Arteaga-Ortiz Luis, Buitrón-Santiago Natalie, Rosas-López Adriana, Rosas-Arzate Guadalupe, Armengolt-Jiménez Alicia, Aguayo Alvaro, López-Karpovitch Xavier, Crespo-Solís Erick
Clinica de Leucemia Aguda, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán.
Rev Invest Clin. 2008 Nov-Dec;60(6):459-69.
Despite therapeutic advances, acute lymphoblastic leukemia (ALL) in adults remains a disease with poor long term outcome and survival rates. Developing countries lack of information about this disease. On the other hand, infections are frequent complications related to mortality and some research studies do not show accurate rates of septic shock or other related factors.
To describe characteristics of adults with acute lymphoblastic leukemia, response to treatment, complications and to evaluate further survival related factors and to compare our experience with other reports of literature.
Between September 2003 to November 2007, the entire cohort of patients with diagnosis of ALL was included. The treatment regimens used were MDACC HyperCVAD (HCVAD) and 0195 (institutional regimen).
Of 40 patients included with the diagnosis of ALL, 92% was B phenotype and 8%, T phenotype, with a median age of 27 years. The median follow up was 28.5 months. Initially, 14% showed central nervous system infiltration; of 51% with available cytogenetics, 16.7% was Philadelphia chromosome positive. There were 36 patients who received treatment: 13 received HCVAD and 23 the 0195 protocol; 78% achieved global complete remission, 85% for the patients with HCVAD and 74% with 0195. The induction death rate was 2.8%. The median disease-free survival was 11.6 months (IC 95%, 2.5-20.8 months) and overall survival was 15 months (IC 95%, 10.6-19.4 months). In 95% of patients, no prophylactic antibiotic therapy was used and treatment related death was 8.4% (2.8% during induction and 5.6% during the rest of treatment). Factors associated with worse survival rate were hyperleukocytosis, T phenotype and lack of early complete remission. During induction, grade 3 to 4 non hematopoietic toxicity was 17%. Incidence of neutropenic febrile episodes was 61% and septic shock was 11%.
With HCVAD, we observed worse complete remission, disease-free survival and overall survival rates compared with the original MDACC reports. Chemotherapy related death rates are similar to other early reports, despite prophylactic antibiotic was not used during myelosuppression.
尽管治疗取得了进展,但成人急性淋巴细胞白血病(ALL)仍然是一种长期预后和生存率较差的疾病。发展中国家缺乏关于这种疾病的信息。另一方面,感染是与死亡率相关的常见并发症,一些研究并未显示出败血症休克或其他相关因素的准确发生率。
描述成人急性淋巴细胞白血病的特征、对治疗的反应、并发症,评估进一步的生存相关因素,并将我们的经验与其他文献报道进行比较。
纳入2003年9月至2007年11月期间所有诊断为ALL的患者。使用的治疗方案为MDACC HyperCVAD(HCVAD)和0195(机构方案)。
在40例诊断为ALL的患者中,92%为B表型,8%为T表型,中位年龄为27岁。中位随访时间为28.5个月。最初,14%的患者出现中枢神经系统浸润;在51%进行了细胞遗传学检测的患者中,16.7%为费城染色体阳性。有36例患者接受了治疗:13例接受HCVAD治疗,23例接受0195方案治疗;78%的患者实现了总体完全缓解,接受HCVAD治疗的患者为85%,接受0195治疗的患者为74%。诱导死亡率为2.8%。无病生存期的中位数为11.6个月(95%置信区间,2.5 - 20.8个月),总生存期为15个月(95%置信区间,10.6 - 19.4个月)。95%的患者未使用预防性抗生素治疗,治疗相关死亡率为8.4%(诱导期为2.8%,治疗其余阶段为5.6%)。与较差生存率相关的因素为白细胞增多、T表型和缺乏早期完全缓解。诱导期3至4级非血液学毒性为17%。中性粒细胞减少伴发热发作的发生率为61%,败血症休克的发生率为11%。
与MDACC的原始报告相比,使用HCVAD时,我们观察到完全缓解率、无病生存期和总生存率更差。尽管在骨髓抑制期间未使用预防性抗生素,但化疗相关死亡率与其他早期报告相似。