Pigneux A, Devergie A, Pochitaloff M, Rio B, Archimbaud E, Cahn J Y, Leblond V, Michallet M, Jouet J P, Guilhot F
Bone Marrow Transplant Laboratory, URA CNRS 1456, University of Bordeaux II, France.
Bone Marrow Transplant. 1995 Jun;15(6):819-24.
Thirty three patients with Philadelphia chromosome positive (Ph+) chronic myelogenous leukemia (CML) in relapse after allogenic bone marrow transplantation (BMT) were treated with recombinant alpha-interferon (IFN). Ten patients received IFN for cytogenetic relapse (group I) and 23 (group II) for hematologic relapse. The starting dose of IFN varied from 1.7 to 6 million units/m2/day (median 3 x 10(6) U/m2/day). Among the 10 group I patients, 3 subsequently developed hematologic relapse. Of the other 7, a cytogenetic response was observed in 6 (complete 4, minor 2). Three of these responders are alive in complete cytogenetic remission. Of the 23 group II patients, 3 did not respond to IFN but 20 achieved a complete (CHR) (n = 14) or a partial hematologic response (PHR) (n = 6). Thirteen of the 14 CHR patients subsequently achieved a cytogenetic response (complete 7, minor 6). Seven of the latter 13 patients are still alive in complete cytogenetic remission (CCR). Thus, for the entire group of 33 patients, IFN was followed by CCR in 11 cases (33%); all these patients are still alive and the median follow-up in CCR is now 60.7 months (range 35.3-72.5 months). The BCR-ABL rearrangement was not detected by RT-PCR in 5 of the 10 patients analyzed. Eleven other patients developed either blast crisis or acceleration. The 3-year probability of survival from the start of IFN therapy probability of survival from the start of IFN therapy was 70 +/- 16% (95% CI) and was statistically higher for patients who achieved CCR than for the others.(ABSTRACT TRUNCATED AT 250 WORDS)
33例异基因骨髓移植(BMT)后复发的费城染色体阳性(Ph+)慢性粒细胞白血病(CML)患者接受了重组α干扰素(IFN)治疗。10例患者因细胞遗传学复发接受IFN治疗(I组),23例(II组)因血液学复发接受治疗。IFN起始剂量为170万至600万单位/平方米/天(中位数3×10⁶单位/平方米/天)。I组10例患者中,3例随后出现血液学复发。另外7例中,6例观察到细胞遗传学反应(完全缓解4例,部分缓解2例)。这些有反应者中有3例仍处于完全细胞遗传学缓解状态存活。II组23例患者中,3例对IFN无反应,但20例实现了完全血液学缓解(CHR)(n = 14)或部分血液学反应(PHR)(n = 6)。14例CHR患者中有13例随后出现细胞遗传学反应(完全缓解7例,部分缓解6例)。后13例患者中有7例仍处于完全细胞遗传学缓解(CCR)状态存活。因此,在33例患者的整个组中,11例(33%)在IFN治疗后实现了CCR;所有这些患者仍存活,CCR状态下的中位随访时间为60.7个月(范围35.3 - 72.5个月)。在分析的10例患者中有5例通过RT-PCR未检测到BCR-ABL重排。另外11例患者发生了急变期或加速期。从IFN治疗开始的3年生存率为70±16%(95%CI),实现CCR的患者的生存率在统计学上高于其他患者。(摘要截断于250字)