Evidence map›Paper›PMID 37443348›Full record

ArticleBritish journal of cancer2023

Combination of pembrolizumab and pelareorep promotes anti-tumour immunity in advanced pancreatic adenocarcinoma (PDAC).

Devalingam Mahalingam, Siqi Chen, Ping Xie, Houra Loghmani, Thomas Heineman, Aparna Kalyan, Sheetal Kircher, Irene B Helenowski, Xinlei Mi, Victoria Maurer and 4 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03723915 (A Phase 2 Study of Pembrolizumab in Combination With Pelareorep in Patients With Advanced Pancreatic Adenocarcinoma), which is not on this map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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.

NCT03723915 phase2terminatednot on this map

A Phase 2 Study of Pembrolizumab in Combination With Pelareorep in Patients With Advanced Pancreatic Adenocarcinoma

TypeinterventionalSponsorNorthwestern UniversityRan2018 to 2021Enrolled17ConditionsPancreatic Adenocarcinoma, Stage III Pancreatic Cancer AJCC v8, Stage IV Pancreatic Cancer AJCC v8ArmsPembrolizumab, Wild-type Reovirus
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Pancreatic cancer in 2025: Have we found a solution?World journal of gastroenterology · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Advancing Immunotherapy in Pancreatic Cancer.International journal of molecular sciences · 2024
    Review
  15. Review
  16. Review
  17. Article
  18. 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

14 authors at 2 institutions in 2 countries.

Devalingam MahalingamRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. mahalingam@northwestern.edu.
Siqi Chen *Robert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Ping Xie *Robert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Houra LoghmaniOncolytics Biotech, Calgary, AB, Canada.
Thomas HeinemanOncolytics Biotech, Calgary, AB, Canada.
Aparna KalyanRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Sheetal KircherRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Irene B HelenowskiQuantitative Data Sciences Core, Department of Preventative Medicine, Biostatistics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Xinlei MiQuantitative Data Sciences Core, Department of Preventative Medicine, Biostatistics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Victoria MaurerRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Matt CoffeyOncolytics Biotech, Calgary, AB, Canada.
Mary MulcahyRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Al- BensonRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Bin ZhangRobert H. Lurie Comprehensive Cancer Center, Division of Hematology & Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. bin.zhang@northwestern.edu.ORCID 0000-0002-6631-7647
Northwestern University · USOncolytics Biotech (Canada) · CA

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Targeting posttranslational modifications of CD73 in TNBCsR01CA258857 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Yong Wan, Bin Zhang · 2021 to 2026
$3.2M
The distinct role of cysteinyl leukotriene receptor for myeloid-derived suppressive cellsR01CA250101 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2020 to 2025
$2.5M
Targeting Posttranslational Modifications in Breast CarcinogenesisR01CA250110 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WAN, YONG · 2020 to 2025
$2.3M
WEE1 inhibition and tumor immunityR01CA222963 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2018 to 2023
$2.2M
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA222963NCI NIH HHS R01 CA250101NCI NIH HHS R01 CA250110NCI NIH HHS R01 CA258857
6 · The paper itself

Abstract

backgroundWe previously reported activity of pelareorep, pembrolizumab and chemotherapy. Patients developed new T-cell clones and increased peripheral T-cell clonality, leading to an inflamed tumour. To evaluate a chemotherapy-free regimen, this study assesses if pelareorep and pembrolizumab has efficacy by inducing anti-tumour immunological changes (NCT03723915).

methodsPDAC patients who progressed after first-line therapy, received iv pelareorep induction with pembrolizumab every 21-days. Primary objective is overall response rate. Secondary objectives included evaluation of immunological changes within tumour and blood.

resultsClinical benefit rate (CBR) was 42% amongst 12 patients. One patient achieved partial response (PR) and four stable disease (SD). Seven progressed, deemed non-responders (NR). VDAC1 expression in peripheral CD8

conclusionPelareorep and pembrolizumab showed modest efficacy in unselected patients, although potential immune and metabolic biomarkers were identified to warrant further evaluation.

Indexed as

AdenocarcinomaPancreatic NeoplasmsAntibodies, Monoclonal, HumanizedB7-H1 AntigenCD8-Positive T-LymphocytesHumansOncolytic VirusesAntibodies, Monoclonal, HumanizedB7-H1 Antigenpembrolizumabreolysin

Identifiers

PMID37443348
PMCPMC10449917
OpenAlexW4384155464

What OpenQuestion holds

Textmetadata
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.