Evidence map›Paper›PMID 38206755›Full record

ArticleBlood advances2024

Patterns of progression after immune checkpoint inhibitors for Hodgkin lymphoma: implications for radiation therapy.

Jessica F Burlile, Kelsey M Frechette, William G Breen, Steven R Hwang, Alexandra S Higgins, Adrienne N Nedved, William S Harmsen, Sydney D Pulsipher, Thomas E Witzig, Ivana N Micallef and 11 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. 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

21 authors at 4 institutions in 1 country.

Jessica F BurlileDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-8653-1045
Kelsey M FrechetteDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN.
William G BreenDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN.
Steven R HwangDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0002-6536-1291
Alexandra S HigginsDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Adrienne N NedvedDepartment of Pharmacy, Mayo Clinic, Rochester, MN.
William S HarmsenDepartment of Biostatistics and Health Sciences Research, Mayo Clinic, Rochester, MN.
Sydney D PulsipherDepartment of Biostatistics and Health Sciences Research, Mayo Clinic, Rochester, MN.ORCID 0000-0002-3193-4565
Thomas E WitzigDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0002-4215-6500
Ivana N MicallefDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Bradford S HoppeDepartment of Radiation Oncology, Mayo Clinic, Jacksonville, FL.ORCID 0000-0002-2312-5418
Thomas M HabermannDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Gita ThanarajasingamDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Patrick B JohnstonDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
David J InwardsDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
N Nora BennaniDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0001-8358-5953
Jennifer L PetersonDepartment of Radiation Oncology, Mayo Clinic, Jacksonville, FL.ORCID 0000-0001-7458-1504
Bradley J StishDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN.
William G RuleDepartment of Radiation Oncology, Mayo Clinic, Phoenix, AZ.
Stephen M AnsellDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Scott C LesterDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN.
Mayo Clinic · USMayo Clinic in Arizona · USMayo Clinic in Florida · USMayo Clinic Health System · US

Funding

Intravenous VSV virotherapy in lymphomaR01CA262613 · NCI · MAYO CLINIC ROCHESTER · PI BENNANI, NABILA NORA, PENG, KAH-WHYE · 2023 to 2025
$1.8M
NCI NIH HHS R01 CA262613
6 · The paper itself

Abstract

abstractImmune checkpoint inhibitors (ICIs) have demonstrated remarkable response rates in relapsed or refractory Hodgkin lymphoma (HL). Still, most patients eventually progress. Patterns of progression after ICIs are not well described and are essential to defining the role of local therapies in combination with ICIs. We identified patients who received ICIs for HL between 2013 and 2022. Fludeoxyglucose-18 positron emission tomography (FDG-PET) before initiating ICI and at progression on/after ICI were reviewed, and areas of active HL were recorded. An exploratory analysis of treatable progression included patients with ≤5 sites of disease on pre-ICI FDG-PET and progression only at pre-ICI sites. Ninety patients were identified; 69 had complete records, and of these, 32 (52%) had relapsed at ICI initiation, 17 (25%) were refractory, and 16 (23%) received ICI as first-line therapy. Forty-five of 69 patients had ≤5 sites of disease (limited) on pre-ICI FDG-PET. Patients with >5 sites of disease had a higher risk of progression, and every site of disease >5 sites conferred an additional 1.2x higher chance of progression. At a median follow-up of 4.0 years, 41 of 69 patients had progressed on/after ICIs (cumulative incidence 66.4%), and of these, 22 of 41 patients progressed only at pre-ICI sites (cumulative incidence 39.4%). In an exploratory analysis, the cumulative incidence of a treatable progression among 45 patients with limited disease was 34%. The cumulative incidence of any progression among this cohort was 58.9%. More than one-third of patients with limited disease before ICIs experienced progression only at pre-ICI sites of disease. These patients could be candidates for radiation during or after ICIs.

Indexed as

Hodgkin DiseaseImmune Checkpoint InhibitorsCognitionFluorodeoxyglucose F18HumansPositron-Emission TomographyFluorodeoxyglucose F18Immune Checkpoint Inhibitors

Identifiers

PMID38206755
PMCPMC10912840
OpenAlexW4390754656

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.