Evidence map›Paper›PMID 27042835›Full record

ArticleBone marrow transplantation2016

Highly favorable outcome in BRCA-mutated metastatic breast cancer patients receiving high-dose chemotherapy and autologous hematopoietic stem cell transplantation.

L Boudin, A Gonçalves, R Sabatier, J Moretta, P Sfumato, P Asseeva, D Livon, F Bertucci, J-M Extra, C Tarpin and 12 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Cytotoxic and targeted therapy for BRCA1/2-driven cancers.Hereditary cancer in clinical practice · 2021
    Review
  3. Review
  4. Review
  5. TargetingCancers · 2018
    Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

L BoudinDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.
A GonçalvesDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.
R SabatierDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.ORCID 0000-0002-5821-682X
J MorettaDépartement d'Anticipation et de Suivi du Cancer, Institut Paoli-Calmettes, Marseille, France.
P SfumatoBiostatistiques, Département de la Recherche Clinique et de l'Innovation (DRCI), Institut Paoli-Calmettes, Marseille, France.
P AsseevaDépartement d'Anticipation et de Suivi du Cancer, Institut Paoli-Calmettes, Marseille, France.
D LivonDépartement d'Anticipation et de Suivi du Cancer, Institut Paoli-Calmettes, Marseille, France.
F BertucciDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.
J-M ExtraDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.
C TarpinDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.
G HouvenaeghelCentre de Recherches en Cancérologie de Marseille (CRCM), Marseille, France.
E LambaudieCentre de Recherches en Cancérologie de Marseille (CRCM), Marseille, France.
A TalletDépartement de Radiothérapie, Institut Paoli-Calmettes, Marseille, France.
M ResbeutDépartement de Radiothérapie, Institut Paoli-Calmettes, Marseille, France.
H SobolAix-Marseille Université, Marseille, France.
E Charafe-JauffretCentre de Recherches en Cancérologie de Marseille (CRCM), Marseille, France.
B CalmelsCentre de Recherches en Cancérologie de Marseille (CRCM), Marseille, France.
C LemarieCentre de Thérapie Cellulaire, Département de Biologie du Cancer, Institut Paoli-Calmettes, Marseille, France.
J-M BoherBiostatistiques, Département de la Recherche Clinique et de l'Innovation (DRCI), Institut Paoli-Calmettes, Marseille, France.
P ViensDépartement d'Oncologie Médicale, Institut Paoli-Calmettes (IPC), Marseille, France.
F EisingerCentre de Recherches en Cancérologie de Marseille (CRCM), Marseille, France.
C ChabannonCentre de Recherches en Cancérologie de Marseille (CRCM), Marseille, France.ORCID 0000-0002-3755-4889

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer carrying BRCA mutation may be highly sensitive to DNA-damaging agents. We hypothesized a better outcome for BRCA-mutated (BRCA(mut)) metastatic breast cancer (MBC) patients receiving high-dose chemotherapy and autologous hematopoietic stem cell transplantation (HDC AHSCT) versus unaffected BRCA (BRCA wild type; (BRCA(wt))) or patients without documented BRCA mutation (BRCA untested (BRCA(ut))). All female patients treated for MBC with AHSCT at Institut Paoli-Calmettes between 2003 and 2012 were included. BRCA(mut) and BRCA(wt) patients were identified from our institutional genetic database. Overall survival (OS) was the primary end point. A total of 235 patients were included. In all, 15 patients were BRCA(mut), 62 BRCA(wt) and 149 BRCA(ut). In multivariate analyses, the BRCA(mut) status was an independent prognostic factor for OS (hazard ratio (HR): 3.08, 95% confidence interval (CI): 1.10-8.64, P=0.0326) and PFS (HR: 2.52, 95% CI :1.29-4.91, P=0.0069). In this large series of MBC receiving HDC AHSCT, we report a highly favorable survival outcome in the subset of patients with documented germline BRCA mutations.

Indexed as

AdultAntineoplastic AgentsBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCombined Modality TherapyFemaleHematopoietic Stem Cell TransplantationHumansMutationNeoplasm MetastasisRetrospective StudiesSurvival AnalysisTreatment OutcomeAntineoplastic AgentsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID27042835

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.