016. In about 3 out of 4 patients the TLN equals a SLN if SLNB is performed simultaneously. The combination of TLNB and SLNB (together so called TAD) seems to further lower FNR. Cases in which tracer uptake in lymph nodes is impaired i.e. by tumor residuals and presumably result in a false negative SLNB can be covered by TLNB.
Clip placement in affected axillary lymph nodes for the purpose of following targeted resection has been implemented into international guidelines. But to date multiple insights into clinical application of TAD are missing. It is not known how often initial CNB/FNA of axillary lymph nodes and following clip placement is successful or has to be abandoned because of technical/medical contraindications. Moreover it is not known how often visualization of the clip after normalization of lymph node structures following NACT and month after initial clip placement is possible. Furthermore information about optimal clip material are lacking. In summary success rates for the targeted resection of the clipped node have to be investigated. Therefore the intraoperative detection rate of the clipped target lymph node is our primary outcome measure.
Patients with clinically affected lymph nodes at initial presentation are planned to be enrolled in multiple german breast centers. In accorndance to german guidelines it is aimed to evaluate the pathologic nodal status via CNB with following clip placement in all of these patients after informed consent. If CNB or clip placement cannot be achieved, technical/medical contraindications are recorded. As the SenTa trial is a registry trial, no strict directives for the further surgical treatment are made. If clip placement is successful, further procedures are left at the investigators choice according to initial pathologic nodal status and potential clinical response to NACT.
If no tumor manifestations are detected in initial CNB, SLNB with simultaneous targeted resection of the clipped node (TLNB) is recommended. The rationale for TLNB in this situation is a FNR of about 20% of initial CNB. On an individual basis upfront ALND can be offered.
If tumor manifestations are detected in initial CNB, targeted resection of the clipped node (TLNB) is strongly recommended because of obvious reasons. If NACT is not planned, upfront ALND should be offered. If patients are planned for NACT further procedures are left at the investigators discretion according to clinical response to NACT. Clinical response after NACT is assessed by axillary ultrasound and an optional needle biopsy if applicable. In case of clinical complete response, TLNB with simultaneous SLNB can be offered on an individual basis.
- Conditions
- Early Stage Breast Cancer
- Being tested
- Not suitable for TAD, Suitable for TAD
- Keywords
- Targeted axillary dissection, Sentinel node biopsy, Neoadjuvant chemotherapy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Not suitable for TADOther
Registry of the rate of patients not suitable for TAD as initial CNB with clip placement of axillary lymph nodes is not possible and underlying medical contraindications, technical obstacles or miscellaneous reasons why needle biopsy and/or clip labeling of clinically affected lymph nodes cannot be done
Suitable for TADProcedure or surgery
Registry of surgical outcome measures of targeted resection of the clipped node with optional sentinel node biopsy or axillary lymph node dissection with or without preceding neoadjuvant chemotherapy
| Study group | Role | What they receive |
|---|---|---|
| CNB biopsy/clip placement not done | Clinically affected lymph nodes cannot be biopsied or clip labeled. Patients are not suitable for TAD Receives: Other: Not suitable for TAD | |
| CNB/clip placement done - benign | Clinically affected lymph nodes can be biopsied and clip labeled. Needle biopsy reveals no axillary tumor spread. Patients are suitable for TAD Receives: Procedure: Suitable for TAD | |
| CNB/clip placement done - malignant | Clinically affected lymph nodes can be biopsied and clip labeled. Needle biopsy reveals axillary tumor spread. Patients are suitable for TAD Receives: Procedure: Suitable for TAD |
What is being measured
The primary outcome is the main question the study is designed to answer.
