Department of Clinical and Experimental Medicine, Unit of Clinical Pharmacology and Pharmacogenetics, University of Pisa, Pisa, Italy.
Oncology Department, IRCCS Istituto Scientifico Romagnolo per lo Studio dei Tumori "Dino Amadori", Meldola, Italy.
Clin Genitourin Cancer. 2024 Oct;22(5):102147. doi: 10.1016/j.clgc.2024.102147. Epub 2024 Jun 27.
The administration of proton pump inhibitors (PPIs) is a common practice to reduce gastro-esophageal adverse events associated with drug treatments but may impair absorption and exposure to oncology drugs. This study investigated the effect of concomitant administration of PPIs and pazopanib, sunitinib and cabozantinib on survival of patients with metastatic clear cell renal carcinoma (mRCC).
Total 451 patients receiving pazopanib, sunitinib and cabozantinib as first line treatment were enrolled in this retrospective study. Patients were defined as "no concomitant PPIs (PPI-)" if no PPIs were administered during TKIs, and as "concomitant PPIs (PPI+)" if the administration of PPIs was at least 75% of the time during which TKIs were given.
Eighty patients administered pazopanib were PPI- and 86 PPI+; no difference in PFS was observed (10.7 vs. 11.9 months, P = .79). If patients were stratified as short (n = 89) and long (n = 77) responders, there was a significant difference in terms of PFS in PPI+ (n = 47) versus PPI- (n = 30) in long responders, being 24.7 versus 38 months (P = .04), respectively. In the sunitinib cohort, no significant difference of PFS in PPI+ (n = 102) versus PPI- (n = 131) was found, being 11.3 versus 18.1 months, respectively (P=0.15). In the cabozantinib cohort, there was a statistically significant difference in PFS of PPI+ versus PPI- (6 months vs. not reached, P = .04). No correlation with adverse events was found.
This study demonstrates an association between PPIs and impaired PFS in mRCC patients given pazopanib and cabozantinib and recommends caution on their concomitant use.
质子泵抑制剂(PPIs)的给药是减少与药物治疗相关的胃食管不良事件的常见做法,但可能会影响肿瘤药物的吸收和暴露。本研究调查了同时给予 PPIs 和帕唑帕尼、舒尼替尼和卡博替尼对转移性透明细胞肾细胞癌(mRCC)患者生存的影响。
这项回顾性研究共纳入了 451 名接受帕唑帕尼、舒尼替尼和卡博替尼一线治疗的患者。如果在 TKI 期间未给予 PPIs,则患者被定义为“无同时使用 PPIs(PPI-)”,如果在给予 TKI 期间至少有 75%的时间给予 PPIs,则患者被定义为“同时使用 PPIs(PPI+)”。
80 名接受帕唑帕尼治疗的患者为 PPI-,86 名患者为 PPI+;无进展生存期(PFS)无差异(10.7 与 11.9 个月,P =.79)。如果将患者分为短(n = 89)和长(n = 77)反应者,在长反应者中,PPI+(n = 47)与 PPI-(n = 30)之间的 PFS 存在显著差异,分别为 24.7 与 38 个月(P =.04)。在舒尼替尼组中,PPI+(n = 102)与 PPI-(n = 131)之间的 PFS 无显著差异,分别为 11.3 与 18.1 个月(P=0.15)。在卡博替尼组中,PPI+与 PPI-之间的 PFS 存在统计学显著差异(6 个月与未达到,P =.04)。未发现与不良事件相关。
本研究表明,PPIs 与接受帕唑帕尼和卡博替尼治疗的 mRCC 患者的 PFS 受损之间存在关联,建议谨慎同时使用。