Evidence map›Paper›PMID 20626396›Full record

Trial reportThe breast journal

Trastuzumab in Primary Inflammatory Breast Cancer (IBC): High Pathological Response Rates and Improved Outcome.

Shaheenah Dawood, Yun Gong, Kristine Broglio, Thomas A Buchholz, Wendy Woodward, Anthony Lucci, Vicente Valero, Ana M Gonzalez-Angulo, Gabriel N Hortobagyi, Massimo Cristofanilli

Abstract readClinical Trial
In one paragraph

Trial report in The breast journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Inflammatory Breast Cancer: a Separate Entity.Current oncology reports · 2019
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
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

10 authors at 3 institutions in 2 countries.

Shaheenah DawoodDepartment of Breast Medical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, Texas; Deparment of Medical Oncology, Dubai Hospital, Dubai, UAE.
Yun Gong
Kristine Broglio
Thomas A Buchholz
Wendy Woodward
Anthony Lucci
Vicente Valero
Ana M Gonzalez-Angulo
Gabriel N Hortobagyi
Massimo Cristofanilli
Dubai Hospital · AEQuantitative BioSciences · USThe University of Texas MD Anderson Cancer Center · US

Funding

CTSA: K12 COMPONENTKL2RR024149 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2011
$6.7M
NCRR NIH HHS KL2 RR024149
6 · The paper itself

Abstract

Inflammatory breast cancer (IBC) represents a rare but aggressive and lethal form of locally advanced breast cancer (LABC) and frequently with HER-2 neu overexpressed or amplified. We retrospectively identified 16 newly diagnosed HER-2 ⁄ neu-positive IBC patients who were treated with preoperative trastuzumab. We determined the pathological complete response rate (pCR) when trastuzumab was added to preoperative chemotherapy in patients with HER2⁄ neupositive IBC. Furthermore, we assessed the expression of CXCR4 in metastatic recurrence sites. Ten patients (62.5%)achieved a pCR. Six patients (37.5%) achieved a partial response. Median follow-up of all patients was 24.2 months. Four(25%) patients have experienced a progression, of which three were in the brain. Two-year progression-free survival was 59.4% (95% CI 35–100). High expression of CXCR4 was detected in the brain metastases. We conclude that in spite of high pCR rates among women with HER-2 ⁄ neu-positive IBC treated with neoadjuvant trastuzumab-based regimens the outcome remains dismal and brain recurrences are frequent. CXCR4 may represent a novel therapeutic target.

Indexed as

AdultAntineoplastic Combined Chemotherapy ProtocolsDisease-Free SurvivalDrug Administration ScheduleErb-b2 Receptor Tyrosine KinasesFemaleHumansInflammatory Breast NeoplasmsMiddle AgedNeoadjuvant TherapyReceptors, CXCR4TrastuzumabTreatment OutcomeCXCR4 protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, CXCR4Trastuzumab

Identifiers

PMID20626396
PMCPMC3097300
OpenAlexW1899019513

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.