Surgical detection rate of the clip labeled target lymph node
Successful intraoperative detection and targeted resection of clip labeled target lymph node as confirmed by specimen radiography and/or surgeon
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Secondary outcomes (13)
Rate of patients not suitable for targeted axillary dissection (TAD)
Rate of patients not suitable for TAD as initial CNB with clip placement of axillary lymph nodes is not possible and underlying medical contraindications, technical obstacles or miscellaneous reasons why needle biopsy and/or clip labeling of clinically affected lymph nodes cannot be done
Measured: 14 days
Rate of representative and successful lymph node CNB
Rate of CNB revealing tumor manifestations or lymph node tissue on histology out of all performed lymph node CNB
Measured: 14 days
Rate of preoperative sonographic clip detection
Essential requirement for targeted resection of the clipped target lymph node is the preoperative visualization of the clip for the purpose of guide wire localization
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Rate of patients treated with TAD after NACT
Rate of patients with intraoperative detection of at least one sentinel lymph node and the clip labeled target lymph node as confirmed by specimen radiography and/or surgeon
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Rate of patients treated with upfront ALND after NACT
Rate of patients treated with upfront axillary dissection including resection of clipped node after completion of NACT
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
False negative rate for target lymph node biopsy (TLNB) alone
Clipped target lymph node does not contain tumor manifestations after NACT but lymph node metastasis is revealed by ALND
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
False negative rate for Sentinel Lymph Node Biopsy (SLN) alone
Sentinel lymph node does not contain tumor manifestations after NACT but lymph node metastasis is revealed by ALND
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Detection Rate for Targeted Axillary Detection (TAD) (SLN and TLN detected)
Successful intraoperative detection and resection of at least one sentinel lymph node and the clip labeled target lymph node as confirmed by specimen radiography and/or surgeon
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Detection Rate for Sentinel Lymph Node Biopsy (SLNB)
Successful intraoperative detection and resection of at least one sentinel lymph node
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Rate of patients,where the clip is found in a sentinel lymph node (SLN)
Clip is located in a sentinel lymph node during TAD, hence the TLN equals a SLN
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Number of excised lymph nodes during targeted axillary dissection (TAD)
Number of excised lymph nodes during targeted axillary dissection (TAD) equals count of sentinel lymph nodes plus target lymph nodes
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Number of excised lymph nodes during sentinel lymph node biopsy (SLNB)
Number of excised lymph nodes during targeted axillary dissection (TAD) equals count of sentinel lymph nodes plus target lymph nodes
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Number of excised target lymph nodes (TLN) which are not a sentinel lymph node
Number of excised clipped lymph nodes during target lymph node biopsy (TLNB) which are not sentinel lymph nodes
Measured: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Apr 2017
- Study start1 Feb 2017
- Primary completion28 Feb 2019
- Study completion1 Oct 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Early Stage Breast CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 548 participants (actual)
Sponsor and investigators
- Lead sponsor
- Kliniken Essen-Mitte
- Sponsor type
- University, hospital or other
- Collaborators
- GBG Forschungs GmbH
- Responsible party
- Sponsor
- Investigators
- Sherko Kümmel, MD, Principal investigator, Kliniken Essen-MitteJohannes Holtschmidt, MD, Study chair, Kliniken Essen-MitteThortsen Kühn, MD, Study chair, Klinikum Esslingen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03102307
- Sponsor's protocol ID
- SenTa
- Status last verified
- Feb 2021
- First submitted
- 27 Mar 2017
- Last updated
- 3 Feb 2021
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Caudle AS, Yang WT, Krishnamurthy S, Mittendorf EA, Black DM, Gilcrease MZ, Bedrosian I, Hobbs BP, DeSnyder SM, Hwang RF, Adrada BE, Shaitelman SF, Chavez-MacGregor M, Smith BD, Candelaria RP, Babiera GV, Dogan BE, Santiago L, Hunt KK, Kuerer HM. Improved Axillary Evaluation Following Neoadjuvant Therapy for Patients With Node-Positive Breast Cancer Using Selective Evaluation of Clipped Nodes: Implementation of Targeted Axillary Dissection. J Clin Oncol. 2016 Apr 1;34(10):1072-8. doi: 10.1200/JCO.2015.64.0094. Epub 2016 Jan 25.
PubMed 26811528Boughey JC, Suman VJ, Mittendorf EA, Ahrendt GM, Wilke LG, Taback B, Leitch AM, Kuerer HM, Bowling M, Flippo-Morton TS, Byrd DR, Ollila DW, Julian TB, McLaughlin SA, McCall L, Symmans WF, Le-Petross HT, Haffty BG, Buchholz TA, Nelson H, Hunt KK; Alliance for Clinical Trials in Oncology. Sentinel lymph node surgery after neoadjuvant chemotherapy in patients with node-positive breast cancer: the ACOSOG Z1071 (Alliance) clinical trial. JAMA. 2013 Oct 9;310(14):1455-61. doi: 10.1001/jama.2013.278932.
