Argiris A, Seropian S, Cooper D L
Section of Medical Oncology, Yale University-School of Medicine, New Haven, Connecticut 06520, USA.
Ann Oncol. 2000 Jun;11(6):665-72. doi: 10.1023/a:1008396525292.
The use of autologous peripheral blood progenitor cells (PBPC) expedites hematologic recovery and reduces the costs of transplantation in comparison with autologous bone marrow; however, its efficacy in patients with Hodgkin's disease has been questioned. We evaluated the results of autologous PBPC transplantation in a population of unselected and uniformly treated patients with primary refractory or relapsed Hodgkin's disease.
Forty consecutive adult patients with primary refractory (n = 7) or relapsed (n = 33) Hodgkin's disease received high-dose BEAM (BCNU, etoposide, ara-C, and melphalan) followed by autologous PBPC infusion. Twenty-four patients (60%) received high-dose BEAM as outpatients. Consolidative radiation therapy was administered to 14 patients (35%).
Thirty-seven patients (92%) achieved a post transplant complete response. The 3-year progression-free survival (PFS) was 69%, and the 3-year overall survival (OS) was 77%, with a median follow-up of surviving patients of 28 months. Severe non-hematologic toxicities included gastrointestinal side effects (diarrhea 17%, mucositis 25%), and interstitial pneumonitis (15%). One patient died of acute transplant-related complications (mortality rate 2.5%). Strong predictors of poor PFS were chemoresistant versus chemosensitive/untested disease (actuarial PFS 89% versus 22%, P = 0.0000) and stage IIB-IV versus I-IIA at relapse/progression (86%, versus 46%, P = 0.005). All five patients with elevated lactate dehydrogenase at the time of transplantation died of their disease. There was a trend toward worse PFS for patients receiving a higher number of CD34+ cells (> or = 11 x 10(6) per kg).
High-dose BEAM chemotherapy with autologous PBPC transplantation is associated with low mortality and results in satisfactory PFS for patients with primary refractory or relapsed Hodgkin's disease. The subset of patients with progressive disease at the time of transplantation performs poorly and may benefit from alternative strategies.
与自体骨髓相比,使用自体外周血祖细胞(PBPC)可加快血液学恢复并降低移植成本;然而,其在霍奇金病患者中的疗效一直受到质疑。我们评估了在未经选择且治疗方案统一的原发性难治性或复发性霍奇金病患者群体中自体PBPC移植的结果。
40例连续的成年原发性难治性(n = 7)或复发性(n = 33)霍奇金病患者接受了大剂量BEAM(卡莫司汀、依托泊苷、阿糖胞苷和美法仑)治疗,随后进行自体PBPC输注。24例患者(60%)作为门诊患者接受了大剂量BEAM治疗。14例患者(35%)接受了巩固性放射治疗。
37例患者(92%)移植后达到完全缓解。3年无进展生存率(PFS)为69%,3年总生存率(OS)为77%,存活患者的中位随访时间为28个月。严重的非血液学毒性包括胃肠道副作用(腹泻17%,黏膜炎25%)和间质性肺炎(15%)。1例患者死于急性移植相关并发症(死亡率2.5%)。PFS差的强烈预测因素是化疗耐药与化疗敏感/未检测疾病(精算PFS 89%对22%,P = 0.0000)以及复发/进展时IIB-IV期与I-IIA期(86%对46%,P = 0.005)。移植时乳酸脱氢酶升高的所有5例患者均死于疾病。接受较高数量CD34+细胞(≥11×10⁶/kg)的患者PFS有变差的趋势。
大剂量BEAM化疗联合自体PBPC移植死亡率低,对于原发性难治性或复发性霍奇金病患者,可带来令人满意的PFS。移植时疾病进展的患者亚组预后较差,可能从替代策略中获益。