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临床试验/NCT05640817
NCT05640817已完成不适用

Clinical Study Evaluating the Nephroprotective Effect of Pentoxifylline Against Cisplatin in Patients With Head and Neck Cancer

Tanta University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2023年1月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
90
试验地点
1
主要终点
nephrotoxicity improvement as measured by CTACE version 5.0

研究概览

简要总结

Head and neck squamous cell carcinoma (HNSCC) encompasses a variety of tumors originating in the lip, oral cavity, hypopharynx, oropharynx, nasopharynx and larynx. It is the sixth most common malignancy worldwide accounting for approximately 6% of all cancer cases (Rettig and D'Souza., 2015). HNSCC represents the third most common cause of cancer death worldwide. Platinum based regimens represent cornerstone in its treatment (Galbiattiet al., 2013).

Cisplatin (cis-diammine dichloroplatinum (II), CDDP) is an inorganic platinum-based chemotherapeutic agent that is widely used in treatment of various solid malignancies as head and neck, lung, testis, ovarian, and bladder cancers (Aparecida et al., 2012). The use of cisplatin is frequently limited by significant side effects including bone marrow suppression, peripheral neuropathy, ototoxicity, anaphylaxis and nephrotoxicity with the latter representing the main dose limiting one (Aparecida et al., 2012).

Acute kidney injury (AKI), distal renal tubular acidosis, renal concentrating defect, transient proteinuria, hyperuricemia, Fanconi-like syndrome, hypomagnesemia, hypocalcemia, renal salt wasting, erythropoietin deficiency, thrombotic microangiopathy, and chronic renal failure are among the renal side effects of cisplatin (Miller et al., 2010).Renal function deterioration is seen in 25% to 35% of patients treated with a single dose of cisplatin (Miller et al., 2010).Cisplatin-induced injury to renal epithelial cells results in the production of various inflammatory factors, including TNF-α. Cisplatin also increases ROS production, which leads to the activation of apoptosis and necrosis pathways (Miller et al., 2010).

Pentoxifylline (PTX), a nonspecific phosphodiesterase inhibitor, was first considered in the treatment of peripheral vascular diseases (Nasiri-Toosi et al., 2013). PTX has anti-inflammatory effects as it down regulates several pro-inflammatory cytokines, including tumor necrosis factor alpha (TNF-α) and interleukin-1 (IL-1) and IL-6 (Mostafa-Hedeab et al., 2022). In addition, PTX has gained considerable interest as a reactive oxygen species (ROS) scavenger, and several studies show its potential antioxidant effects (Zhang et al., 2016). Several studies evaluate the renoprotective effects of PTX against drug-induced nephrotoxicity (Ramesh and Reeves, 2002; Kasap et al., 2013;Nasiri-Toosi et al.,2013; Panahi-Shokouh etal., 2020; Alorabi et al., 2022).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient aged 18 years or more with head and neck cancer who will receive cisplatin for the first time.
  • Baseline estimated glomerular filtration rate (eGFR) ≥ 59 ml/min/1.73 m
  • Eastern Cooperative Oncology Group performance status (ECOG) <
  • Patients with normal organic function as defined for the following criteria:
  • Aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤ 2.5 times the upper normal limit of the local laboratory ;
  • Total serum bilirubin ≤ 2.0 x ULN-LL;
  • Absolute neutrophil count ≥ 1,500 / mm3;
  • Platelet count ≥ 100,000 / mm3;
  • Hemoglobin ≥ 8.0 g / dl;
  • Serum creatinine ≤ 1.5 x ULN-LL

排除标准

  • Pregnant or nursing women, or females intending pregnancy were all prohibited
  • Patients with concurrent other malignancy or history of other malignancy treated within the past 3 years.
  • Baseline estimated glomerular filtration rate (eGFR) < 59 ml/min/1.73 m
  • Alanine aminotransferase (ALT) > 3× times ULN.
  • Eastern Cooperative Oncology Group performance status (ECOG) ≥
  • Patients have Diabetes mellitus.
  • Patients have current participation in other protocols with experimental drugs.
  • Patients with no ability to ingest food orally.
  • Pentoxifylline hypersensitivity.
  • Use of other nephrotoxic drugs as aminoglycosides, non-steroidal anti-inflammatory drugs and contrast media.

研究组 & 干预措施

Group 1 as control group

Active Comparator

cisplatin with standard hydration with normal saline

干预措施: cisplatin with standard hydration with normal saline (Drug)

Group two as Pentoxifylline

Active Comparator

receive cisplatin with standard hydration with normal saline and Pentoxifylline 400 mg SR tablets twice daily for three cycles.

干预措施: Pentoxifylline 400 mg SR tablets (Drug)

结局指标

主要结局

nephrotoxicity improvement as measured by CTACE version 5.0

时间窗: up to 6 months

次要结局

  • Kidney injury molecule 1 decrease serum level(up to 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eman Elberri

Lecturer of Clinical Pharmacy

Tanta University

研究点 (1)

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