A striking elevation of CA19-9 after preoperative therapy negates prognostic benefit from radical surgery in resectable and borderline resectable pancreatic cancer.


Journal

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

Informations de publication

Date de publication:
29 Jul 2024
Historique:
received: 29 04 2024
revised: 28 05 2024
accepted: 23 06 2024
medline: 31 7 2024
pubmed: 31 7 2024
entrez: 30 7 2024
Statut: aheadofprint

Résumé

Identifying patients who can be spared nonbeneficial surgery is crucial, as pancreatic cancer surgery is highly invasive, with substantial negative effects on quality of life. The study objective was to investigate a useful indicator of patients who do not gain prognostic benefit from radical surgery after neoadjuvant therapy for resectable and borderline resectable pancreatic cancer. We compared factors among 609 patients with resectable or borderline resectable pancreatic cancer receiving neoadjuvant therapy during 2005-2019. Patients were divided into a poor-prognosis group (no surgery or postresection recurrence within a year) and a good-prognosis group (no recurrence or recurrence >1 year after resection). Patients who experience a recurrence within a year of resection (poor-prognosis group) did no better than patients who received neoadjuvant therapy and progressed but never made it to surgery. The value of carbohydrate antigen 19-9 after neoadjuvant therapy was the most significant indicator to predict the poor prognosis group and the elevation of carbohydrate antigen 19-9 (>200 U/mL) identified only poor prognosis group with high specificity of 96.6%. The overall survival of patients with more than 200 of carbohydrate antigen 19-9 after neoadjuvant therapy was significantly very poor and their 2-year survival rate was only 41.4%. A striking elevation of carbohydrate antigen 19-9 after neoadjuvant therapy for resectable or borderline resectable pancreatic cancer is a good indicator of poor prognosis. Patients with carbohydrate antigen 19-9 >200 U/mL after neoadjuvant therapy should not undergo radical surgery.

Sections du résumé

BACKGROUND BACKGROUND
Identifying patients who can be spared nonbeneficial surgery is crucial, as pancreatic cancer surgery is highly invasive, with substantial negative effects on quality of life. The study objective was to investigate a useful indicator of patients who do not gain prognostic benefit from radical surgery after neoadjuvant therapy for resectable and borderline resectable pancreatic cancer.
METHOD METHODS
We compared factors among 609 patients with resectable or borderline resectable pancreatic cancer receiving neoadjuvant therapy during 2005-2019. Patients were divided into a poor-prognosis group (no surgery or postresection recurrence within a year) and a good-prognosis group (no recurrence or recurrence >1 year after resection).
RESULTS RESULTS
Patients who experience a recurrence within a year of resection (poor-prognosis group) did no better than patients who received neoadjuvant therapy and progressed but never made it to surgery. The value of carbohydrate antigen 19-9 after neoadjuvant therapy was the most significant indicator to predict the poor prognosis group and the elevation of carbohydrate antigen 19-9 (>200 U/mL) identified only poor prognosis group with high specificity of 96.6%. The overall survival of patients with more than 200 of carbohydrate antigen 19-9 after neoadjuvant therapy was significantly very poor and their 2-year survival rate was only 41.4%.
CONCLUSION CONCLUSIONS
A striking elevation of carbohydrate antigen 19-9 after neoadjuvant therapy for resectable or borderline resectable pancreatic cancer is a good indicator of poor prognosis. Patients with carbohydrate antigen 19-9 >200 U/mL after neoadjuvant therapy should not undergo radical surgery.

Identifiants

pubmed: 39079828
pii: S0039-6060(24)00473-2
doi: 10.1016/j.surg.2024.06.049
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Auteurs

Hirofumi Akita (H)

Department of Surgery, Osaka International Cancer Institute, Japan. Electronic address: hirofumi.akita@oici.jp.

Yosuke Mukai (Y)

Department of Surgery, Osaka International Cancer Institute, Japan.

Masahiko Kubo (M)

Department of Surgery, Osaka International Cancer Institute, Japan.

Hidenori Takahashi (H)

Department of Surgery, Osaka International Cancer Institute, Japan.

Shinichiro Hasegawa (S)

Department of Surgery, Osaka International Cancer Institute, Japan.

Masatoshi Kitakaze (M)

Department of Surgery, Osaka International Cancer Institute, Japan.

Norihiro Matsuura (N)

Department of Surgery, Osaka International Cancer Institute, Japan.

Yasunori Masuike (Y)

Department of Surgery, Osaka International Cancer Institute, Japan.

Takahito Sugase (T)

Department of Surgery, Osaka International Cancer Institute, Japan.

Naoki Shinno (N)

Department of Surgery, Osaka International Cancer Institute, Japan.

Takashi Kanemura (T)

Department of Surgery, Osaka International Cancer Institute, Japan.

Hisashi Hara (H)

Department of Surgery, Osaka International Cancer Institute, Japan.

Toshinori Sueda (T)

Department of Surgery, Osaka International Cancer Institute, Japan.

Junichi Nishimura (J)

Department of Surgery, Osaka International Cancer Institute, Japan.

Masayoshi Yasui (M)

Department of Surgery, Osaka International Cancer Institute, Japan.

Takeshi Omori (T)

Department of Surgery, Osaka International Cancer Institute, Japan.

Hiroshi Miyata (H)

Department of Surgery, Osaka International Cancer Institute, Japan.

Masayuki Ohue (M)

Department of Surgery, Osaka International Cancer Institute, Japan.

Hiroshi Wada (H)

Department of Surgery, Osaka International Cancer Institute, Japan.

Classifications MeSH