Evidence map›Paper›PMID 37432985›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

Clinical and Molecular Features of Long-term Response to Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer.

Rohit Thummalapalli, Biagio Ricciuti, Chaitanya Bandlamudi, Daniel Muldoon, Hira Rizvi, Arielle Elkrief, Jia Luo, Joao V Alessi, Federica Pecci, Giuseppe Lamberti and 18 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Review
  5. Article
  6. Distinct Clinicogenomic Features and Immunotherapy Associations in Pulmonary Sarcomatoid Carcinoma: A Multicenter Retrospective Study.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Article
  7. Article
  8. Article
  9. Targeted therapy combined with immunotherapyWorld journal of gastroenterology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
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  20. 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

28 authors at 4 institutions in 2 countries.

Rohit Thummalapalli *Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-8865-0299
Biagio Ricciuti *Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-0651-2678
Chaitanya BandlamudiDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-1108-4919
Daniel MuldoonDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-7936-4365
Hira RizviDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-8007-096X
Arielle ElkriefDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-1981-1535
Jia LuoLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-3606-827X
Joao V AlessiLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-8072-5946
Federica PecciLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0009-0000-9289-2007
Giuseppe LambertiLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-3069-7630
Alessandro Di FedericoLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-8877-4315
Lingzhi HongDepartment of Thoracic/Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-6553-3279
Jianjun ZhangDepartment of Thoracic/Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-7872-3477
John V HeymachDepartment of Thoracic/Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-9068-8942
Don L GibbonsDepartment of Thoracic/Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0003-2362-3094
Andrew J PlodkowskiDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-3772-370X
Vignesh RavichandranMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-1532-2593
Mark T A DonoghueMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-4538-6069
Chad VanderbiltDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-8114-0237
Marc LadanyiDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-9055-7213
Charles M RudinDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-5204-3465
Mark G KrisDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-7317-5341
Gregory J RielyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-5357-4313
Jamie E ChaftDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-5838-9982
Matthew D HellmannDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-2670-9777
Natalie I Vokes *Department of Thoracic/Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-3766-5335
Mark M Awad *Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-0928-5244
Adam J Schoenfeld *Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-2644-1416
Memorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · USHarvard University · USDana-Farber Cancer Institute · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Investigational Cancer Therapeutics Training Program (ICTTP)T32CA009207 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Omar Abdel-Wahab, Alexander Drilon · 1985 to 2026
$13.7M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016672NCI NIH HHS T32 CA009207
6 · The paper itself

Abstract

purposeWe sought to identify features of patients with advanced non-small cell lung cancer (NSCLC) who achieve long-term response (LTR) to immune checkpoint inhibitors (ICI), and how these might differ from features predictive of short-term response (STR). EXPERIMENTAL

designWe performed a multicenter retrospective analysis of patients with advanced NSCLC treated with ICIs between 2011 and 2022. LTR and STR were defined as response ≥ 24 months and response < 12 months, respectively. Tumor programmed death ligand 1 (PD-L1) expression, tumor mutational burden (TMB), next-generation sequencing (NGS), and whole-exome sequencing (WES) data were analyzed to identify characteristics enriched in patients achieving LTR compared with STR and non-LTR.

resultsAmong 3,118 patients, 8% achieved LTR and 7% achieved STR, with 5-year overall survival (OS) of 81% and 18% among LTR and STR patients, respectively. High TMB (≥50th percentile) enriched for LTR compared with STR (P = 0.001) and non-LTR (P < 0.001). Whereas PD-L1 ≥ 50% enriched for LTR compared with non-LTR (P < 0.001), PD-L1 ≥ 50% did not enrich for LTR compared with STR (P = 0.181). Nonsquamous histology (P = 0.040) and increasing depth of response [median best overall response (BOR) -65% vs. -46%, P < 0.001] also associated with LTR compared with STR; no individual genomic alterations were uniquely enriched among LTR patients.

conclusionsAmong patients with advanced NSCLC treated with ICIs, distinct features including high TMB, nonsquamous histology, and depth of radiographic improvement distinguish patients poised to achieve LTR compared with initial response followed by progression, whereas high PD-L1 does not.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenBiomarkers, TumorHumansImmune Checkpoint InhibitorsRetrospective StudiesAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorImmune Checkpoint Inhibitors

Identifiers

PMID37432985
PMCPMC10618656
OpenAlexW4383897132

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.