Evidence map›Paper›PMID 38461929›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2024

Evaluation of Major Pathologic Response and Pathologic Complete Response as Surrogate End Points for Survival in Randomized Controlled Trials of Neoadjuvant Immune Checkpoint Blockade in Resectable in NSCLC.

Jacobi B Hines, Robert B Cameron, Alessandra Esposito, Leeseul Kim, Luca Porcu, Antonio Nuccio, Giuseppe Viscardi, Roberto Ferrara, Giulia Veronesi, Patrick M Forde and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 4 pooled it
36.1field-weighted citation impact, top 1% of its field
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

56 citing papers in PubMed, 4 syntheses or guidelines pooled it, 63 citations in OpenAlex.

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  13. A systematic review and meta-analysis on survival, pathological response, and safety of durvalumab in early-stage non-small cell lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  15. Prognostic value ofCancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Article
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  18. Current and future immunotherapies for NSCLC.Journal of hematology & oncology · 2026
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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

19 authors at 9 institutions in 3 countries.

Jacobi B HinesDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
Robert B CameronDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois. Electronic address: robert.cameron@uchicagomedicine.org.
Alessandra EspositoDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
Leeseul KimDepartment of Medicine, Ascension Saint Francis Hospital, Chicago, Illinois.
Luca PorcuCancer Research United Kingdom, Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.
Antonio NuccioDepartment of Medical Oncology, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), San Raffaele Scientific Institute, Milan, Italy.
Giuseppe ViscardiDepartment of Pneumology and Oncology, Azienda Ospedaliera di Rilievo Nazionale (AORN) Ospedali dei Colli, Naples, Italy.
Roberto FerraraDepartment of Medical Oncology, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), San Raffaele Scientific Institute, Milan, Italy.
Giulia VeronesiSchool of Medicine and Surgery, Vita-Salute San Raffaele University, Milan, Italy; Department of Thoracic Surgery, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS) San Raffaele Scientific Institute, Milan, Italy.
Patrick M FordeDepartment of Oncology, Division of Upper Aerodigestive Malignancies, Bloomberg-Kimmel Institute for Cancer Immunotherapy, John Hopkins Kimmel Cancer Center, Baltimore, Maryland.
Janis TaubeDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Everett VokesDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
Christine M BestvinaDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
James M DolezalDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
Matteo SaccoDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
Marta MonteforteDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Tina CasconeDepartment of Thoracic/Head and Neck Medical Oncology, Division of Cancer Medicine, The University of Texas, Monroe Dunaway (MD) Anderson Cancer Center, Houston, Texas.
Marina C GarassinoDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
Valter TorriDepartment of Clinical Oncology, "Mario Negri" Institute for Pharmacological Research- IRCCS, Milan, Italy.
University of Chicago · USVita-Salute San Raffaele University · ITJohns Hopkins University · USAzienda di Rilievo Nazionale ed Alta Specializzazione · ITBloomberg (United States) · USMario Negri Institute for Pharmacological Research · ITSaint Francis Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity of Cambridge · GB

Funding

CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
NIGMS NIH HHS T32 GM007019
6 · The paper itself

Abstract

introductionControversy remains as to whether pathologic complete response (pCR) and major pathologic response (MPR) represent surrogate end points for event-free survival (EFS) and overall survival (OS) in neoadjuvant trials for resectable NSCLC.

methodsA search of PubMed and archives of international conference abstracts was performed from June 2017 through October 31, 2023. Studies incorporating a neoadjuvant arm with immune checkpoint blockade alone or in combination with chemotherapy were included. Those not providing information regarding pCR, MPR, EFS, or OS were excluded. For trial-level surrogacy, log ORs for pCR and MPR and log hazard ratios for EFS and OS were analyzed using a linear regression model weighted by sample size. The regression coefficient and R

resultsSeven randomized clinical trials were identified for a total of 2385 patients. At the patient level, the R

conclusionsOur analyses reveal a robust correlation between pCR and MPR with 2-year EFS but not OS. Trial-level surrogacy was moderate but imprecise. More mature follow-up and data to assess the impact of study crossover are needed.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsNeoadjuvant TherapyHumansPathologic Complete ResponseRandomized Controlled Trials as TopicSurvival RateImmune Checkpoint InhibitorsChemoimmunotherapyImmunotherapyNeoadjuvantNSCLCPathologic responseSurrogate end points

Identifiers

PMID38461929
PMCPMC12697759
OpenAlexW4392603763

What OpenQuestion holds

Textmetadata
LicenceTDM
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.