Rivera G K, Pinkel D, Simone J V, Hancock M L, Crist W M
Department of Hematology-Oncology, St. Jude Children's Research Hospital, Memphis, TN.
N Engl J Med. 1993 Oct 28;329(18):1289-95. doi: 10.1056/NEJM199310283291801.
Therapy for childhood lymphoblastic leukemia has evolved during the past three decades, but key questions about what are the least toxic, most effective forms of treatment remain unanswered because of the lack of comprehensive follow-up information.
To assess long-term outcome in the series of clinical trials conducted at St. Jude Hospital, we compared the results of treatment typical of four eras: exploratory combination chemotherapy (era 1, 1962 to 1966; 91 patients), regimens for the control of meningeal leukemia (era 2, 1967 to 1979; 825 patients), limited intensification of therapy (era 3, 1979 to 1983; 428 patients), and extended intensification of therapy (era 4, 1984 to 1988; 358 patients). ("Intensification" refers to strategies of systemic chemotherapy that are more aggressive than conventional ones.) The major end points were survival and event-free survival; we also calculated the relative risk of treatment failure and the rate of relapse or death after treatment ended (post-treatment failure rate).
The probability of event-free survival improved significantly in each successive era (P < 0.001 by the log-rank test), reaching 71 percent in era 4. There was a decrease of approximately 50 percent in the risk of treatment failure from one era to the next in each subgroup of patients defined according to different combinations of the leukocyte count, race, age, and sex. Leukemia appeared to be eradicated in patients who remained in complete remission for three years or more after treatment in era 4. The incidence of death due to nonleukemic causes remained 4 to 6 percent despite the trend toward more intensive treatment. An estimated 765 patients (45 percent) are long-term survivors; most of them (80 percent) have no health problems related to leukemia or its treatment.
The development and successful application of preventive therapy for meningeal leukemia, followed by the intensification of systemic chemotherapy, has progressively improved the rate of cure of childhood lymphoblastic leukemia, with relatively few adverse sequelae.
在过去三十年中,儿童淋巴细胞白血病的治疗方法不断演变,但由于缺乏全面的随访信息,关于毒性最小、最有效的治疗形式的关键问题仍未得到解答。
为了评估在圣裘德医院进行的一系列临床试验的长期结果,我们比较了四个时期典型治疗的结果:探索性联合化疗(时期1,1962年至1966年;91例患者)、控制脑膜白血病的方案(时期2,1967年至1979年;825例患者)、有限强化治疗(时期3,1979年至1983年;428例患者)以及强化治疗(时期4,1984年至1988年;358例患者)。(“强化”指的是比传统全身化疗更积极的策略。)主要终点是生存率和无事件生存率;我们还计算了治疗失败的相对风险以及治疗结束后复发或死亡的发生率(治疗后失败率)。
在每个连续时期,无事件生存率的概率均显著提高(对数秩检验P<0.001),在时期4达到71%。根据白细胞计数、种族、年龄和性别的不同组合定义的每个患者亚组中,从一个时期到下一个时期,治疗失败的风险降低了约50%。在时期4治疗后完全缓解三年或更长时间的患者中,白血病似乎已被根除。尽管有强化治疗的趋势,但非白血病原因导致的死亡率仍为4%至6%。估计有765名患者(45%)为长期幸存者;其中大多数(80%)没有与白血病或其治疗相关的健康问题。
脑膜白血病预防性治疗的发展和成功应用,随后强化全身化疗,已逐步提高了儿童淋巴细胞白血病的治愈率,且不良后遗症相对较少。