Evidence map›Paper›PMID 42288908›Full record

ArticleJournal of pharmaceutical health care and sciences2026

Prolongation of prothrombin time-international normalized ratio by concomitant use of warfarin and combination therapy with lenvatinib and pembrolizumab in a patient with renal cell carcinoma on dialysis: a case report.

Shota Torii, Tomoya Narita, Aya Torii-Goto, Takamasa Homma, Hideki Esaki, Takashi Sakakibara, Atsuya Kondo, Norio Takimoto

Abstract read
In one paragraph

Article in Journal of pharmaceutical health care and sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shota ToriiDepartment of Pharmacy, Kariya Toyota General Hospital, 5-15 Sumiyoshi-cho , Kariya-City, Aichi, 448- 8505, Japan. toriishota1007@gmail.com.
Tomoya NaritaDepartment of Urology, Kariya Toyota General Hospital, Aichi, 448- 8505, Japan.
Aya Torii-GotoDepartment of Pharmacy, College of Pharmacy, Kinjo Gakuin University, Nagoya, 463-8521, Japan.
Takamasa HommaDepartment of Pharmacy, Kariya Toyota General Hospital, 5-15 Sumiyoshi-cho , Kariya-City, Aichi, 448- 8505, Japan.
Hideki EsakiDepartment of Pharmacy, Kariya Toyota General Hospital, 5-15 Sumiyoshi-cho , Kariya-City, Aichi, 448- 8505, Japan.
Takashi SakakibaraDepartment of Pharmacy, Kariya Toyota General Hospital, 5-15 Sumiyoshi-cho , Kariya-City, Aichi, 448- 8505, Japan.
Atsuya KondoDepartment of Urology, Kariya Toyota General Hospital, Aichi, 448- 8505, Japan.
Norio TakimotoDepartment of Pharmacy, Kariya Toyota General Hospital, 5-15 Sumiyoshi-cho , Kariya-City, Aichi, 448- 8505, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcquired polycystic kidney disease is associated with an increased risk of developing renal cell carcinoma (RCC), which is commonly observed in patients on dialysis and may present with inferior vena cava tumor thrombus. However, there are no prior reports on the use of warfarin for inferior vena cava tumor thrombus in patients on dialysis with RCC receiving combination therapy with lenvatinib and pembrolizumab. CASE PRESENTATION: We describe a 64-year-old Japanese man with RCC complicated by tumor thrombus extending into the renal vein and inferior vena cava who was undergoing hemodialysis. Warfarin was initiated at 2 mg/day due to the risk of thrombus progression. His baseline prothrombin time-international normalized ratio (PT-INR) was 1.80 before the initiation of combination therapy with lenvatinib and pembrolizumab. After 8 days of warfarin administration, combination therapy with lenvatinib (10 mg/day) and pembrolizumab (200 mg every 3 weeks) was initiated. Nine days later, the PT-INR elevated to 3.02 despite no change in warfarin dose. The patient remained asymptomatic. Adjusting warfarin to 2-2.5 mg/day and close PT-INR monitoring successfully restored values to the therapeutic range of 1.6-2.6 by day 80, without reducing the lenvatinib dose.

conclusionsNeither warfarin nor lenvatinib is eliminated by dialysis; therefore, potential pharmacokinetic interactions should be managed with the same caution as in non-dialysis patients. Concomitant use of warfarin and combination therapy with lenvatinib and pembrolizumab in patients with RCC undergoing hemodialysis may enhance anticoagulant effects via multiple interacting factors, including cytochrome P-450-related interactions, systemic inflammation, and hypoalbuminemia. Therefore, careful follow-up, including shorter intervals between outpatient visits (e.g., weekly monitoring), is essential for safe PT-INR management.

Indexed as

DialysisDrug interactionLenvatinib and pembrolizumabRenal cell carcinomaWarfarin

Identifiers

PMID42288908
PMCPMC13491841

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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 Socratic graph.