Russo D, Malagola M, Skert C, Cancelli V, Turri D, Pregno P, Bergamaschi M, Fogli M, Testoni N, De Vivo A, Castagnetti F, Pungolino E, Stagno F, Breccia M, Martino B, Intermesoli T, Cambrin G R, Nicolini G, Abruzzese E, Tiribelli M, Bigazzi C, Usala E, Russo S, Russo-Rossi A, Lunghi M, Bocchia M, D'Emilio A, Santini V, Girasoli M, Lorenzo R Di, Bernardi S, Palma A Di, Cesana B M, Soverini S, Martinelli G, Rosti G, Baccarani M
Unit of Blood Diseases and Stem Cell Transplantation, University of Brescia, Brescia, Italy.
Ematologia 1-TMO, AOR Villa Sofia-Cervello, Palermo, Italy.
Blood Cancer J. 2015 Sep 18;5(9):e347. doi: 10.1038/bcj.2015.75.
The aim of this study was to investigate the effects of a non-standard, intermittent imatinib treatment in elderly patients with Philadelphia-positive chronic myeloid leukaemia and to answer the question on which dose should be used once a stable optimal response has been achieved. Seventy-six patients aged ⩾65 years in optimal and stable response with ⩾2 years of standard imatinib treatment were enrolled in a study testing a regimen of intermittent imatinib (INTERIM; 1-month on and 1-month off). With a minimum follow-up of 6 years, 16/76 patients (21%) have lost complete cytogenetic response (CCyR) and major molecular response (MMR), and 16 patients (21%) have lost MMR only. All these patients were given imatinib again, the same dose, on the standard schedule and achieved again CCyR and MMR or an even deeper molecular response. The probability of remaining on INTERIM at 6 years was 48% (95% confidence interval 35-59%). Nine patients died in remission. No progressions were recorded. Side effects of continuous treatment were reduced by 50%. In optimal and stable responders, a policy of intermittent imatinib treatment is feasible, is successful in about 50% of patients and is safe, as all the patients who relapsed could be brought back to optimal response.
本研究的目的是调查非标准的间歇性伊马替尼治疗对老年费城染色体阳性慢性髓系白血病患者的影响,并回答在达到稳定的最佳反应后应使用何种剂量的问题。76例年龄≥65岁、接受标准伊马替尼治疗≥2年且处于最佳和稳定反应状态的患者参加了一项测试间歇性伊马替尼方案(INTERIM;1个月用药、1个月停药)的研究。在至少6年的随访中,16/76例患者(21%)失去了完全细胞遗传学反应(CCyR)和主要分子反应(MMR),16例患者(21%)仅失去了MMR。所有这些患者再次按照标准方案给予相同剂量的伊马替尼,再次获得了CCyR和MMR或更深的分子反应。6年时继续使用INTERIM方案的概率为48%(95%置信区间35-59%)。9例患者在缓解期死亡。未记录到病情进展。持续治疗的副作用减少了50%。在最佳和稳定反应者中,间歇性伊马替尼治疗策略是可行的,约50%的患者治疗成功且安全,因为所有复发的患者都能恢复到最佳反应状态。