Evidence map›Paper›PMID 34313025›Full record

ArticleCancer medicine2021

Outcomes of axitinib versus sunitinib as first-line therapy to patients with metastatic renal cell carcinoma in the immune-oncology era.

Kazuyuki Numakura, Yumin Muto, Sei Naito, Shingo Hatakeyama, Renpei Kato, Tomoyuki Koguchi, Takahiro Kojima, Yoshihide Kawasaki, Syuya Kandori, Sadafumi Kawamura and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Effect of active anticancer therapy on serologic response to SARS-CoV-2 BNT162b2 vaccine in patients with urothelial and renal cell carcinoma.International journal of urology : official journal of the Japanese Urological Association · 2022
    Article
  6. No Time to Die: How Kidney Cancer Evades Cell Death.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

18 authors at 8 institutions in 1 country.

Kazuyuki NumakuraDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.ORCID 0000-0002-5899-1738
Yumin MutoDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.
Sei NaitoDepartment of Urology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Shingo HatakeyamaDepartment of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Renpei KatoDepartment of Urology, Iwate Medical University, Morioka, Japan.ORCID 0000-0001-6089-7620
Tomoyuki KoguchiDepartment of Urology, Fukushima Medical University, Fukushima, Japan.
Takahiro KojimaDepartment of Urology and Andrology, Tsukuba University Graduate School of Comprehensive Human Sciences, Tsukuba, Japan.
Yoshihide KawasakiDepartment of Urology, Tohoku University Graduate School of Medicine, Tohoku, Japan.
Syuya KandoriDepartment of Urology and Andrology, Tsukuba University Graduate School of Comprehensive Human Sciences, Tsukuba, Japan.ORCID 0000-0003-4621-8470
Sadafumi KawamuraDepartment of Urology, Miyagi Cancer Center, Natori, Japan.
Yoichi AraiDepartment of Urology, Miyagi Cancer Center, Natori, Japan.
Akihiro ItoDepartment of Urology, Tohoku University Graduate School of Medicine, Tohoku, Japan.
Hiroyuki NishiyamaDepartment of Urology and Andrology, Tsukuba University Graduate School of Comprehensive Human Sciences, Tsukuba, Japan.
Yoshiyuki KojimaDepartment of Urology, Fukushima Medical University, Fukushima, Japan.
Wataru ObaraDepartment of Urology, Iwate Medical University, Morioka, Japan.
Chikara OhyamaDepartment of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Norihiko TsuchiyaDepartment of Urology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Tomonori HabuchiDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.
Akita University · JPUniversity of Tsukuba · JPFukushima Medical University · JPHirosaki University · JPIwate Medical University · JPMiyagi Prefectural Hospital Organization · JPTohoku University · JPYamagata University · JP

Funding

Grants-in-Aid for Scientific Research, Japan 17K11121Grants-in-Aid for Scientific Research, Japan 20K09553
6 · The paper itself

Abstract

Although combination immune checkpoint inhibitor (immuno-oncology [IO]) therapy is the first-line treatment for metastatic renal cell carcinoma (mRCC), it mostly causes resistance and tumor regrowth. Therefore, an optimal second-line therapy is necessary. Such therapy typically comprises vascular endothelial growth factor receptor-tyrosine kinase inhibitors (VEGFR-TKIs). This study was aimed at comparing the efficacy of two TKIs-axitinib and sunitinib-in mRCC patients. From January 2008 to October 2018, we registered 703 mRCC patients from 8 Japanese institutes. Of these, 408 patients received axitinib or sunitinib as the first-line treatment. Thereafter, efficacy and survival rate were compared between the axitinib and sunitinib groups. To reduce the effects of selection bias and potential confounders, propensity score matching analysis was performed. Axitinib and sunitinib were administered in 274 and 134 patients, respectively. More than 25% of the patients received nivolumab sequence therapy. To calculate the propensity scores for each patient, we performed multivariate logistic regression analysis. The objective response rate, progression-free survival (PFS), cause-specific survival, and overall survival (OS) were significantly better in the axitinib group than in the sunitinib group. Furthermore, the OS was better in the nivolumab-treated patients in the axitinib group. Axitinib showed higher efficacy and afforded greater survival benefits than did sunitinib when administered as first-line therapy in mRCC patients. Thus, from among VEGFR-TKIs, axitinib might be a possible option for application in the middle of IO drug-based treatment sequences.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsAxitinibCarcinoma, Renal CellFemaleHumansKidney NeoplasmsMaleMiddle AgedNeoplasm MetastasisSunitinibYoung AdultAxitinibSunitinibaxitinibmetastatic renal cell carcinomanivolumab

Identifiers

PMID34313025
PMCPMC8419787
OpenAlexW3183900543

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.