Evidence map›Paper›PMID 21252716›Full record

SynthesisJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2011

International association for the study of lung cancer/american thoracic society/european respiratory society international multidisciplinary classification of lung adenocarcinoma.

William D Travis, Elisabeth Brambilla, Masayuki Noguchi, Andrew G Nicholson, Kim R Geisinger, Yasushi Yatabe, David G Beer, Charles A Powell, Gregory J Riely, Paul E Van Schil and 38 more

2 registry-linked trialsOpen access · bronzeAbstract readSystematic Review
In one paragraph

Synthesis in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 2,136 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2,136citing papers in PubMed, 4 pooled it
320.4field-weighted citation impact, top 1% 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.

NCT02853006 nacompletednot on this mapstarted 2015, after this paper: background citation

Study on Fluids Associated to Lung Cancer, of the Ectopic Expression of Cancer Testis Gene and Mutation as Diagnostics and Prognosis Biomarkers

TypeinterventionalSponsorUniversity Hospital, GrenobleRan2015 to 2020Enrolled31ConditionsLung CancerArmsBlood and respiratory fluids sampling, Biopsy, Excised tissues
NCT05816499 phase1 / phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

A Phase Ib/II Trial of Cadonilimab (PD-1/CTLA-4 Bispecific Antibody) in Combination With Anlotinib and Docetaxel in Patients (Pts) With Checkpoint Inhibitor (CPI)-Experienced Advanced Non-small Cell Lung Cancer (NSCLC)

TypeinterventionalSponsorShanghai Chest HospitalRan2023 to 2025Enrolled50ConditionsNSCLC Stage IV, NSCLC Stage IIIB, NSCLC Stage IIICArmsCadonilimab, Anlotinib, Docetaxel
3 · Its place in the literature

Who cites it

2,136 citing papers in PubMed, 4 syntheses or guidelines pooled it, 4,802 citations in OpenAlex.

  1. Recent advances in diagnostic and therapeutic approaches for pulmonary enteric adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  7. Dielectric properties, thermal properties, blood perfusion rate: which biophysical parameter is the leading source of variability of microwave ablation models in lung?International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2026
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2,076 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

48 authors at 17 institutions in 9 countries.

William D TravisDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. travisw@mskcc.org
Elisabeth Brambilla
Masayuki Noguchi
Andrew G Nicholson
Kim R Geisinger
Yasushi Yatabe
David G Beer
Charles A Powell
Gregory J Riely
Paul E Van Schil
Kavita Garg
John H M Austin
Hisao Asamura
Valerie W Rusch
Fred R Hirsch
Giorgio Scagliotti
Tetsuya Mitsudomi
Rudolf M Huber
Yuichi Ishikawa
James Jett
Montserrat Sanchez-Cespedes
Jean-Paul Sculier
Takashi Takahashi
Masahiro Tsuboi
Johan Vansteenkiste
Ignacio Wistuba
Pan-Chyr Yang
Denise Aberle
Christian Brambilla
Douglas Flieder
Wilbur Franklin
Adi Gazdar
Michael Gould
Philip Hasleton
Douglas Henderson
Bruce Johnson
David Johnson
Keith Kerr
Keiko Kuriyama
Jin Soo Lee
Vincent A Miller
Iver Petersen
Victor Roggli
Rafael Rosell
Nagahiro Saijo
Erik Thunnissen
Ming Tsao
David Yankelevitz
Thoracic Surgery Foundation · USAichi Cancer Center · JPClinica de Pneumologie Iaşi · ROColumbia University · USFlinders Medical Centre · AUGenesis Foundation · USHarvard University · USInserm · FRInstitut d'Investigació Biomédica de Bellvitge · ESMemorial Sloan Kettering Cancer Center · USNational Cancer Center · KRPulmonary and Critical Care Associates · USPulmonary Associates · USTaipei Institute of Pathology · TWUniversity of Antwerp · BEUniversity of Colorado Boulder · USUniversity of Michigan–Ann Arbor · US

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V., MINNA, JOHN D. · 1996 to 2024
$57.4M
NCI NIH HHS P50 CA070907
6 · The paper itself

