Evidence map›Paper›PMID 41324568›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2026

Addition of Ipatasertib to Dual Anti-HER2 Maintenance Therapy in HER2-Positive Metastatic Breast Tumors with PIK3CA Mutations: The Phase Ib SOLTI-1507 IPATHER Trial.

Mafalda Oliveira, Eva Ciruelos, Guillermo Villacampa, Serafín Morales, Javier Salvador Bofill, Vanesa Quiroga, Joaquín Gavilá, Alexandra Cortegoso, Estela Vega, Fernando Henao and 10 more

Abstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

20 authors.

Mafalda OliveiraMedical Oncology Department, Vall d'Hebron University Hospital, and Breast Cancer Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.ORCID 0000-0001-9152-8799
Eva CiruelosSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-2796-1042
Guillermo VillacampaSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0003-4868-6585
Serafín MoralesMedical Oncology Department, Hospital Universitario Arnau de Vilanova, Lleida, Spain.ORCID 0000-0001-7445-4193
Javier Salvador BofillMedical Oncology Department, Hospital Virgen del Rocío, Sevilla, Spain/Instituto de BioMedicina de Sevilla (IBIS), Seville, Spain.ORCID 0000-0003-3043-4398
Vanesa QuirogaMedical Oncology Department, Badalona-Applied Research Group in Oncology (B-ARGO Group), Catalan Institute of Oncology, Barcelona, Spain.ORCID 0000-0002-7852-474X
Joaquín GaviláSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-6768-3833
Alexandra CortegosoMedical Oncology Department, Complejo Hospitalario Universitario de Santiago, Santiago de Compostela, Spain.ORCID 0000-0003-4098-9266
Estela VegaMedical Oncology Department, Centro Integral Oncológico Clara Campal, Madrid, Spain.ORCID 0009-0005-5652-6460
Fernando HenaoMedical Oncology Department, Hospital Virgen de Macarena, Sevilla, Spain.ORCID 0000-0003-3819-9572
Sonia ServitjaMedical Oncology Department, Hospital del Mar, Hospital del Mar Research Institute, Universitat Pompeu Fabra, Barcelona, Spain.ORCID 0000-0001-6988-4519
Pablo TolosaSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-3747-4766
Samyukta ChillaraSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-6072-5455
Milana BergaminoMedical Oncology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.ORCID 0000-0002-1091-2711
Fernando SalvadorSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-5442-1754
Mariana Paes DiasSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-5757-4211
Juan M Ferrero-CafieroSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0001-8796-8812
Xavier Gonzalez FarreSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0002-5797-7037
Tomás PascualSOLTI Cancer Research Group, Barcelona, Spain.ORCID 0000-0001-8431-3183
Cristina SauraMedical Oncology Department, Vall d'Hebron University Hospital, and Breast Cancer Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.ORCID 0000-0001-8296-5065

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to evaluate the safety and feasibility of ipatasertib combined with trastuzumab and pertuzumab (HP) as maintenance therapy after first-line treatment in patients with HER2-positive metastatic breast cancer harboring PIK3CA mutations (PIK3CAmut). PATIENTS AND

methodsThis prospective, multicenter, single-arm, phase Ib study evaluated the safety and preliminary efficacy of ipatasertib, an AKT inhibitor, combined with HP, with or without endocrine therapy as maintainance therapy, in patients with unresectable locally advanced or metastatic PIK3CAmut, HER2-positive breast cancer following first-line induction chemotherapy and HP.

resultsSeventeen patients were enrolled, with a median follow-up of 27.7 months. During the dose-selection phase, ipatasertib at 400 mg daily (21 days on and 7 days off) with standard HP was established as the recommended phase II dosage. This decision was based on the absence of dose-limiting toxicities in the first six patients treated at this dosage during the initial 28-day cycle, which constituted the primary endpoint. Grade 3 treatment-related adverse events (TRAE) occurred in seven patients (41.2%), most commonly diarrhea and nausea. Two (11.8%) reported four serious TRAE (diarrhea, vomiting, ischemic stroke, and pneumonitis, one case each) related to ipatasertib, from which they recovered. The confirmed overall response rate was 31.1% [95% confidence interval (CI), 12.1%-58.5%], clinical benefit rate 84.6% (95% CI, 53.7%-97.3%), and median progression-free survival 16.4 months (95% CI, 9.4-NR); 47.3% of patients were progression free at 18 months.

conclusionsThese results support ipatasertib plus HP as a safe and promising maintenance strategy for HER2-positive breast tumors harboring PIK3CAmut.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsClass I Phosphatidylinositol 3-KinasesErb-b2 Receptor Tyrosine KinasesMutationAdultAgedAntibodies, Monoclonal, HumanizedFemaleHumansMiddle AgedPiperazinesProspective StudiesPyrimidinesAntibodies, Monoclonal, HumanizedClass I Phosphatidylinositol 3-KinasesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesipatasertibpertuzumabPIK3CA protein, humanPiperazinesPyrimidines

Identifiers

PMID41324568
PMCPMC12869161

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.