Evidence map›Paper›PMID 38637966›Full record

Trial reportCancer research and treatment2024

Analysis of Response and Progression Patterns of Tyrosine Kinase Inhibitors in Recurrent or Metastatic Adenoid Cystic Carcinoma: A Post Hoc Analysis of Two KCSG Phase II Trials.

Youjin Kim, Bhumsuk Keam, Eun Joo Kang, Jin-Soo Kim, Hye Ryun Kim, Keun-Wook Lee, Jung Hye Kwon, Kyoung Eun Lee, Yaewon Yang, Yoon Hee Choi and 7 more

Open access · diamondAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer research and treatment, 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, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

17 authors at 14 institutions in 4 countries.

Youjin KimDepartment of Hematology and Oncology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.
Bhumsuk KeamDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Eun Joo KangDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea.
Jin-Soo KimDepartment of Internal Medicine, SMG-SNU Boramae Medical Center, Seoul, Korea.
Hye Ryun KimDepartment of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.
Keun-Wook LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
Jung Hye KwonDivision of Hematology-Oncology, Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.
Kyoung Eun LeeEwha Womans University Medical Center, Seoul, Korea.
Yaewon YangDepartment of Internal Medicine, Chungbuk University Hospital, Chungbuk University College of Medicine, Cheongju, Korea.
Yoon Hee ChoiDivision of Hematology-Oncology, Department of Internal Medicine, Dongnam Institute of Radiological and Medical Sciences, Busan, Korea.
Min Kyoung KimDivision of Hematology-Oncology, Department of Internal Medicine, Yeungnam University Hospital, Yeungnam University College of Medicine, Daegu, Korea.
Jun Ho JiDivision of Hematology-Oncology, Department of Internal Medicine, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
Tak YunRare Cancers Clinic, Center for Specific Organs Cancer, National Cancer Center, Goyang, Korea.
Moon Young ChoiDepartment of Internal Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
Ki Hyeong LeeDepartment of Internal Medicine, Chungbuk University Hospital, Chungbuk University College of Medicine, Cheongju, Korea.
Sung-Bae KimDivision of Oncology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Myung-Ju AhnDivision of Hematology-Oncology, Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Chungbuk National University Hospital · KRNew Generation University College · ETSungkyunkwan University · KRAsan Medical Center · KRDongnam Institute of Radiological & Medical Sciences · KRInje University Busan Paik Hospital · KRKorea University · KRNational Cancer Center · KRNational University College · PRSeoul National University Hospital · KRSNUH SMG-SNU Boramae Medical Center · KRUlsan University Hospital · KRYeungnam University · KRYonsei University · KR

Funding

NTP INFORMATION SYSTEMS SUPPORT27305C0011 · NIEHS · Z-TECH CORPORATION · 2007 to 2009
$4.3M
PROVIDE RABBITS, RATS MICE, HAMSTERS GERBILS, GUINEA PIGS27307C0012 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$1.0M
PROVIDE RABBITS, RATS, MICE, HAMSTERS, GERBILS, GUINEA PIGS27307C0011 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$500k
Ministry of Health and Welfare HA22C0011Ministry of Health and Welfare HA22C0012National Cancer CenterNIEHS NIH HHS 27305C0011NIEHS NIH HHS 27307C0011NIEHS NIH HHS 27307C0012NIEHS NIH HHS 27398C0011
6 · The paper itself

Abstract

purposeIn this study, we evaluated 66 patients diagnosed with adenoid cystic carcinoma (ACC) enrolled in two Korean Cancer Study Group trials to investigate the response and progression patterns in recurrent and/or metastatic ACC treated with vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKIs). MATERIALS AND

methodsWe evaluated 66 patients diagnosed with ACC who were enrolled in the Korean Cancer Study Group trials. The tumor measurements, clinical data, treatment outcomes, and progression patterns of therapy were analyzed.

resultsIn the 66 patients (53 receiving axitinib and 13 receiving nintedanib), the disease control rate was 61%, and three patients achieved partial response. The median follow-up, median progression-free survival (PFS), overall survival, and 6-month PFS rate were 27.6%, 12.4%, and 18.1% months and 62.1%, respectively. Among 42 patients who experienced progression, 27 (64.3%) showed target lesion progression. Bone metastasis was an independent poor prognostic factor.

conclusionOverall, most patients demonstrated stable disease with prolonged PFS; however, prominent target lesion progression occurred in some patients. Thus, PFS may capture VEGFR-TKI efficacy better than the objective response rate.

Indexed as

Carcinoma, Adenoid CysticDisease ProgressionNeoplasm Recurrence, LocalProtein Kinase InhibitorsAdultAgedAxitinibFemaleHumansIndolesMaleMiddle AgedNeoplasm MetastasisPrognosisTreatment OutcomeTyrosine Kinase InhibitorsAxitinibIndolesnintedanibProtein Kinase InhibitorsTyrosine Kinase InhibitorsAdenoid cystic carcinomaAxitinibNintedanibTyrosine kinase inhibitorsVascular endothelial growth factor receptors

Identifiers

PMID38637966
PMCPMC11491249
OpenAlexW4394797335

What OpenQuestion holds

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LicenceCC BY-NC
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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.