Evidence map›Paper›PMID 27752361›Full record

ArticleCell death discovery

Immune-modulating effects of bevacizumab in metastatic non-small-cell lung cancer patients.

E C Martino, G Misso, P Pastina, S Costantini, F Vanni, C Gandolfo, C Botta, F Capone, A Lombardi, L Pirtoli and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
3.3field-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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
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  5. JCO precision oncology · 2026
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8 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

E C MartinoRadiotherapy Unit, Department of Oncology, Siena University Hospital , Siena, Italy.
G MissoDepartment of Biochemistry, Biophysics and General Pathology, Second Naples University , Naples, Italy.
P PastinaRadiotherapy Unit, Department of Oncology, Siena University Hospital , Siena, Italy.
S CostantiniCROM, Mercogliano , Italy.
F VanniRadiotherapy Unit, Department of Oncology, Siena University Hospital , Siena, Italy.
C GandolfoMicrobiology and Virology Unit, Department of Medical Biotechnology , Siena, Italy.
C BottaMedical Oncology Unit, 'Magna Graecia' University and AUO 'Materdomini' , Catanzaro, Italy.
F CaponeCROM, Mercogliano , Italy.
A LombardiDepartment of Biochemistry, Biophysics and General Pathology, Second Naples University , Naples, Italy.
L PirtoliRadiotherapy Unit, Department of Oncology, Siena University Hospital , Siena, Italy.
P TassoneMedical Oncology Unit, 'Magna Graecia' University and AUO 'Materdomini' , Catanzaro, Italy.
C UlivieriDepartment of Science of Life; University of Siena , Siena, Italy.
P TagliaferriMedical Oncology Unit, 'Magna Graecia' University and AUO 'Materdomini' , Catanzaro, Italy.
M G CusiMicrobiology and Virology Unit, Department of Medical Biotechnology , Siena, Italy.
M CaragliaDepartment of Biochemistry, Biophysics and General Pathology, Second Naples University , Naples, Italy.
P CorrealeRadiotherapy Unit, Department of Oncology, Siena University Hospital , Siena, Italy.
University of Siena · ITMagna Graecia University · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mPEBev is an anticancer regimen which combines a chemotherapy doublet, based on cisplatin and oral etoposide (mPE), with bevacizumab (mPEBev), a mAb targeting the vasculo-endothelial growth factor (VEGF). In previous studies, this regimen showed powerful anti-angiogenetic effects and significant antitumor activity in metastatic non-small-cell lung cancer (mNSCLC) patients. We also recorded the best benefit in patients exhibiting low-systemic inflammatory profile at baseline. On these bases, we hypothesized that mPEBev antitumor activity could be partially related to bevacizumab-associated immunological effects. For this reason, we performed an immunological monitoring in 59 out of 120 stage IIIb-IV NSCLC patients enrolled in the BEVA2007 phase II trial, who received fractioned cisplatin (30 mg/sqm days 1-3q21) and oral etoposide (50 mg, days 1-15q21) (mPE doublet) ±bevacizumab. In this group of patients, 12 received the mPE doublet alone and 47 the doublet in combination with bevacizumab (5 mg/kg on the day 3q21; mPEBev regimen). Blood cell counts, serum analysis, multiplex cytokine assay and immunocytofluorimetric analysis, performed on baseline and post-treatment on blood samples from these patients, revealed that bevacizumab addition to the doublet decreased levels of pro-angiogenic (VEGF, Angiostatin-1 and Follistatin) and inflammatory cytokines (interferon (IFN)γ, IL4 and IL17), improved

Identifiers

PMID27752361
PMCPMC5045963
OpenAlexW2528647848

What OpenQuestion holds

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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.