Evidence map›Paper›PMID 35848053›Full record

ArticleCancer medicine2023

Clinical impact of tumour burden on the efficacy of PD-1/PD-L1 inhibitors plus chemotherapy in non-small-cell lung cancer.

Taichi Miyawaki, Hirotsugu Kenmotsu, Kosei Doshita, Hiroaki Kodama, Naoya Nishioka, Yuko Iida, Eriko Miyawaki, Nobuaki Mamesaya, Haruki Kobayashi, Shota Omori and 10 more

Abstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
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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.

Taichi MiyawakiDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Hirotsugu KenmotsuDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0003-0590-9259
Kosei DoshitaDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Hiroaki KodamaDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0002-0953-3183
Naoya NishiokaDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Yuko IidaDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Eriko MiyawakiDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Nobuaki MamesayaDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Haruki KobayashiDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0002-3386-8063
Shota OmoriDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0003-1407-9779
Ryo KoDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.
Kazushige WakudaDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0002-6369-2388
Akira OnoDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0001-5705-9423
Tateaki NaitoDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0003-4047-2929
Haruyasu MurakamiDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.ORCID 0000-0003-2416-546X
Keita MoriClinical Research Support Center, Shizuoka Cancer Centre, Shizuoka, Japan.
Hideyuki HaradaRadiation and Proton Therapy Centre, Shizuoka Cancer Centre, Shizuoka, Japan.
Masahiro EndoDivision of Diagnostic Radiology, Shizuoka Cancer Centre, Shizuoka, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Toshiaki TakahashiDivision of Thoracic Oncology, Shizuoka Cancer Centre, Shizuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProgrammed cell death 1 (PD-1)/programmed cell death ligand (PD-L1) inhibitors plus chemotherapy (ICI + Chemo) is the standard treatment for advanced non-small-cell lung cancer (NSCLC). However, the impact of tumour burden on the efficacy of ICI + Chemo remains unknown.

methodsWe retrospectively evaluated 92 patients with advanced NSCLC treated with ICI + Chemo. Tumour burden was assessed as the sum of the longest diameter of the target lesion (BSLD) and number of metastatic lesions (BNMLs). We categorised the patients into three groups based on the combined BSLD and BNML values.

resultsSixty-eight patients (74%) had progressive disease or died. Forty-four patients (48%) in the low-BSLD group had a median progression-free survival (PFS) of 9.5 months, whereas patients in the high-BSLD group had a median PFS of 4.6 months (hazard ratio [HR] = 0.54, p = 0012). Twenty-five patients (27%) in the low-BNML group had a median PFS of 9.6 months, whereas patients in the high-BNML group had a median PFS of 6.5 months (HR = 0.51, p = 0.029). Low-BSLD and low-BNML were associated independently with improved PFS in multivariate analysis. Analysis of the tumour burden combined with BSLD and BNML revealed a trend towards improved PFS as the tumour burden decreased, with median PFS of 22.3, 8.7, and 3.9 months in the low- (N = 13), medium- (N = 42) and high-burden (N = 37) groups respectively.

conclusionsOur findings demonstrated that a high tumour burden negatively impacts the efficacy of ICI + Chemo in patients with advanced NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenHumansImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorRetrospective StudiesTumor BurdenB7-H1 AntigenImmune Checkpoint InhibitorsProgrammed Cell Death 1 Receptorclinical cancer researchimmunologylung cancermetastasisnon-small-cell lung cancer

Identifiers

PMID35848053
PMCPMC9883568

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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.