Minimum and Optimal CA19-9 Response After Two Months Induction Chemotherapy in Patients with Locally Advanced Pancreatic Cancer: A Nationwide Multicenter Study.


Journal

Annals of surgery
ISSN: 1528-1140
Titre abrégé: Ann Surg
Pays: United States
ID NLM: 0372354

Informations de publication

Date de publication:
21 Jul 2023
Historique:
medline: 21 7 2023
pubmed: 21 7 2023
entrez: 21 7 2023
Statut: aheadofprint

Résumé

This nationwide multicenter study aimed to define clinically relevant thresholds of relative serum CA19-9 response after 2 months induction chemotherapy in patients with locally advanced pancreatic cancer (LAPC). CA19-9 is seen as leading biomarker for response evaluation in patients with LAPC, but early clinically useful cut-offs are lacking. All consecutive patients with LAPC after 4 cycles (m)FOLFIRINOX or 2 cycles gemcitabine-nab-paclitaxel induction chemotherapy (±radiotherapy) with CA19-9 ≥5 U/mL at baseline were analyzed (2015-2019). The association of CA19-9 response with median OS (mOS) was evaluated for different CA19-9 cut-off points. Minimum and optimal CA19-9 response were established via log-rank test. Predictors for OS were analyzed, using cox regression analysis. Overall, 212 patients were included of whom 42 (19.8%) underwent resection. Minimum CA19-9 response demonstrating a clinically significant mOS difference (12.7 vs. 19.6 mo) was seen at ≥40% CA19-9 decrease. The optimal cut-off for CA19-9 response was ≥60% decrease (21.7 vs. 14.0 mo, P=0.021). Only for patients with elevated CA19-9 levels at baseline (n=184), CA19-9 decrease ≥60% (HR=0.59, 95%CI 0.36-0.98, P=0.042) was independently associated with prolonged OS, as were SBRT (HR=0.42, 95%CI 0.25-0.70; P=0.001), and resection (HR=0.25, 95%CI 0.14-0.46, P<0.001), and duration of chemotherapy (HR=0.75, 95%CI 0.69-0.82, P<0.001). CA19-9 decrease of ≥60% following induction chemotherapy as optimal response cut-off in patients with LAPC is an independent predictor for OS when CA19-9 is increased at baseline. Furthermore, ≥40% is the minimum cut-off demonstrating survival benefit. These cut-offs may be used when discussing treatment strategies during early response evaluation.

Sections du résumé

OBJECTIVE OBJECTIVE
This nationwide multicenter study aimed to define clinically relevant thresholds of relative serum CA19-9 response after 2 months induction chemotherapy in patients with locally advanced pancreatic cancer (LAPC).
SUMMARY BACKGROUND DATA BACKGROUND
CA19-9 is seen as leading biomarker for response evaluation in patients with LAPC, but early clinically useful cut-offs are lacking.
METHODS METHODS
All consecutive patients with LAPC after 4 cycles (m)FOLFIRINOX or 2 cycles gemcitabine-nab-paclitaxel induction chemotherapy (±radiotherapy) with CA19-9 ≥5 U/mL at baseline were analyzed (2015-2019). The association of CA19-9 response with median OS (mOS) was evaluated for different CA19-9 cut-off points. Minimum and optimal CA19-9 response were established via log-rank test. Predictors for OS were analyzed, using cox regression analysis.
RESULTS RESULTS
Overall, 212 patients were included of whom 42 (19.8%) underwent resection. Minimum CA19-9 response demonstrating a clinically significant mOS difference (12.7 vs. 19.6 mo) was seen at ≥40% CA19-9 decrease. The optimal cut-off for CA19-9 response was ≥60% decrease (21.7 vs. 14.0 mo, P=0.021). Only for patients with elevated CA19-9 levels at baseline (n=184), CA19-9 decrease ≥60% (HR=0.59, 95%CI 0.36-0.98, P=0.042) was independently associated with prolonged OS, as were SBRT (HR=0.42, 95%CI 0.25-0.70; P=0.001), and resection (HR=0.25, 95%CI 0.14-0.46, P<0.001), and duration of chemotherapy (HR=0.75, 95%CI 0.69-0.82, P<0.001).
CONCLUSION CONCLUSIONS
CA19-9 decrease of ≥60% following induction chemotherapy as optimal response cut-off in patients with LAPC is an independent predictor for OS when CA19-9 is increased at baseline. Furthermore, ≥40% is the minimum cut-off demonstrating survival benefit. These cut-offs may be used when discussing treatment strategies during early response evaluation.

Identifiants

pubmed: 37477009
doi: 10.1097/SLA.0000000000006021
pii: 00000658-990000000-00581
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest.

Auteurs

Leonard W F Seelen (LWF)

Department of Surgery, UMC Utrecht Cancer Center and St Antonius Hospital Nieuwegein: Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.

Deesje Doppenberg (D)

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

Thomas F Stoop (TF)

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.
Division of Surgical Oncology, Department of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.

Anne Nagelhout (A)

Department of Surgery, UMC Utrecht Cancer Center and St Antonius Hospital Nieuwegein: Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.

Lilly J H Brada (LJH)

Department of Surgery, UMC Utrecht Cancer Center and St Antonius Hospital Nieuwegein: Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.

Koop Bosscha (K)

Department of Surgery, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.

Olivier R Busch (OR)

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

Geert A Cirkel (GA)

Department of Medical Oncology, Regional Academic Cancer Center Utrecht, Meander Medical Center Amersfoort, University Medical Center, Utrecht, The Netherlands.

Marcel den Dulk (M)

Department of Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.
Department of General, Visceral and Transplant Surgery, University Hospital Aachen, Germany.

Freek Daams (F)

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

Susan van Dieren (S)

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

Casper H J van Eijck (CHJ)

Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Sebastiaan Festen (S)

Department of Surgery, OLVG, Amsterdam, The Netherlands.

Bas Groot Koerkamp (B)

Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Nadia Haj Mohammad (N)

Department of Medical Oncology, Regional Academic Cancer Center Utrecht, University Medical Center, Utrecht, The Netherlands.

Ignace H J T de Hingh (IHJT)

Department of Surgery, Catharina Hospital, Eindhoven, The Netherlands.

Daan J Lips (DJ)

Department of Surgery, Medisch Spectrum Twente, Enschede, The Netherlands.

Maartje Los (M)

Department of Medical Oncology, Regional Academic Cancer Center Utrecht, St. Antonius Hospital Nieuwegein, University Medical Center, Utrecht, The Netherlands.

Vincent E de Meijer (VE)

Department of Surgery, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands.

Gijs A Patijn (GA)

Department of Surgery, Isala Clinics, Zwolle, The Netherlands.

Marco B Polée (MB)

Department of Medical Oncology, Medical Center Leeuwarden, Leeuwarden, The Netherlands.

Martijn W J Stommel (MWJ)

Department of Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.

Marieke S Walma (MS)

Department of Surgery, UMC Utrecht Cancer Center and St Antonius Hospital Nieuwegein: Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.

Roeland F de Wilde (RF)

Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Johanna W Wilmink (JW)

Cancer Center Amsterdam, Amsterdam, The Netherlands.
Amsterdam UMC, location University of Amsterdam, Department of Medical Oncology, Amsterdam, The Netherlands.

I Quintus Molenaar (IQ)

Department of Surgery, UMC Utrecht Cancer Center and St Antonius Hospital Nieuwegein: Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.

Hjalmar C van Santvoort (HC)

Department of Surgery, UMC Utrecht Cancer Center and St Antonius Hospital Nieuwegein: Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.

Marc G Besselink (MG)

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

Classifications MeSH