ASO Author Reflections: Sentinel Lymph Node Biopsy for Patients with a Non-classic Lobular Carcinoma In Situ Breast Biopsy
Pieter J. Westenend, Claudia J. C. Meurs, Sabine Siesling, Marian B. E. Menke-Pluijmers

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsBreast Cancer Treatment Studies · Breast Lesions and Carcinomas · Breast Implant and Reconstruction
As a primary diagnosis, pleomorphic or florid lobular carcinoma in situ (LCIS), also known as non-classic LCIS, is a rare finding on breast biopsy. A population-based study in the Netherlands found 160 cases during 10 years.^1^ At resection, 31–32 % of the patients were upstaged to invasive carcinoma.
Based on expert opinion and consensus, guidelines recommend that these patients should be treated similarly to patients with a ductal carcinoma in situ (DCIS) biopsy (i.e., by surgery). Like many other guidelines, the Dutch guideline does not specify whether this means that performing a sentinel lymph node biopsy (SLNB) in selected cases is part of this recommendation.^2^ According to this guideline, SLNB should be considered for patients with DCIS biopsy at high risk for upstaging who are scheduled for breast-conserving surgery (BCS). We found that SLNB was performed for 48 (36 %) of the 133 surgically treated patients with a non-classic LCIS biopsy. This is lower than the SLNB rate of 67 % for patients with a DCIS biopsy.^3^
The role of an SLNB for patients with a DCIS biopsy is the subject of an ongoing debate. In a recent guideline, the European Society of Breast Cancer Specialists (EUSOMA) set the SLNB target for patients treated with breast-conserving surgery (BCS) at 10 %, with a maximum of 20 %.^4^ In our LCIS study, we found an SLNB rate of 28 % (30 of 106) for patients undergoing BCS and 67 % (18 of 27) for patients undergoing mastectomy (unpublished analysis).^1^.
Selection of patients based on risk factors for upstaging is critical to lowering the SLNB rate. Unfortunately, because non-classic LCIS is so rare, there are no data on risk factors for upstaging in non-classic LCIS. On the other hand, it is reassuring that we found a metastasis rate of 6 % (2 patients with a micro-metastasis and 1 patient with a macro-metastasis, excluding 3 patients with isolated tumour cells)^1^. For patients treated by BCS, we found only one micro-metastasis.
The recently published SOUND trial demonstrated no difference in distant metastasis, survival, or local recurrence between patients with small (<2 cm), clinically node-negative invasive cancers treated with an SLNB and those treated without an SLNB.^5^ The metastasis rate for patients treated with an SLNB was 13.7 %, twice as high as in our LCIS study. In our study, 34 patients had invasive breast cancer at surgery, 4 of whom had a tumor larger than 2 cm.
In our opinion, this means that the SLNB target rate for non-classic LCIS can be the same 10 % as for DCIS, and that not performing a SLNB is also an option. We encourage researchers studying non-classic LCIS to report not only on the upstage rate, but also on the use and outcomes of SLNB because the data are sparse.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Federation of medical specialists. Federatie Medisch Specialisten, Kv K: 40483480. https://richtlijnendatabase.nl/richtlijn/borstkanker/startpagina_-_borstkanker.html.
- 2Gentilini OD, Botteri E, Sangalli C, Galimberti V, Porpiglia M, Agresti R, et al; SOUND Trial Group. Sentinel lymph node biopsy vs no axillary surgery in patients with small breast cancer and negative results on ultrasonography of axillary lymph nodes: the SOUND randomized clinical trial. JAMA Oncol. 2023;9:1557–64.10.1001/jamaoncol.2023.3759 PMC 1051487337733364 · doi ↗ · pubmed ↗
