Evidence map›Paper›PMID 23792567›Full record

ArticleCancer biology & therapy2013

FOLFIRI plus dulanermin (rhApo2L/TRAIL) in a patient with BRAF-mutant metastatic colon cancer.

Bora Lim, Angelique Scicchitano, Cheryl Beachler, Niraj Gusani, Nabeel Sarwani, Zhaohai Yang, Kevin Staveley-O'Carroll, Avi Ashkenazi, Chia Portera, Wafik S El-Deiry

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Cancer biology & therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Advances in the study of death receptor 5.Frontiers in pharmacology · 2025
    Review
  2. Therapeutic targeting of TRAIL death receptors.Biochemical Society transactions · 2023
    Review
  3. Article
  4. Article
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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

10 authors at 5 institutions in 2 countries.

Bora LimHematology/Oncology Division, Penn State Hershey Cancer Institute, Penn State Hershey Medical Center, Hershey, PA USA.
Angelique Scicchitano
Cheryl Beachler
Niraj Gusani
Nabeel Sarwani
Zhaohai Yang
Kevin Staveley-O'Carroll
Avi Ashkenazi
Chia Portera
Wafik S El-Deiry
Penn State Milton S. Hershey Medical Center · USHershey (United States) · USCancer Institute (WIA) · INGenesys (United States) · USPalmetto Hematology Oncology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer patients with BRAF-mutant tumors have a more aggressive, rapidly progressing disease that is in critical need of novel therapeutic approaches. Indeed, whereas the median overall survival (OS) of colorectal cancer (CRC) patients receiving standard-of-care therapy is approximately two years or more if their tumors express wild-type BRAF and wild-type KRAS, median OS is less than twelve months with tumors expressing V600E-mutant BRAF and wild-type KRAS. Pro-apoptotic receptor agonists are a class of biologic agents under development to induce tumor-specific apoptosis and are being combined with classical chemotherapy or targeted agents in clinical trials. Herein, we present the case of a patient with bulky V600E-mutant BRAF hepatic flexure colon carcinoma, treated initially with FOLFOX plus bevacizumab neoadjuvant therapy and surgery. The patient had a rapid tumor relapse with metastatic disease to the liver and lung, and was enrolled in a phase 1b open-label clinical study, where he received the FOLFIRI regimen in combination with the pro-apoptotic receptor agonist dulanermin (rhApo2L/TRAIL). The patient maintained stable disease through 25 doses administered every two weeks before his disease progressed. After coming off study, the patient underwent surgical debulking and received intraperitoneal hyperthermic chemotherapy. He subsequently relapsed and was treated with FOLFIRI plus cetuximab. At the time of this report, the patient remains on active treatment. It is unclear what effect dulanermin may have had on the course of his disease, but it is noteworthy that the patient remained on FOLFIRI plus dulanermin therapy for a period that exceeded the median OS for patients with advanced, aggressive BRAF-mutant CRC. It is also noteworthy that at the time of this report the patient's overall survival since diagnosis has exceeded 30 months, which is beyond what is generally observed even for patients with CRC harboring wild-type BRAF and wild-type KRAS.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCamptothecinColorectal NeoplasmsFluorouracilHumansLeucovorinMaleMiddle AgedMutationNeoplasm MetastasisProto-Oncogene Proteins B-rafTNF-Related Apoptosis-Inducing LigandBRAF protein, humanCamptothecinFluorouracilLeucovorinProto-Oncogene Proteins B-rafTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanApo2LBRAFcancer therapyclinical experiencecolon cancerdulanerminpatientTRAIL

Identifiers

PMID23792567
PMCPMC3841210
OpenAlexW2128794616

What OpenQuestion holds

Textmetadata
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.