High thromboembolic event rate in patients with locally advanced oesophageal cancer during neoadjuvant therapy. An exploratory analysis of the prospective, randomised intergroup phase III trial SAKK 75/08.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
28 Feb 2020
Historique:
received: 13 10 2019
accepted: 11 02 2020
entrez: 1 3 2020
pubmed: 1 3 2020
medline: 23 10 2020
Statut: epublish

Résumé

High rates of venous thromboembolic events (VTEs), mainly in advanced disease, are reported for patients with cancer of the upper gastrointestinal tract (stomach, pancreas) and for treatment with cisplatin. Exploratory analysis of VTEs reported as adverse events and serious adverse events in a prospective, randomised, multicentre, multimodal phase III trial according to VTEs reported as adverse events and severe adverse events. Patients with resectable oesophageal cancer (T2N1-3, T3-4aNx) were randomized to 2 cycles of chemotherapy with docetaxel 75 mg/m VTEs occurred in 26 of 300 patients included in the trial, resulting in an incidence rate (IR) of 8.7% [95% CI 5.7-12.4%]. A total of 29 VTEs were reported:13 (45%) VTEs were grade 2, 13 (45%) grade 3 and three (10%) fatal grade 5 events. 72% (21/29) of all VTEs occurred preoperatively (IR 6.7%): 14% (4/29) during chemotherapy and 59% (17/29) during CRT. In multivariable logistic regression only adenocarcinoma (IR 11.1%, 21/189 patients) compared to squamous cell cancer (IR 4.5%, 5/111 patients) was significantly associated with VTE-risk during treatment, OR 2.9 [95%CI 1.0-8.4], p = 0.046. Baseline Khorana risk score was 0 in 73% (19/26), 1-2 in 23% (6/26) and 3 in only 4% (1/26) of patients with VTEs. A high incidence of VTEs during preoperative therapy of resectable oesophageal cancer is observed in this analysis, especially in patients with adenocarcinoma. The role of prophylactic anticoagulation during neoadjuvant therapy in resectable esophageal cancer should be further evaluated in prospective clinical trials. According to our data, which are in line with other analysis of VTE-risk in patients with oesophageal cancer patients treated with neoadjuvant cisplatin-based chemotherapy and CRT, prophylactic anticoagluation could be considered balanced against individual bleeding risks, especially in patients with adenocarcinoma. In addition to the established risk factors, oesophageal adenocarcinoma treated with neoadjuvant cisplatin-based therapy may be regarded as a high-risk situation for VTEs. Registered at clinicaltrials.gov, NCT01107639, on 21 April 2010.

Sections du résumé

BACKGROUND BACKGROUND
High rates of venous thromboembolic events (VTEs), mainly in advanced disease, are reported for patients with cancer of the upper gastrointestinal tract (stomach, pancreas) and for treatment with cisplatin.
METHODS METHODS
Exploratory analysis of VTEs reported as adverse events and serious adverse events in a prospective, randomised, multicentre, multimodal phase III trial according to VTEs reported as adverse events and severe adverse events. Patients with resectable oesophageal cancer (T2N1-3, T3-4aNx) were randomized to 2 cycles of chemotherapy with docetaxel 75 mg/m
RESULTS RESULTS
VTEs occurred in 26 of 300 patients included in the trial, resulting in an incidence rate (IR) of 8.7% [95% CI 5.7-12.4%]. A total of 29 VTEs were reported:13 (45%) VTEs were grade 2, 13 (45%) grade 3 and three (10%) fatal grade 5 events. 72% (21/29) of all VTEs occurred preoperatively (IR 6.7%): 14% (4/29) during chemotherapy and 59% (17/29) during CRT. In multivariable logistic regression only adenocarcinoma (IR 11.1%, 21/189 patients) compared to squamous cell cancer (IR 4.5%, 5/111 patients) was significantly associated with VTE-risk during treatment, OR 2.9 [95%CI 1.0-8.4], p = 0.046. Baseline Khorana risk score was 0 in 73% (19/26), 1-2 in 23% (6/26) and 3 in only 4% (1/26) of patients with VTEs.
CONCLUSION CONCLUSIONS
A high incidence of VTEs during preoperative therapy of resectable oesophageal cancer is observed in this analysis, especially in patients with adenocarcinoma. The role of prophylactic anticoagulation during neoadjuvant therapy in resectable esophageal cancer should be further evaluated in prospective clinical trials. According to our data, which are in line with other analysis of VTE-risk in patients with oesophageal cancer patients treated with neoadjuvant cisplatin-based chemotherapy and CRT, prophylactic anticoagluation could be considered balanced against individual bleeding risks, especially in patients with adenocarcinoma. In addition to the established risk factors, oesophageal adenocarcinoma treated with neoadjuvant cisplatin-based therapy may be regarded as a high-risk situation for VTEs.
TRIAL REGISTRATION BACKGROUND
Registered at clinicaltrials.gov, NCT01107639, on 21 April 2010.

