Evidence map›Paper›PMID 34155351›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

Breast implant-associated anaplastic large cell lymphoma: clinical follow-up and analysis of sequential pathologic specimens of untreated patients shows persistent or progressive disease.

Mark G Evans, L Jeffrey Medeiros, Mario L Marques-Piubelli, Huan-You Wang, Carlos Ortiz-Hidalgo, Sergio Pina-Oviedo, Angela Morine, Mark W Clemens, Kelly K Hunt, Swaminathan Iyer and 13 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Guideline
  2. Programmed Death Ligand 1 (PD-L1) Expression in Lymphomas: State of the Art.International journal of molecular sciences · 2024
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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

23 authors at 13 institutions in 5 countries.

Mark G EvansDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
L Jeffrey MedeirosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-6577-8006
Mario L Marques-PiubelliDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-6324-2096
Huan-You WangUniversity of California San Diego, La Jolla, CA, USA.
Carlos Ortiz-HidalgoDepartamento de Anatomía Patológica, Hospital y Fundación Médica Sur, Ciudad de México, Mexico.
Sergio Pina-OviedoDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Angela MorineCounties Manukau District Health Board, Auckland, New Zealand.
Mark W ClemensDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Kelly K HuntDepartment of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-9156-8723
Swaminathan IyerDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Qinglong HuTucson Pathology Associates, Tucson, AZ, USA.
Claudia RecavarrenLaboratorio Recavarren Emanuel, Clinica Ricardo Palma, Lima, Peru.
Roberta DemichelisInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Martha RomeroPathology Department, Hospital Universitario Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Aliyah R SohaniHarvard Medical School Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-6307-4854
Michael MisialekNewton-Wellesley Hospital, Newton, MA, USA.
Mitual B AminBeaumont Hospital, Royal Oak, MI, USA.
Carlos E Bueso-RamosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Adrian A Carballo-ZarateDepartment of Pathology, Hospital Español de México, Mexico City, Mexico.
Hun J LeeDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Chi Young OkDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-6822-7880
Jie XuDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-9163-3898
Roberto N MirandaDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Roberto.miranda@mdanderson.org.ORCID 0000-0002-8467-5464
The University of Texas MD Anderson Cancer Center · USBeaumont Hospital, Royal Oak · USBrigham and Women's Hospital · USCounties Manukau District Health Board · NZFundación Santa Fe de Bogotá · COHarvard University · USHospital Español · MXHospital Médica Sur · MXInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXNewton Wellesley Hospital · USUniversidad Ricardo Palma · PEUniversity of Arkansas for Medical Sciences · USUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast implant-associated anaplastic large cell lymphoma (ALCL) is a distinctive type of T-cell lymphoma that arises around textured-surface breast implants. In a subset of patients, this disease can involve surrounding tissues, spread to regional lymph nodes, and rarely metastasize to distant sites. The aim of this study was to assess sequential pathologic specimens from patients with breast implant-associated ALCL to better understand the natural history of early-stage disease. To achieve this goal, we searched our files for patients who had breast implant-associated ALCL and who had undergone earlier surgical intervention with assessment of biopsy or cytologic specimens. We then focused on the patient subset in whom a definitive diagnosis was not established, and patients did not receive current standard-of-care therapy at that time. We identified a study group of ten patients with breast implant-associated ALCL in whom pathologic specimens were collected 0.5 to 4 years before a definitive diagnosis was established. A comparison of these serial biopsy specimens showed persistent disease without change in pathologic stage in three patients, progression in five patients, and persistence versus progression in two patients. Eventually, six patients underwent implant removal with complete capsulectomy and four underwent partial capsulectomy. Seven patients also received chemotherapy because of invasive disease, three of whom also received radiation therapy, two brentuximab vedotin after chemotherapy failure, and one allogeneic stem cell transplant. Eight patients achieved complete remission and two had partial remission after definitive therapy. At time of last follow-up, six patients were alive without disease, one had evidence of disease, one died of disease, and two patients died of unrelated cancers. In summary, this analysis of sequential specimens from patients with breast implant-associated ALCL suggests these neoplasms persist or progress over time if not treated with standard-of-care therapy.

Indexed as

BiopsyBreast ImplantationBreast ImplantsDisease ProgressionFemaleHumansLymphoma, Large-Cell, AnaplasticMiddle AgedPredictive Value of TestsProsthesis DesignRemission InductionRetrospective StudiesRisk FactorsSurface PropertiesTime FactorsTreatment Outcome

Identifiers

PMID34155351
OpenAlexW3175116291

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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.