Evidence map›Paper›PMID 20697067›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2010

In situ vaccination with a TLR9 agonist induces systemic lymphoma regression: a phase I/II study.

Joshua D Brody, Weiyun Z Ai, Debra K Czerwinski, James A Torchia, Mia Levy, Ranjana H Advani, Youn H Kim, Richard T Hoppe, Susan J Knox, Lewis K Shin and 3 more

7 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 7 registered trials, which are not on this map. Cited by 276 papers.

0numbers the graph read from it
0cells of the map it votes in
276citing papers in PubMed
10.6field-weighted citation impact, top 1% 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.

NCT00185965 phase1 / phase2completednot on this map

Le23 CPG: A Phase 1-2 Study of Intratumoral Injection of CPG 7909, A TLR 9 Agonist, Combined With Local Radiation in Recurrent Low-Grade Lymphomas

TypeinterventionalSponsorRonald LevyRan2004 to 2010Enrolled30ConditionsNon-Hodgkin Lymphoma, Mycosis FungoidesArmsCPG 7909
NCT01976585 phase1 / phase2completednot on this mapstarted 2014, after this paper: background citation

A Phase I/II Study of Intratumoral Injection of rhuFlt3L/CDX-301 and Poly-ICLC in Combination With Low-Dose Radiotherapy in Low-Grade B-cell Lymphomas

TypeinterventionalSponsorJoshua BrodyRan2014 to 2020Enrolled21ConditionsLow-Grade B-cell LymphomaArmsrhuFlt3L/CDX-301, Poly-ICLC
NCT01984892 phase2terminatednot on this mapstarted 2013, after this paper: background citation

Treatment of Solid Tumors With Intratumoral Hiltonol® (Poly-ICLC): A Phase II Clinical Study

TypeinterventionalSponsorNina BhardwajRan2013 to 2014Enrolled8ConditionsMelanoma, Squamous Cell Carcinoma of the Head and Neck, Squamous Cell Carcinoma of the Skin, Sarcoma of the SkinArmsPoly-ICLC
NCT02579005 phase1suspendednot on this mapstarted 2018, after this paper: background citation

Radio-Immuno-Modulation for Advanced Lung Cancer: a Pilot Study Evaluating Tolerance and Immune Responses

TypeinterventionalSponsorCentre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de MontrealRan2018 to 2025Enrolled24ConditionsLung CancerArmsPatients with a living donor, Patients with a UCB donor
NCT03262103 phase1completednot on this mapstarted 2017, after this paper: background citation

Phase I Study of In Situ Autologous Vaccination Against Prostate Cancer With Intratumoral and Systemic Hiltonol® (Poly-ICLC) Prior To Radical Prostatectomy

TypeinterventionalSponsorAshutosh Kumar TewariRan2017 to 2022Enrolled13ConditionsProstate CancerArmsIntratumoral (IT) Poly ICLC 0.5 mg, Intratumoral (IT) Poly ICLC 1.0 mg, Intramuscular (IM) Poly ICLC, Radical Prostatectomy
NCT03721679 phase1 / phase2terminatednot on this mapstarted 2018, after this paper: background citation

Poly-ICLC (Hiltonol®) Plus Anti-PD1 or Anti-PD-L1 in Unresectable Solid Cancers An Adaptive Phase I/II Clinical Pilot Study

TypeinterventionalSponsorOncovir, Inc.Ran2018 to 2021Enrolled7ConditionsSolid CancerArmsPoly-ICLC combination treatment with aPD-1 (Nivolumab or Pembrolizumab) or aPD-L1 (Atezolizumab or Durvalumab) over 6 months
NCT03792724 phase1 / phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Phase I-II Study of Intratumoral Urelumab Combined With Nivolumab in Patients With Solid Tumors

TypeinterventionalSponsorClinica Universidad de Navarra, Universidad de NavarraRan2019 to 2023Enrolled32ConditionsNeoplasmsArmsUrelumab + Nivolumab
3 · Its place in the literature

Who cites it

276 citing papers in PubMed, 482 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Cancer discovery · 2018
    Trial
  5. Trial
  6. Trial
  7. Review
  8. Article
  9. Targeting prostate adenocarcinoma tumor microenvironment via cancer nanotheranostics: a comprehensive update on improved roadmap for disease diagnosis, therapy and management.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  10. Review
  11. Article
  12. Frontiers in immunology · 2026
    Review
  13. Review
  14. Article
  15. Article
  16. Dendritic cell maturation in cancer.Nature reviews. Cancer · 2025
    Review
  17. Article
  18. TLR9: A Double-Dealing Toll-Like Receptor.ImmunoTargets and therapy · 2025
    Review
  19. Article
  20. The Tumor Immune Environment: Advances in the Cancer Immunotherapy Era.Methods in molecular biology (Clifton, N.J.) · 2025
    Review

216 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Joshua D Brody269 Campus Dr - CCSR rm 1105, Stanford, CA 94305, USA.
Weiyun Z Ai
Debra K Czerwinski
James A Torchia
Mia Levy
Ranjana H Advani
Youn H Kim
Richard T Hoppe
Susan J Knox
Lewis K Shin
Irene Wapnir
Robert J Tibshirani
Ronald Levy
Ford Motor Company (United States) · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
TRIGGERING CELL DEATH IN B CELL LYMPHOMAP01CA034233 · NCI · STANFORD UNIVERSITY · PI TIBSHIRANI, ROB · 1985 to 2010
$19.5M
NCI NIH HHS P01 CA034233NCI NIH HHS P01-CA34233NIAID NIH HHS T32 AI007290
6 · The paper itself

Abstract

purposeCombining tumor antigens with an immunostimulant can induce the immune system to specifically eliminate cancer cells. Generally, this combination is accomplished in an ex vivo, customized manner. In a preclinical lymphoma model, intratumoral injection of a Toll-like receptor 9 (TLR9) agonist induced systemic antitumor immunity and cured large, disseminated tumors. PATIENTS AND

methodsWe treated 15 patients with low-grade B-cell lymphoma using low-dose radiotherapy to a single tumor site and-at that same site-injected the C-G enriched, synthetic oligodeoxynucleotide (also referred to as CpG) TLR9 agonist PF-3512676. Clinical responses were assessed at distant, untreated tumor sites. Immune responses were evaluated by measuring T-cell activation after in vitro restimulation with autologous tumor cells.

resultsThis in situ vaccination maneuver was well-tolerated with only grade 1 to 2 local or systemic reactions and no treatment-limiting adverse events. One patient had a complete clinical response, three others had partial responses, and two patients had stable but continually regressing disease for periods significantly longer than that achieved with prior therapies. Vaccination induced tumor-reactive memory CD8 T cells. Some patients' tumors were able to induce a suppressive, regulatory phenotype in autologous T cells in vitro; these patients tended to have a shorter time to disease progression. One clinically responding patient received a second course of vaccination after relapse resulting in a second, more rapid clinical response.

conclusionIn situ tumor vaccination with a TLR9 agonist induces systemic antilymphoma clinical responses. This maneuver is clinically feasible and does not require the production of a customized vaccine product.

Indexed as

AdultAgedCancer VaccinesFemaleHumansImmunity, InnateInjections, IntralesionalLogistic ModelsLymphoma, B-CellMaleMiddle AgedOligodeoxyribonucleotidesPhenotypePrognosisProportional Hazards ModelsRemission InductionCancer VaccinesOligodeoxyribonucleotidesProMuneToll-Like Receptor 9

Identifiers

PMID20697067
PMCPMC2954133
OpenAlexW2170612601

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 1 more above

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.