Evidence map›Paper›PMID 33835222›Full record

ArticleCancer immunology, immunotherapy : CII2021

Tumour draining lymph node-generated CD8 T cells play a role in controlling lung metastases after a primary tumour is removed but not when adjuvant immunotherapy is used.

Vanessa S Fear, Catherine A Forbes, Samuel A Neeve, Scott A Fisher, Jonathan Chee, Jason Waithman, Shao Kang Ma, Richard Lake, Anna K Nowak, Jenette Creaney and 3 more

Erratum issued Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT06815705 (An Exploratory Study of Reconstruction of Cervical Lymphatic System by Vascularized Lymphoid Tissue Transplantation During Head and Neck Squamous Cell Carcinoma Surgery), which is not on this map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.4field-weighted citation impact, top 8% 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.

NCT06815705 nanot yet recruitingnot on this mapstarted 2025, after this paper: background citation

An Exploratory Study of Reconstruction of Cervical Lymphatic System by Vascularized Lymphoid Tissue Transplantation During Head and Neck Squamous Cell Carcinoma Surgery

TypeinterventionalSponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityRan2025 to 2027Enrolled23ConditionsHead and Neck Squamous Cell Carcinoma, Lymphedema, Secondary, Neck Lymph Dissection, Vascularized Lymph Node TransplantationArmsVascularized lymphatic transplantation
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 40 citations in OpenAlex.

  1. Decoding B-cell Signatures of Complete Pathologic Response to Perioperative Chemoimmunotherapy in Non-Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  10. Bioresponsive immunomodulator nanocomplex for selective immunoengineering in metastatic lymph nodes.Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Vanessa S FearInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia. Vanessa.Fear@telethonkids.org.au.ORCID http://orcid.org/0000-0001-8363-6685
Catherine A ForbesInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Samuel A NeeveInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Scott A FisherInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Jonathan CheeInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Jason WaithmanTelethon Kids Institute, Perth, Australia.
Shao Kang MaInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Richard LakeInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Anna K NowakInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Jenette CreaneyInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
Matthew D BrownFiona Stanley Hospital, Murdoch, Australia.
Christobel SaundersDivision of Surgery, Medical School, University of Western Australia, Perth, Australia.
Bruce W S RobinsonInstitute for Respiratory Health, National Centre for Asbestos Related Diseases, University of Western Australia, Perth, Australia.
The University of Western Australia · AUThe Kids Research Institute Australia · AUFiona Stanley Hospital · AU

Funding

National Health and Medical Research Council APP1107043 CRENational Health and Medical Research Council APP1107091National Health and Medical Research Council APP1108638 Practitioner FellowshipNational Health and Medical Research Council APP1144209
6 · The paper itself

Abstract

Surgical resection of cancer remains the frontline therapy for millions of patients annually, but post-operative recurrence is common, with a relapse rate of around 45% for non-small cell lung cancer. The tumour draining lymph nodes (dLN) are resected at the time of surgery for staging purposes, and this cannot be a null event for patient survival and future response to immune checkpoint blockade treatment. This project investigates cancer surgery, lymphadenectomy, onset of metastatic disease, and response to immunotherapy in a novel model that closely reflects the clinical setting. In a murine metastatic lung cancer model, primary subcutaneous tumours were resected with associated dLNs remaining intact, completely resected or partially resected. Median survival after surgery was significantly shorter with complete dLN resection at the time of surgery (49 days (95%CI)) compared to when lymph nodes remained intact (> 88 days; p < 0.05). Survival was partially restored with incomplete lymph node resection and CD8 T cell dependent. Treatment with aCTLA4 whilst effective against the primary tumour was ineffective for metastatic lung disease. Conversely, aPD-1/aCD40 treatment was effective in both the primary and metastatic disease settings and restored the detrimental effects of complete dLN resection on survival. In this pre-clinical lung metastatic disease model that closely reflects the clinical setting, we observe decreased frequency of survival after complete lymphadenectomy, which was ameliorated with partial lymph node removal or with early administration of aPD-1/aCD40 therapy. These findings have direct relevance to surgical lymph node resection and adjuvant immunotherapy in lung cancer, and perhaps other cancer, patients.

Indexed as

Lymph Node ExcisionAnimalsCD8-Positive T-LymphocytesChemotherapy, AdjuvantImmune Checkpoint InhibitorsLung NeoplasmsLymph NodesMiceNeoplasm MetastasisNeoplasm Recurrence, LocalImmune Checkpoint InhibitorsCancer surgeryImmunotherapyLymph nodesMetastatic disease

Identifiers

PMID33835222
PMCPMC8505306
OpenAlexW3151107652

What OpenQuestion 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 OpenQuestion graph.