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TroFuse-020/GOG-3101/ENGOT-cx20: A phase 3, randomized, active-controlled, open-label, multicenter study comparing sacituzumab tirumotecan monotherapy vs treatment of physician’s choice as second-line treatment for recurrent or metastatic cervical cancer.

2025· article· en· W4410815665 on OpenAlexaff
Ritu Salani, Mansoor Raza Mirza, Zhongqiu Lin, Shin Nishio, Ana Oaknin, Jean‐Emmanuel Kurtz, Giorgio Valabrega, Valeria Cáceres, Philipp Harter, Lucy Gilbert, Azmat Sadozye, Lillian Barros, Toon Van Gorp, Ingrid Boere, Christian Marth, Linda Duska, Bradley J. Monk, Xin Tong Li, Cumhur Tekin, Kristina Lindemann

Bibliographic record

VenueJournal of Clinical Oncology · 2025
Typearticle
Languageen
FieldMedicine
TopicEndometrial and Cervical Cancer Treatments
Canadian institutionsMcGill University Health Centre
Fundersnot available
KeywordsMedicineOpen labelSurgeryRandomized controlled trial

Abstract

fetched live from OpenAlex

TPS5618 Background: Sacituzumab tirumotecan (sac-TMT; formerly MK-2870/SKB264) is an antibody‒drug conjugate comprising a trophoblast cell-surface antigen 2 (TROP2)–antibody, a hydrolytically-cleavable linker, and the cytotoxic drug KL610023 (average drug/antibody ratio, 7.4). In an ongoing phase 1/2 study (MK-2870-001), sac-TMT monotherapy showed promising antitumor activity in participants with locally advanced unresectable/metastatic solid tumors that were refractory to standard therapies. This phase 3, randomized, open-label, multicenter study (NCT06459180) evaluates the efficacy and safety of sac-TMT monotherapy vs treatment of physician’s choice (TPC) as second-line treatment in participants with recurrent/metastatic cervical cancer. Methods: Eligible participants are aged ≥18 years with progressive recurrent/metastatic cervical cancer, measurable per RECIST version 1.1 by the investigator, and had received 1 prior line of platinum doublet chemotherapy (±bevacizumab) and anti‒PD-1/anti‒PD-L1 therapy as a part of cervical cancer regimens. Participants must provide tissue from a core or excisional biopsy of a not previously irradiated tumor lesion. Approximately 666 participants will be randomly assigned 1:1 to receive either sac-TMT 4 mg/kg intravenously (IV) Q2W or TPC (pemetrexed 500 mg/m 2 IV Q3W; tisotumab vedotin 2 mg/kg IV Q3W; topotecan 1 or 1.25 mg/m 2 on days 1–5 of each 3-week treatment cycle; vinorelbine 30 mg/m 2 on days 1 and 8 of each 3-week treatment cycle; gemcitabine 1000 mg/m 2 on days 1 and 8 of each 3-week treatment cycle; or irinotecan 100 or 125 mg/m 2 on days 1, 8, 15, and 22 of each 6-week treatment cycle). Tumor imaging will be performed ≤28 days before treatment allocation/randomisation, then Q9W until week 54 and Q12W thereafter. The primary endpoint is OS; secondary endpoints include PFS assessed by blinded independent central review, objective response, duration of response, safety, time to deterioration, and patient-reported outcomes. Enrollment began in Q3 2024. Clinical trial information: NCT06459180 .

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.008
Threshold uncertainty score0.028

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.001
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0020.002
Bibliometrics0.0010.000
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0020.004
Insufficient payload (model declined to judge)0.0080.002

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 head0.263
GPT teacher head0.559
Teacher spread0.295 · 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 source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
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

Citations1
Published2025
Admission routes1
Has abstractyes

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