Evidence map›Paper›PMID 37278395›Full record

ArticleCancer medicine2023

The role of nanoliposomal irinotecan plus fluorouracil/leucovorin in the continuum of care of patients with metastatic pancreatic ductal adenocarcinoma.

Letizia Procaccio, Valeria Merz, Morena Fasano, Vanja Vaccaro, Elisa Giommoni, Andrea Pretta, Silvia Noventa, Maria Antonietta Satolli, Guido Giordano, Clizia Zichi and 14 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 11 institutions in 1 country.

Letizia ProcaccioMedical Oncology 1 Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Valeria MerzDigestive Molecular Clinical Oncology Research Unit, Università degli Studi di Verona, Verona, Italy.ORCID 0000-0002-2120-1923
Morena FasanoMedical Oncology Unit, Department of Precision Medicine, School of Medicine, University of study of Campania "L. Vanvitelli", Naples, Italy.
Vanja VaccaroRegina Elena National Cancer Institute, Rome, Italy.
Elisa GiommoniClinical Oncology Unit, Careggi University Hospital, Florence, Italy.ORCID 0000-0002-1715-8440
Andrea PrettaMedical Oncology Department, University Hospital, University of Cagliari, Cagliari, Italy.
Silvia NoventaMedical Oncology Unit, Casa di Cura Poliambulanza, Brescia, Italy.
Maria Antonietta SatolliDepartment of Oncology, University of Turin, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Turin, Italy.
Guido GiordanoUO di Oncologia Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Clizia ZichiDepartment of Oncology, University of Turin, Ordine Mauriziano Hospital, Turin, Italy.
Carmine PintoHigh-Complexity Oncology Unit, Clinical Cancer Center, IRCCS Reggio Emilia, Reggio Emilia, Italy.
Camilla ZecchettoDigestive Molecular Clinical Oncology Research Unit, Università degli Studi di Verona, Verona, Italy.
Giulia BarsottiMedical Oncology 1 Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Ferdinando De VitaMedical Oncology Unit, Department of Precision Medicine, School of Medicine, University of study of Campania "L. Vanvitelli", Naples, Italy.
Michele MilellaRegina Elena National Cancer Institute, Rome, Italy.
Lorenzo AntonuzzoClinical Oncology Unit, Careggi University Hospital, Florence, Italy.
Mario ScartozziMedical Oncology Department, University Hospital, University of Cagliari, Cagliari, Italy.
Alberto ZaniboniMedical Oncology Unit, Casa di Cura Poliambulanza, Brescia, Italy.
Rosella SpadiMedical Oncology 1, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Turin, Italy.
Simona CasalinoDigestive Molecular Clinical Oncology Research Unit, Università degli Studi di Verona, Verona, Italy.
Francesca BergamoMedical Oncology 1 Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Chiara De ToniMedical Oncology 1 Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Davide MelisiDigestive Molecular Clinical Oncology Research Unit, Università degli Studi di Verona, Verona, Italy.
Sara LonardiMedical Oncology 3 Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.ORCID 0000-0002-7593-8138
University of Verona · ITIstituto Oncologico Veneto · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITAzienda Ospedaliero-Universitaria Careggi · ITGruppo di Ricerca Geriatrica · ITUniversity of Cagliari · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Padua · ITA. O. Ordine Mauriziano di Torino · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITCasa Sollievo della Sofferenza · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe NAPOLI-I trial showed better outcome of nanoliposomal irinotecan (nal-IRI) plus 5-fluorouracil/leucovorin (5-FU/LV) compared to 5-FU/LV in patients with advanced pancreatic ductal adenocarcinoma cancer (advPDAC) progressed to gemcitabine-based therapy. This study aims to explore the real-world efficacy and safety of 5-FU/LV-nal-IRI.

methodsThis is a retrospective multicenter analysis including advPDAC patients receiving 5-FU/LV-nal-IRI after failure of gemcitabine-based therapy. Survival analyses were performed using Kaplan-Meier method, univariate and multivariate analyses by Cox regression.

resultsA total of 296 patients (median age 64.4 years, ECOG PS ≥1 in 56% of cases) were treated at 11 Italian institutions between 2016 and 2018. 34% of them underwent primary tumor resection, and 79% received gemcitabine-nabpaclitaxel as first line. 5-FU/LV-nal-IRI was administered as second-line in 73% of cases. Objective response and disease control rate were 12% and 41%, respectively. Treatment was well tolerated with dose reductions in 50% of patients but no one permanent discontinuation; the commonest grade ≥3 toxicities were neutropenia (14%) and diarrhea (12%). Median PFS and OS from 5-FU/LV-nal-IRI initiation was 3.2 and 7.1 months, respectively.

conclusionsThese real-world data confirm the 5-FU/LV-nal-IRI efficacy and safety in advPDAC patients progressed to gemcitabine-based therapy, with outcomes comparable to NAPOLI-1, even in a less-selected population and with more modern therapeutic algorithm.

Indexed as

AdenocarcinomaPancreatic NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsCamptothecinContinuity of Patient CareFluorouracilGemcitabineHumansIrinotecanLeucovorinMiddle AgedCamptothecinFluorouracilGemcitabineIrinotecanLeucovorin

Identifiers

PMID37278395
PMCPMC10358242
OpenAlexW4379507911

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.