Evidence map›Paper›PMID 37621684›Full record

ArticleFrontiers in oncology2023

LM02 trial Perioperative treatment with panitumumab and FOLFIRI in patients with wild-type RAS, potentially resectable colorectal cancer liver metastases-a phase II study.

Gudrun Piringer, Thomas Gruenberger, Josef Thaler, Irene Kührer, Klaus Kaczirek, Friedrich Längle, Istvan Viragos-Toth, Arno Amann, Wolfgang Eisterer, Reinhold Függer and 6 more

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Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 57% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

16 authors at 11 institutions in 1 country.

Gudrun PiringerDepartment of Internal Medicine IV, Klinikum Wels-Grieskirchen, Wels, Austria.
Thomas GruenbergerDepartment of Surgery, Clinic Favoriten, Hepato-Pancreato-Biliary Center, Health Network Vienna and Sigmund Freud University, Vienna, Austria.
Josef ThalerDepartment of Internal Medicine IV, Klinikum Wels-Grieskirchen, Wels, Austria.
Irene KührerDivision of General Surgery, Department of Surgery, Medical University of Vienna, Vienna, Austria.
Klaus KaczirekDivision of General Surgery, Department of Surgery, Medical University of Vienna, Vienna, Austria.
Friedrich LängleDepartment of Surgery, Landesklinikum Wiener Neustadt, Wiener Neustadt, Austria.
Istvan Viragos-TothDepartment of Surgery, Landesklinikum Wiener Neustadt, Wiener Neustadt, Austria.
Arno AmannDepartment of Haematology and Oncology, Medical University of Innsbruck, Innsbruck, Austria.
Wolfgang EistererDepartment of Internal Medicine and Oncology, Klinikum Klagenfurt, Klagenfurt, Austria.
Reinhold FüggerDepartment of General and Visceral Surgery, Congregation Hospital, Linz, Austria.
Johannes AndelDepartment of Internal Medicine II, Landeskrankenhaus Steyr, Steyr, Austria.
Angelika PichlerDepartment of Hematology and Oncology, Landeskrankenhaus Hochsteiermark, Leoben, Austria.
Judith StiftDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Lidija SölknerDepartment of Statistics, Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria.
Michael GnantComprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Dietmar ÖfnerDepartment of Visceral-, Transplant- and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
Medical University of Vienna · ATFachhochschule Wiener Neustadt · ATInnsbruck Medical University · ATJohannes Kepler University of Linz · ATComprehensive Cancer Center Vienna · ATKlinikum Klagenfurt · ATLandeskrankenhaus Feldkirch · ATLKH Hochsteiermark · ATSigmund Freud Privatuniversität Wien · ATStatistics Austria · ATWomen's General Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Twenty percent of colorectal cancer liver metastases (CLMs) are initially resectable with a 5-year survival rate of 25%-40%. Perioperative folinic acid, 5-fluorouracil, oxaliplatin (FOLFOX) increases progression-free survival (PFS). In advanced disease, the addition of targeting therapies results in an overall survival (OS) advantage. The aim of this study was to evaluate panitumumab and FOLFIRI as perioperative therapy in resectable CLM. Methods: Patients with previously untreated, wild-type Rat sarcoma virus (RAS), and resectable CLM were included. Preoperative four and postoperative eight cycles of panitumumab and folinic acid, 5-fluorouracil, irinotecan (FOLFIRI) were administered. Primary objectives were efficacy and safety. Secondary endpoints included PFS and OS. Results: We enrolled 36 patients in seven centers in Austria (intention-to-treat analyses, 35 patients). There were 28 men and seven women, and the median age was 66 years. About 91.4% completed preoperative therapy and 82.9% underwent liver resection. The R0 resection rate was 82.7%. Twenty patients started and 12 patients completed postoperative chemotherapy. The objective radiological response rate after preoperative therapy was 65.7%. About 20% and 5.7% of patients had stable disease and progressive disease, respectively. The most common grade 3 adverse events were diarrhea, rash, and leukopenia during preoperative therapy. One patient died because of sepsis, and one had a pulmonary embolism grade 4. After surgery, two patients died because of hepatic failure. Most common grade 3 adverse events during postoperative therapy were skin toxicities/rash and leukopenia/neutropenia, and the two grade 4 adverse events were stroke and intestinal obstruction. Median PFS was 13.2 months. The OS rate at 12 and 24 months were 85.6% and 73.3%, respectively. Conclusions: Panitumumab and FOLFIRI as perioperative therapy for resectable CLM result in a radiological objective response rate in 65.7% of patients with a manageable grade 3 diarrhea rate of 14.3%. Median PFS was 13.2 months, and the 24-month OS rate was 73.3%. These data are insufficient to widen the indication of panitumumab from the unresectable setting to the setting of resectable CLM.

Indexed as

anti-EGFR-therapyCRLMLM02-trialpanitumumab-FOLFIRIperioperative therapy

Identifiers

PMID37621684
PMCPMC10446765
OpenAlexW4385704921

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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.