Evidence map›Paper›PMID 31175167›Full record

Trial reportThe oncologist2019

Regorafenib in Patients with Antiangiogenic-Naïve and Chemotherapy-Refractory Advanced Colorectal Cancer: Results from a Phase IIb Trial.

Rachel P Riechelmann, Luiz S Leite, Giovanni M Bariani, Joao Glasberg, Thomas G Rivelli, Leonardo Gomes da Fonseca, Daniela R Nebuloni, Maria I Braghiroli, Marcelo A Queiroz, Alice M Isejima and 3 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02465502 (An Uncontrolled, Open-label Phase IIb Trial of Regorafenib in Subjects With Antiangiogenic-naive and Chemotherapy-refractory Advanced Colorectal Cancer), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 19% 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.

NCT02465502 phase2completednot on this map

An Uncontrolled, Open-label Phase IIb Trial of Regorafenib in Subjects With Antiangiogenic-naive and Chemotherapy-refractory Advanced Colorectal Cancer

TypeinterventionalSponsorBayerRan2015 to 2017Enrolled59ConditionsColorectal NeoplasmsArmsRegorafenib (Stivarga, BAY73-4506)
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
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  6. Review
  7. Review
  8. 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

13 authors at 2 institutions in 2 countries.

Rachel P RiechelmannDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil rachel.riechelmann@accamargo.org.br.
Luiz S LeiteDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Giovanni M BarianiDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Joao GlasbergDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Thomas G RivelliDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Leonardo Gomes da FonsecaDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Daniela R NebuloniDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Maria I BraghiroliDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Marcelo A QueirozDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Alice M IsejimaMedical Affairs Study Support, SBU Oncology, Bayer S.A., São Paulo, Brazil.
Christian KappelerClinical Statistics, Global Clinical Oncology, Bayer AG, Berlin, Germany.
Luciana KikuchiMedical and Data Management, SBU Oncology, Bayer S.A., São Paulo, Brazil.
Paulo M HoffDepartment of Radiology and Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.
Instituto do Câncer do Estado de São Paulo · BRBayer (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegorafenib is a multikinase inhibitor with antiangiogenic effects that improves overall survival (OS) in metastatic colorectal cancer (mCRC) after failure of standard therapies. We investigated the efficacy and safety of regorafenib in antiangiogenic therapy-naïve chemotherapy-refractory advanced colorectal cancer. PATIENTS AND

methodsThis single-center, single-arm, phase IIb study (NCT02465502) enrolled adults with mCRC whose disease had progressed on, or who were intolerant to, standard therapy, but who were antiangiogenic therapy-naïve. Patients received regorafenib 160 mg once daily for 3 weeks per 4-week cycle. The primary endpoint was progression-free survival (PFS) rate at week 8.

resultsOf 59 treated patients, almost half had received at least four prior lines of therapy. Patients received a median of 86% of the planned dose. The week 8 PFS rate was 53% (95% confidence interval [CI], 39.1-64.3); median PFS was 3.5 months (95% CI, 1.8-3.6). Median OS was 7.4 months (95% CI, 5.3-8.9). Tumor response (RECIST version 1.1) was 2%, and metabolic response rate (criteria from the European Organisation for Research and Treatment of Cancer) was 41%. The most frequently reported regorafenib-related grade ≥3 adverse events were hypertension (36%), hand-foot skin reaction (HFSR, 25%), and hypophosphatemia (24%). There were no regorafenib-related deaths. An exploratory analysis showed that patients with grade ≥2 HFSR had longer OS (10.2 months) with regorafenib treatment versus those with grades 0-1 (5.4 months).

conclusionThese findings support the antitumor activity of regorafenib in antiangiogenic-naïve patients with chemotherapy-refractory mCRC. IMPLICATIONS FOR PRACTICE: The multikinase inhibitor regorafenib improved overall survival in the phase III CORRECT and CONCUR trials in heavily pretreated patients with treatment-refractory metastatic colorectal cancer (mCRC). Exploratory subgroup analysis from CONCUR suggested that regorafenib treatment prior to targeted therapy (including bevacizumab) may improve outcomes. In this single-center, single-arm phase IIb study, regorafenib demonstrated antitumor activity in 59 antiangiogenic-naïve patients with chemotherapy-refractory mCRC. Further studies should assess the efficacy of regorafenib in this patient population, as well as explore the reasons behind improved outcomes among patients who had a metabolic response and those who developed hand-foot skin reaction.

Indexed as

Salvage TherapyAdultAgedAngiogenesis InhibitorsColorectal NeoplasmsDrug Resistance, NeoplasmFemaleHumansMaleMiddle AgedNeovascularization, PathologicPhenylurea CompoundsPyridinesSurvival RateTreatment OutcomeAngiogenesis InhibitorsPhenylurea CompoundsPyridinesregorafenibAngiogenesis inhibitorsColorectal neoplasmsComputed tomographyPositron emission tomographyRegorafenib

Identifiers

PMID31175167
PMCPMC6738304
OpenAlexW2948524598

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.