Evidence map›Paper›PMID 33234578›Full record

Trial reportCancer discovery2021

Personalized Antibodies for Gastroesophageal Adenocarcinoma (PANGEA): A Phase II Study Evaluating an Individualized Treatment Strategy for Metastatic Disease.

Daniel V T Catenacci, Stephanie Moya, Samantha Lomnicki, Leah M Chase, Bryan F Peterson, Natalie Reizine, Lindsay Alpert, Namrata Setia, Shu-Yuan Xiao, John Hart and 14 more

Open access · bronzeAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Cancer discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
6.2field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Prognostic implications of tissue-based homologous recombination deficiency in metastatic gastric cancer treated with immune checkpoint inhibitor plus chemotherapy.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2026
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  17. Neoadjuvant Immunotherapy in Gastroesophageal Cancer: A Promising Early Signal?Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
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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

24 authors at 3 institutions in 1 country.

Daniel V T CatenacciThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois. dcatenac@bsd.uchicago.edu.
Stephanie MoyaThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Samantha LomnickiThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Leah M ChaseThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Bryan F PetersonThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Natalie ReizineThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Lindsay AlpertThe University of Chicago, Department of Pathology, Chicago, Illinois.
Namrata SetiaThe University of Chicago, Department of Pathology, Chicago, Illinois.
Shu-Yuan XiaoThe University of Chicago, Department of Pathology, Chicago, Illinois.
John HartThe University of Chicago, Department of Pathology, Chicago, Illinois.
Uzma D SiddiquiThe University of Chicago, Department of Medicine, Center for Endoscopic Research and Therapeutics (CERT), Chicago, Illinois.
D Kyle HogarthThe University of Chicago, Department of Medicine, Section of Pulmonology, Chicago, Illinois.ORCID 0000-0001-8925-7360
Oliver S EngThe University of Chicago, Department of Surgery, Chicago, Illinois.ORCID 0000-0003-0226-5005
Kiran TuragaThe University of Chicago, Department of Surgery, Chicago, Illinois.
Kevin RogginThe University of Chicago, Department of Surgery, Chicago, Illinois.
Mitchell C PosnerThe University of Chicago, Department of Surgery, Chicago, Illinois.
Paul ChangThe University of Chicago, Department of Radiology, Chicago, Illinois.ORCID 0000-0002-9083-1435
Sunil NarulaThe University of Chicago, New Lennox, Illinois.
Murtuza RampurwalaThe University of Chicago, Orland Park, Illinois.
Yuan JiThe University of Chicago, Department of Public Health Sciences, Chicago, Illinois.ORCID 0000-0003-4712-5567
Theodore KarrisonThe University of Chicago, Department of Public Health Sciences, Chicago, Illinois.
Chih-Yi LiaoThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Blase N PoliteThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
Hedy L KindlerThe University of Chicago, Section of Hematology/Oncology, Department of Medicine, Chicago, Illinois.
University of Chicago · USChicago Department of Public Health · USNorth Park University · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
PANGEA: Personalized Antibodies for GastroEsophageal Adenocarcinoma Pilot TrialK23CA178203 · NCI · UNIVERSITY OF CHICAGO · PI CATENACCI, DANIEL · 2014 to 2016
$507k
NCI NIH HHS K23 CA178203NCI NIH HHS P30 CA014599
6 · The paper itself

Abstract

The one-year and median overall survival (mOS) rates of advanced gastroesophageal adenocarcinomas (GEA) are ∼50% and <12 months, respectively. Baseline spatial and temporal molecular heterogeneity of targetable alterations may be a cause of failure of targeted/immunooncologic therapies. This heterogeneity, coupled with infrequent incidence of some biomarkers, has resulted in stalled therapeutic progress. We hypothesized that a personalized treatment strategy, applied at first diagnosis then serially over up to three treatment lines using monoclonal antibodies combined with optimally sequenced chemotherapy, could contend with these hurdles. This was tested using a novel clinical expansion-platform type II design with a survival primary endpoint. Of 68 patients by intention-to-treat, the one-year survival rate was 66% and mOS was 15.7 months, meeting the primary efficacy endpoint (one-sided

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalChicagoEsophageal NeoplasmsFemaleHumansMaleMiddle AgedMolecular Targeted TherapyProgression-Free SurvivalStomach NeoplasmsTreatment OutcomeAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunological

Identifiers

PMID33234578
PMCPMC7858231
OpenAlexW3108411734

What OpenQuestion holds

Textmetadata
LicenceTDM
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.