Evidence map›Paper›PMID 35834010›Full record

ArticleJournal of cancer research and clinical oncology2023

Safety and efficacy of pembrolizumab for advanced nonsmall cell lung cancer: before and during the COVID-19 pandemic.

Doran Ksienski, Sapna Gupta, Pauline T Truong, Jeffrey Bone, Angela Chan, Deepu Alex, Jason Hart, Philip Pollock, Tiffany Patterson, Melissa Clarkson and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

13 authors at 3 institutions in 1 country.

Doran KsienskiBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada. dksienski@bccancer.bc.ca.ORCID http://orcid.org/0000-0001-6300-8294
Sapna GuptaBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada.
Pauline T TruongBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada.
Jeffrey BoneBC Children's Hospital Research Institute, Vancouver, BC, Canada.
Angela ChanUniversity of British Columbia, Victoria, BC, Canada.
Deepu AlexBC Cancer-Vancouver, Vancouver, BC, Canada.
Jason HartBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada.
Philip PollockBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada.
Tiffany PattersonBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada.
Melissa ClarksonBC Cancer-Victoria, 2410 Lee Avenue, Victoria, BC, V8R 6V5, Canada.
Dushanthi DissanayakeFaculty of Medicine, University of British Columbia, Victoria, BC, Canada.
Eric SonkeDepartment of Internal Medicine, University of British Columbia, Victoria, BC, Canada.
Mary LesperanceDepartment of Mathematics and Statistics, University of Victoria, Victoria, BC, Canada.
University of British Columbia · CAUniversity of Victoria · CABC Children's Hospital · CA

Funding

BC Cancer Foundation F21-02290
6 · The paper itself

Abstract

purposeThe COVID-19 pandemic changed diagnostic and treatment pathways in oncology. We compared the safety and efficacy of pembrolizumab amongst advanced nonsmall cell lung cancer (NSCLC) patients with a PD-L1 tumor proportion score (TPS) ≥ 50% before and during the pandemic.

methodsAdvanced NSCLC patients initiating pembrolizumab between June 2015 and December 2019 ("pre-pandemic cohort") and between March 2020 and March 2021 ("pandemic cohort") at BC Cancer were identified retrospectively. Multivariable logistic regression evaluated risk factors for immune-related adverse events (irAE) ≥ grade 3 at the 6 week, 3 month, and 6 month landmarks. Cox regression models of overall survival (OS) were constructed.

resultsThe study population comprised 417 patients in the pre-pandemic cohort and 111 patients in the pandemic cohort. Between March and May 2020, 48% fewer advanced NSCLC cases with PD-L1 TPS ≥ 50% were diagnosed compared to similar intervals in 2018-2019. Telemedicine assessment [new patient consultations (p < 0.001) and follow-up (p < 0.001)] and extended interval pembrolizumab dosing (p < 0.001) were more common in the pandemic cohort. Patients initiating pembrolizumab after February 2020 (vs. before January 2020) experienced similar odds of developing severe irAE. 2/111 (1.8%) patients receiving pembrolizumab during the pandemic tested positive for COVID-19. On multivariable analysis, no association between pembrolizumab treatment period (before vs. during the COVID-19 pandemic) and OS was observed (p = 0.18).

conclusionSignificant changes in healthcare delivery in response to the pandemic did not result in increased high grade toxicity or lower survival outcomes in patients with advanced NSCLC treated with pembrolizumab.

Indexed as

Carcinoma, Non-Small-Cell LungCOVID-19Lung NeoplasmsAntibodies, Monoclonal, HumanizedB7-H1 AntigenHumansPandemicsRetrospective StudiesAntibodies, Monoclonal, HumanizedB7-H1 AntigenpembrolizumabCOVID-19Lung cancerPembrolizumabSafetyToxicity

Identifiers

PMID35834010
PMCPMC9281358
OpenAlexW4285390563

What OpenQuestion holds

Textmetadata
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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.