Skip to main content
Erschienen in: Gastric Cancer 4/2020

26.02.2020 | Original Article

Development and internal validation of a diagnostic score for gastric linitis plastica

verfasst von: J. Vivier-Chicoteau, J. Lambert, R. Coriat, P. E. Bonnot, D. Goere, B. Roche, M. Dior, G. Goujon, S. Morgant, M. Pocard, O. Glehen, T. Aparicio, Jean-Marc Gornet

Erschienen in: Gastric Cancer | Ausgabe 4/2020

Einloggen, um Zugang zu erhalten

Abstract

Background

There is no consensual definition for gastric linitis plastica (GLP). We aim to construct a diagnostic score to distinguish this rare tumor from usual gastric adenocarcinomas.

Methods

In this retrospective study, all patients who had gastrectomy for cancer between 2007 and 2017 in French tertiary centers were included. The outcome was a diagnosis of GLP based on pathological review of the surgical specimen. The diagnostic score was created by using variables that were most frequently associated with GLP using penalized logistic regression on multiply imputed datasets. We used discrimination measures to assess the performances of the score. Internal validation was performed using bootstrapping methods to correct for over-optimism.

Results

220 patients including 71 linitis plastica (female 49%, median age 57 years) were analyzed. The six parameters retained in the diagnosis score were the presence of large folds and/or parietal thickening on at least one segment, pangastric infiltration and presence of gastric stenosis on the upper endoscopy, circumferential thickening on at least one segment and thickening of the third hyperechogenic layer on endoscopic ultrasound and the presence of signet ring cells on endoscopic biopsies. The area under the ROC curve (AUC) was 0.967 with a sensitivity of 94% [89.9–97.3] and a specificity of 88.7% [81.7–95.8] for a threshold of 2.75. After internal validation, the corrected AUC was 0.959.

