Malignant Features in Pretreatment Metastatic Lateral Lymph Nodes in Locally Advanced Low Rectal Cancer Predict Distant Metastases.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 19 02 2021
accepted: 15 08 2021
pubmed: 8 9 2021
medline: 6 1 2022
entrez: 7 9 2021
Statut: ppublish

Résumé

Pretreatment enlarged lateral lymph nodes (LLN) in patients with locally advanced low rectal cancer are predictive for local recurrences after neoadjuvant (chemo)radiotherapy (n(C)RT) followed by total mesorectal excision (TME). Not much is known of the impact on oncological outcomes when in addition malignant features are present in enlarged LLN. A multicenter retrospective cohort study was conducted at five tertiary referral centers in the Netherlands and Australia. All patients were diagnosed with locally advanced low rectal cancer with LLN on pretreatment magnetic resonance imaging (MRI) and underwent n(C)RT followed by TME. LLN were considered enlarged with a short axis of ≥ 5 mm. Malignant features were defined as nodes with internal heterogeneity and/or border irregularity. Outcomes of interest were local recurrence-free survival (LRFS), distant metastatic-free survival (DMFS), and overall survival (OS). Out of 115 patients, the majority was male (75%) and the median age was 64 years (range 26-85 years). Median pretreatment LLN short axis was 7 mm (range 5-28 mm), and 60 patients (52%) had malignant features. After a median follow-up of 47 months, patients with larger LLN (7 + mm) had a worse LRFS (p = 0.01) but no difference in DMFS (p = 0.37) and OS (p = 0.54) compared with patients with smaller LLN (5-6 mm). LLN patients with malignant features had no difference in LRFS (p = 0.20) but worse DMFS (p = 0.004) and OS (p = 0.006) compared with patients without malignant features in the LLN. Cox regression analysis identified LLN short axis as an independent factor for LR. Malignant features in LLN were an independent factor for DMFS. The current study suggests that pretreatment enlarged LLN that also harbor malignant features are predictive of a worse DMFS. More studies will be required to further explore the role of malignant features in LLN.

Identifiants

pubmed: 34490529
doi: 10.1245/s10434-021-10762-z
pii: 10.1245/s10434-021-10762-z
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1194-1203

Subventions

Organisme : Royal Adelaide Hospital Research Committee 2020 Florey Fellowship
ID : MYIP: 12471

Informations de copyright

© 2021. Society of Surgical Oncology.

Références

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Auteurs

Hidde M Kroon (HM)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia. Hidde.Kroon@sa.gov.au.
Faculty of Health and Medical Sciences, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia. Hidde.Kroon@sa.gov.au.

Nagendra N Dudi-Venkata (NN)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia.
Faculty of Health and Medical Sciences, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.

Sergei Bedrikovetski (S)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia.
Faculty of Health and Medical Sciences, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.

Jianliang Liu (J)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia.

Anouck Haanappel (A)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia.

Atsushi Ogura (A)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Department of Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Cornelis J H van de Velde (CJH)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Harm J T Rutten (HJT)

Department of Surgery, Catharina Hospital, Eindhoven, The Netherlands.
GROW, School of Oncology and Developmental Biology, University of Maastricht, Maastricht, The Netherlands.

Geerard L Beets (GL)

Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands.

Michelle L Thomas (ML)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia.

Miranda Kusters (M)

Department of Surgery, Amsterdam University Medical Centers, Location VUmc, Amsterdam, The Netherlands.

Tarik Sammour (T)

Colorectal Unit, Department of Surgery, Royal Adelaide Hospital, Adelaide, SA, Australia.
Faculty of Health and Medical Sciences, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.

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