Evidence map›Paper›PMID 40421804›Full record

ArticleClinical pharmacology and therapeutics2025

Folinic Acid Prophylaxis and Dose Adjustments Enable Safe Treatment with Pemetrexed in Patients with Renal Impairment.

Nikki de Rouw, Leila-Sophie Otten, Mart P Kicken, Berber Piet, Bonne Biesma, Bianca van Veggel, Christi M J Steendam, Ben van den Borne, Lizza E L Hendriks, Sander Croes and 9 more

Abstract read
In one paragraph

Article in Clinical pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

19 authors.

Nikki de RouwDepartment of Clinical Pharmacy, Amphia Hospital, Breda, The Netherlands.ORCID 0000-0002-1991-0552
Leila-Sophie OttenDepartment of Pharmacy, Pharmacology & Toxicology, Research Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0002-1225-4740
Mart P KickenDepartment of Pharmacy, Pharmacology & Toxicology, Research Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0002-5321-0816
Berber PietDepartment of Pulmonary Diseases, Research Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0002-9069-3597
Bonne BiesmaDepartment of Pulmonary Diseases, Jeroen Bosch Hospital's, Hertogenbosch, The Netherlands.ORCID 0000-0001-5386-170X
Bianca van VeggelDepartment of Pulmonary Diseases, Jeroen Bosch Hospital's, Hertogenbosch, The Netherlands.ORCID 0000-0002-3223-1255
Christi M J SteendamDepartment of Pulmonary Diseases, Catharina Hospital, Eindhoven, The Netherlands.ORCID 0000-0002-8487-9344
Ben van den BorneDepartment of Pulmonary Diseases, Catharina Hospital, Eindhoven, The Netherlands.ORCID 0009-0006-3086-1591
Lizza E L HendriksDepartment of Pulmonary Diseases, GROW-School for Oncology and Reproduction, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-3521-2535
Sander CroesDepartment of Clinical Pharmacy & Toxicology, CARIM-School for Cardiovascular Disease, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID 0009-0003-5799-1415
Anne-Marie C DingemansDepartment of Respiratory Medicine, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0001-6105-182X
Daphne W DumoulinDepartment of Respiratory Medicine, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0001-5578-7902
Ron H J MathijssenDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-5667-5697
Jacobus A BurgersDepartment of Thoracic Oncology, Antoni Van Leeuwenhoek-The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-0218-8436
Alwin D R HuitemaDepartment of Pharmacy & Pharmacology, Antoni Van Leeuwenhoek-The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0003-1939-4639
Hieronymus J DerijksDepartment of Pharmacy, Jeroen Bosch Hospital, S-Hertogenbosch, The Netherlands.ORCID 0000-0003-1658-3100
Maarten J DeenenDepartment of Clinical Pharmacy, Catharina Hospital, Eindhoven, The Netherlands.ORCID 0000-0002-4389-6420
Michel M van den HeuvelDepartment of Pulmonary Diseases, Research Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0002-6372-2153
Rob Ter HeineDepartment of Pharmacy, Pharmacology & Toxicology, Research Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0003-2185-8201

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pemetrexed is a cornerstone in chemo(immunotherapy) of non-small cell lung cancer and mesothelioma; however, it is contraindicated in patients with renal impairment due to severe toxicity concerns. Therefore, a large proportion of patients is withheld from effective chemo(immunotherapy). We performed an intra-patient 3 + 3 dose escalation renal impairment study (eGFR < 45 mL/min). The pemetrexed dose was calculated based on renal function to reach a target AUC, and patients received oral folinic acid prophylaxis 45 mg four times daily on Days 2-15 of each cycle. Endpoints included safety (incidence of hematological and non-hematological toxicity, treatment delays) and pharmacokinetics in line with regulatory guidance for renal impairment trials. Six patients with an estimated glomerular filtration rate (eGFR) between 26 and 41 mL/min were included. All patients were successfully escalated to the full dose. Adverse event patterns and pharmacokinetics were comparable to those in patients with normal renal function. Grade I/II anemia occurred in five patients (already present at baseline). One occurrence of grade IV neutropenia was observed, which resolved without intervention. Moreover, in three patients, a 1-week treatment delay occurred. Treatment resulted in a response in four patients (n = 1 complete response, n = 2 partial response, n = 1 stable disease). Pemetrexed can be safely administered in patients with impaired renal function when the dose is calculated based on renal function and folinic acid prophylaxis is administered, thereby enabling an effective treatment modality for patients that, thus far, could not be treated.

Indexed as

Antineoplastic AgentsLeucovorinLung NeoplasmsPemetrexedRenal InsufficiencyAgedCarcinoma, Non-Small-Cell LungDose-Response Relationship, DrugFemaleGlomerular Filtration RateHumansMaleMiddle AgedAntineoplastic AgentsLeucovorinPemetrexed

Identifiers

PMID40421804
PMCPMC12355014

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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.