PubMed 24101169Kuehn T, Bauerfeind I, Fehm T, Fleige B, Hausschild M, Helms G, Lebeau A, Liedtke C, von Minckwitz G, Nekljudova V, Schmatloch S, Schrenk P, Staebler A, Untch M. Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy (SENTINA): a prospective, multicentre cohort study. Lancet Oncol. 2013 Jun;14(7):609-18. doi: 10.1016/S1470-2045(13)70166-9. Epub 2013 May 15.
PubMed 23683750Kuemmel S, Heil J, Rueland A, Seiberling C, Harrach H, Schindowski D, Lubitz J, Hellerhoff K, Ankel C, Grasshoff ST, Deuschle P, Hanf V, Belke K, Dall P, Dorn J, Kaltenecker G, Kuehn T, Beckmann U, Potenberg J, Blohmer JU, Kostara A, Breit E, Holtschmidt J, Traut E, Reinisch M. A Prospective, Multicenter Registry Study to Evaluate the Clinical Feasibility of Targeted Axillary Dissection (TAD) in Node-positive Breast Cancer Patients. Ann Surg. 2022 Nov 1;276(5):e553-e562. doi: 10.1097/SLA.0000000000004572. Epub 2020 Nov 4.
PubMed 33156057
Study at a glance
From the registry record, last updated by the sponsor on 3 Feb 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective, Multicenter, Registry Trial to Evaluate Utilization Frequency and Feasibility of Targeted Axillary Dissection (TAD) After Needle Biopsy and Clip Placement in Early Breast Cancer With Clinically Affected Lymph Nodes
- ClinicalTrials.gov ID
- NCT03102307
- Acronym / sponsor ID
- SenTa
- Conditions
- Early Stage Breast Cancer
- Keywords
- Targeted axillary dissection, Sentinel node biopsy, Neoadjuvant chemotherapy
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 548 participants (actual)
- Lead sponsor
- Kliniken Essen-MitteUniversity, hospital or other
- Collaborators
- GBG Forschungs GmbH
- Study start
- 1 Feb 2017 (actual)
- Primary completion
- 28 Feb 2019 (actual)
- Study completion
- 1 Oct 2019 (actual)
- First posted
- 5 Apr 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A downstaging of axillary tumor-spread can be achieved in about 40% of the patients receiving neoadjuvant chemotherapy (NACT). The impact of NACT on loco-regional tumor control has not yet been sufficiently investigated. Moreover the pathologic nodal status after NACT is a strong prognostic marker. Therefore it is most desirable to identify the approximately 40% of patients with pathologic complete response of the axilla, that could be spared from a potentially non beneficial axillary lymph node dissection (ALND). Attempts to identify these patients via sentinel lymph node biopsy (SLNB) after NACT have failed to provide acceptable false negative rates (FNR). The new concept of targeted axillary dissection (TAD) following NACT has shown promising results. Still multiple information about the clinical adoption of this procedure into clinical practice are missing. The SenTa registry trial is designed to assess the clinical implementation of TAD into general practice.
Detailed description
For decades the pathologic nodal status in early breast cancer has been of paramount importance, when evaluating the need for further adjuvant therapies. Nowadays tumor characteristics as receptor status and gene expression essays are increasingly included in this decision process. An increasing number of breast cancer patients are treated with neoadjuvant chemotherapy (NACT). A downstaging of axillary tumor-spread can be achieved in about 40% of the patients receiving NACT. The contribution of NACT to loco-regional tumor control is not fully integrated into the surgical treatment plan. The introduction of sentinel lymph node biopsy (SLNB) and the results of the ACOSOG (American College of Surgeons Oncology Group) Z0011 trial led to a reduction in radicalness of axillary surgery in the adjuvant setting. The impact of NACT on loco-regional tumor control in the neoadjuvant setting has not yet been sufficiently investigated. Moreover the pathologic nodal status after NACT is a strong prognostic marker. Therefore it is most desirable to identify the approximately 40% of patients with pathologic complete response of the axilla and distinguish these patients from those with tumor residuals which might need additional postneoadjuvant treatment. So far attempts to identify these patients via SLNB after NACT have failed to provide acceptable false negative rates (FNR) as reported in the SENTINA (Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy) trial and ACOSOG Z1071 trial.
