Lymph Node Metastases from Visceral Peritoneal Colorectal Metastases are Associated with Systemic Recurrence.


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:
Mar 2022
Historique:
received: 11 05 2021
accepted: 13 09 2021
pubmed: 9 10 2021
medline: 8 2 2022
entrez: 8 10 2021
Statut: ppublish

Résumé

Visceral peritoneal colorectal metastases (VPCMs) may further metastasize to lymph nodes that drain those organs. The rate of lymph node metastases (LNMs) from VPCMs and their clinical and prognostic significance are unknown. This study retrospectively analyzed the authors' institutional databases of 160 patients with peritoneal colorectal metastases who underwent cytoreductive surgery and hyperthermic intraperitoneal chemotherapy. Patients with LNM-VPCM (n = 12) were identified by pathologic reports, and both their short- and long-term outcomes were compared with those of patients without LNM-VPCM. The clinical presentation and primary tumor pathologic characteristics did not differ between the two groups. The patients with LNM-VPCM had a higher tumor burden (measured by the peritoneal carcinomatosis index [PCI]) and visible remnant disease compared with those who had no LNM-VPI (10 vs 5.5 [p = 0.03] vs 33.3% vs 6.8% [p = 0.007], respectively). The postoperative outcomes also were comparable. The patients with LNM-VPCM had a shorter overall survival (OS) than those without LNM-VPCM (median OS, 22.5 months; 95% confidence interval [CI], 15.1-29.9 months vs 40.1 months; 95% CI, 38.1-42 months; p = 0.02). However, only tumor grade and PCI were predictors of OS in the multivariate analysis (hazard ratio [HR], 2.33 [p = 0.001]; 1.77 [p = 0.03], respectively). The study showed that LNM-VPCM was associated with systemic but not peritoneal recurrence compared with non-LNM-VPCM (81.8% vs 51.6% for systemic recurrence, respectively; p = 0.05). The small distinct group of patients defined by LNM-VPCM were prone to systemic recurrence. Given its correlation with systemic recurrence, LNM-VPCM may indicate the need for adjuvant treatment.

Sections du résumé

BACKGROUND BACKGROUND
Visceral peritoneal colorectal metastases (VPCMs) may further metastasize to lymph nodes that drain those organs. The rate of lymph node metastases (LNMs) from VPCMs and their clinical and prognostic significance are unknown.
METHODS METHODS
This study retrospectively analyzed the authors' institutional databases of 160 patients with peritoneal colorectal metastases who underwent cytoreductive surgery and hyperthermic intraperitoneal chemotherapy. Patients with LNM-VPCM (n = 12) were identified by pathologic reports, and both their short- and long-term outcomes were compared with those of patients without LNM-VPCM.
RESULTS RESULTS
The clinical presentation and primary tumor pathologic characteristics did not differ between the two groups. The patients with LNM-VPCM had a higher tumor burden (measured by the peritoneal carcinomatosis index [PCI]) and visible remnant disease compared with those who had no LNM-VPI (10 vs 5.5 [p = 0.03] vs 33.3% vs 6.8% [p = 0.007], respectively). The postoperative outcomes also were comparable. The patients with LNM-VPCM had a shorter overall survival (OS) than those without LNM-VPCM (median OS, 22.5 months; 95% confidence interval [CI], 15.1-29.9 months vs 40.1 months; 95% CI, 38.1-42 months; p = 0.02). However, only tumor grade and PCI were predictors of OS in the multivariate analysis (hazard ratio [HR], 2.33 [p = 0.001]; 1.77 [p = 0.03], respectively). The study showed that LNM-VPCM was associated with systemic but not peritoneal recurrence compared with non-LNM-VPCM (81.8% vs 51.6% for systemic recurrence, respectively; p = 0.05).
CONCLUSION CONCLUSIONS
The small distinct group of patients defined by LNM-VPCM were prone to systemic recurrence. Given its correlation with systemic recurrence, LNM-VPCM may indicate the need for adjuvant treatment.

Identifiants

pubmed: 34622371
doi: 10.1245/s10434-021-10869-3
pii: 10.1245/s10434-021-10869-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2069-2075

Informations de copyright

© 2021. Society of Surgical Oncology.

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Auteurs

Eran Nizri (E)

Peritoneal Surface Malignancy and Melanoma Unit, Department of Surgery A, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel. eran.nizri@mail.huji.ac.il.
The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel. eran.nizri@mail.huji.ac.il.

Yaniv Berger (Y)

The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Department of Surgery B, Chaim Sheba Medical Center, Tel Hashomer, Israel.

Eraan Green (E)

Peritoneal Surface Malignancy and Melanoma Unit, Department of Surgery A, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Matan Kyzer (M)

The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Department of Surgery B, Chaim Sheba Medical Center, Tel Hashomer, Israel.

Asaf Aizic (A)

Institute of Pathology, Tel- Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Nadav Nevo (N)

Peritoneal Surface Malignancy and Melanoma Unit, Department of Surgery A, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Fabian Gerstenhaber (F)

Peritoneal Surface Malignancy and Melanoma Unit, Department of Surgery A, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Joseph M Klausner (JM)

Peritoneal Surface Malignancy and Melanoma Unit, Department of Surgery A, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Mordechai Gutman (M)

The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Department of Surgery B, Chaim Sheba Medical Center, Tel Hashomer, Israel.

Guy Lahat (G)

Peritoneal Surface Malignancy and Melanoma Unit, Department of Surgery A, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Aviad Hoffman (A)

Department of General Surgery, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

Ravit Geva (R)

The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Oncology Division, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

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