Use of self-expandable metallic stents for endoscopic biliary decompression decreases stent complications in pancreatic cancer patients receiving chemotherapy.


Journal

Surgical endoscopy
ISSN: 1432-2218
Titre abrégé: Surg Endosc
Pays: Germany
ID NLM: 8806653

Informations de publication

Date de publication:
01 2022
Historique:
received: 01 10 2020
accepted: 13 01 2021
pubmed: 4 2 2021
medline: 3 3 2022
entrez: 3 2 2021
Statut: ppublish

Résumé

Both plastic stents and self-expandable metallic stents (SEMSes) are used for endoscopic biliary decompression (BD) among patients with pancreatic cancer (PAC). Cholangitis or stent occlusion often interrupts or ends chemotherapy. We investigated cholangitis, stent occlusion, and chemotherapy interruption rates for SEMSes and plastic stents among patients receiving chemotherapy for PAC. We retrospectively analyzed data for 293 PAC patients who received a biliary stent at Helsinki University Hospital during 2000-2017. Patients received chemotherapy as palliative treatment (PT: n = 187) or neoadjuvant treatment (NAT: n = 106). Among participants, 229 had a plastic stent (PT: n = 138, NAT: n = 91) and 64 had a SEMS (PT: n = 49, NAT: n = 15). Overall, 15.6% (n = 10) of patients with SEMSes (PT: 20.4%, n = 10, NAT: 0%) and 53.0% (n = 121) of patients with plastic stents (PT: 69.3%, n = 95, NAT: 28.5%, n = 26) experienced one or more stent complications (p < 0.001). Cholangitis developed in 6.3% (n = 8) of PT patients with SEMSes. No patients with SEMSes receiving NAT (n = 15) experienced cholangitis. However, 31.9% (PT: 42.8%, n = 59, p = 0.001; NAT: 15.4%, n = 14, p = 0.211) of patients with plastic stents developed cholangitis. Among all patients receiving NAT or PT, cholangitis interrupted chemotherapy 6 times (9.4%) in SEMS patients and 61 times (26.6%) in plastic stent patients (p = 0.004). Stent occlusion without cholangitis interrupted NAT or PT 2 times (2.1%) in SEMS patients and 31 times (13.5%) in plastic stent patients (p = 0.023). SEMS is recommended for BD among patients with PAC receiving chemotherapy. Among both PT and NAT patients, patients with SEMS experience a lower stent failure rate, lower rate of cholangitis, and fewer chemotherapy interruptions than patients with plastic stents.

Sections du résumé

BACKGROUND
Both plastic stents and self-expandable metallic stents (SEMSes) are used for endoscopic biliary decompression (BD) among patients with pancreatic cancer (PAC). Cholangitis or stent occlusion often interrupts or ends chemotherapy. We investigated cholangitis, stent occlusion, and chemotherapy interruption rates for SEMSes and plastic stents among patients receiving chemotherapy for PAC.
MATERIALS AND METHODS
We retrospectively analyzed data for 293 PAC patients who received a biliary stent at Helsinki University Hospital during 2000-2017. Patients received chemotherapy as palliative treatment (PT: n = 187) or neoadjuvant treatment (NAT: n = 106). Among participants, 229 had a plastic stent (PT: n = 138, NAT: n = 91) and 64 had a SEMS (PT: n = 49, NAT: n = 15).
RESULTS
Overall, 15.6% (n = 10) of patients with SEMSes (PT: 20.4%, n = 10, NAT: 0%) and 53.0% (n = 121) of patients with plastic stents (PT: 69.3%, n = 95, NAT: 28.5%, n = 26) experienced one or more stent complications (p < 0.001). Cholangitis developed in 6.3% (n = 8) of PT patients with SEMSes. No patients with SEMSes receiving NAT (n = 15) experienced cholangitis. However, 31.9% (PT: 42.8%, n = 59, p = 0.001; NAT: 15.4%, n = 14, p = 0.211) of patients with plastic stents developed cholangitis. Among all patients receiving NAT or PT, cholangitis interrupted chemotherapy 6 times (9.4%) in SEMS patients and 61 times (26.6%) in plastic stent patients (p = 0.004). Stent occlusion without cholangitis interrupted NAT or PT 2 times (2.1%) in SEMS patients and 31 times (13.5%) in plastic stent patients (p = 0.023).
CONCLUSIONS
SEMS is recommended for BD among patients with PAC receiving chemotherapy. Among both PT and NAT patients, patients with SEMS experience a lower stent failure rate, lower rate of cholangitis, and fewer chemotherapy interruptions than patients with plastic stents.

Identifiants

pubmed: 33534073
doi: 10.1007/s00464-021-08327-y
pii: 10.1007/s00464-021-08327-y
pmc: PMC8741707
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

614-620

Informations de copyright

© 2021. The Author(s).

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Auteurs

Sini Vehviläinen (S)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland. sini.vehvilainen@hus.fi.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland. sini.vehvilainen@hus.fi.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland. sini.vehvilainen@hus.fi.

Hanna Seppänen (H)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland.

Anna Nurmi (A)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland.

Caj Haglund (C)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland.

Harri Mustonen (H)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland.

Marianne Udd (M)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland.

Leena Kylänpää (L)

Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki, Helsinki, Finland.
Department of Surgery, Meilahti Hospital, University of Helsinki, Haartmaninkatu 4, PO Box 340, HUS, 00029, Helsinki, Finland.

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