Evidence map›Paper›PMID 31368078›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2020

Treatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensus.

D Isla, J de Castro, R García-Campelo, P Lianes, E Felip, P Garrido, L Paz-Ares, J M Trigo

Open access · hybridAbstract readConsensus Statement
PubMed Publisher
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 23 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

8 authors at 8 institutions in 1 country.

D IslaMedical Oncology Department, University Hospital Lozano Blesa, Avda. San Juan Bosco, 15, 50009, Zaragoza, Spain. lola.isla@gmail.com.ORCID http://orcid.org/0000-0002-2483-198X
J de CastroMedical Oncology Department, Hospital Universitario La Paz-IDIPAZ, Madrid, Spain.ORCID http://orcid.org/0000-0002-3622-6306
R García-CampeloMedical Oncology Department, Complexo Hospitalario Universitario A Coruña, Coruña, Spain.
P LianesMedical Oncology Department, Hospital de Mataró, Mataró, Spain.ORCID http://orcid.org/0000-0002-4976-9246
E FelipOncology Department, Vall d'Hebron University, Vall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID http://orcid.org/0000-0002-7620-0098
P GarridoMedical Oncology Department, Ramón y Cajal University Hospital, Madrid, Spain.ORCID http://orcid.org/0000-0002-5899-6125
L Paz-AresDepartment of Medical Oncology, Hospital Universitario 12 de Octubre, H12o-CNIO Lung Cancer Unit, Universidad Complutense and Ciberonc, Madrid, Spain.ORCID http://orcid.org/0000-0002-1947-3364
J M TrigoMedical Oncology Department, Hospital Universitario Virgen de la Victoria, IBIMA, Málaga, Spain.
Complexo Hospitalario Universitario A Coruña · ESHospital Clínico Universitario Lozano Blesa · ESHospital Clínico Universitario Virgen de la Victoria · ESHospital de Mataró · ESHospital Universitario 12 De Octubre · ESHospital Universitario La Paz · ESInstituto Cajal · ESVall d'Hebron Institute of Oncology · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmunotherapy-based approaches are standard first-line treatments for advanced/metastatic lung cancer or for chemoradiotherapy consolidation in locally advanced disease. Uncertainty on how to treat patients at disease progression prompted us to develop a consensus document on post-immunotherapy options in Spain for patients with advanced wild-type lung adenocarcinoma.

methodsAfter extensive literature review, a 5-member scientific committee generated 33 statements in 4 domains: general aspects (n = 4); post-durvalumab in locally advanced disease (n = 6); post-first-line immunotherapy ± chemotherapy in advanced/metastatic disease (n = 11); and post-first-line platinum-based chemotherapy in advanced/metastatic disease (n = 12). A panel of 26 lung cancer experts completed 2 Delphi iterations through an online platform rating their degree of agreement/disagreement (first-round scale 1-5 and second-round scale 1-4, 1 = strongly disagree, 4/5 = strongly agree) for each statement. Second-round consensus: ≥ 70% of responses were in categories 1/2 (disagreement) or 3/4 (agreement).

resultsConsensus was reached for 2/33 statements in the first Delphi round and in 29/31 statements in the second round. Important variables informing treatment at disease progression with an immunotherapy-based treatment include: disease aggressiveness, previous treatment, accumulated toxicity, progression-free interval, PD-L1 expression, and tumour mutational burden. A platinum-based chemotherapy should follow a first-line immunotherapy treatment without chemotherapy. Treatment with docetaxel + nintedanib may be appropriate post-durvalumab in refractory patients or following progression to first-line chemotherapy + immunotherapy, or second-line chemotherapy after first-line immunotherapy, or first-line chemotherapy in some patients with low/negative PD-L1 expression, or second-line immunotherapy after first-line chemotherapy.

conclusionsTo support decision making following progression to immunotherapy-based treatment in patients with advanced wild-type lung adenocarcinoma, a consensus document has been developed.

Indexed as

Adenocarcinoma of LungAntineoplastic Combined Chemotherapy ProtocolsImmunotherapyLung NeoplasmsAntibodies, MonoclonalB7-H1 AntigenClinical Decision-MakingDelphi TechniqueDisease ProgressionDocetaxelHumansIndolesMutationSpainAntibodies, MonoclonalB7-H1 AntigenCD274 protein, humanDocetaxeldurvalumabIndolesnintedanibAccumulated toxicityChemotherapyDelphi consensusDisease aggressivenessImmunotherapyLung adenocarcinomaNintedanibPD-L1 expressionPrior treatmentProgression-free intervalTreatment decisionsTumour mutational burden

Identifiers

PMID31368078
OpenAlexW2966144876

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.