Evidence map›Paper›PMID 38920621›Full record

ArticleBiomolecules & biomedicine2024

Which factors help to determine the long-term response to first-line tyrosine kinase inhibitors in patients with metastatic renal cell carcinoma: A Turkish multi-centre study.

Nargiz Majidova, Mustafa Seyyar, Demet Işık Bayraktar, Gülhan Dinç, Elfag İsgandarov, Javid Huseynov, Alper Yaşar, Abdussamet Çelebi, Nadiye Sever, Erkam Kocaaslan and 11 more

Abstract readMulticenter Study
In one paragraph

Article in Biomolecules & biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Nargiz MajidovaDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Mustafa SeyyarDepartment of Internal Medicine, Division of Medical Oncology, Kocaeli University, Kocaeli, Turkey.
Demet Işık BayraktarDepartment of Internal Medicine, Division of Medical Oncology, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey.
Gülhan DinçDepartment of Internal Medicine, Division of Medical Oncology, Professor Dr Cemil Tascioglu City Hospital, Istanbul, Turkey.
Elfag İsgandarovDepartment of Internal Medicine, Division of Medical Oncology, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey.
Javid HuseynovDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Alper YaşarDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Abdussamet ÇelebiDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Nadiye SeverDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Erkam KocaaslanDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Pınar ErelDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Yeşim AğyolDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Ali Kaan GürenDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Rukiye ArıkanDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Selver IşıkDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Özlem ErcelepDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Güzin DemirağDepartment of Internal Medicine, Division of Medical Oncology, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey.
Umut KefeliDepartment of Internal Medicine, Division of Medical Oncology, Kocaeli University, Kocaeli, Turkey.
Osman KöstekDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
İbrahim Vedat BayoğluDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.
Murat SarıDepartment of Internal Medicine, Division of Medical Oncology, Marmara University School of Medicine, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many developing countries lack access to recommended first-line treatments for metastatic renal cell carcinoma (mRCC), such as immune checkpoint inhibitors (ICIs) or ICI-tyrosine kinase inhibitor (TKI) combinations. As a result, predictive markers are necessary to identify patients who may benefit from single-agent TKIs for long-term response. This study aims to identify such parameters. This was a multi-centre, retrospective study of patients with mRCC who were undergoing first-line treatment with sunitinib or pazopanib. Patients who had been diagnosed with mRCC and had not experienced disease progression for 36 months or more were deemed to have achieved a long-term response. Predictive clinical and pathological characteristics of patients who did not experience long-term disease progression were investigated. A total of 320 patients from four hospitals were included in the study. The median age of the patients was 60 years (range 20-89 years). According to the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk classification, 109 patients were classified as having favourable risk and 211 were in the intermediate-poor risk group. The median progression-free survival (PFS) and overall survival (OS) for all patients were 12.5 months and 76.4 months, respectively. In the long-term responder's group, the median PFS was 78.4 months. Among all patients, prior nephrectomy, the Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) <1, and the absence of brain metastasis were predictive factors for long-term response. For patients in the favourable risk group, the lack of brain metastasis was a predictor of long-term response. In the intermediate-poor risk group, prior nephrectomy and ECOG PS <1 were predictive factors for long-term response. Some individuals with mRCC may experience a durable response to TKIs. The likelihood of a long-term response can be determined by factors such as nephrectomy, ECOG PS < 1, and the absence of brain metastases.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsProtein Kinase InhibitorsSunitinibAdultAgedAged, 80 and overFemaleHumansIndazolesMaleMiddle AgedNeoplasm MetastasisPyrimidinesRetrospective StudiesSulfonamidesIndazolespazopanibProtein Kinase InhibitorsPyrimidinesSulfonamidesSunitinibTyrosine Kinase Inhibitors

Identifiers

PMID38920621
PMCPMC11496851

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