Evidence map›Paper›PMID 33062062›Full record

ArticleTherapeutic advances in medical oncology2020

FOLFIRINOX after first-line gemcitabine-based chemotherapy in advanced pancreatic cancer: a retrospective comparison with FOLFOX and FOLFIRI schedules.

Francesca Foschini, Fabiana Napolitano, Alberto Servetto, Roberta Marciano, Eleonora Mozzillo, Anna Chiara Carratù, Antonio Santaniello, Pietro De Placido, Priscilla Cascetta, Giovanni Butturini and 10 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. GSK3βGut · 2026
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  5. Observational
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  13. Pancreatic adenocarcinoma: Beyond first line, where are we?World journal of gastroenterology · 2021
    Review
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

20 authors at 5 institutions in 1 country.

Francesca FoschiniDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.ORCID https://orcid.org/0000-0001-5389-7390
Fabiana NapolitanoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Alberto ServettoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Roberta MarcianoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Eleonora MozzilloDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Anna Chiara CarratùDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Antonio SantanielloDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Pietro De PlacidoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Priscilla CascettaDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Giovanni ButturiniPancreatic Surgery Unit, Pederzoli Hospital, Peschiera del Garda, Verona, Italy.
Isabella FrigerioPancreatic Surgery Unit, Pederzoli Hospital, Peschiera del Garda, Verona, Italy.
Paolo RegiPancreatic Surgery Unit, Pederzoli Hospital, Peschiera del Garda, Verona, Italy.
Nicola SilvestrisMedical Oncology Unit, IRCCS Istituto Tumori Giovanni Paolo II of Bari, Bari, Italy.
Sabina DelcuratoloMedical Oncology Unit, IRCCS Istituto Tumori Giovanni Paolo II of Bari, Bari, Italy.
Enrico VasileUnit of Oncology 2, University Hospital of Pisa, Italy.
Caterina VivaldiUnit of Oncology 2, University Hospital of Pisa, Italy.
Cataldo BiancoDepartment of Experimental and Clinical Medicine, University of Catanzaro Magna Graecia, Catanzaro, Italy.
Sabino De PlacidoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, 80131 Naples, Italy.
Luigi FormisanoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, Via Pansini 5, Naples, 80131, Italy.
Roberto BiancoDepartment of Clinical Medicine and Surgery, Oncology Division, University of Naples Federico II, Via Pansini 5, Naples, 80131, Italy.
University of Naples Federico II · ITCasa di Cura Villa Garda · ITAzienda Ospedaliera Universitaria Pisana · ITIstituto Tumori Bari · ITMagna Graecia University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic adenocarcinoma is the fourth leading cause of cancer-related death. In cases with metastasis, the combination of 5-fluorouracil, irinotecan, and oxaliplatin (FOLFIRINOX) or gemcitabine-based chemotherapy regimens are considered the standard of care. However, the optimal sequence of these regimens is unclear.

methodsThis retrospective study initially evaluated 186 patients with locally advanced/metastatic pancreatic cancer at three Italian institutions between February 2013 and October 2019. All patients had progressed after receiving gemcitabine-based first-line chemotherapy and were subsequently offered second-line FOLFIRINOX, FOLFOX-6, or FOLFIRI treatment. This study evaluated progression-free survival (PFS), overall survival from the start of second-line treatment (OS2), overall survival from the start of first-line treatment (OS1), and safety outcomes.

resultsA total of 77 patients received ⩾4 cycles of second-line chemotherapy and were considered eligible: 15 patients received FOLFIRINOX, 32 patients received FOLFOX-6, and 30 patients received FOLFIRI. The FOLFIRINOX group had median PFS of 26.29 weeks and median OS2 of 47.86 weeks, while the FOLFIRI group had median PFS of 10.57 weeks and median OS2 of 25.00 weeks (

conclusionRelative to the FOLFIRI regimen, the FOLFIRINOX regimen had a favorable toxicity profile and better survival outcomes. No significant differences were observed relative to the FOLFOX-6 regimen.

Indexed as

FOLFIRINOXgemcitabinepancreatic adenocarcinomasafetysecond line

Identifiers

PMID33062062
PMCPMC7533956
OpenAlexW3091097272

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.