Advertisement
Research Article|Articles in Press

The involvement of axillary reverse mapping nodes in patients with node-positive breast cancer

      Abstract

      Introduction

      Axillary reverse mapping (ARM) procedure is useful in reducing lymphedema. However, concerns regarding oncologic safety have limited the adoption of the ARM procedure. This study aimed to evaluate the involvement of ARM nodes in node-positive breast cancer patients.

      Materials and methods

      Two hundred twenty-three node-positive patients were enrolled in this study: 90 were clinically node-negative, but had one or more positive sentinel lymph nodes (SLNs) (SLN-positive group); 68 were clinicopathologically node-positive (CpN-positive group); and 65 had confirmed nodal involvement and received neoadjuvant chemotherapy (NAC) (NAC group). All patients underwent axillary lymph node dissection with fluorescent ARM.

      Results

      ARM nodes were involved in 33 (36.7%) patients of the SLN-group. Residual ARM nodes after SLN biopsy were involved in 11 patients (12.2%), including 5 patients (19.2%) with crossover type nodes and 6 patients (9.4%) with non-crossover type nodes. However, the difference in involvement rates between the two types was not high enough to be significant. Of these 11 patients, moreover, four patients had three or more than 3 involved SLNs. On the other hand, the involvement rate of ARM nodes in the NAC group was significantly lower than that of the CpN-positive group (35.4% vs. 64.7%: p < 0.01). Despite lower involvement, the risk of metastases in the ARM nodes was still too high to spare ARM nodes in both the NAC group and CpN-positive group.

      Conclusions

      Suspicious or involved ARM nodes should be removed even when detected in ARM procedure, particularly in NAC-group and CpN-positive-group patients.

      Keywords

      Abbreviations:

