Neoadjuvant Chemotherapy Enhances Local Postoperative Histopathological Tumour Stage in Borderline Resectable Pancreatic Cancer - A Matched-Pair Analysis.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 29 08 2019
revised: 14 09 2019
accepted: 17 09 2019
entrez: 2 10 2019
pubmed: 2 10 2019
medline: 8 10 2019
Statut: ppublish

Résumé

Neoadjuvant chemotherapy (NAC) is established in the treatment of ductal pancreatic adenocarcinoma for downsizing borderline-resectable pancreatic cancer (BRPC) and may affect nodal positivity and rates of R0 resection. This study aimed to identify the impact of NAC on postoperative histopathological parameters with a prognostic relevance. A one-to-three matched-pair analysis, including an overall total of 132 patients (25% treated with NAC and subsequent resection and 75% undergoing upfront surgery) was performed. Influence of NAC on nodal positivity, lymphatic, vascular and perineural invasion, as well as resection stage and grading, was examined. Furthermore, perioperative complications, in-hospital stay, re-admission rates, mortality, as well as preoperative body mass index and American Association of Anesthesiologist classification scores, were evaluated. Patients treated with NAC significantly less frequently had lymphatic tissue invasion (lymph node invasion: 51.5% vs. 72.7%; p=0.032, and lymphatic vessel invasion 9.4% vs. 55.3%; p=0.0004), whereas vascular and perineural invasion, as well as grading and resection state were not significantly different. Carbohydrate antigen 19-9 regression in correlation with nodal positivity also did not differ, and both groups showed comparable perioperative complication rates. Occurrence and severity of postoperative pancreatic fistula (18.2% vs. 24.3%; p=0.034) were significantly lower in patients who had undergone NAC. NAC significantly affects postoperative histopathological tumour stage in BRPC and appears to be a safe treatment option without increased perioperative complications, re-admission, in-hospital stay, or mortality. Further studies are mandatory to underline the suitability of NAC for ductal pancreatic adenocarcinoma subgroups in order to guide clinicians in their daily decision-making comprehensively.

Sections du résumé

BACKGROUND BACKGROUND
Neoadjuvant chemotherapy (NAC) is established in the treatment of ductal pancreatic adenocarcinoma for downsizing borderline-resectable pancreatic cancer (BRPC) and may affect nodal positivity and rates of R0 resection. This study aimed to identify the impact of NAC on postoperative histopathological parameters with a prognostic relevance.
PATIENTS AND METHODS METHODS
A one-to-three matched-pair analysis, including an overall total of 132 patients (25% treated with NAC and subsequent resection and 75% undergoing upfront surgery) was performed. Influence of NAC on nodal positivity, lymphatic, vascular and perineural invasion, as well as resection stage and grading, was examined. Furthermore, perioperative complications, in-hospital stay, re-admission rates, mortality, as well as preoperative body mass index and American Association of Anesthesiologist classification scores, were evaluated.
RESULTS RESULTS
Patients treated with NAC significantly less frequently had lymphatic tissue invasion (lymph node invasion: 51.5% vs. 72.7%; p=0.032, and lymphatic vessel invasion 9.4% vs. 55.3%; p=0.0004), whereas vascular and perineural invasion, as well as grading and resection state were not significantly different. Carbohydrate antigen 19-9 regression in correlation with nodal positivity also did not differ, and both groups showed comparable perioperative complication rates. Occurrence and severity of postoperative pancreatic fistula (18.2% vs. 24.3%; p=0.034) were significantly lower in patients who had undergone NAC.
CONCLUSION CONCLUSIONS
NAC significantly affects postoperative histopathological tumour stage in BRPC and appears to be a safe treatment option without increased perioperative complications, re-admission, in-hospital stay, or mortality. Further studies are mandatory to underline the suitability of NAC for ductal pancreatic adenocarcinoma subgroups in order to guide clinicians in their daily decision-making comprehensively.

Identifiants

pubmed: 31570482
pii: 39/10/5781
doi: 10.21873/anticanres.13781
doi:

Substances chimiques

CA-19-9 Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5781-5787

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Lea Timmermann (L)

Department of Surgery, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany Lea.Timmermann@charite.de.

Nathalie Rosumeck (N)

Department of Hematology, Oncology and Tumor Immunology, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany.

Fritz Klein (F)

Department of Surgery, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany.

Johann Pratschke (J)

Department of Surgery, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany.

Uwe Pelzer (U)

Department of Hematology, Oncology and Tumor Immunology, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany.

Marcus Bahra (M)

Department of Surgery, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany.

Thomas Malinka (T)

Department of Surgery, Charité University of Medicine Berlin, corporate member of University of Berlin and Berlin Institute of Health, Berlin, Germany.

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Classifications MeSH