Evidence map›Paper›PMID 36493333›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2023

Molecular Classification of Appendiceal Adenocarcinoma.

Michael B Foote, Henry Walch, Walid Chatila, Efsevia Vakiani, Chris Chandler, Felix Steinruecke, Garrett M Nash, Zsofia Stadler, Sebastian Chung, Rona Yaeger and 12 more

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
11.1field-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.

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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Guideline
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  10. KRAS inhibition is an effective therapy for appendiceal adenocarcinoma.bioRxiv : the preprint server for biology · 2026
    Article
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  16. KRAS/ABHD17C/ALOX15B Axis Promotes Pancreatic Cancer Progression via Ferroptosis Evasion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 2 institutions in 2 countries.

Michael B FooteDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-3027-2405
Henry WalchHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1188-350X
Walid ChatilaHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-5474-218X
Efsevia VakianiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Chris ChandlerDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
Felix SteinrueckeDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-4597-8232
Garrett M NashDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
Zsofia StadlerDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-6985-2864
Sebastian ChungDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-5165-4360
Rona YaegerDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-7233-5454
Maria Ignez BraghrioliDivision of Medical Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.ORCID 0000-0001-6366-8786
Jinru ShiaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-4351-2511
Yelena KemelNiehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-5042-5651
Anna MaioNiehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
Margaret SheehanNiehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
Benoit RousseauDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1594-4827
Guillem ArgilésDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1487-7108
Michael BergerHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-3882-5000
David SolitHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-6614-802X
Nikolaus SchultzHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-0131-4904
Luis A DiazDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-7079-8914
Andrea CercekDivision of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-5054-8192
Memorial Sloan Kettering Cancer Center · USInstituto do Câncer do Estado de São Paulo · BR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
CLINICAL SCHOLARS BIOMEDICAL RESEARCH TRAINING PROGRAMT32CA009512 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Ping Chi · 1985 to 2026
$6.3M
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA009512
6 · The paper itself

Abstract

purposeAppendiceal adenocarcinomas (ACs) are rare, histologically diverse malignancies treated as colorectal cancers despite having distinct biology and clinical behavior. To guide clinical decision making, we defined molecular subtypes of AC associated with patient survival, metastatic burden, and chemotherapy response. PATIENTS AND

methodsA comprehensive molecular analysis was performed in patients with AC to define molecular subtypes. Associations between molecular subtype and overall survival, intraoperative peritoneal cancer index, and first-line chemotherapy response were assessed adjusting for histopathologic and clinical variables using multivariable Cox proportional hazards, linear regression, and logistic regression models.

resultsWe defined distinct molecular lineages of mucinous appendiceal adenocarcinoma (MAAP) from co-occurring mutations in

conclusionAC molecular patterns identify distinct molecular subtypes: a clinically indolent RAS-mut/GNAS-wt/TP53-wt subtype; a chemotherapy-resistant GNAS-mut predominant subtype; and an aggressive, highly aneuploid TP53-mut predominant subtype. Each subtype exhibits conserved clinical behavior irrespective of histopathology.

Indexed as

AdenocarcinomaAdenocarcinoma, MucinousAppendiceal NeoplasmsPeritoneal NeoplasmsHumansMutation

Identifiers

PMID36493333
PMCPMC10043565
OpenAlexW4311027359

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.