Identifiants

pubmed: 32111181
doi: 10.1186/s12885-020-6623-z
pii: 10.1186/s12885-020-6623-z
pmc: PMC7048062
doi:

Substances chimiques

Docetaxel 15H5577CQD
Cetuximab PQX0D8J21J
Cisplatin Q20Q21Q62J

Banques de données

ClinicalTrials.gov
['NCT01107639']

Types de publication

Clinical Trial, Phase III Comparative Study Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

166

Subventions

Organisme : Staatssekretariat für Bildung, Forschung und Innovation
ID : No grant number applies
Organisme : Merck KGaA, Darmstadt, Germany
ID : No grant numer applies

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Auteurs

Martin Fehr (M)

Department of Medical Oncology and Haematology, Cantonal Hospital St. Gallen, Rorschacherstrasse 95, 9007, St. Gallen, Switzerland. Martin.Fehr@kssg.ch.

Hanne Hawle (H)

SAKK Coordinating Center, Bern, Switzerland.

Stefanie Hayoz (S)

SAKK Coordinating Center, Bern, Switzerland.

Peter Thuss-Patience (P)

Charité - Universitätsmedizin Berlin, Berlin, Germany.

Sabina Schacher (S)

Kantonsspital Winterthur, Winterthur, Switzerland.

Jorge Riera Knorrenschild (J)

Universitätsklinikum Giessen und Marburg, Marburg, Germany.

Donat Dürr (D)

Stadtspital Triemli, Zürich, Switzerland.

Wolfram T Knoefel (WT)

Universitätsklinikum Düsseldorf, Düsseldorf, Germany.

Holger Rumpold (H)

Krankenhaus der barmherzigen Schwestern, Linz, Austria.
Landeskrankenhaus Feldkirch, Feldkirch, Austria.

Michael Bitzer (M)

Universitätsklinikum Tübingen, Tübingen, Germany.

Martin Zweifel (M)

Inselspital Bern, Bern, Switzerland.

Panagiotis Samaras (P)

Universitätsspital Zürich, Zürich, Switzerland.

Ulrich Mey (U)

Kantonsspital Graubünden, Chur, Switzerland.

Marc Küng (M)

Hôpital Fribourgeois, Villars-sur-Glâne, Switzerland.

Ralph Winterhalder (R)

Luzerner Kantonsspital, Luzern, Switzerland.

Wolfgang Eisterer (W)

Medizinische Universität Innsbruck, Innsbruck, Austria.
Klinikum Klagenfurt am Wörthersee, Klagenfurt, Austria.

Viviane Hess (V)

Universitätsspital Basel, Basel, Switzerland.

Marie-Aline Gérard (MA)

SAKK Coordinating Center, Bern, Switzerland.

Arnoud Templeton (A)

Claraspital Basel, Basel, Switzerland.

Michael Stahl (M)

Evang. Kliniken Essen-Mitte, Essen, Germany.

Thomas Ruhstaller (T)

Department of Medical Oncology and Haematology, Cantonal Hospital St. Gallen, Rorschacherstrasse 95, 9007, St. Gallen, Switzerland.
University of Basel, Basel, Switzerland.

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Classifications MeSH