Seibel Nita L, Steinherz Peter G, Sather Harland N, Nachman James B, Delaat Cynthia, Ettinger Lawrence J, Freyer David R, Mattano Leonard A, Hastings Caroline A, Rubin Charles M, Bertolone Kathy, Franklin Janet L, Heerema Nyla A, Mitchell Torrey L, Pyesmany Allan F, La Mei K, Edens Cheryl, Gaynon Paul S
Hematology/Oncology, Children's National Medical Center and George Washington University School of Medicine and Public Health, 111 Michigan Avenue NW, Washington, DC 20010, USA.
Blood. 2008 Mar 1;111(5):2548-55. doi: 10.1182/blood-2007-02-070342. Epub 2007 Nov 26.
Longer and more intensive postinduction intensification (PII) improved the outcome of children and adolescents with "higher risk" acute lymphoblastic leukemia (ALL) and a slow marrow response to induction therapy. In the Children's Cancer Group study (CCG-1961), we tested longer versus more intensive PII, using a 2 x 2 factorial design for children with higher risk ALL and a rapid marrow response to induction therapy. Between November 1996 and May 2002, 2078 children and adolescents with newly diagnosed ALL (1 to 9 years old with white blood count 50 000/mm3 or more, or 10 years of age or older with any white blood count) were enrolled. After induction, 1299 patients with marrow blasts less than or equal to 25% on day 7 of induction (rapid early responders) were randomized to standard or longer duration (n = 651 + 648) and standard or increased intensity (n = 649 + 650) PII. Stronger intensity PII improved event-free survival (81% vs 72%, P < .001) and survival (89% vs 83%, P = .003) at 5 years. Differences were most apparent after 2 years from diagnosis. Longer duration PII provided no benefit. Stronger intensity but not prolonged duration PII improved outcome for patients with higher-risk ALL. This study is registered at http://clinicaltrials.gov as NCT00002812.
诱导后强化治疗(PII)时间延长及强度增加可改善“高危”急性淋巴细胞白血病(ALL)患儿及青少年的预后,这类患儿对诱导治疗的骨髓反应缓慢。在儿童癌症研究组(CCG - 1961)的研究中,我们针对诱导治疗后骨髓反应迅速的高危ALL患儿,采用2×2析因设计,对PII时间延长与强度增加进行了测试。1996年11月至2002年5月,共纳入2078例新诊断的ALL患儿及青少年(年龄1至9岁,白细胞计数≥50000/mm³;或年龄10岁及以上,白细胞计数任意)。诱导治疗后,1299例在诱导第7天骨髓原始细胞≤25%的患者(早期快速反应者)被随机分为标准或延长疗程组(n = 651 + 648)以及标准或增加强度组(n = 649 + 650)进行PII。强度更大的PII可改善5年无事件生存率(81%对72%,P <.001)及总生存率(89%对83%,P =.003)。差异在诊断后2年最为明显。延长疗程的PII未显示出益处。对于高危ALL患者,强度增加而非疗程延长的PII可改善预后。本研究已在http://clinicaltrials.gov注册,注册号为NCT00002812。