Evidence map›Paper›PMID 29082359›Full record

ArticleJCO precision oncology2017

Initiative for Molecular Profiling and Advanced Cancer Therapy (IMPACT): An MD Anderson Precision Medicine Study.

Apostolia-Maria Tsimberidou, David S Hong, Yang Ye, Carrie Cartwright, Jennifer J Wheler, Gerald S Falchook, Aung Naing, Siqing Fu, Sarina Piha-Paul, Filip Janku and 8 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 3 pooled it
5.5field-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

108 citing papers in PubMed, 3 syntheses or guidelines pooled it, 160 citations in OpenAlex.

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48 more citing papers are in PubMed but not listed here.

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

18 authors at 1 institution in 1 country.

Apostolia-Maria TsimberidouThe University of Texas MD Anderson Cancer Center, Houston, TX.
David S HongThe University of Texas MD Anderson Cancer Center, Houston, TX.
Yang YeThe University of Texas MD Anderson Cancer Center, Houston, TX.
Carrie CartwrightThe University of Texas MD Anderson Cancer Center, Houston, TX.
Jennifer J WhelerThe University of Texas MD Anderson Cancer Center, Houston, TX.
Gerald S FalchookThe University of Texas MD Anderson Cancer Center, Houston, TX.
Aung NaingThe University of Texas MD Anderson Cancer Center, Houston, TX.
Siqing FuThe University of Texas MD Anderson Cancer Center, Houston, TX.
Sarina Piha-PaulThe University of Texas MD Anderson Cancer Center, Houston, TX.
Filip JankuThe University of Texas MD Anderson Cancer Center, Houston, TX.
Funda Meric-BernstamThe University of Texas MD Anderson Cancer Center, Houston, TX.
Patrick HwuThe University of Texas MD Anderson Cancer Center, Houston, TX.
Bryan KeeThe University of Texas MD Anderson Cancer Center, Houston, TX.
Merrill S KiesThe University of Texas MD Anderson Cancer Center, Houston, TX.
Russell BroaddusThe University of Texas MD Anderson Cancer Center, Houston, TX.
John MendelsohnThe University of Texas MD Anderson Cancer Center, Houston, TX.
Kenneth R HessThe University of Texas MD Anderson Cancer Center, Houston, TX.
Razelle KurzrockRazelle Kurzrock, University of California, San Diego, San Diego, CA.
Carrier (United States) · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposeGenomic profiling is increasingly used in the management of cancer. We have previously reported preliminary results of our precision medicine program. Here, we present response and survival outcomes for 637 additional patients who were referred for phase I trials and were treated with matched targeted therapy (MTT) when available. PATIENTS AND

methodsPatients with advanced cancer who underwent tumor genomic analyses were treated with MTT when available.

resultsOverall, 1,179 (82.1%) of 1,436 patients had one or more alterations (median age, 59.7 years; men, 41.2%); 637 had one or more actionable aberrations and were treated with MTT (n = 390) or non-MTT (n = 247). Patients who were treated with MTT had higher rates of complete and partial response (11%

conclusionOur results support the use of genomic matching. Subset analyses indicate that matching patients who harbor a PI3K and mitogen-activated protein kinase pathway alteration to only a PI3K pathway inhibitor does not improve outcome. We have initiated IMPACT2, a randomized trial to compare treatment with and without genomic selection.

Identifiers

PMID29082359
PMCPMC5659750
OpenAlexW2700576167

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.