Evidence map›Paper›PMID 39225092›Full record

ReviewThe Journal of clinical investigation2024

Cancer therapy-related salivary dysfunction.

Cristina Paz, Annemarie Glassey, Abigail Frick, Sarah Sattar, Nicholas G Zaorsky, Grace C Blitzer, Randall J Kimple

Abstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Organoid-based modeling and regenerative strategies for salivary gland dysfunction.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Review
  11. Article
  12. Article
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

7 authors.

Cristina PazDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Annemarie GlasseyDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Abigail FrickDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Sarah SattarDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Nicholas G ZaorskyUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio, USA.
Grace C BlitzerDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Randall J KimpleDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Project 3: Modulation of the head and neck tumor immune microenvironment by targeting the TAM family of receptorsP50CA278595 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI David J Beebe · 2022 to 2026
$12.5M
Intra-salivary gland autotransplantation of marrow mesenchymal stromal cells for treatment of radiation induced xerostomiaUH3DE030431 · NIDCR · UNIVERSITY OF WISCONSIN-MADISON · PI Jacques Galipeau, Randall J. Kimple · 2023 to 2026
$2.0M
Intra-salivary gland autotransplantation of marrow mesenchymal stromal cells for treatment of radiation induced xerostomiaUG3DE030431 · NIDCR · UNIVERSITY OF WISCONSIN-MADISON · PI KIMPLE, RANDALL J. · 2021 to 2021
$312k
Planning a phase I study of minor salivary gland derived autologous MSCs for prevention of long-term radiation induced xerostomiaR34DE033042 · NIDCR · UNIVERSITY OF WISCONSIN-MADISON · PI KIMPLE, RANDALL J., MCCOY, SARA · 2023 to 2024
$298k
Mesenchymal stromal cells for treatment of radiation-induced xerostomiaF31DE031180 · NIDCR · UNIVERSITY OF WISCONSIN-MADISON · PI PAZ, CRISTINA · 2022 to 2024
$112k
NCI NIH HHS P30 CA014520NCI NIH HHS P50 CA278595NIDCR NIH HHS F31 DE031180NIDCR NIH HHS R34 DE033042NIDCR NIH HHS UG3 DE030431NIDCR NIH HHS UH3 DE030431
6 · The paper itself

Abstract

Salivary gland dysfunction is a common side effect of cancer treatments. Salivary function plays key roles in critical daily activities. Consequently, changes in salivary function can profoundly impair quality of life for cancer patients. We discuss salivary gland anatomy and physiology to understand how anticancer therapies such as chemotherapy, bone marrow transplantation, immunotherapy, and radiation therapy impair salivary function. We discuss approaches to quantify xerostomia in the clinic, including the advantages and limitations of validated quality-of-life instruments and approaches to directly measuring salivary function. Current and emerging approaches to treat cancer therapy-induced dry mouth are presented using radiation-induced salivary dysfunction as a model. Limitations of current sialagogues and salivary analogues are presented. Emerging approaches, including cellular and gene therapy and novel pharmacologic approaches, are described.

Indexed as

NeoplasmsSalivary GlandsXerostomiaAnimalsAntineoplastic AgentsHumansImmunotherapyQuality of LifeRadiotherapyAntineoplastic Agents

Identifiers

PMID39225092
PMCPMC11364403

What OpenQuestion holds

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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.