Evidence map›Paper›PMID 39624249›Full record

ArticleJTO clinical and research reports2024

CRYOVATE: A Pilot Study of Lung Cancer Cryoactivation in Combination With Immunotherapy in Advanced NSCLC.

Antoine Desilets, Gabryella Pinheiro, Wiam Belkaid, Olivier Salko, Julie Malo, Eleyine Zarour, Adeline Jouquan, Anne-Julie Thibaudeau, Marc-Antoine Nolin, John Stagg and 10 more

Abstract read
In one paragraph

Article in JTO clinical and research reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
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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

20 authors.

Antoine DesiletsDepartment of Medicine, Division of Hematology-Oncology, Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Gabryella PinheiroCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Wiam BelkaidCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Olivier SalkoCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Julie MaloCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Eleyine ZarourDepartment of Radiology, CHUM, Montreal, Canada.
Adeline JouquanCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Anne-Julie ThibaudeauCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Marc-Antoine NolinCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
John StaggCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Marie FlorescuDepartment of Medicine, Division of Hematology-Oncology, Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Mustapha TehfeDepartment of Medicine, Division of Hematology-Oncology, Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Normand BlaisDepartment of Medicine, Division of Hematology-Oncology, Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Samer TabchiDepartment of Medicine, Division of Hematology-Oncology, Rouyn-Noranda Hospital, Rouyn-Noranda, Canada.
Jean ChalaouiDepartment of Radiology, CHUM, Montreal, Canada.
Philippe StephensonDepartment of Pathology, CHUM, Montreal, Canada.
Arielle ElkriefDepartment of Medicine, Division of Hematology-Oncology, Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Vincent Quoc-Huy TrinhCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.
Bertrand RoutyDepartment of Medicine, Division of Hematology-Oncology, Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Moishe LibermanCentre de recherche du CHUM (CRCHUM), University of Montreal, Montreal, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: NSCLC is the leading cause of cancer-related mortality. Although immune-checkpoint inhibitors (ICIs) have improved survival in patients with advanced NSCLC, treatment resistance remains a challenge. Cryoactivation, a technique inducing cell death by cycles of freezing and thawing, has the potential to augment tumor responses when combined with ICIs. Methods: This single-arm phase 1 clinical trial enrolled patients with previously untreated advanced NSCLC and 50% or higher programmed cell death ligand-1 (PD-L1). Patients underwent cryoactivation followed by ICI monotherapy initiated 5 days later. The primary end point was the objective response rate. Co-secondary end points included the safety and feasibility of the procedure and overall survival. Immune cell infiltration by immunohistochemistry was performed on paired pre- and post-treatment samples, with patients dichotomized according to clinical benefit (CB) rate (CB versus no CB [NCB]). Results: Eight patients were enrolled. Two patients achieved a partial response, yielding an objective response rate of 25%. Median progression-free survival and overall survival were 3.8 and 13.0 months, respectively. The cryoactivation procedure was well tolerated, without grade 3 to 4 adverse events. Post-hoc analysis reported a CB rate of 50%. Immunohistochemistry analysis reported a numerical difference in the cluster of differentiation 8-positive (CD8 Conclusions: Although cryoactivation combined with pembrolizumab was safe and well tolerated in patients with NSCLC, therapeutic benefits were not evident compared with historical cohorts of ICI monotherapy. Correlative analyses validated CD8

Indexed as

CryoactivationImmune checkpoint inhibitorsImmunotherapyNon–small cell lung cancer

Identifiers

PMID39624249
PMCPMC11609556

What OpenQuestion holds

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Registered trials

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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.