Evidence map›Paper›PMID 40507234›Full record

ReviewCancers2025

Efficacy and Safety of TROP-2-Targeting Antibody-Drug Conjugate Treatment in Previously Treated Patients with Advanced Non-Small Cell Lung Cancer: A Systematic Review and Pooled Analysis of Reconstructed Patient Data.

Sara Stumpo, Andrea Carlini, Francesco Mantuano, Alessandro Di Federico, Barbara Melotti, Francesca Sperandi, Valentina Favorito, Andrea De Giglio

Abstract readReview
In one paragraph

Review in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. 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

8 authors.

Sara StumpoDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.ORCID 0009-0006-7433-4347
Andrea CarliniDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.ORCID 0009-0006-4575-8300
Francesco MantuanoDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.ORCID 0009-0005-3111-5067
Alessandro Di FedericoDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.ORCID 0000-0001-8877-4315
Barbara MelottiMedical Oncology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via P. Albertoni 15, 40138 Bologna, Italy.ORCID 0000-0003-1041-391X
Francesca SperandiMedical Oncology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via P. Albertoni 15, 40138 Bologna, Italy.ORCID 0000-0002-1581-3456
Valentina FavoritoDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.ORCID 0009-0001-5282-260X
Andrea De GiglioDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Via Zamboni 33, 40126 Bologna, Italy.ORCID 0000-0002-0731-5721

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDocetaxel is the standard of care for advanced non-small cell lung cancer (NSCLC) after platinum-based chemotherapy and/or immunotherapy but is associated with modest clinical outcomes and considerable toxicity. Sacituzumab govitecan and datopotamab deruxtecan are trophoblast cell surface antigen (TROP)-2-directed antibody-drug conjugates (ADCs) that showed encouraging activity in pretreated patients with advanced NSCLC. This systematic review and pooled analysis aims to comprehensively assess the efficacy and safety of anti-TROP-2 ADCs compared to docetaxel in pretreated patients with advanced NSCLC.

methodsA systematic search through PubMed and EMBASE before 31 January 2025 was performed to identify eligible studies. Randomized controlled phase III trials comparing an anti-TROP-2 regimen to docetaxel in patients with pretreated advanced NSCLC were included. Overall survival (OS), progression-free survival (PFS), and grade ≥ 3 treatment-related adverse events (TRAEs) were extracted from the identified trials. A pooled analysis of reconstructed patient data and meta-analysis employing the random-effect model were used to summarize the efficacy and safety outcomes.

resultsAcross the two trials included, 1207 patients were enrolled, 598 in the TROP-2 ADC arm and 609 in the docetaxel arm. Anti-TROP-2 treatment did not produce significant improvements in OS (HR: 0.90; 95% CI, 0.78-1.03; P = 0.13) and PFS (HR: 0.84; 95% CI, 0.68-1.02; P = 0.08), compared to docetaxel, even in patients with a nonsquamous histology (OS HR: 0.86; 95% CI, 0.73-1.01; P = 0.06; PFS HR: 0.76; 95% CI, 0.52-1.12; P = 0.17). Across the subgroup analyses, a statistically significant improvement in OS was observed in patients with actionable genomic alterations (AGAs) (HR: 0.63; 95% CI, 0.41-0.95; P = 0.03). Compared to docetaxel, the anti-TROP-2 regimen demonstrated a lower risk of developing grade ≥ 3 TRAEs (RR: 0.76; 95% CI, 0.55-1.05; P = 0.09).

conclusionsThe anti-TROP-2 regimen showed a better safety profile but failed to demonstrate a relevant clinical improvement over docetaxel. Anti-TROP-2 ADCs could find a role in the management of patients with AGAs.

Indexed as

antibody–drug conjugatesdatopotamabnon-small cell lung cancersacituzumabTROP2

Identifiers

PMID40507234
PMCPMC12153610

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.