Evidence map›Paper›PMID 36776373›Full record

ArticleFrontiers in oncology2022

Tumor regression rate, PD-L1 expression, pembrolizumab/nab-paclitaxel-based regimens, squamous cell carcinoma, and comorbidities were independently associated with efficacy of neoadjuvant chemoimmunotherapy in non-small cell lung cancer.

Xingsheng Hu, Chunhong Hu, Xianling Liu, Fang Ma, Junpeng Xie, Ping Zhong, Chenxi Tang, Dan Fan, Yuan Gao, Xiang Feng and 3 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, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  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

13 authors.

Xingsheng HuDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Chunhong HuDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Xianling LiuDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Fang MaDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Junpeng XieDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Ping ZhongDepartment of Dermatology, North Sichuan Medical College Affiliated Nanchong Central Hospital, Nanchong, China.
Chenxi TangDepartment of Nursing, North Sichuan Medical College Affiliated Nanchong Central Hospital, Nanchong, China.
Dan FanDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Yuan GaoDepartment of Basic Science, Logan University, Chesterfield, MO, United States.
Xiang FengDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Mengge DingDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.
Dezhi LiDepartment of Oncology, The Fourth Affiliated Hospital of Zhejiang University School of Medicine, Yiwu, China.
Chaoyuan LiuDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neoadjuvant chemoimmunotherapy (NCIO) is more effective than neoadjuvant immunotherapy alone for pathological response in non-small cell lung cancer (NSCLC) patients, but the processes for determining patient suitability for its implementation are not clear. We aimed to identify the most relevant factors and build a convenient model to select NSCLC patients who would benefit most from NCIO. Methods: Results: A total of 101 eligible stage IIB-IIIC NSCLC patients were included. After NCIO, all patients successfully underwent surgical resection. A total of 46.53% (47/101) of patients achieved pathological complete response (pCR), and 70.30% (71/101) achieved major pathologic response (MPR). Tumor regression rate (adjusted odds ratio OR = 12.33), PD-L1 expression (adjusted odds ratio (OR) = 9.66), pembrolizumab/nab-paclitaxel-based regimens (adjusted OR = 4.92), and comorbidities (adjusted OR = 0.16) were independently associated with pCR rate (all Conclusions: The tumor regression rate, PD-L1 expression, pembrolizumab/nab-paclitaxel-based regimens, presence of squamous cell carcinoma, and comorbidities were the main influential factors for incidence of pCR/MPR in patients with stage IIB-IIIC NSCLC in the present study. Through predictive models, we can predict who will benefit most from NCIO prior to the emergence of clinical outcomes in locally advanced NSCLC.

Indexed as

major pathologic responseneoadjuvant chemoimmunotherapynon-small cell lung cancerpathologic complete responsesurgery

Identifiers

PMID36776373
PMCPMC9911863

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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.