- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07579286
Refusal of Sentinel Lymph Node Biopsy in Patients With Luminal A Subtype Early Breast Cancer (LumiNOde)
Sentinel lymph node biopsy (SLNB) is the standard of axillary lymph node surgical staging in patients with early breast cancer.
The main goal of the study is to abandon axillary surgery in patients over 59 years old with early, luminal A, clinical lymph node negative breast cancer.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Sentinel lymph node biopsy (SLNB) has replaced axillary lymph node dissection (ALND) in early breast cancer and has been widely implemented in clinical practice worldwide. The primary goal of SLNB is to reduce the complications associated with ALND while maintaining high anti-tumor efficacy.
However, many studies have shown that although SLNB reduces the complications typical of ALND, the incidence of these complications remains high: the risk of developing lymphedema is 7.5%, sensory disturbances and restrictions in arm movement occur in 5-8% of cases. It is well known that these complications negatively affect the physical, psychological, and emotional well-being of women, thereby reducing their quality of life.
It is also noteworthy that there is a relatively high rate of false-negative results in SLNB (ranging from 4.6% to 16.7%).
Due to advances in imaging diagnostic methods, the accuracy of preoperative assessment of lymph node status has significantly improved. According to studies, the sensitivity and specificity of ultrasound examination of the axillary lymph nodes in diagnosing lymph node involvement are 85% and 78%, respectively. Other sources, however, report a 15.5% of false-negative rate in preoperative ultrasound examinations. Consequently, the diagnostic field of standard radiological methods (ultrasound, CT, MRI) in assessing axillary lymph node status is deemed 'insufficient'. Mammolymphoscintigraphy is an additional diagnostic method based on the detection of pathophysiological alterations in the energy metabolism of tumor cells at the subcellular and molecular levels. Moreover, since metabolic changes usually precede anatomical reorganization, functional imaging methods are regarded as having greater sensitivity in identifying neoplastic changes. Our own experience with radiolabeled 99mTc lipophilic cations in diagnosing axillary lymph node metastasis breast cancer demonstrated that the sensitivity, specificity, and overall accuracy of the method were 80%, 84%, and 76%, respectively. Therefore, in this study, we are incorporating mammolymphoscintigraphy as an essential method for determining lymph node status.
In recent years, the status of axillary lymph nodes has played a diminishing role for adjuvant therapy in early breast cancer patients. Furthermore, in the luminal A subtype of early breast cancer, hormone therapy will be prescribed in the adjuvant setting regardless of axillary lymph node status.
Thus, the existing clinical data do not allow for a definitive conclusion regarding the role of SLNB in early breast cancer patients with the luminal A subtype. To address this and other questions, the present study was initiated
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Petr Krivorotko, Degree
- Telefonnummer: +79219597722
- E-mail: dr.krivorotko@mail.ru
Undersøgelse Kontakt Backup
- Navn: Arina Gorina
- Telefonnummer: +79185374992
- E-mail: dr.arina_olegovna@mail.ru
Studiesteder
-
-
Russian Federation
-
Saint Petersburg, Russian Federation, Rusland, 197758
- Rekruttering
- N.N. Petrov National Medical Research Center of Oncology
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- HER2-negative breast cancer (ER +/ PR +), Ki67 <= 30%, G1-2
- age> 59 years.
- morphologically confirmed diagnosis of breast cancer, IA-IIA stage
- ECOG score 0-2.
- the absence of contraindications to surgical intervention (including anesthetic risk is taken into account).
- patient is able to provide informed consent and sign approved consent forms to participate in the study.
- patients after surgical treatment in the scope of breast resection with sentinel lymph node biopsy (SLNB, group 1) or without axillary surgery (without SLNB, group 2).
- N0 status of axillary lymph nodes according to ultrasound and SPECT-CT of the breast with 99mTc-Technetril.
Exclusion Criteria:
- Inconsistency with inclusion criteria.
- stage T2-4, N1 or M1 cancer
- severe uncontrolled concomitant chronic diseases or acute diseases
- previous/concurrent malignancy or history of radiation therapy to the chest wall region
- any condition that is a contraindication to radiation therapy
5. pregnancy
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Group 2:breast resection without sentinel lymph node biopsy, radiotherapy to the breast area and SLN
|
breast resection without sentinel lymph node biopsy, radiotherapy to the breast area and sentinel lymph nodes
|
|
Aktiv komparator: Group 1: Breast resection with biopsy of the sentinel lymph node, radiotherapy
|
Breast resection with sentinel lymph node biopsy, radiotherapy to the breast and axilla according to current treatment standards
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Axillary recurrence rate.
Tidsramme: 2, 3, 5 years
|
Compare the rate of axillary recurrences in patients with early breast cancer who did not undergo sentinel lymph node biopsy (SLNB) versus those who received standard treatment with SLNB.
|
2, 3, 5 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
locoregional recurrence-free survival
Tidsramme: 5 and 10 years
|
Compare locoregional recurrence-free survival in the study groups of patients with early breast cancer
|
5 and 10 years
|
|
overall survival and recurrence-free survival
Tidsramme: 5 and 10 years
|
Compare overall survival and recurrence-free survival in the study groups of patients with early breast cancer
|
5 and 10 years
|
|
frequency and severity of adverse events
Tidsramme: 3, 5 and 10 years
|
Compare the frequency and severity of adverse events, using the current version 5.0 of the CTCAE
|
3, 5 and 10 years
|
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Neoplasmer efter sted
- Neoplasmer
- Hudsygdomme
- Brystsygdomme
- Hud- og bindevævssygdomme
- Brystneoplasmer
- Undersøgelsesteknikker
- Håndtering af eksemplar
- Kliniske laboratorieteknikker
- Diagnostiske teknikker og procedurer
- Diagnose
- Kirurgiske procedurer, operative
- Cytologiske teknikker
- Biopsi
- Cytodiagnose
- Mastektomi
- Diagnostiske teknikker, kirurgisk
- Lymfeknude excision
- Mastektomi, segmental
- Sentinel lymfeknude biopsi
Andre undersøgelses-id-numre
- 2417313
- 24/173 (Anden identifikator: N.N. Petrov National Medical Research Center of Oncology)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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