A1 Refereed original research article in a scientific journal

Donor-site safety in microvascular lymph node transfer for breast cancer-related lymphedema using reverse lymphatic mapping—A prospective study




AuthorsPajula, Susanna; Saarikko, Anne; Suominen, Sinikka; Kaartinen, Ilkka; Kiiski, Juha; Mani, Maria; Halle, Martin; Hartiala, Pauliina

PublisherElsevier

Publication year2024

JournalJournal of Plastic, Reconstructive and Aesthetic Surgery

Journal name in sourceJournal of Plastic, Reconstructive & Aesthetic Surgery

Volume98

First page 20

Last page31

ISSN1748-6815

eISSN1878-0539

DOIhttps://doi.org/10.1016/j.bjps.2024.08.063

Web address https://doi.org/10.1016/j.bjps.2024.08.063

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/457685359


Abstract

Background: Vascularized lymph node transfer (VLNT) is one option among other surgical treatments in the management of breast cancer-related lymphedema (BCRL). The cause of concern regarding VLNT harvested from the groin has been the potential development of secondary lower-extremity lymphedema. This study explored the risks associated with donor-site morbidity following groin VLNT, with or without concomitant breast reconstruction.

Method: The cohort comprised data from the Lymfactin® Phase I and II trials, conducted from 2016 to 2019, that used perioperative reverse lymphatic mapping. The volume of the lower extremities was measured preoperatively and at 3, 6, and 12 months postoperative, and the adverse events were documented during study visits.

Results: Altogether, 51 women with a mean age of 55.5 years were recruited. The mean duration of BCRL was 31.8 months. Among these, 25 (49%) underwent VLNT (VLNT-group) and 26 (51%) underwent VLNT in combination with breast reconstruction (VLNT-BR group). The groups were similar in terms of age, (p = 0.766), BMI (p = 0.316), and duration of BCRL (p = 0.994). Across a period of one year, the volume difference between the lower extremities changed by 22.6 ml (range: -813 to 860.2 ml) (p = 0.067). None of the patients had lower-extremity volume difference exceeding 10% at the 12-month follow-up visit. The most frequent adverse events were postoperative pain (17.7%), wound healing issues (11.8%), and seroma formation (11.8%). Most adverse events (64.6%) were classified as minor.

Conclusions: This prospective study demonstrated that groin VLNT with reverse lymphatic mapping appears safe and does not increase the risk of secondary donor-site lymphedema within one year postoperatively.


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Funding information in the publication
The Lymfactin® phases I and II were supported by Herantis Pharma Plc. (Espoo Finland).


Last updated on 2025-27-01 at 19:19