Klion Amy D, Robyn Jamie, Maric Irina, Fu Weiming, Schmid Laura, Lemery Steven, Noel Pierre, Law Melissa A, Hartsell Marilyn, Talar-Williams Cheryl, Fay Michael P, Dunbar Cynthia E, Nutman Thomas B
Laboratory of Parasitic Diseases, National Institutes of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Blood. 2007 Nov 15;110(10):3552-6. doi: 10.1182/blood-2007-07-100164. Epub 2007 Aug 20.
Although imatinib is clearly the treatment of choice for FIP1L1/PDGFRA-positive chronic eosinophilic leukemia (CEL), little is known about optimal dosing, duration of treatment, and the possibility of cure in this disorder. To address these questions, 5 patients with FIP1L1/PDGFRA-positive CEL with documented clinical, hematologic, and molecular remission on imatinib (400 mg daily) and without evidence of cardiac involvement were enrolled in a dose de-escalation trial. The imatinib dose was tapered slowly with close follow-up for evidence of clinical, hematologic, and molecular relapse. Two patients with endomyocardial fibrosis were maintained on imatinib 300 to 400 mg daily and served as controls. All 5 patients who underwent dose de-escalation, but neither of the control patients, experienced molecular relapse (P < .05). None developed recurrent symptoms, and eosinophil counts, serum B12, and tryptase levels remained suppressed. Reinitiation of therapy at the prior effective dose led to molecular remission in all 5 patients, although 2 patients subsequently required increased dosing to maintain remission. These data are consistent with suppression rather than elimination of the clonal population in FIP1L1/PDGFRA-positive CEL and suggest that molecular monitoring may be the most useful method in determining optimal dosing without the risk of disease exacerbation. This trial was registered at http://www.clinicaltrials.gov as no. NCT00044304.
尽管伊马替尼显然是FIP1L1/PDGFRA阳性慢性嗜酸性粒细胞白血病(CEL)的首选治疗药物,但对于该疾病的最佳剂量、治疗持续时间以及治愈的可能性却知之甚少。为了解决这些问题,5例FIP1L1/PDGFRA阳性CEL患者,在接受伊马替尼(每日400 mg)治疗后有记录的临床、血液学和分子学缓解,且无心脏受累证据,被纳入剂量递减试验。伊马替尼剂量缓慢递减,同时密切随访以寻找临床、血液学和分子学复发的证据。2例患有心内膜纤维化的患者继续每日服用300至400 mg伊马替尼作为对照。所有5例接受剂量递减的患者均出现分子学复发,而2例对照患者均未出现(P <.05)。所有患者均未出现复发症状,嗜酸性粒细胞计数、血清B12和类胰蛋白酶水平仍受到抑制。以先前的有效剂量重新开始治疗使所有5例患者均实现分子学缓解,尽管有2例患者随后需要增加剂量以维持缓解。这些数据与FIP1L1/PDGFRA阳性CEL中克隆群体的抑制而非消除一致,并表明分子监测可能是确定最佳剂量且无疾病恶化风险的最有用方法。该试验已在http://www.clinicaltrials.gov上注册,编号为NCT00044304。