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Rechallenge with first-generation RET inhibitors in <i>RET</i> -rearranged NSCLC pre-treated with selpercatinib or pralsetinib: Results from the RET MAP registry.

2025· article· en· W4410803003 on OpenAlexaff
Arianna Marinello, Julia Rotow, Meghanne Lomibao, Rita Leporati, Jamie Feng, Giulio Metro, Mariana Brandão, Amin Nassar, Fabrizio Citarella, David Planchard, Laura Mezquita, Benjamin Besse, Alexander Drilon, Mihaela Aldea

Bibliographic record

VenueJournal of Clinical Oncology · 2025
Typearticle
Languageen
FieldMedicine
TopicLung Cancer Treatments and Mutations
Canadian institutionsPrincess Margaret Cancer CentreUniversity Health Network
Fundersnot available
KeywordsMedicineProto-Oncogene Proteins c-retOncologyCancer researchInternal medicineReceptor

Abstract

fetched live from OpenAlex

8646 Background: RET fusions occur in 1-2% of patients with advanced non-small cell lung cancer (aNSCLC). First-generation RET inhibitors (RETi, selpercatinib and pralsetinib), have improved outcomes across treatment lines. Options at progression remain limited, especially in the absence of novel generation RETi. In real-world settings, rechallenge with the same class RETi is sometimes attempted, though efficacy and safety data are lacking. Methods: This multicenter retrospective analysis of the RET MAP registry included patients with RET -rearranged aNSCLC initially treated with selpercatinib or pralsetinib, followed by rechallenge with the same or a different first-generation RETi, as a single agent or in combination therapy. Clinical features, reasons for initial RETi discontinuation, treatment outcomes, and toxicity were assessed for both treatment courses. Results: Among 354 patients treated with first-generation RETi, same class RETi were re-administered in later lines in 33 (9.3 %) patients. At first RETi administration vs rechallenge, median prior lines were 2 (IQR 2–3) vs 4 (IQR 3–5), ECOG PS 0–1 was observed in 26 (78%) vs 25 (76%) patients, and brain metastases in 9 (27%) vs 13 (39%). Reasons for discontinuation of the first RETi were disease progression in 25 (76%) patients and toxicity in 8 (24%). RETi re-administration involved a change of first-generation RETi in 14 (42%) patients, monotherapy in 22 (67%), combination therapy in 11 (33%) (8 with other targeted agents for by-pass resistance, 3 with chemotherapy). It was given immediately after a prior RETi in 13 (39%) patients. At subsequent RETi treatment after progression on a prior RETi, ORR and median PFS were 18% and 2.17 months (95% CI 1.63–NR), respectively, with single-agent RETi (N=17), and 20% and 4 months (95% CI 3.55–NR), respectively, with RETi combined with other targeted agents (N=8). Patients who previously discontinued RETi due to toxicity (N=8) received a different RETi, with ORR and median PFS of 57% and 9.89 months (95% CI 5.33–NR), respectively. In this subgroup, 3 (37.5%) experienced serious side effects at re-administration of a different first-generation RETi. Conclusions: Rechallenge a different RETi of the same class is effective after initial discontinuation due to toxicity, though recurrent toxicity may occur in one-third of patients. In contrast, RETi rechallenge after progression demonstrates limited efficacy, primarily in selected cases treated with combination therapies.

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)0.002
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.002
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.093
GPT teacher head0.452
Teacher spread0.359 · 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 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".

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Citations0
Published2025
Admission routes1
Has abstractyes

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