Two-stage hepatectomy for colorectal liver metastases: Pathologic response to preoperative chemotherapy is associated with second-stage completion and longer survival.


Journal

Surgery
ISSN: 1532-7361
Titre abrégé: Surgery
Pays: United States
ID NLM: 0417347

Informations de publication

Date de publication:
04 2019
Historique:
received: 22 06 2018
revised: 21 09 2018
accepted: 09 10 2018
pubmed: 20 11 2018
medline: 19 12 2019
entrez: 20 11 2018
Statut: ppublish

Résumé

Two-stage hepatectomy of bilobar colorectal liver metastases is widely used and shows encouraging survival results. However, the risk of dropout after the first stage remains high and is associated with poor survival. The objective of our study was to evaluate the factors associated with long-term survival based on the pathologic response to preoperative systemic chemotherapy in colorectal liver metastases patients who underwent two-stage hepatectomy. The pathologic response to preoperative chemotherapy and its effect on second-stage completion and survival were retrospectively evaluated in 67 patients treated between 2003 and 2013. A total of 56 patients underwent two-stage hepatectomy for initially nonresectable colorectal liver metastases. Chemotherapy was combined with a biotherapy in 32 cases. The tumor regression grade, modified tumor regression grade, and Blazer grade were used to classify patients as responders (tumor regression grade and modified tumor regression grade 1-3, Blazer 0-1) or nonresponders (tumor regression grade and modified tumor regression grade 4-5, Blazer 2) after the first stage. Tumor response in the three classifications was associated with second-stage completion (tumor regression grade 1-3: OR = 4.01, 95% CI: 1.12-14.36, P = .033; modified tumor regression grade 1-3: OR = 3.8, 95% CI: 1.13-12.6, P = .03; Blazer 0-1: OR = 5.45, 95% CI: 1.66-17.85, P = .005). Triple chemotherapy was also associated with responders. The median overall survival of responders was significantly higher (Blazer 0-1: 42.9 months versus Blazer 2: 20.1 months, P = .018; tumor regression grade 1-3: 42.9 months versus tumor regression grade 4-5: 25.1 months, P = .04). A pathologic response to chemotherapy is associated with second-stage completion and longer survival. Further studies are needed to achieve the early identification of patients for whom the benefit of the second surgical stage is less straightforward.

Sections du résumé

BACKGROUND
Two-stage hepatectomy of bilobar colorectal liver metastases is widely used and shows encouraging survival results. However, the risk of dropout after the first stage remains high and is associated with poor survival. The objective of our study was to evaluate the factors associated with long-term survival based on the pathologic response to preoperative systemic chemotherapy in colorectal liver metastases patients who underwent two-stage hepatectomy.
METHODS
The pathologic response to preoperative chemotherapy and its effect on second-stage completion and survival were retrospectively evaluated in 67 patients treated between 2003 and 2013.
RESULTS
A total of 56 patients underwent two-stage hepatectomy for initially nonresectable colorectal liver metastases. Chemotherapy was combined with a biotherapy in 32 cases. The tumor regression grade, modified tumor regression grade, and Blazer grade were used to classify patients as responders (tumor regression grade and modified tumor regression grade 1-3, Blazer 0-1) or nonresponders (tumor regression grade and modified tumor regression grade 4-5, Blazer 2) after the first stage. Tumor response in the three classifications was associated with second-stage completion (tumor regression grade 1-3: OR = 4.01, 95% CI: 1.12-14.36, P = .033; modified tumor regression grade 1-3: OR = 3.8, 95% CI: 1.13-12.6, P = .03; Blazer 0-1: OR = 5.45, 95% CI: 1.66-17.85, P = .005). Triple chemotherapy was also associated with responders. The median overall survival of responders was significantly higher (Blazer 0-1: 42.9 months versus Blazer 2: 20.1 months, P = .018; tumor regression grade 1-3: 42.9 months versus tumor regression grade 4-5: 25.1 months, P = .04).
CONCLUSION
A pathologic response to chemotherapy is associated with second-stage completion and longer survival. Further studies are needed to achieve the early identification of patients for whom the benefit of the second surgical stage is less straightforward.

Identifiants

pubmed: 30449697
pii: S0039-6060(18)30717-7
doi: 10.1016/j.surg.2018.10.006
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

703-711

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

François Quénet (F)

Surgical Oncology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France. Electronic address: François.quenet@icm.unicancer.fr.

Marie-Hélène Pissas (MH)

Surgical Oncology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Hugo Gil (H)

Anatomopathology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Lise Roca (L)

Biometrics Unit, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Sébastien Carrère (S)

Surgical Oncology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Olivia Sgarbura (O)

Surgical Oncology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Philippe Rouanet (P)

Surgical Oncology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Hélène de Forges (H)

Clinical Research Unit, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Lakhdar Khellaf (L)

Anatomopathology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Emmanuel Deshayes (E)

Nuclear Medicine Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Marc Ychou (M)

Medical Oncology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France.

Frédéric Bibeau (F)

Anatomopathology Department, Institut Régional du Cancer de Montpellier (ICM), Université de Montpellier, France; Anatomopathology Department, Centre Hospitalier Universitaire de Caen, Caen, France.

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Classifications MeSH