Evidence map›Paper›PMID 37188668›Full record

ArticleNature communications2023

Clinical efficacy and biomarker analysis of dual PD-1/CTLA-4 blockade in recurrent/metastatic EBV-associated nasopharyngeal carcinoma.

Darren Wan-Teck Lim, Hsiang-Fong Kao, Lisda Suteja, Constance H Li, Hong Sheng Quah, Daniel Shao-Weng Tan, Sze-Huey Tan, Eng-Huat Tan, Wan-Ling Tan, Justina Nadia Lee and 10 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
9.4field-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.

NCT03097939 phase2active not recruitingnot on this map

A Phase II Trial Of Ipilimumab In Combination With Nivolumab In Patients With Advanced Nasopharyngeal Carcinoma

TypeinterventionalSponsorNational Cancer Centre, SingaporeRan2017 to 2027Enrolled113ConditionsNasopharyngeal CarcinomaArmsIpilimumab, Nivolumab
NCT07756190 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Phase II Study of Radscopal Radiotherapy Combined With Immunotherapy as First-Line Treatment for Chemotherapy-Ineligible Patients With De Novo Metastatic Nasopharyngeal Carcinoma

TypeinterventionalSponsorSun Yat-sen UniversityRan2026 to 2030Enrolled28ConditionsNasopharyngeal Carcinoma (NPC), Metastatic Nasopharyngeal CarcinomaArmsSintilimab, ipilimumab, Radscopal Radiotherapy
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Platelet-to-lymphocyte ratio and systemic inflammation response index are the optimal combination for risk stratification in patients with nasopharyngeal carcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  8. Review
  9. Review
  10. Review
  11. Applications of single-cell transcriptomics: updated insights in endometrial cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  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

20 authors at 7 institutions in 2 countries.

Darren Wan-Teck LimNational Cancer Centre Singapore, Singapore, Singapore. darren.lim.w.t@singhealth.com.sg.ORCID 0000-0002-4655-0206
Hsiang-Fong KaoNational Taiwan University Hospital, Taipei, Taiwan.
Lisda SutejaNational Cancer Centre Singapore, Singapore, Singapore.ORCID 0000-0002-4548-2766
Constance H LiNational Cancer Centre Singapore, Singapore, Singapore.
Hong Sheng QuahNational Cancer Centre Singapore, Singapore, Singapore.ORCID 0000-0001-8430-8528
Daniel Shao-Weng TanNational Cancer Centre Singapore, Singapore, Singapore.ORCID 0000-0002-6514-6786
Sze-Huey TanNational Cancer Centre Singapore, Singapore, Singapore.ORCID 0000-0002-3089-7379
Eng-Huat TanNational Cancer Centre Singapore, Singapore, Singapore.
Wan-Ling TanNational Cancer Centre Singapore, Singapore, Singapore.
Justina Nadia LeeInstitute of Molecular and Cell Biology, A*STAR, Singapore, Singapore.
Felicia Yu-Ting WeeInstitute of Molecular and Cell Biology, A*STAR, Singapore, Singapore.
Amit JainNational Cancer Centre Singapore, Singapore, Singapore.
Boon-Cher GohNational University Health System, Singapore, Singapore.
Melvin L K ChuaNational Cancer Centre Singapore, Singapore, Singapore.ORCID 0000-0002-1648-1473
Bin-Chi LiaoNational Taiwan University Hospital, Taipei, Taiwan.
Quan Sing NgNational Cancer Centre Singapore, Singapore, Singapore.
Ruey-Long HongNational Taiwan University Hospital, Taipei, Taiwan.
Mei-Kim AngNational Cancer Centre Singapore, Singapore, Singapore.
Joe Poh-Sheng YeongInstitute of Molecular and Cell Biology, A*STAR, Singapore, Singapore.ORCID 0000-0002-6674-7153
N Gopalakrishna IyerNational Cancer Centre Singapore, Singapore, Singapore. gmsngi@nus.edu.sg.ORCID 0000-0002-8812-6219
Duke-NUS Medical School · SGNational Cancer Centre Singapore · SGAgency for Science, Technology and Research · SGNational Taiwan University · TWNational University Health System · SGSingapore General Hospital · SGSingHealth · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-agent checkpoint inhibitor (CPI) activity in Epstein-Barr Virus (EBV) related nasopharyngeal carcinoma (NPC) is limited. Dual CPI shows increased activity in solid cancers. In this single-arm phase II trial (NCT03097939), 40 patients with recurrent/metastatic EBV-positive NPC who failed prior chemotherapy receive nivolumab 3 mg/kg every 2 weeks and ipilimumab 1 mg/kg every 6 weeks. Primary outcome of best overall response rate (BOR) and secondary outcomes (progression-free survival [PFS], clinical benefit rate, adverse events, duration of response, time to progression, overall survival [OS]) are reported. The BOR is 38% with median PFS and OS of 5.3 and 19.5 months, respectively. This regimen is well-tolerated and treatment-related adverse events requiring discontinuation are low. Biomarker analysis shows no correlation of outcomes to PD-L1 expression or tumor mutation burden. While the BOR does not meet pre-planned estimates, patients with low plasma EBV-DNA titre (<7800 IU/ml) trend to better response and PFS. Deep immunophenotyping of pre- and on-treatment tumor biopsies demonstrate early activation of the adaptive immune response, with T-cell cytotoxicity seen in responders prior to any clinically evident response. Immune-subpopulation profiling also identifies specific PD-1 and CTLA-4 expressing CD8 subpopulations that predict for response to combined immune checkpoint blockade in NPC.

Indexed as

Epstein-Barr Virus InfectionsNasopharyngeal NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsCTLA-4 AntigenHerpesvirus 4, HumanHumansNasopharyngeal CarcinomaNeoplasm Recurrence, LocalProgrammed Cell Death 1 ReceptorTreatment OutcomeCTLA-4 AntigenProgrammed Cell Death 1 Receptor

Identifiers

PMID37188668
PMCPMC10184620
OpenAlexW4376642794

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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 Socratic graph.