Evidence map›Paper›PMID 35158794›Full record

ArticleCancers2022

Pancreatic Cancer Organoids in the Field of Precision Medicine: A Review of Literature and Experience on Drug Sensitivity Testing with Multiple Readouts and Synergy Scoring.

Lotta Mäkinen, Markus Vähä-Koskela, Matilda Juusola, Harri Mustonen, Krister Wennerberg, Jaana Hagström, Pauli Puolakkainen, Hanna Seppänen

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 14% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Clinical significance of non-invasive in vitro drug sensitivity profiling using pancreatic cancer organoids derived from saline flushes collected during routine EUS-FNA.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  5. Review
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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

8 authors at 1 institution in 1 country.

Lotta MäkinenDepartment of Surgery, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.ORCID 0000-0003-1553-1915
Markus Vähä-KoskelaInstitute for Molecular Medicine Finland FIMM, Helsinki Institute for Life Science HiLIFE, University of Helsinki, 00290 Helsinki, Finland.ORCID 0000-0001-7764-7820
Matilda JuusolaDepartment of Surgery, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Harri MustonenDepartment of Surgery, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Krister WennerbergInstitute for Molecular Medicine Finland FIMM, Helsinki Institute for Life Science HiLIFE, University of Helsinki, 00290 Helsinki, Finland.
Jaana HagströmDepartment of Pathology, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.ORCID 0000-0001-6079-7881
Pauli PuolakkainenDepartment of Surgery, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Hanna SeppänenDepartment of Surgery, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
University of Helsinki · FI

Funding

Cancer Foundations Finland 2018-2021Georg C. and Mary Ehrnrooth foundation 2021Medicinska Understödsföreningen Liv och Hälsa 2017-2021Sigrid Jusélius Foundation 2017-2021Waldemar von Frenckells stiftelse 2019
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a silent killer, often diagnosed late. However, it is also dishearteningly resistant to nearly all forms of treatment. New therapies are urgently needed, and with the advent of organoid culture for pancreatic cancer, an increasing number of innovative approaches are being tested. Organoids can be derived within a short enough time window to allow testing of several anticancer agents, which opens up the possibility for functional precision medicine for pancreatic cancer. At the same time, organoid model systems are being refined to better mimic the cancer, for example, by incorporation of components of the tumor microenvironment. We review some of the latest developments in pancreatic cancer organoid research and in novel treatment design. We also summarize our own current experiences with pancreatic cancer organoid drug sensitivity and resistance testing (DSRT) in 14 organoids from 11 PDAC patients. Our data show that it may be necessary to include a cell death read-out in ex vivo DSRT assays, as metabolic viability quantitation does not capture actual organoid killing. We also successfully adapted the organoid platform for drug combination synergy discovery. Lastly, live organoid culture 3D confocal microscopy can help identify individual surviving tumor cells escaping cell death even during harsh combination treatments. Taken together, the organoid technology allows the development of novel precision medicine approaches for PDAC, which paves the way for clinical trials and much needed new treatment options for pancreatic cancer patients.

Indexed as

cancer precision medicinedrug combinationsorganoidpancreatic ductal adenocarcinoma

Identifiers

PMID35158794
PMCPMC8833348
OpenAlexW4206766967

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.