Conclusion

It is the first study validating a pre-therapeutic diagnostic score (Saint Louis linitis score) with an excellent ability to discriminate GLP from non-GLP adenocarcinomas. An external validation is necessary to confirm our data.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):359–86.CrossRef Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):359–86.CrossRef
2.
Zurück zum Zitat Karimi P, Islami F, Anandasabapathy S, Freedman ND, Kamangar F. Gastric cancer: descriptive epidemiology, risk factors, screening, and prevention. Cancer Epidemiol Biomark Prev. 2014;23(5):700–13.CrossRef Karimi P, Islami F, Anandasabapathy S, Freedman ND, Kamangar F. Gastric cancer: descriptive epidemiology, risk factors, screening, and prevention. Cancer Epidemiol Biomark Prev. 2014;23(5):700–13.CrossRef
3.
Zurück zum Zitat Lauren P. The two histological main types of gastric carcinoma: diffuse and so-called intestinal-type carcinoma An attempt at a histo-clinical classification. Acta Pathol Microbiol Scand. 1965;64:31–49.CrossRef Lauren P. The two histological main types of gastric carcinoma: diffuse and so-called intestinal-type carcinoma An attempt at a histo-clinical classification. Acta Pathol Microbiol Scand. 1965;64:31–49.CrossRef
4.
Zurück zum Zitat Bosman FT, Carneiro F, Hruban RH, Theise ND (2010) World Health Organization (WHO) classification of tumours of the digestive system, 4th Edition. International Agency for Research on Cancer (IARC), Lyon, pp 45–79. Bosman FT, Carneiro F, Hruban RH, Theise ND (2010) World Health Organization (WHO) classification of tumours of the digestive system, 4th Edition. International Agency for Research on Cancer (IARC), Lyon, pp 45–79.
5.
Zurück zum Zitat Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English edition. Gastric Cancer. 2011;14(2):101–12. Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English edition. Gastric Cancer. 2011;14(2):101–12.
6.
Zurück zum Zitat Borrmann R. Geschwülste Des Magens und Des Duodenums, vol. 1. Berlin: Springer; 1926. Borrmann R. Geschwülste Des Magens und Des Duodenums, vol. 1. Berlin: Springer; 1926.
7.
Zurück zum Zitat Siewert J, Stein H. Carcinoma of the gastroesophageal junction—classification, pathology and extent of resection. Dis Esophagus. 1996;9:173–82.CrossRef Siewert J, Stein H. Carcinoma of the gastroesophageal junction—classification, pathology and extent of resection. Dis Esophagus. 1996;9:173–82.CrossRef
8.
Zurück zum Zitat Mastoraki A, Papanikolaou IS, Sakorafas G, Safioleas M. Facing the challenge of managing linitis plastic—review of the literature. Hepatogastroenterology. 2009;56(96):1773–8.PubMed Mastoraki A, Papanikolaou IS, Sakorafas G, Safioleas M. Facing the challenge of managing linitis plastic—review of the literature. Hepatogastroenterology. 2009;56(96):1773–8.PubMed
9.
Zurück zum Zitat Agnes A, Estrella JS, Badgwell B. The significance of a nineteenth century definition in the era of genomics: linitis plastica. World J Surg Oncol. 2017;15(1). Agnes A, Estrella JS, Badgwell B. The significance of a nineteenth century definition in the era of genomics: linitis plastica. World J Surg Oncol. 2017;15(1).
10.
Zurück zum Zitat Chang JM, Lara KA, Gray RJ, Pockaj BA, Wasif N. Clinical outcomes after surgery for linitis plastica of the stomach: analysis of a population cancer registry. Am Surg. 2017;83(1):23–9.PubMed Chang JM, Lara KA, Gray RJ, Pockaj BA, Wasif N. Clinical outcomes after surgery for linitis plastica of the stomach: analysis of a population cancer registry. Am Surg. 2017;83(1):23–9.PubMed
11.
Zurück zum Zitat Blackham AU, Swords DS, Levine EA, Fino NF, Squires MH, Poultsides G, et al. Is linitis plastica a contraindication for surgical resection: a multi-institution study of the US gastric cancer collaborative. Ann Surg Oncol. 2016;23(4):1203–11.CrossRef Blackham AU, Swords DS, Levine EA, Fino NF, Squires MH, Poultsides G, et al. Is linitis plastica a contraindication for surgical resection: a multi-institution study of the US gastric cancer collaborative. Ann Surg Oncol. 2016;23(4):1203–11.CrossRef
12.
Zurück zum Zitat Mariette C, Carneiro F, Grabsch HI, van der Post RS, Allum W, de Manzoni G, et al. Consensus on the pathological definition and classification of poorly cohesive gastric carcinoma. Gastric Cancer Off J Int Gastric Cancer Assoc Jpn Gastric Cancer Assoc. 2018;15:123. Mariette C, Carneiro F, Grabsch HI, van der Post RS, Allum W, de Manzoni G, et al. Consensus on the pathological definition and classification of poorly cohesive gastric carcinoma. Gastric Cancer Off J Int Gastric Cancer Assoc Jpn Gastric Cancer Assoc. 2018;15:123.
