Evidence map›Paper›PMID 33240992›Full record

ArticleAnnals of translational medicine2020

Efficacy and safety of concurrent anti-tuberculosis treatment and chemotherapy in lung cancer patients with co-existent tuberculosis.

Mei-Feng Ye, Shan Su, Zhi-Hao Huang, Jian-Jun Zou, Duo-Hua Su, Xiao-Hui Chen, Long-Feng Zeng, Wei-Xiang Liao, Hui-Yi Huang, Yun-Yun Zeng and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  7. Frontiers in immunology · 2025
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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

15 authors at 3 institutions in 1 country.

Mei-Feng YeGuangzhou Medical University, Guangzhou, China.
Shan SuDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Zhi-Hao HuangDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Jian-Jun ZouDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Duo-Hua SuDepartment of Tuberculosis, Guangzhou Chest Hospital, Guangzhou, China.
Xiao-Hui ChenDepartment of Thoracic Surgery, Guangzhou Chest Hospital, Guangzhou, China.
Long-Feng ZengDepartment of Tuberculosis, Guangzhou Chest Hospital, Guangzhou, China.
Wei-Xiang LiaoDepartment of Tuberculosis, Guangzhou Chest Hospital, Guangzhou, China.
Hui-Yi HuangDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Yun-Yun ZengDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Wen-Chang CenDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Xian-Lan ZhangDepartment of Oncology, Guangzhou Chest Hospital, Guangzhou, China.
Chun-Xin LiaoDepartment of Tuberculosis, Guangzhou Chest Hospital, Guangzhou, China.
Jian ZhangDepartment of Oncology, Zhujiang Hospital, Guangzhou, China.
Yan-Bin ZhangDepartment of Tuberculosis, Guangzhou Chest Hospital, Guangzhou, China.
Guangzhou Chest Hospital · CNGuangzhou Medical University · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis retrospective study evaluated the safety and efficacy of concurrent anti-tuberculosis (TB) and chemotherapy treatment in patients with advanced lung cancer and active TB.

methodsWe retrospectively analyzed patients who were first diagnosed with advanced lung cancer and received first-line chemotherapy in Guangzhou Chest Hospital from 2015 to 2017. Patients were categorized into two groups (2:1): lung cancer patients without active TB (Group A), and lung cancer patients with active TB (Group B). Primary endpoints included adverse events (AEs), objective response rate (ORR), time to treatment failure, and overall survival (OS).

resultsA total of 99 patients were eligible (Group A, n=66; Group B, n=33). Grade ≥3 treatment-related AEs, primarily hematologic toxicity, occurred in 39.4% and 51.5% of patients in Groups A and B, respectively. The hypohepatia in both groups was generally at grade 1 or 2, with similar incidences (26% and 27%, respectively). After two cycles of chemotherapy, the ORR was 42.4% and 33.3% in Group A and B, respectively (P=0.383). The median time to treatment failure (TTF) was 7.0 and 5.6 months for Groups A and B, respectively (P=0.175). The median OS was 17.0 and 14.0 months for Groups A and B, respectively (P=0.312). After 3 months of anti-TB treatment, all patients achieved sputum acid-fast bacilli (AFB) smear conversion and absorption on imaging, and the end of follow-up observed no recurrence.

conclusionsConcurrent anti-TB and chemotherapy treatment did not increase hematological toxicity or hypohepatia in lung cancer patients with pulmonary TB.

Indexed as

chemotherapyLung cancerpulmonary tuberculosis (pulmonary TB)

Identifiers

PMID33240992
PMCPMC7576042
OpenAlexW3087153778

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.