Nab-paclitaxel/gemcitabine combination is more effective than gemcitabine alone in locally advanced, unresectable pancreatic cancer - A GISCAD phase II randomized trial.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
05 2021
Historique:
received: 04 09 2020
revised: 10 02 2021
accepted: 15 02 2021
pubmed: 4 4 2021
medline: 26 10 2021
entrez: 3 4 2021
Statut: ppublish

Résumé

The role of combination chemotherapy has not yet been established in unresectable locally advanced pancreatic cancer (LAPC) lacking dedicated randomized trials. This phase II trial tested the efficacy of Nab-paclitaxel (NAB-P)/Gemcitabine (G) versus G alone. Patients were randomized, 1:1 to G 1000 mg/m A total of124 patients were enrolled. The study showed a reduction of a progressive disease from 45.6% with G to 25.4% with NAB-P/G (P = 0.01) at 3 months. Noteworthy, at 6 months in the G arm, 35.6% of patients present a metastatic spread versus 20.8% in the NAB/G arm. The response rate was 5.3% in the G arm and 27% in the NAB/G arm. Median PFS was 4 months for the G arm and 7 months for the NAB-P/G arm. Median OS was 10.6 in the G arm and 12.7 months in the NAB-P/G arm. One patient died during treatment with G due to a stroke. NAB-P/G reduced the rate of LAPC patients progressing after three cycles of chemotherapy compared with G, especially in terms of distant relapses. It positively affects PFS. To the best of our knowledge, this is the first randomized trial providing evidence that combination chemotherapy is superior to gemcitabine alone in this setting. CLINICALTRIALS. NCT02043730.

Sections du résumé

BACKGROUND
The role of combination chemotherapy has not yet been established in unresectable locally advanced pancreatic cancer (LAPC) lacking dedicated randomized trials.
METHODS
This phase II trial tested the efficacy of Nab-paclitaxel (NAB-P)/Gemcitabine (G) versus G alone. Patients were randomized, 1:1 to G 1000 mg/m
FINDINGS
A total of124 patients were enrolled. The study showed a reduction of a progressive disease from 45.6% with G to 25.4% with NAB-P/G (P = 0.01) at 3 months. Noteworthy, at 6 months in the G arm, 35.6% of patients present a metastatic spread versus 20.8% in the NAB/G arm. The response rate was 5.3% in the G arm and 27% in the NAB/G arm. Median PFS was 4 months for the G arm and 7 months for the NAB-P/G arm. Median OS was 10.6 in the G arm and 12.7 months in the NAB-P/G arm. One patient died during treatment with G due to a stroke.
INTERPRETATION
NAB-P/G reduced the rate of LAPC patients progressing after three cycles of chemotherapy compared with G, especially in terms of distant relapses. It positively affects PFS. To the best of our knowledge, this is the first randomized trial providing evidence that combination chemotherapy is superior to gemcitabine alone in this setting. CLINICALTRIALS.
GOV IDENTIFIER
NCT02043730.

Identifiants

pubmed: 33812334
pii: S0959-8049(21)00106-4
doi: 10.1016/j.ejca.2021.02.023
pii:
doi:

Substances chimiques

130-nm albumin-bound paclitaxel 0
Albumins 0
Deoxycytidine 0W860991D6
Paclitaxel P88XT4IS4D
Gemcitabine 0

Banques de données

ClinicalTrials.gov
['NCT02043730']

Types de publication

Clinical Trial, Phase II Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

422-429

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement Dr Cascinu reports grants from Celegne during the conduct of the study; other from Celegne; other from Servier, outside the submitted work; and the remaining authors have nothing to disclose.

Auteurs

Stefano Cascinu (S)

Medical Oncology Department, Università Vita-Salute, IRCCS-Ospedale San Raffaele, Milano, Italy. Electronic address: cascinu.stefano@hsr.it.

Rossana Berardi (R)

Medical Oncology Unit, Università Politecnica delle Marche, Azienda Ospedaliera Umberto I, Salesi, Lancisi, Ancona, Italy.

Roberto Bianco (R)

Università Federico II Napoli, Italy.

Domenico Bilancia (D)

Medical Oncology Unit, Ospedale San Carlo, Potenza, Italy.

Alberto Zaniboni (A)

Medical Oncology Unit, Fondazione Poliambulanza, Brescia, Italy.

Daris Ferrari (D)

Medical Oncology Unit, Azienda Ospedaliera San Paolo, Milano, Italy.

Stefania Mosconi (S)

Cancer Center ASST Papa Giovanni XXIII, Bergamo, Italy.

Andrea Spallanzani (A)

Medical Oncology Unit, Azienda Ospedaliero-Universitaria di Modena, Modena, Italy.

Luigi Cavanna (L)

Medical Oncology Unit, Ospedale di Piacenza, Italy.

Silvana Leo (S)

Medical Oncology Unit, Ospedale di Lecce, Italy.

Francesca Negri (F)

Medical Oncology Unit, Azienda Ospedaliero-Universitaria di Parma, Italy.

Giordano D Beretta (GD)

Medical Oncology Unit, Humanitas Gavazzeni, Bergamo, Italy.

Alberto Sobrero (A)

Medical Oncology Unit, IRCCS San Martino-IST, Genova, Italy.

Maria Banzi (M)

Medical Oncology Unit, Ospedale-IRCCS di Reggio Emilia, Italy.

Alberto Morabito (A)

Medical Oncology Unit Ospedale di Camposampiero, Italy.

Alessandro Bittoni (A)

Medical Oncology Unit, Università Politecnica delle Marche, Azienda Ospedaliera Umberto I, Salesi, Lancisi, Ancona, Italy.

Roberta Marciano (R)

Università Federico II Napoli, Italy.

Domenica Ferrara (D)

Medical Oncology Unit, Ospedale San Carlo, Potenza, Italy.

Silvia Noventa (S)

Medical Oncology Unit, Fondazione Poliambulanza, Brescia, Italy.

Maria C Piccirillo (MC)

Fondazione Istituto Nazionale Tumori-IRCCS G. Pascale, Napoli, Italy.

Roberto Labianca (R)

Cancer Center ASST Papa Giovanni XXIII, Bergamo, Italy.

Cristina Mosconi (C)

Istituto di Radiologia, Policlinico S. Orsola, Università di Bologna, Italy.

Andrea Casadei Gardini (A)

Medical Oncology Department, Università Vita-Salute, IRCCS-Ospedale San Raffaele, Milano, Italy.

Ciro Gallo (C)

Statistica Medica Università degli Studi della Campania Luigi Vanvitelli, Italy.

Francesco Perrone (F)

Fondazione Istituto Nazionale Tumori-IRCCS G. Pascale, Napoli, Italy.

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Classifications MeSH