13.
Zurück zum Zitat Palli D, Bianchi S, Cipriani F, Duca P, Amorosi A, Avellini C, et al. Reproducibility of histologic classification of gastric cancer. Br J Cancer. 1991;63(5):765.CrossRef Palli D, Bianchi S, Cipriani F, Duca P, Amorosi A, Avellini C, et al. Reproducibility of histologic classification of gastric cancer. Br J Cancer. 1991;63(5):765.CrossRef
14.
Zurück zum Zitat Flucke U, Mönig SP, Baldus SE, Zirbes TK, Bollschweiler E, Thiele J, et al. Differences between biopsy- or specimen-related Laurén and World Health Organization classification in gastric cancer. World J Surg. 2002;26(2):137–40.CrossRef Flucke U, Mönig SP, Baldus SE, Zirbes TK, Bollschweiler E, Thiele J, et al. Differences between biopsy- or specimen-related Laurén and World Health Organization classification in gastric cancer. World J Surg. 2002;26(2):137–40.CrossRef
15.
Zurück zum Zitat Amin MB, Edge SB, Greene FL, et al., editors. AJCC cancer staging manual. 8th ed. New York: Springer; 2017. Amin MB, Edge SB, Greene FL, et al., editors. AJCC cancer staging manual. 8th ed. New York: Springer; 2017.
16.
Zurück zum Zitat Jung K, Park MI, Kim SE, Park SJ. Borrmann type 4 advanced gastric cancer: focus on the development of scirrhous gastric cancer. Clin Endosc. 2016;49(4):336–45.CrossRef Jung K, Park MI, Kim SE, Park SJ. Borrmann type 4 advanced gastric cancer: focus on the development of scirrhous gastric cancer. Clin Endosc. 2016;49(4):336–45.CrossRef
17.
Zurück zum Zitat Pernot S. Signet-ring cell carcinoma of the stomach: Impact on prognosis and specific therapeutic challenge. World J Gastroenterol. 2015;21(40):11428.CrossRef Pernot S. Signet-ring cell carcinoma of the stomach: Impact on prognosis and specific therapeutic challenge. World J Gastroenterol. 2015;21(40):11428.CrossRef
18.
Zurück zum Zitat Golembeski CP, Genta RM. Signet-ring cell carcinoma in gastric biopsies: expecting the unexpected. J Clin Pathol. 2013;66(2):136–9.CrossRef Golembeski CP, Genta RM. Signet-ring cell carcinoma in gastric biopsies: expecting the unexpected. J Clin Pathol. 2013;66(2):136–9.CrossRef
19.
Zurück zum Zitat Piessen G, Amielh D, Messager M, Vinatier E, Leteurtre E, Triboulet JP, et al. Is pretreatment endoscopic biopsy a good predictor of signet ring cell histology in gastric carcinoma? World J Surg. 2012;36(2):346–54.CrossRef Piessen G, Amielh D, Messager M, Vinatier E, Leteurtre E, Triboulet JP, et al. Is pretreatment endoscopic biopsy a good predictor of signet ring cell histology in gastric carcinoma? World J Surg. 2012;36(2):346–54.CrossRef
20.
Zurück zum Zitat Pedrazzani C, Marrelli D, Pacelli F, Di Cosmo M, Mura G, Bettarini F, et al. Gastric linitis plastica: which role for surgical resection? Gastric Cancer. 2012;15(1):56–60.CrossRef Pedrazzani C, Marrelli D, Pacelli F, Di Cosmo M, Mura G, Bettarini F, et al. Gastric linitis plastica: which role for surgical resection? Gastric Cancer. 2012;15(1):56–60.CrossRef
21.
Zurück zum Zitat Endo K, Sakurai M, Kusumoto E, Uehara H, Yamaguchi S, Tsutsumi N, et al. Biological significance of localized Type IV scirrhous gastric cancer. Oncol Lett. 2012;3(1):94–9.CrossRef Endo K, Sakurai M, Kusumoto E, Uehara H, Yamaguchi S, Tsutsumi N, et al. Biological significance of localized Type IV scirrhous gastric cancer. Oncol Lett. 2012;3(1):94–9.CrossRef
22.
Zurück zum Zitat Mocellin S, Pasquali S. Diagnostic accuracy of endoscopic ultrasonography (EUS) for the preoperative locoregional staging of primary gastric cancer. Cochrane Database Syst Rev. 2015;2:1–173. Mocellin S, Pasquali S. Diagnostic accuracy of endoscopic ultrasonography (EUS) for the preoperative locoregional staging of primary gastric cancer. Cochrane Database Syst Rev. 2015;2:1–173.
23.
Zurück zum Zitat Liu Y, Chen K, Yang X-J. Endoscopic ultrasound guided fine needle aspiration used in diagnosing gastric linitis plastica: metastatic lymph nodes can be valuable targets. J Gastroenterol Hepatol. 2018;34:202–6.CrossRef Liu Y, Chen K, Yang X-J. Endoscopic ultrasound guided fine needle aspiration used in diagnosing gastric linitis plastica: metastatic lymph nodes can be valuable targets. J Gastroenterol Hepatol. 2018;34:202–6.CrossRef
24.
