Evidence map›Paper›PMID 36523994›Full record

ArticleFrontiers in oncology2022

Immune checkpoint inhibitors alone or in combination with chemotherapy for treatment of advanced non-small cell lung cancer after first-line platinum-based chemotherapy: A propensity score matching analysis.

Lupeng Qiu, Shan Gao, Sicheng Du, Shengjie Sun, Yanjie Liang, Zhuoya Sun, Tao Li, Guhe Jia, Ke Li, Xiaohui Sun and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2022. 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. Review
  2. Article
  3. Article
  4. Article
  5. 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

12 authors.

Lupeng QiuDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Shan GaoDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Sicheng DuDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Shengjie SunDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Yanjie LiangDepartment of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Zhuoya SunDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Tao LiDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Guhe JiaDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Ke LiDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiaohui SunDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Shunchang JiaoDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiao ZhaoDepartment of Oncology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitors (ICIs) have changed the treatment landscape of several cancer types. However, data are lacking with regard to the clinical responsiveness of ICIs in patients with advanced non-small cell lung cancer (NSCLC) after standard first-line chemotherapy. Therefore, we aimed to evaluate the clinical efficacy of ICI alone or in combination with chemotherapy for patients with advanced NSCLC after first-line platinum-based chemotherapy. Methods: We retrospectively collected patients with confirmed advanced NSCLC who underwent ICI monotherapy or ICI plus chemotherapy after first-line platinum-based chemotherapy between January 2018 and December 2020. A propensity score matching analysis was used to balance baseline characteristics between the two treatment groups. Kaplan-Meier methods and multivariable Cox regressions were used for survival analyses. Results: Among 832 eligible patients, 222 received ICI monotherapy and 610 received ICI plus chemotherapy. The median overall survival (OS) of patients who received ICI plus chemotherapy was 16.0 months compared with 13.1 months in patients who received ICI monotherapy (HR: 0.64, 95% CI: 0.49-0.85, P = 0.002). After 1:1 propensity score matching, all baseline characteristics were well-balanced between the two treatment groups. Patients who received ICI plus chemotherapy had significantly longer OS than those who received ICI monotherapy (NR vs. 13.1 months, HR: 0.50, 95% CI: 0.34-0.71, P < 0.001). Meanwhile, the median time to treatment discontinuation was 4.4 months in the ICI-chemo group and 3.5 months in the ICI-mono group (HR: 0.72, 95% CI: 0.58-0.89, P = 0.002). The multivariate analysis indicated that treatment regimen was an independent prognostic factor for OS (HR: 0.488, 95% CI: 0.337-0.707, P < 0.001). Moreover, a nomogram that integrated both treatment regimens and clinicopathological factors was created for survival prediction. Conclusion: Our study indicated that patients with advanced NSCLC who received ICI plus chemotherapy after first-line platinum-based chemotherapy tended to have longer OS than those who received ICI monotherapy. The multivariate analysis showed that treatment regimen was an independent prognostic factor for OS. Future prospective studies are needed to confirm these findings.

Indexed as

chemotherapyimmune checkpoint inhibitornon-small cell lung canceroverall survivalpropensity score matching

Identifiers

PMID36523994
PMCPMC9745307

What OpenQuestion holds

Textmetadata
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.