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Record W4416971674 · doi:10.1186/s12885-025-15224-3

Tucatinib, trastuzumab, and capecitabine with stereotactic radiosurgery in patients with brain metastases from HER-2 positive breast cancer (TUTOR): Study protocol for a multicenter phase 1 clinical trial

2025· article· en· W4416971674 on OpenAlexaff
Zouina Sarfraz, Ahmad Ozair, Mainak Bardhan, Amy Starosciak, Dilanis Perche, Lydia Hodgson, Yazmín Odia, Minesh P. Mehta, Rupesh Kotecha, Michael McDermott, Arun Maharaj, Ana Cristina Sandoval Leon, Reshma Mahtani, Manmeet S. Ahluwalia

Bibliographic record

VenueBMC Cancer · 2025
Typearticle
Languageen
FieldMedicine
TopicBrain Metastases and Treatment
Canadian institutionsMcGill UniversityMontreal Neurological Institute and Hospital
FundersPfizer
KeywordsCapecitabineRadiosurgeryBreast cancerRegimenNeutropeniaClinical trialClinical endpointMetastatic breast cancer

Abstract

fetched live from OpenAlex

BACKGROUND: Approximately 30-50% of patients with HER-2 + breast cancer develop brain metastases (BM). Stereotactic radiosurgery (SRS) is frequently used for local disease control. Tucatinib, an oral HER-2-selective tyrosine kinase inhibitor, has been demonstrated to be safe and efficacious in HER-2 + breast cancer in combination with capecitabine and trastuzumab. The synergy between these three drugs and radiation may enhance DNA damage and increase apoptosis. We hypothesize that this chemoradiation regimen in patients with HER-2 + breast cancer BM (BCBM), is safe and provides superior long-term control of intracranial and systemic disease. METHODS: This is a prospective, single-arm, multicenter, ongoing, phase-1 clinical trial. Eligible patients are aged ≥ 18 years, have an Eastern Cooperative Oncology Group (ECOG) score 0-2, normal organ function, and up to ten newly diagnosed BM will be enrolled at six centers in the United States. Any number of prior systemic therapies are allowed, except prior use of tucatinib or capecitabine. Key exclusion criteria include leptomeningeal metastases, intra-tumoral or peri-tumoral hemorrhage, and BM within 5 mm of the optic chiasm/nerve. Patients receive oral tucatinib alongside SRS, followed by a two-week dose-limiting toxicity (DLT) period. Beginning in Cycle 2, they receive capecitabine (days 1-14 of each 21-day cycle) and trastuzumab (day 1 of each cycle), continuing the regimen until disease progression or intolerable toxicity. DLTs are defined by grade 3 or 4 thrombocytopenia, grade 4 anemia, grade 4 neutropenia lasting more than seven days, febrile neutropenia, and grade ≥three non-hematologic toxicity. The primary study endpoint is a maximum tolerated dose (MTD) of tucatinib in combinatorial therapy. This de-escalation study starts at a 300 mg dose level DL(0), with DL(-1) 250 mg, and DL(-2) of 200 mg, based on a 3 + 3 design. Cohort expansion at the MTD is to include 40 patients. Secondary endpoints include efficacy as determined by response rate, intracranial progression-free survival (per investigator-assessed), extracranial PFS, overall survival, quality of life as assessed by FACT-Br, toxicity, and neurocognitive function. DISCUSSION: This trial has been approved by the Institutional Review Board (IRB) and began patient enrollment in January 2024. The trial will provide insights into the safety and effectiveness of a novel combinatorial therapy for BCBM. TRIAL REGISTRATION: ClinicalTrials.Gov identifier NCT05553522. Registered on 09-22-2022 https://clinicaltrials.gov/ct2/show/NCT05553522 .

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.160
Threshold uncertainty score0.974

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.047
GPT teacher head0.426
Teacher spread0.380 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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