Attempts have bee made to further improve FNR of SLNB after NACT in patients with clinically affected lymph nodes at initial presentation. A new concept of surgical axillary staging after NACT is the targeted axillary dissection (TAD). First results have shown to reduce FNR far below the desired threshold of 10%. In this procedure clinically suspicious lymph nodes are evaluated by core needle biopsy (CNB) or fine needle aspiration (FNA) before NACT. A clip is placed into the most suspicious appearing lymph node (target lymph node TLN) directly after biopsy. In case of proven metastasis surgical staging of the axilla is postponed to after completion of NACT. The targeted resection of the clipped node after NACT (target lymph node biopsy TLNB) displays a FNR of 2 - 4.2% according to first results published by Caudle et al. in 2016. In about 3 out of 4 patients the TLN equals a SLN if SLNB is performed simultaneously. The combination of TLNB and SLNB (together so called TAD) seems to further lower FNR. Cases in which tracer uptake in lymph nodes is impaired i.e. by tumor residuals and presumably result in a false negative SLNB can be covered by TLNB.
Clip placement in affected axillary lymph nodes for the purpose of following targeted resection has been implemented into international guidelines. But to date multiple insights into clinical application of TAD are missing. It is not known how often initial CNB/FNA of axillary lymph nodes and following clip placement is successful or has to be abandoned because of technical/medical contraindications. Moreover it is not known how often visualization of the clip after normalization of lymph node structures following NACT and month after initial clip placement is possible. Furthermore information about optimal clip material are lacking. In summary success rates for the targeted resection of the clipped node have to be investigated. Therefore the intraoperative detection rate of the clipped target lymph node is our primary outcome measure.
Patients with clinically affected lymph nodes at initial presentation are planned to be enrolled in multiple german breast centers. In accorndance to german guidelines it is aimed to evaluate the pathologic nodal status via CNB with following clip placement in all of these patients after informed consent. If CNB or clip placement cannot be achieved, technical/medical contraindications are recorded. As the SenTa trial is a registry trial, no strict directives for the further surgical treatment are made. If clip placement is successful, further procedures are left at the investigators choice according to initial pathologic nodal status and potential clinical response to NACT.
If no tumor manifestations are detected in initial CNB, SLNB with simultaneous targeted resection of the clipped node (TLNB) is recommended. The rationale for TLNB in this situation is a FNR of about 20% of initial CNB. On an individual basis upfront ALND can be offered.
If tumor manifestations are detected in initial CNB, targeted resection of the clipped node (TLNB) is strongly recommended because of obvious reasons. If NACT is not planned, upfront ALND should be offered. If patients are planned for NACT further procedures are left at the investigators discretion according to clinical response to NACT. Clinical response after NACT is assessed by axillary ultrasound and an optional needle biopsy if applicable. In case of clinical complete response, TLNB with simultaneous SLNB can be offered on an individual basis.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| CNB biopsy/clip placement not done | – | Other: Not suitable for TADClinically affected lymph nodes cannot be biopsied or clip labeled. Patients are not suitable for TAD |
| CNB/clip placement done - benign | – | Procedure: Suitable for TADClinically affected lymph nodes can be biopsied and clip labeled. Needle biopsy reveals no axillary tumor spread. Patients are suitable for TAD |
| CNB/clip placement done - malignant | – | Procedure: Suitable for TADClinically affected lymph nodes can be biopsied and clip labeled. Needle biopsy reveals axillary tumor spread. Patients are suitable for TAD |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with newly diagnosed invasive breast cancer with clinically affected lymph nodes
Key inclusion criteria (5 listed)
- informed consent
- invasive mamma carcinoma verified by needle biopsy of the primary tumor
- nodal positive (cN+) verified by axillary ultrasound
- cT stage 1-4c, multifocality allowed
- no sign of distant metastasis (cM0)
Key exclusion criteria (6 listed)
- prior history of breast cancer
- prior ipsilateral extensive surgery of breast or axilla
- inflammatory or extramammary breast cancer
- pregnancy
- inability to understand the studies purpose
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Not suitable for TADRegistry of the rate of patients not suitable for TAD as initial CNB with clip placement of axillary lymph nodes is not possible and underlying medical contraindications, technical obstacles or miscellaneous reasons why needle biopsy and/or clip labeling of clinically affected lymph nodes cannot be done | Other | CNB biopsy/clip placement not done |
| Suitable for TADRegistry of surgical outcome measures of targeted resection of the clipped node with optional sentinel node biopsy or axillary lymph node dissection with or without preceding neoadjuvant chemotherapy | Procedure or surgery | CNB/clip placement done - benign, CNB/clip placement done - malignant |
Primary outcome
Surgical detection rate of the clip labeled target lymph node
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Successful intraoperative detection and targeted resection of clip labeled target lymph node as confirmed by specimen radiography and/or surgeon
13 secondary outcomes
Rate of patients not suitable for targeted axillary dissection (TAD)
Time frame: 14 days
Rate of representative and successful lymph node CNB
Time frame: 14 days
Rate of preoperative sonographic clip detection
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Rate of patients treated with TAD after NACT
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Rate of patients treated with upfront ALND after NACT
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
False negative rate for target lymph node biopsy (TLNB) alone
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
False negative rate for Sentinel Lymph Node Biopsy (SLN) alone
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Detection Rate for Targeted Axillary Detection (TAD) (SLN and TLN detected)
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Detection Rate for Sentinel Lymph Node Biopsy (SLNB)
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Rate of patients,where the clip is found in a sentinel lymph node (SLN)
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Number of excised lymph nodes during targeted axillary dissection (TAD)
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Number of excised lymph nodes during sentinel lymph node biopsy (SLNB)
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Number of excised target lymph nodes (TLN) which are not a sentinel lymph node
Time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Feb 2021.
