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急性髓系白血病患者首次复发后长期无病生存的概率:单中心经验

Probability of long-term disease-free survival for acute myeloid leukemia patients after first relapse: A single-centre experience.

作者信息

Vignetti M, Orsini E, Petti M C, Moleti M L, Andrizzi C, Pinto R M, Amadori S, Meloni G

机构信息

Department of Human Biopathology, Università La Sapienza, Rome, Italy.

出版信息

Ann Oncol. 1996 Nov;7(9):933-8. doi: 10.1093/oxfordjournals.annonc.a010796.

Abstract

BACKGROUND

Various polichemotherapy regimens, including either high- or intermediate-dose Ara-C, are generally utilized to reinduce remission in relapsed AML patients. After achieving second CR, bone marrow transplantation (either allogeneic or autologous) represents the treatment of choice for eligible patients, with the aim of prolonging remission duration and improving disease-free survival.

PATIENTS AND METHODS

Fifty AML patients in first hematological relapse were treated with MEC regimen, consisting of a 6-day induction cycle [mitoxantrone 6 mg/m2/day, cytarabine (Ara-C) 1 g/m2/day and VP-16 80 mg/m2/day] followed by a 4-day cycle with the same drugs for patients achieving complete remission (CR); allogeneic or autologous bone marrow transplantation (BMT) were planned as post-consolidation treatment.

RESULTS

Thirty-four patients (68%) achieved second CR, 3 (6%) died during induction and 13 were refractory. CR rate was significantly higher in patients with a first CR lasting > 6 months (82% vs. 41%, P < 0.001). Out of the 34 patients in CR after the 4-day cycle, 18 (53%) were not eligible to transplant and did not receive any further therapy and 16 (47%) received autologous (15 cases) or allogeneic (1 case) BMT at a median time of 2 months from second CR. Twenty-two patients relapsed after a median time of 6 months (range 1-31), 1 patient died from transplant-related toxicity and 11 are in continuous CR [7 out of 16 (44%) in the transplanted and 4 out of 11 (36%) in the non-transplanted group]. Overall survival and event-free survival for the 50 patients were 29% and 19% at 70 months, respectively. The disease-free survival for the 34 patients who obtained second CR is 29% projected at 69 months [41% at 69 months for 16 transplanted patients versus 18% at 49 months for the remaining 18 patients (P = 0.007)].

CONCLUSIONS

These results show that MEC followed by high-dose post-consolidation treatment is a promising approach in relapsed AML; however, alternative strategies are to be investigated for the relevant fraction of patients that, even achieving second CR, are not eligible for BMT.

摘要

背景

各种联合化疗方案,包括高剂量或中剂量阿糖胞苷,通常用于使复发的急性髓系白血病(AML)患者再次诱导缓解。在获得第二次完全缓解(CR)后,骨髓移植(异基因或自体)是符合条件患者的首选治疗方法,目的是延长缓解期并提高无病生存率。

患者和方法

50例首次血液学复发的AML患者接受MEC方案治疗,诱导周期为6天[米托蒽醌6mg/m²/天、阿糖胞苷(Ara-C)1g/m²/天和依托泊苷80mg/m²/天],达到完全缓解(CR)的患者随后进行4天相同药物的周期治疗;计划进行异基因或自体骨髓移植(BMT)作为巩固治疗后的治疗。

结果

34例患者(68%)获得第二次CR,3例(6%)在诱导期间死亡,13例难治。首次CR持续时间>6个月的患者CR率显著更高(82%对41%,P<0.001)。在4天周期后达到CR的34例患者中,18例(53%)不符合移植条件且未接受任何进一步治疗,16例(47%)在第二次CR后中位2个月接受了自体(15例)或异基因(1例)BMT。22例患者在中位6个月(范围1-31个月)后复发,1例患者死于移植相关毒性,11例持续CR[移植组16例中的7例(44%)和未移植组11例中的4例(36%)]。50例患者的总生存率和无事件生存率在70个月时分别为29%和19%。获得第二次CR的34例患者的无病生存率预计在69个月时为29%[16例移植患者在69个月时为41%,其余18例患者在49个月时为18%(P=0.007)]。

结论

这些结果表明,MEC方案后进行高剂量巩固治疗是复发AML的一种有前景的方法;然而,对于即使获得第二次CR但不符合BMT条件的相关部分患者,仍需研究替代策略。

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