Abstract

introductionAdenocarcinoma is the most common histologic type of lung cancer. To address advances in oncology, molecular biology, pathology, radiology, and surgery of lung adenocarcinoma, an international multidisciplinary classification was sponsored by the International Association for the Study of Lung Cancer, American Thoracic Society, and European Respiratory Society. This new adenocarcinoma classification is needed to provide uniform terminology and diagnostic criteria, especially for bronchioloalveolar carcinoma (BAC), the overall approach to small nonresection cancer specimens, and for multidisciplinary strategic management of tissue for molecular and immunohistochemical studies.

methodsAn international core panel of experts representing all three societies was formed with oncologists/pulmonologists, pathologists, radiologists, molecular biologists, and thoracic surgeons. A systematic review was performed under the guidance of the American Thoracic Society Documents Development and Implementation Committee. The search strategy identified 11,368 citations of which 312 articles met specified eligibility criteria and were retrieved for full text review. A series of meetings were held to discuss the development of the new classification, to develop the recommendations, and to write the current document. Recommendations for key questions were graded by strength and quality of the evidence according to the Grades of Recommendation, Assessment, Development, and Evaluation approach.

resultsThe classification addresses both resection specimens, and small biopsies and cytology. The terms BAC and mixed subtype adenocarcinoma are no longer used. For resection specimens, new concepts are introduced such as adenocarcinoma in situ (AIS) and minimally invasive adenocarcinoma (MIA) for small solitary adenocarcinomas with either pure lepidic growth (AIS) or predominant lepidic growth with ≤ 5 mm invasion (MIA) to define patients who, if they undergo complete resection, will have 100% or near 100% disease-specific survival, respectively. AIS and MIA are usually nonmucinous but rarely may be mucinous. Invasive adenocarcinomas are classified by predominant pattern after using comprehensive histologic subtyping with lepidic (formerly most mixed subtype tumors with nonmucinous BAC), acinar, papillary, and solid patterns; micropapillary is added as a new histologic subtype. Variants include invasive mucinous adenocarcinoma (formerly mucinous BAC), colloid, fetal, and enteric adenocarcinoma. This classification provides guidance for small biopsies and cytology specimens, as approximately 70% of lung cancers are diagnosed in such samples. Non-small cell lung carcinomas (NSCLCs), in patients with advanced-stage disease, are to be classified into more specific types such as adenocarcinoma or squamous cell carcinoma, whenever possible for several reasons: (1) adenocarcinoma or NSCLC not otherwise specified should be tested for epidermal growth factor receptor (EGFR) mutations as the presence of these mutations is predictive of responsiveness to EGFR tyrosine kinase inhibitors, (2) adenocarcinoma histology is a strong predictor for improved outcome with pemetrexed therapy compared with squamous cell carcinoma, and (3) potential life-threatening hemorrhage may occur in patients with squamous cell carcinoma who receive bevacizumab. If the tumor cannot be classified based on light microscopy alone, special studies such as immunohistochemistry and/or mucin stains should be applied to classify the tumor further. Use of the term NSCLC not otherwise specified should be minimized.

conclusionsThis new classification strategy is based on a multidisciplinary approach to diagnosis of lung adenocarcinoma that incorporates clinical, molecular, radiologic, and surgical issues, but it is primarily based on histology. This classification is intended to support clinical practice, and research investigation and clinical trials. As EGFR mutation is a validated predictive marker for response and progression-free survival with EGFR tyrosine kinase inhibitors in advanced lung adenocarcinoma, we recommend that patients with advanced adenocarcinomas be tested for EGFR mutation. This has implications for strategic management of tissue, particularly for small biopsies and cytology samples, to maximize high-quality tissue available for molecular studies. Potential impact for tumor, node, and metastasis staging include adjustment of the size T factor according to only the invasive component (1) pathologically in invasive tumors with lepidic areas or (2) radiologically by measuring the solid component of part-solid nodules.

Indexed as

AdenocarcinomaHumansLung NeoplasmsNeoplasm StagingSocieties, Medical

Identifiers

PMID21252716
PMCPMC4513953
OpenAlexW2049674541

What OpenQuestion holds

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LicenceTDM
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Registered trials

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.