Kothari Shalin, Ud-Din Najam, Lisi Michele, Coyle Thomas
Department of Medicine, SUNY Upstate Medical University, 750 E Adams St., Syracuse, NY, 13210, USA.
Division of Hematology/Oncology, Department of Medicine, SUNY Upstate Medical University, 750 E Adams St., Syracuse, NY, 13210, USA.
J Med Case Rep. 2016 Jun 14;10:176. doi: 10.1186/s13256-016-0963-y.
In vitro studies confirmed cytoreductive anti-tumor activity of crizotinib in experimental models of anaplastic large cell lymphoma in 2007. One case series and a few case reports describe the use of crizotinib in relapsed or refractory anaplastic lymphoma kinase-positive anaplastic large cell lymphoma. Even though data are limited regarding the dose of crizotinib in renal insufficiency, our case was successfully treated with a lower dose of crizotinib.
We report the case of a 48-year-old white man who had progressive disease after three prior cycles of cyclophosphamide, doxorubicin, vincristine and prednisone and three cycles of ifosfamide, carboplatin, and etoposide, and was not a candidate for high-dose chemotherapy and transplant due to poor performance status and renal insufficiency; he had a complete and durable response to single agent crizotinib. Crizotinib was given at a reduced dose (250 mg once daily) due to his renal insufficiency. He has been in complete remission for more than 2 years.
Our experience confirms the activity of crizotinib in this disease; it suggests that long-term treatment with crizotinib is a reasonable option in patients who are not candidates for more aggressive therapy and indicates that crizotinib can be used successfully at reduced doses in patients with pre-existing renal insufficiency. The role and timing of crizotinib in anaplastic lymphoma kinase-positive anaplastic large cell lymphoma is unclear, but the current literature that we review here provides promising results that may lead to studies of crizotinib earlier in the course of disease.
2007年的体外研究证实了克唑替尼在间变性大细胞淋巴瘤实验模型中的细胞减灭抗肿瘤活性。一个病例系列和一些病例报告描述了克唑替尼在复发或难治性间变性淋巴瘤激酶阳性间变性大细胞淋巴瘤中的应用。尽管关于肾功能不全患者使用克唑替尼的剂量数据有限,但我们的病例使用较低剂量的克唑替尼成功得到了治疗。
我们报告了一名48岁白人男性的病例,他在接受了三个周期的环磷酰胺、阿霉素、长春新碱和泼尼松以及三个周期的异环磷酰胺、卡铂和依托泊苷治疗后病情进展,由于身体状况不佳和肾功能不全,他不适合进行大剂量化疗和移植;他对单药克唑替尼有完全且持久的反应。由于他肾功能不全,克唑替尼以降低剂量(每日一次250毫克)给药。他已完全缓解超过2年。
我们的经验证实了克唑替尼在这种疾病中的活性;这表明对于不适合更积极治疗的患者,长期使用克唑替尼是一个合理的选择,并且表明克唑替尼可以在已有肾功能不全的患者中成功以降低剂量使用。克唑替尼在间变性淋巴瘤激酶阳性间变性大细胞淋巴瘤中的作用和时机尚不清楚,但我们在此回顾的当前文献提供了有希望的结果,可能会促使在疾病过程中更早地对克唑替尼进行研究。