Evidence map›Paper›PMID 8912545›Full record

Trial reportBritish journal of cancer1996

Primary chemotherapy in breast invasive carcinoma: predictive value of the immunohistochemical detection of hormonal receptors, p53, c-erbB-2, MiB1, pS2 and GST pi.

G MacGrogan, L Mauriac, M Durand, F Bonichon, M Trojani, I de Mascarel, J M Coindre

Registry-linked trialOpen access · bronzeAbstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in British journal of cancer, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00005908 (A Pilot Trial of Sequential Primary), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.6field-weighted citation impact, top 5% 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.

NCT00005908 phase2completednot on this mapstarted 2000, after this paper: background citation

A Pilot Trial of Sequential Primary (Neoadjuvant) Combination Chemotherapy With Docetaxel/Capecitabine (TX) and Doxorubicin/Cyclophosphamide (AC) in Primary Breast Cancer With Evaluation of Chemotherapy Effects on Gene Expression

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2000 to 2008Enrolled30ConditionsBreast Cancer, Breast NeoplasmArmsDocetaxel - Dose A, Anastrozole, cyclophosphamide, Docetaxel - Dose B, Doxorubicin hydrochloride
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 193 citations in OpenAlex.

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  14. Prognostic value of proliferation markers expression in breast cancer.Medical oncology (Northwood, London, England) · 2013
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  15. Article
  16. Review
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  18. Ki-67 biomarker in breast cancer of Indian women.North American journal of medical sciences · 2011
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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

7 authors at 1 institution in 1 country.

G MacGroganInstitut Bergonié, Comprehensive Cancer Center, Bordeaux, France.
L Mauriac
M Durand
F Bonichon
M Trojani
I de Mascarel
J M Coindre
Institut Bergonié · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary chemotherapy in operable breast invasive carcinoma enables tumour reduction and conservative surgery. In order to search for one or more biological factors capable of predicting tumour behaviour under primary chemotherapy, and subsequent patient survival, an immunohistochemical study was performed with specific antibodies to p53, c-erbB-2 (Her-2/neu), Mib1 (antiKi-67), pS2, GST pi, oestrogen receptors (ERs) and progesterone receptors (PRs). Core biopsies, obtained before primary chemotherapy, were available from a series of 128 breast invasive carcinomas treated between January 1985 and April 1989, with a median follow-up of 93.3 months. Univariate statistical analysis showed that negative ER detection by immunohistochemistry (IHC) was highly correlated with chemosensitivity (P = 0.001). A high percentage of Mib1-positive tumour cells (> 40%), as well as initial tumour size less than 4 cm, were also correlated with tumour responsiveness to chemotherapy (P = 0.009 and P = 0.03). By multivariate analysis IHC-ER, Mib1 and initial tumour size were independent predictors, the last parameter being the most important. Concerning subsequent patient survival, c-erbB-2 overexpression, as detected by IHC, was significant with respect to overall survival (OS) (P = 0.0006), disease-free interval (DFI) (P = 0.03) and metastasis-free interval (MFI) (P = 0.008) by univariate analysis. Furthermore, c-erbB-2 was the major independent prognostic factor for OS and MFI by multivariate analysis.

Indexed as

ProteinsAdultAgedAntibodies, NeoplasmAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBreast NeoplasmsEpirubicinErb-b2 Receptor Tyrosine KinasesFemaleGlutathione TransferaseHumansImmunohistochemistryMethotrexateMiddle AgedMitomycinAntibodies, NeoplasmBiomarkers, TumorEpirubicinErb-b2 Receptor Tyrosine KinasesGlutathione TransferaseMethotrexateMitomycinNeoplasm ProteinsProteinsReceptors, EstrogenReceptors, ProgesteroneTFF1 protein, humanThiotepaTrefoil Factor-1Tumor Suppressor Protein p53Tumor Suppressor ProteinsVincristineVindesine

Identifiers

PMID8912545
PMCPMC2074756
OpenAlexW2062421538

What OpenQuestion holds

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Registered trials

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.