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Cited by 451

The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.

Antitumor Activity of Nivolumab in Recurrent and Metastatic Nasopharyngeal Carcinoma: An International, Multicenter Study of the Mayo Clinic Phase 2 Consortium (NCI-9742)

Open access
Ma, Brigette B.Y., Lim, Wan-Teck, Goh, Boon-Cher, Hui, Edwin P., Lo, Kwok-Wai, Pettinger, Adam, Foster, Nathan R., Riess, Jonathan W., Agulnik, Mark, Chang, Alex Y.C., Chopra, Akhil, Kish, Julie A., Chung, Christine H., Adkins, Douglas R., Cullen, Kevin J., Gitlitz, Barbara J., Lim, Dean W., To, Ka-Fai, Chan, K.C. Allen, Lo, Y.M. Dennis, King, Ann D., Erlichman, Charles, Yin, Jun, Costello, Brian A., Chan, Anthony T.C.·2018·Journal of Clinical Oncology

Abstract

Purpose: This multinational study evaluated the antitumor activity of nivolumab in nasopharyngeal carcinoma (NPC). Tumor and plasma-based biomarkers were investigated in an exploratory analysis. Patients and Methods: Patients with multiply pretreated recurrent or metastatic NPC were treated with nivolumab until disease progression. The primary end point was objective response rate (ORR) and secondary end points included survival and toxicity. The expression of programmed death-ligand 1 (PD-L1) and human leukocyte antigens A and B in archived tumors and plasma clearance of Epstein-Barr virus DNA were correlated with ORR and survival. Results: A total of 44 patients were evaluated and the overall ORR was 20.5% (complete response, n = 1; partial response, n = 8). Nine patients received nivolumab for > 12 months (20%). The 1-year overall survival rate was 59% (95% CI, 44.3% to 78.5%) and 1-year progression-free survival (PFS) rate was 19.3% (95% CI, 10.1% to 37.2%). There was no statistical correlation between ORR and the biomarkers; however, a descriptive analysis showed that the proportion of patients who responded was higher among those with PD-L1 positive tumors (> 1% expression) than those with PD-L1-negative tumors. The loss of expression of one or both human leukocyte antigen class 1 proteins was associated with better PFS than when both proteins were expressed (1-year PFS, 30.9% v 5.6%; log-rank P = .01). There was no association between survival and PD-L1 expression or plasma Epstein-Barr virus DNA clearance. There was no unexpected toxicity to nivolumab. Conclusion: Nivolumab has promising activity in NPC and the 1-year overall survival rate compares favorably with historic data in similar populations. Additional evaluation in a randomized setting is warranted. The biomarker results were hypothesis generating and validation in larger cohorts is needed.

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Metadata

Authors
Ma, B. B. Y., Lim, W.-T., Goh, B.-C., Hui, E. P., Lo, K.-W., Pettinger, A., Foster, N. R., Riess, J. W., Agulnik, M., Chang, A. Y. C., Chopra, A., Kish, J. A., Chung, C. H., Adkins, D. R., Cullen, K. J., Gitlitz, B. J., Lim, D. W., To, K.-F., Chan, K. C. A., Lo, Y. M. D., King, A. D., Erlichman, C., Yin, J., Costello, B. A., & Chan, A. T. C.
Venue
Journal of Clinical Oncology
Published
2018-05-10
Volume
36
Issue
14
Pages
1412-1418
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2794739281
Cited by
451
References
32
FWCI
15.42
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Antitumor Activity of Nivolumab in Recurrent and Metastatic Nasopharyngeal Carcinoma: An International, Multicenter Study of the Mayo Clinic Phase 2 Consortium (NCI-9742). https://app.cochat.ai/papers/10.1200/jco.2017.77.0388
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Ma, B. B. Y., Lim, W.-T., Goh, B.-C., Hui, E. P., Lo, K.-W., Pettinger, A., Foster, N. R., Riess, J. W., Agulnik, M., Chang, A. Y. C., Chopra, A., Kish, J. A., Chung, C. H., Adkins, D. R., Cullen, K. J., Gitlitz, B. J., Lim, D. W., To, K.-F., Chan, K. C. A., . . . Chan, A. T. C. (2018). Antitumor Activity of Nivolumab in Recurrent and Metastatic Nasopharyngeal Carcinoma: An International, Multicenter Study of the Mayo Clinic Phase 2 Consortium (NCI-9742). Journal of Clinical Oncology. https://doi.org/10.1200/jco.2017.77.0388

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.