Evidence map›Paper›PMID 29893790›Full record

Trial reportAnnals of oncology : official journal of the European Society for Medical Oncology2018

Palbociclib as single agent or in combination with the endocrine therapy received before disease progression for estrogen receptor-positive, HER2-negative metastatic breast cancer: TREnd trial.

L Malorni, G Curigliano, A M Minisini, S Cinieri, C A Tondini, K D'Hollander, G Arpino, A Bernardo, A Martignetti, C Criscitiello and 12 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Annals of oncology : official journal of the European Society for Medical Oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02549430 (Phase 2,Open-label,Multicenter,Randomized Study of PD0332991), which is not on this map. Cited by 59 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 3 pooled it
14.3field-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.

NCT02549430 phase2completednot on this map

Phase 2,Open-label,Multicenter,Randomized Study of PD0332991 (Oral CDK4/6 Inhibitor) Monotherapy and in Combination With the HT to Which the pt Has Progressed in the Previous Line for ER+,Her2- Post-menopausal Advanced Breast Cancer Pts

TypeinterventionalSponsorFondazione Sandro PitiglianiRan2012 to 2017Enrolled115ConditionsBreast CancerArmsPalbociclib, Anastrozole, Letrozole, Exemestane, Fulvestrant
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 3 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
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  11. CDK4/6 Inhibitor Resistance in ER+ Breast Cancer.Advances in experimental medicine and biology · 2025
    Review
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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

22 authors at 12 institutions in 3 countries.

L Malorni"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy. Electronic address: luca.malorni@uslcentro.toscana.it.
G CuriglianoDivision of Early Drug Development, Department of Haematology and Haemato-Oncology, Istituto Europeo di Oncologia, University of Milan, Milan, Italy.
A M MinisiniDepartment of Oncology, Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy.
S CinieriMedical Oncology Department, ASL Brindisi, Brindisi, Italy.
C A TondiniHospital Papa Giovanni XXIII, Bergamo, Italy.
K D'HollanderInternational Drug Development Institute, Louvain-La-Neuve, Belgium.
G ArpinoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples.
A BernardoMedical Oncology Department, ICS Maugeri IRCCS, Pavia, Italy.
A MartignettiOncology Department, Azienda USL Toscana Sud Est, Hospital Alta Val D'Elsa, Poggibonsi Siena, Italy.
C CriscitielloDivision of Early Drug Development, Istituto Europeo di Oncologia, Milan, Italy.
F PuglisiMedical Oncology and Cancer Prevention Unit, IRCCS, CRO National Cancer Institute, Aviano; Department of Medicine, University of Udine, Udine, Italy.
M Pestrin"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
G Sanna"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
E Moretti"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
E Risi"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
C Biagioni"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
A McCartney"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
L BoniClinical Trial Coordinating Center, AOU Careggi, Istituto Toscano Tumori, Florence, Italy.
M BuyseInternational Drug Development Institute, San Francisco, USA.
I Migliaccio"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
L Biganzoli"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
A Di Leo"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
Hospital of Prato · ITAzienda Usl Toscana Centro · ITEuropean Institute of Oncology · ITInternational Drug Development Institute (Belgium) · BEIstituti Clinici Scientifici Maugeri · ITOspedale A. Perrino · ITOspedale Papa Giovanni XXIII · ITOspedale Santa Maria della Misericordia di Udine · ITTumour Institute of Tuscany · ITUniversity of Milan · ITUniversity of Naples Federico II · ITUniversity of Udine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The activity of palbociclib as a single agent in advanced breast cancer has not been extensively studied, with the only available clinical data limited to heavily pretreated patients. Preclinical data suggests palbociclib may partially reverse endocrine resistance, though this hypothesis has not been evaluated in previous clinical studies. This phase II, open-label, multicenter study examined the activity of palbociclib monotherapy, as well as palbociclib given in combination with the same endocrine therapy (ET) that was received prior to disease progression, in postmenopausal women with moderately pretreated, estrogen receptor-positive, HER2 negative advanced breast cancer. Patients and methods: Eligible women with advanced disease which had progressed on one or two prior ETs were randomized 1 : 1 to receive either palbociclib alone, or palbociclib in combination with the ET as previously received. Primary end point was clinical benefit rate (CBR); secondary end points included progression-free survival (PFS). Results: Between October 2012 and July 2016, a total of 115 patients were randomized. The CBR was 54% [95% confidence interval (CI): 41.5-63.7] for combination therapy, and 60% (95% CI: 47.8-72.9) for monotherapy. Median PFS was 10.8 months (95% CI: 5.6-12.7) for combination therapy, and 6.5 months (95% CI: 5.4-8.5) for monotherapy [hazard ratio (HR) 0.69; 95% CI: 0.4-1.1, exploratory P-value = 0.12]. Exploratory analyses revealed the PFS advantage for combination therapy was seen in the subgroup of patients who received prior ET for >6 months (HR 0.53; 95% CI: 0.3-0.9, exploratory P-value = 0.02), but not in those who received prior ET for ≤6 months. Conclusion: Palbociclib has clinical activity as a single agent in women with moderately pretreated, oestrogen receptor-positive, HER2-negative advanced breast cancer. Palbociclib may have potential to reverse endocrine resistance in patients with a history of previous durable response to ET. Clinical trial information: NCT02549430.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsDisease ProgressionDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesEstrogen AntagonistsFemaleHumansMiddle AgedPiperazinesProgression-Free SurvivalPyridinesReceptors, EstrogenERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesEstrogen AntagonistspalbociclibPiperazinesPyridinesReceptors, Estrogen

Identifiers

PMID29893790
PMCPMC6454527
OpenAlexW2807927321

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.