Cited by 618Cancer Immunotherapy and BiomarkersLung Cancer Diagnosis and TreatmentLung Cancer Treatments and Mutations

The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index; 4 of the 45 sources its claims cite were checked for support.

Neoadjuvant nivolumab or nivolumab plus ipilimumab in operable non-small cell lung cancer: the phase 2 randomized NEOSTAR trial

Open access

Abstract

Ipilimumab improves clinical outcomes when combined with nivolumab in metastatic non-small cell lung cancer (NSCLC), but its efficacy and impact on the immune microenvironment in operable NSCLC remain unclear. We report the results of the phase 2 randomized NEOSTAR trial (NCT03158129) of neoadjuvant nivolumab or nivolumab + ipilimumab followed by surgery in 44 patients with operable NSCLC, using major pathologic response (MPR) as the primary endpoint. The MPR rate for each treatment arm was tested against historical controls of neoadjuvant chemotherapy. The nivolumab + ipilimumab arm met the prespecified primary endpoint threshold of 6 MPRs in 21 patients, achieving a 38% MPR rate (8/21). We observed a 22% MPR rate (5/23) in the nivolumab arm. In 37 patients resected on trial, nivolumab and nivolumab + ipilimumab produced MPR rates of 24% (5/21) and 50% (8/16), respectively. Compared with nivolumab, nivolumab + ipilimumab resulted in higher pathologic complete response rates (10% versus 38%), less viable tumor (median 50% versus 9%), and greater frequencies of effector, tissue-resident memory and effector memory T cells. Increased abundance of gut Ruminococcus and Akkermansia spp. was associated with MPR to dual therapy. Our data indicate that neoadjuvant nivolumab + ipilimumab-based therapy enhances pathologic responses, tumor immune infiltrates and immunologic memory, and merits further investigation in operable NSCLC.

Overview

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Registry

Crossref · 10.1038/s41591-020-01224-2

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49 of 49 references verified0 citation errors · 0 not checkable

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  • It may state two separate claims as one. 54
  • Probably not a substantial claim. 32
80 of 80
  • The paper relies on this without support.

    The efficacy and impact of ipilimumab on the immune microenvironment in operable NSCLC were unclear before this study.

    “Ipilimumab improves clinical outcomes when combined with nivolumab in metastatic non-small cell lung cancer (NSCLC), but its efficacy and impact on the immune microenvironment in operable NSCLC remain unclear.”
  • The paper relies on this without support.

    The impact of dual ICI therapy on the immune microenvironment of resectable NSCLC had not been established.

    “Although the addition of ipilimumab to nivolumab therapy has dramatically altered care of patients with advanced NSCLC, the impact of this dual ICI therapy on the immune microenvironment of resectable NSCLC has not been established.”
  • The paper relies on this without support.

    NEOSTAR is the first reported randomized phase 2 trial testing neoadjuvant nivolumab and nivolumab plus ipilimumab in resectable NSCLC using MPR as the primary endpoint.

    “NEOSTAR is the first reported, randomized phase 2 trial testing neoadjuvant nivolumab and nivolumab + ipilimumab in patients with resectable NSCLC using MPR as the primary endpoint.”
  • The authors state this as an assumption.

    This is the first report of neoadjuvant ICIs imparting immunologic memory in clinical specimens of resected NSCLC.

    “To our knowledge, this is the first report of neoadjuvant ICIs imparting immunologic memory in clinical specimens of resected NSCLC.”
  • The paper relies on this without support.

    This trial is the first completed randomized study to compare neoadjuvant nivolumab alone with nivolumab plus ipilimumab in resectable NSCLC.

    “Despite these limitations, to our knowledge, this is the first completed randomized study comparing the impact of neoadjuvant nivolumab monotherapy and combined nivolumab + ipilimumab in resectable NSCLC.”
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Metadata

Authors
Cascone, T., William, W. N., Weissferdt, A., Leung, C. H., Lin, H. Y., Pataer, A., Godoy, M. C. B., Carter, B. W., Federico, L., Reuben, A., Khan, M. A. W., Dejima, H., Francisco-Cruz, A., Parra, E. R., Solis, L. M., Fujimoto, J., Tran, H. T., Kalhor, N., Fossella, F. V., Mott, F. E., Tsao, A. S., Blumenschein, G., Le, X., Zhang, J., Skoulidis, F., Kurie, J. M., Altan, M., Lu, C., Glisson, B. S., Byers, L. A., Elamin, Y. Y., Mehran, R. J., Rice, D. C., Walsh, G. L., Hofstetter, W. L., Roth, J. A., Antonoff, M. B., Kadara, H., Haymaker, C., Bernatchez, C., Ajami, N. J., Jenq, R. R., Sharma, P., Allison, J. P., Futreal, A., Wargo, J. A., Wistuba, I. I., Swisher, S. G., Lee, J. J., Gibbons, D. L., Vaporciyan, A. A., Heymach, J. V., & Sepesi, B.
Affiliations
The University of Texas MD Anderson Cancer Center (US)
Corresponding author
Cascone, Tina
Venue
Nature Medicine
Published
2021-02-18
Volume
27
Issue
3
Pages
504-514
ISSN
  • 1078-8956 (ISSN-L)
  • 1546-170X
OpenAlex
W3132841322
Cited by
618
References
46
Citations by year
2026: 54 · 2025: 92 · 2024: 124 · 2023: 160 · 2022: 141 · 2021: 47
FWCI
42.92
Type
journal article
Language
en
Open access
Locations
  • Nature Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Cancer Institute (P50CA070907, P30CA016672)
Topics
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Diagnosis and Treatment
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
Keywords
neoadjuvant immunotherapy, nivolumab, ipilimumab, major pathological response, tumor immune microenvironment, T cell memory, gut microbiota, Ruminococcus, Akkermansia, tumor immune infiltrate
MeSH terms
Ipilimumab, Nivolumab, Adult, Aged, Antineoplastic Combined Chemotherapy Protocols, Carcinoma, Non-Small-Cell Lung, Female, Humans, Lung Neoplasms, Male, Middle Aged, Biomarkers, Tumor, Neoadjuvant Therapy

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