      ARM (axillary reverse mapping), NAC (neoadjuvant chemotherapy), SLN (sentinel lymph node), ALND (axillary lymph node dissection), ALN (axillary lymph node), ICG (indocyanine green), BCS (breast conserving surgery), FNAC (fine needle aspiration cytology), FEC (fluorouracil, epirubicin and cyclophosphamide), DOC (docetaxel), H & E (hematoxylin and eosin), CpN-positive (clinicopathologically node-positive)
      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to European Journal of Surgical Oncology
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Noguchi M.
        • Miwa K.
        • Michigishi T.
        • et al.
        The role of axillary lymph node dissection in breast cancer management.
        Breast Cancer. 1997; 4: 143-153https://doi.org/10.1007/BF02967068
        • Giuliano A.E.
        • McCall L.
        • Beitsch P.
        • et al.
        Locoregional recurrence after sentinel lymph node dissection with or without axillary dissection in patients with sentinel lymph node metastases: the American College of Surgeons Oncology Group Z0011 randomized trial.
        Ann Surg. 2011; 252: 426-433https://doi.org/10.1097/SLA.0b013e3181f08f32
        • Donker M.
        • van Tienhoven G.
        • Straver M.E.
        • et al.
        Raditherapy or surgery of the axilla after a positive sentinel node in breast cancer (EORTC 10981-22023 AMAROS): a randomised, multicentre, open-label, phase 3 non-inferiority trial.
        Lancet Oncol. 2014; 15: 1303-1310https://doi.org/10.1016/S1470-2045(14)70460-7
        • Maggi N.
        • Nussbaumer R.
        • Holzer L.
        • Weber W.P.
        Axillary surgery in node-positive breast cancer.
        Breast. 2022; 62: S50-S53https://doi.org/10.1016/j.breast.2021.08.018
        • Noguchi M
        • Inokuchi M
        • Yokoi-Noguchi M
        • Morioka E
        • Haba Y
        Conservative axillary surgery is emerging in the surgical management of breast cancer.
        Breast Cancer. 2023 Jan; 30: 14-22
        • Thompson M.
        • Korourian S.
        • Henry-Tillman R.
        • et al.
        Axillary reverse mapping (ARM): a new concept to identify and enhance lymphatic preservation.
        Ann Surg Oncol. 2007; 14: 1890-1895https://doi.org/10.1245/s10434-007-9412-x
        • Nos C.
        • Lesieur B.
        • Clough K.B.
        • Lecuru F.
        Blue dye injection in the arm in order to conserve the lymphatic drainage of the arm in breast cancer patients requiring an axillary dissection.
        Ann Surg Oncol. 2007; 14: 2490-2496https://doi.org/10.1245/s10434-007-9450-4
        • Yue T.
        • Zhuang D.
        • Zhou P.
        • et al.
        A prospective study to assess the feasibility of axillary reverse mapping and evaluate its effect on preventing lymphedema in breast cancer patients.
        Clin Breast Cancer. 2015; 15: 301-306https://doi.org/10.1016/j.clbc.2015.01.010
        • Yuan Q.
        • Wu G.
        • Xiao S.Y.
        • et al.
        Identification and preservation of arm lymphatic system in axillary dissection for breast cancer to reduce arm lymphedema events: a randomized clinical trial.
        Ann Surg Oncol. 2019; 26 (3446-3354)https://doi.org/10.1245/s10434-019-07569-4
        • Faisal M.
        • Sayed M.G.
        • Antonious K.
        • Bakr A.A.
        • Farag S.H.
        Prevention of lymphedema via axillary reverse mapping for arm lymph-node preservation following breast cancer surgery: a randomized controlled trial.
        Patient Saf Surg. 2019; 13: 35https://doi.org/10.1186/s13037-019-0217-1
        • Abdelhamid M.I.
        • Bari A.A.
        • Farid M.
        • Nour H.
        Evaluation of axillary reverse mapping (ARM) in clinically axillary node negative breast cancer patients -randomized controlled trial.
        Int J Surg. 2020; 75: 174-178https://doi.org/10.1016/j.ijsu.2020.01.152
        • Gennaro M.
        • Maccairo M.
        • Mariani L.
        • et al.
        Occurrence of breast-cancer-related lymphedema after reverse lymphatic mapping and selective axillary dissection versus standard surgical treatment of axilla: a two-arm randomized clinical trial.
        Cancer. 2022; : 1-9https://doi.org/10.1002/cncr:34498
        • Noguchi M.
        Axillary reverse mapping for breast cancer.
        Breast Cancer Res Treat. 2010; 119: 529-535https://doi.org/10.1007/s10549-009-0578-8
        • Suami H.
        • Taylor G.I.
        • Pan W.-R.
        The lymphatic territories of the upper limb: anatomical study and clinical implications.
        Plast Reconstr Surg. 2007; 119: 1813-1822https://doi.org/10.1097/01.prs.0000246516.64780.61
        • Pavlista D.
        • Eliska O.
        Relationship between the lymphatic drainage of the breast and the upper extremity: a postmortem study.
        Ann Surg Oncol. 2012; 19: 3410-3415https://doi.org/10.1245/s10434-012-2363-x
        • Noguchi M.
        • Miura S.
        • Morioka E.
        • et al.
        Is axillary reverse mapping feasible in breast cancer patients?.
        Eur J Surg Oncol. 2015; 41: 442-449https://doi.org/10.1016/j.ejso.2015.01.029
        • Noguchi M.
        • Yokoi M.
        • Nakano Y.
        Axillary reverse mapping with indocyanine fluorescence imaging in patients with breast cancer.
        J Surg Oncol. 2010; 101: 217-221https://doi.org/10.1002/jso.21473
        • Foster D.
        • Choy N.
        • Porter C.
        • Ahmed S.
        • Wapnir I.
        Axillary reverse mapping with indocyanine green or isosulfan blue demonstrate similar crossover rates to radiotracer identified sentinel nodes.
        J Surg Oncol. 2018; https://doi.org/10.1002/jso.24859
        • Sakurai T.
        • Endo M.
        • Shimizu K.
        • et al.
        Axillary reverse mapping using fluorescence imaging is useful for identifying the risk group of postoperative lymphedema in breast cancer patients undergoing sentinel node biopsies.
        J Surg Oncol. 2014; 109: 612-615https://doi.org/10.1002/jso.23528
        • Conversano A.
        • Abbaci M.
        • Karimi M.
        • Mathieu M.C.
        • de Keeuw F.
        • Michiels S.
        • et al.
        Axillary reverse mapping near-infrared fluorescence imaging in invasive breast cancer (ARMONIC study).
        Eur J Surg Oncol. 2022; https://doi.org/10.1016/j.ejso.2022.07.004
        • Noguchi M.
        • Inokuchi M.
        • Yokoi-Noguchi M.
        • Morioka E.
        The involvement of axillary reverse mapping nodes in patients with clinically node-negative breast cancer.
        Breast Cancer. 2022; 29: 209-215https://doi.org/10.1007/s12282-021-01300-6
        • Nakano Y.
        • Noguchi M.
        • Yokoi-Noguchi M.
        • et al.
        The roles of 18F-FDG-PET/CT and US-guided FNAC in assessment of axillary nodal metastases in breast cancer patients.
        Breast Cancer. 2017; 24: 121-127https://doi.org/10.1007/s12282-016-0684-5
        • Noguchi M.
        • Inokuchi M.
        • Zen Y.
        Complement of peritumoral and subareolar injection in breast cancer sentinel lymph node biopsy.
        J Surg Oncol. 2009; 100: 100-105https://doi.org/10.1002/jso.21308
        • Lyman G.H.
        • Giuliano A.E.
        • Somerfield M.R.
        • Benson III, A.B.
        • Bodurka D.C.
        • Burstein H.J.
        • et al.
        American society of clinical oncology guideline. Recommendations for sentinel lymph node biopsy in early-stage breast cancer.
        J Clin Oncol. 2005; 23: 7703-7720https://doi.org/10.1200/JCO.2005.08.001
        • Tummel E.
        • Ochoa D.
        • Korourian S.
        • et al.
        Does axillary reverse mapping prevent lymphedema after lymphadenectomy.
        Ann Surg. 2017; 265: 987-992https://doi.org/10.1097/SLA.000000000001778
        • Montagna G.
        • Mamtani A.
        • Knezevic A.
        • Brogi E.
        • Barrio A.V.
        • Morrow M.
        Selecting node-positive patients for axillary downstaging with neoadjuvant chemotherapy.
        Ann Surg Oncol. 2020; 27: 4515-4522https://doi.org/10.1245/s10434-020-08650-z
        • Beek M.A.
        • Gobardhan P.D.
        • Klompenhouwer E.G.
        • Rutten H.J.T.
        • Voogd A.C.
        • Luiten E.J.T.
        Axillary reverse mapping (ARM) in clinically node positive breast cancer patients.
        EJSO. 2015; 41: 59-63https://doi.org/10.1016/j.ejso.2014.09.012
        • Abbaci M.
        • Conversano A.
        • Karimi M.
        • et al.
        Near-infrared fluorescece axillary reverse mapping (ARM) procedure in invasive breast cancer: relationship between fluorescence signal in ARM lymph nodes and clinical outcomes.
        Cancers. 2022; 14: 2614https://doi.org/10.3390/cancers14112614
        • Frasier L.L.
        • Holden S.
        • Holden T.
        • Schumacher J.R.
        • Leverson G.
        • Anderson B.
        • et al.
        Temporal trends in postmastectomy radiation therapy and breast reconstruction associated with changes in national comprehensive cancer network guidelines.
        JAMA Onco. 2016; 2: 95-101