Zurück zum Zitat Morgant S, Artru P, Oudjit A, Lourenco N, Pasquer A, Walter T, et al. Computed tomography scan efficacy in staging gastric linitis plastica lesion: a retrospective multicentric French study. Cancer Manag Res. 2018;10:3825–31.CrossRef Morgant S, Artru P, Oudjit A, Lourenco N, Pasquer A, Walter T, et al. Computed tomography scan efficacy in staging gastric linitis plastica lesion: a retrospective multicentric French study. Cancer Manag Res. 2018;10:3825–31.CrossRef
25.
Zurück zum Zitat Han D-S, Suh Y-S, Kong S-H, Lee H-J, Choi Y, Aikou S, et al. Nomogram predicting long-term survival after d2 gastrectomy for gastric cancer. J Clin Oncol Off J Am Soc Clin Oncol. 2012;30(31):3834–40.CrossRef Han D-S, Suh Y-S, Kong S-H, Lee H-J, Choi Y, Aikou S, et al. Nomogram predicting long-term survival after d2 gastrectomy for gastric cancer. J Clin Oncol Off J Am Soc Clin Oncol. 2012;30(31):3834–40.CrossRef
26.
Zurück zum Zitat Hirabayashi S, Kosugi S, Isobe Y, Nashimoto A, Oda I, Hayashi K, et al. Development and external validation of a nomogram for overall survival after curative resection in serosa-negative, locally advanced gastric cancer. Ann Oncol Off J Eur Soc Med Oncol. 2014;25(6):1179–84.CrossRef Hirabayashi S, Kosugi S, Isobe Y, Nashimoto A, Oda I, Hayashi K, et al. Development and external validation of a nomogram for overall survival after curative resection in serosa-negative, locally advanced gastric cancer. Ann Oncol Off J Eur Soc Med Oncol. 2014;25(6):1179–84.CrossRef
27.
Zurück zum Zitat Zheng Z-F, Lu J, Wang W, Desiderio J, Li P, Xie J-W, et al. Development and external validation of a simplified nomogram predicting individual survival after R0 resection for gastric cancer: an international, multicenter study. Ann Surg Oncol. 2018;25:2383–90.CrossRef Zheng Z-F, Lu J, Wang W, Desiderio J, Li P, Xie J-W, et al. Development and external validation of a simplified nomogram predicting individual survival after R0 resection for gastric cancer: an international, multicenter study. Ann Surg Oncol. 2018;25:2383–90.CrossRef
28.
Zurück zum Zitat Narita Y, Kadowaki S, Oze I, Kito Y, Kawakami T, Machida N, et al. Establishment and validation of prognostic nomograms in first-line metastatic gastric cancer patients. J Gastrointest Oncol. 2018;9(1):52–63.CrossRef Narita Y, Kadowaki S, Oze I, Kito Y, Kawakami T, Machida N, et al. Establishment and validation of prognostic nomograms in first-line metastatic gastric cancer patients. J Gastrointest Oncol. 2018;9(1):52–63.CrossRef
29.
Zurück zum Zitat Kim SY, Yoon MJ, Park YI, Kim MJ, Nam B-H, Park SR. Nomograms predicting survival of patients with unresectable or metastatic gastric cancer who receive combination cytotoxic chemotherapy as first-line treatment. Gastric Cancer Off J Int Gastric Cancer Assoc Jpn Gastric Cancer Assoc. 2018;21(3):453–63. Kim SY, Yoon MJ, Park YI, Kim MJ, Nam B-H, Park SR. Nomograms predicting survival of patients with unresectable or metastatic gastric cancer who receive combination cytotoxic chemotherapy as first-line treatment. Gastric Cancer Off J Int Gastric Cancer Assoc Jpn Gastric Cancer Assoc. 2018;21(3):453–63.
30.
Zurück zum Zitat Messager M, Lefevre JH, Pichot-Delahaye V, Souadka A, Piessen G, Mariette C, et al. The impact of perioperative chemotherapy on survival in patients with gastric signet ring cell adenocarcinoma: a multicenter comparative study. Ann Surg. 2011;254(5):684–93.CrossRef Messager M, Lefevre JH, Pichot-Delahaye V, Souadka A, Piessen G, Mariette C, et al. The impact of perioperative chemotherapy on survival in patients with gastric signet ring cell adenocarcinoma: a multicenter comparative study. Ann Surg. 2011;254(5):684–93.CrossRef
Metadaten
Titel
Development and internal validation of a diagnostic score for gastric linitis plastica
verfasst von
J. Vivier-Chicoteau
J. Lambert
R. Coriat
P. E. Bonnot
D. Goere
B. Roche
M. Dior
G. Goujon
S. Morgant
M. Pocard
O. Glehen
T. Aparicio
Jean-Marc Gornet
Publikationsdatum
26.02.2020
Verlag
Springer Singapore
Erschienen in
Gastric Cancer / Ausgabe 4/2020
Print ISSN: 1436-3291
Elektronische ISSN: 1436-3305
DOI
https://doi.org/10.1007/s10120-020-01051-x

Weitere Artikel der Ausgabe 4/2020

Gastric Cancer 4/2020 Zur Ausgabe

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

Karpaltunnelsyndrom BDC Leitlinien Webinare
CME: 2 Punkte

Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

Radiusfraktur BDC Leitlinien Webinare
CME: 2 Punkte

Das Webinar beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

Appendizitis BDC Leitlinien Webinare
CME: 2 Punkte

Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.