Signet ring cell features with peritoneal carcinomatosis in patients undergoing cytoreductive surgery and hyperthermic intraperitoneal chemotherapy are associated with poor overall survival.


Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
May 2019
Historique:
received: 08 09 2018
accepted: 26 12 2018
pubmed: 17 1 2019
medline: 18 4 2019
entrez: 17 1 2019
Statut: ppublish

Résumé

Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS/HIPEC) is effective in select patients with peritoneal carcinomatosis (PC). Signet ring cell (SRC) pathology is associated with poor prognosis. The role of CRS/HIPEC in this population is unclear. Patients diagnosed with PC due to appendiceal (AC), colorectal (CRC), and gastric cancer (GC) undergoing CRS/HIPEC 2007-2016 were included. A total of 268 patients were referred for CRS/HIPEC. Of the 204 patients who underwent complete CRS/HIPEC, 101 (49.5%) had AC, 85 (41.7%) CRC, and 18 (8.8%) GC. Patients with GC had higher rates of SRC pathology than AC and CRC: 12 (66.7%) vs 16 (15.8%) and 10 (11.7%). The 3-year survival rate after CRS/HIPEC was 5.7% for the SRC group and 66.1% for the non-SRC group (P < 0.001). This was true for both AC and CRC subgroups (P < 0.001 for both). Overall, patients with SRC were more likely to have a peritoneal carcinomatosis index (PCI) score > 15 (P = 0.046). Upon multivariate analysis of the SRC population, PCI > 20 (P = 0.007) and GC (P = 0.008) were found to be independent predictors of poor overall survival. Performing CRS/HIPEC for PC from gastrointestinal malignancies presenting SRC features is recommended on patients with select diseases of appendiceal and colorectal origins.

Sections du résumé

BACKGROUND BACKGROUND
Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS/HIPEC) is effective in select patients with peritoneal carcinomatosis (PC). Signet ring cell (SRC) pathology is associated with poor prognosis. The role of CRS/HIPEC in this population is unclear.
METHODS METHODS
Patients diagnosed with PC due to appendiceal (AC), colorectal (CRC), and gastric cancer (GC) undergoing CRS/HIPEC 2007-2016 were included.
RESULTS RESULTS
A total of 268 patients were referred for CRS/HIPEC. Of the 204 patients who underwent complete CRS/HIPEC, 101 (49.5%) had AC, 85 (41.7%) CRC, and 18 (8.8%) GC. Patients with GC had higher rates of SRC pathology than AC and CRC: 12 (66.7%) vs 16 (15.8%) and 10 (11.7%). The 3-year survival rate after CRS/HIPEC was 5.7% for the SRC group and 66.1% for the non-SRC group (P < 0.001). This was true for both AC and CRC subgroups (P < 0.001 for both). Overall, patients with SRC were more likely to have a peritoneal carcinomatosis index (PCI) score > 15 (P = 0.046). Upon multivariate analysis of the SRC population, PCI > 20 (P = 0.007) and GC (P = 0.008) were found to be independent predictors of poor overall survival.
CONCLUSIONS CONCLUSIONS
Performing CRS/HIPEC for PC from gastrointestinal malignancies presenting SRC features is recommended on patients with select diseases of appendiceal and colorectal origins.

Identifiants

pubmed: 30650185
doi: 10.1002/jso.25379
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

758-765

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Daniel Solomon (D)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Natasha DeNicola (N)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Daniela Feingold (D)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Peter H Liu (PH)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Samantha Aycart (S)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Benjamin J Golas (BJ)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Umut Sarpel (U)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Daniel M Labow (DM)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

Deepa R Magge (DR)

Division of Surgical Oncology, Icahn School of Medicine at Mount Sinai, New York City, New York.

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Classifications MeSH