- Background: PubMed 26811528Caudle AS, Yang WT, Krishnamurthy S, Mittendorf EA, Black DM, Gilcrease MZ, Bedrosian I, Hobbs BP, DeSnyder SM, Hwang RF, Adrada BE, Shaitelman SF, Chavez-MacGregor M, Smith BD, Candelaria RP, Babiera GV, Dogan BE, Santiago L, Hunt KK, Kuerer HM. Improved Axillary Evaluation Following Neoadjuvant Therapy for Patients With Node-Positive Breast Cancer Using Selective Evaluation of Clipped Nodes: Implementation of Targeted Axillary Dissection. J Clin Oncol. 2016 Apr 1;34(10):1072-8. doi: 10.1200/JCO.2015.64.0094. Epub 2016 Jan 25.
- Background: PubMed 24101169Boughey JC, Suman VJ, Mittendorf EA, Ahrendt GM, Wilke LG, Taback B, Leitch AM, Kuerer HM, Bowling M, Flippo-Morton TS, Byrd DR, Ollila DW, Julian TB, McLaughlin SA, McCall L, Symmans WF, Le-Petross HT, Haffty BG, Buchholz TA, Nelson H, Hunt KK; Alliance for Clinical Trials in Oncology. Sentinel lymph node surgery after neoadjuvant chemotherapy in patients with node-positive breast cancer: the ACOSOG Z1071 (Alliance) clinical trial. JAMA. 2013 Oct 9;310(14):1455-61. doi: 10.1001/jama.2013.278932.
- Background: PubMed 23683750Kuehn T, Bauerfeind I, Fehm T, Fleige B, Hausschild M, Helms G, Lebeau A, Liedtke C, von Minckwitz G, Nekljudova V, Schmatloch S, Schrenk P, Staebler A, Untch M. Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy (SENTINA): a prospective, multicentre cohort study. Lancet Oncol. 2013 Jun;14(7):609-18. doi: 10.1016/S1470-2045(13)70166-9. Epub 2013 May 15.
- Results publication: PubMed 33156057Kuemmel S, Heil J, Rueland A, Seiberling C, Harrach H, Schindowski D, Lubitz J, Hellerhoff K, Ankel C, Grasshoff ST, Deuschle P, Hanf V, Belke K, Dall P, Dorn J, Kaltenecker G, Kuehn T, Beckmann U, Potenberg J, Blohmer JU, Kostara A, Breit E, Holtschmidt J, Traut E, Reinisch M. A Prospective, Multicenter Registry Study to Evaluate the Clinical Feasibility of Targeted Axillary Dissection (TAD) in Node-positive Breast Cancer Patients. Ann Surg. 2022 Nov 1;276(5):e553-e562. doi: 10.1097/SLA.0000000000004572. Epub 2020 Nov 4.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sherko Kümmel, MD principal investigator
Kliniken Essen-Mitte
Johannes Holtschmidt, MD study chair
Kliniken Essen-Mitte
Thortsen Kühn, MD study chair
Klinikum Esslingen
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Early Stage Breast Cancer, run by Kliniken Essen-Mitte at 3 sites in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 3 Feb 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Surgical detection rate of the clip labeled target lymph node (time frame: 6 month for patients undergoing NACT after initial needle biopsy/clip placement and subsequent surgical resection of the clipped node). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03102307, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2021.