Evidence map›Paper›PMID 37702716›Full record

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

Circulating Tumor DNA Monitoring on Chemo-immunotherapy for Risk Stratification in Advanced Non-Small Cell Lung Cancer.

Bruna Pellini, Russell W Madison, Merrida A Childress, Shoshana T Miller, Ole Gjoerup, Jason Cheng, Richard S P Huang, Michael Krainock, Pratyush Gupta, Wei Zou and 8 more

Open access · hybridAbstract read
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 35 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 4 pooled it
10.0field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 4 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Circulating Tumor DNA Assessment for Treatment Monitoring Adds Value to PSA in Metastatic Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Trial
  8. Trial
  9. Applications of circulating tumor DNA in unresectable and advanced non-small cell lung cancer immunotherapy: from stratification to therapeutic guidance.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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  11. Article
  12. Review
  13. Article
  14. Observational
  15. Article
  16. Article
  17. ctDNA in Pancreatic Adenocarcinoma: A Critical Appraisal.Current oncology (Toronto, Ont.) · 2025
    Review
  18. Article
  19. Article
  20. Chemoimmunotherapy synergism: mechanisms and clinical applications.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    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

18 authors at 6 institutions in 1 country.

Bruna Pellini *Department of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0003-0898-0202
Russell W Madison *Foundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0002-7838-2526
Merrida A ChildressFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0002-0854-784X
Shoshana T MillerFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0009-0004-2353-4547
Ole GjoerupFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0001-9127-8769
Jason ChengGenentech, Inc., South San Francisco, California.ORCID 0000-0002-4008-6019
Richard S P HuangFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0001-8395-5168
Michael KrainockNatera, Inc., San Carlos, California.ORCID 0000-0003-0081-4584
Pratyush GuptaGenentech, Inc., South San Francisco, California.ORCID 0000-0003-3927-6496
Wei ZouGenentech, Inc., South San Francisco, California.ORCID 0000-0002-3639-9821
David S ShamesGenentech, Inc., South San Francisco, California.ORCID 0000-0002-5900-1177
Solomon MoshkevichNatera, Inc., San Carlos, California.ORCID 0009-0009-8612-1308
Marcus BallingerGenentech, Inc., South San Francisco, California.ORCID 0009-0009-9006-5433
Minetta C LiuNatera, Inc., San Carlos, California.ORCID 0000-0002-8206-5232
Amanda YoungFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0002-2199-1873
Minu K SrivastavaGenentech, Inc., South San Francisco, California.ORCID 0009-0000-3827-9180
Geoffrey R OxnardFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0003-1054-8240
Mark A SocinskiAdventHealth Cancer Institute, Orlando, Florida.ORCID 0000-0003-2915-9325
GlobalFoundries (United States) · USNatera (United States) · USFlorida Hospital Cancer Institute · USSan Francisco Foundation · USUniversity of South Florida · USVanderbilt University · US

Funding

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6 · The paper itself

Abstract

purposeChemoimmunotherapy (chemoIO) is a prevalent first-line treatment for advanced driver-negative non-small cell lung cancer (NSCLC), with maintenance therapy given after induction. However, there is significant clinical variability in the duration, dosing, and timing of maintenance therapy after induction chemoIO. We used circulating tumor DNA (ctDNA) monitoring to inform outcomes in patients with advanced NSCLC receiving chemoIO. EXPERIMENTAL

designThis retrospective study included 221 patients from a phase III trial of atezolizumab+carboplatin+nab-paclitaxel versus carboplatin+nab-paclitaxel in squamous NSCLC (IMpower131). ctDNA monitoring used the FoundationOne Tracker involving comprehensive genomic profiling of pretreatment tumor tissue, variant selection using an algorithm to exclude nontumor variants, and multiplex PCR of up to 16 variants to detect and quantify ctDNA.

resultsctDNA was detected (ctDNA+) in 96% of pretreatment samples (median, 93 mean tumor molecules/mL), and similar ctDNA dynamics were noted across treatment arms during chemoIO. ctDNA decrease from baseline to C4D1 was associated with improved outcomes across multiple cutoffs for patients treated with chemoIO. When including patients with missing plasma or ctDNA- at baseline, patients with ctDNA- at C4D1 (clearance), had more favorable progression-free survival (median 8.8 vs. 3.5 months; HR, 0.32;0.20-0.52) and OS (median not reached vs. 8.9 months; HR, 0.22; 0.12-0.39) from C4D1 than ctDNA+ patients.

conclusionsctDNA monitoring during induction chemoIO can inform treatment outcomes in patients with advanced NSCLC. Importantly, monitoring remains feasible and informative for patients missing baseline ctDNA. ctDNA testing during induction chemoIO identifies patients at higher risk for disease progression and may inform patient selection for novel personalized maintenance or second-line treatment strategies.

Indexed as

Carcinoma, Non-Small-Cell LungCirculating Tumor DNALung NeoplasmsCarboplatinHumansImmunotherapyPaclitaxelRetrospective StudiesRisk AssessmentCarboplatinCirculating Tumor DNAPaclitaxel

Identifiers

PMID37702716
PMCPMC10643998
OpenAlexW4386704751

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.