Evidence map›Paper›PMID 36505826›Full record

ArticleFrontiers in oncology2022

Efficacy of dabrafenib/trametinib in pancreatic ductal adenocarcinoma with BRAF NVTAP deletion: A case report.

Ji Eun Shin, Ho Jung An, Hyung Soon Park, Hyunho Kim, Byoung Yong Shim

Open access · goldAbstract readCase Reports
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 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% 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

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

  1. Pooled it
  2. Unravelling the pathogenesis and therapeutic approaches of pancreatic ductal adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Chemotherapy-free treatment targeting fusions and driver mutations inTherapeutic advances in medical oncology · 2024
    Article
  9. BRAFScience advances · 2023
    Article
  10. 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

5 authors at 2 institutions in 1 country.

Ji Eun ShinDivision of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, Catholic University of Korea, Suwon-si, Gyeonggi-do, South Korea.
Ho Jung AnDivision of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, Catholic University of Korea, Suwon-si, Gyeonggi-do, South Korea.
Hyung Soon ParkDivision of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, Catholic University of Korea, Suwon-si, Gyeonggi-do, South Korea.
Hyunho KimDivision of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, Catholic University of Korea, Suwon-si, Gyeonggi-do, South Korea.
Byoung Yong ShimDivision of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, Catholic University of Korea, Suwon-si, Gyeonggi-do, South Korea.
St. Vincent's Hospital · KRCatholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have been actively conducted to identify actionable mutations and incorporate them into clinical practice in pancreatic ductal adenocarcinoma (PDAC), which is known to have a poor prognosis with traditional cytotoxic chemotherapy. A BRAF point mutation in V600E is commonly reported in KRAS wild-type PDAC, and targeting BRAF_V600E is already being applied to various carcinomas, including PDAC. Accumulated evidence also shows that not only BRAF_V600E but also short in-frame deletions of BRAF have an oncogenic function. Here, we report that a patient with BRAF N486_P490 deletion initiated on dabrafenib or trametinib, a BRAF inhibitor, and a MEK inhibitor, respectively, after cytotoxic chemotherapy failure. The patient then presented with a partial response.

Indexed as

BRAF mutationBRAF short in-frame deletiondabrafenib/trametinibNGSpancreatic ductal adenocarcinoma

Identifiers

PMID36505826
PMCPMC9731151
OpenAlexW4309899638

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.