Janicek M, Kaplan W, Neuberg D, Canellos G P, Shulman L N, Shipp M A
Dana-Farber Cancer Institute, Boston, MA 02115, USA.
J Clin Oncol. 1997 Apr;15(4):1631-7. doi: 10.1200/JCO.1997.15.4.1631.
This prospective study assessed the predictive value of early restaging gallium (Ga) and computed tomographic (CT) scans in poor-prognosis patients with aggressive non-Hodgkin's lymphoma (NHL) who were treated with high-dose cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy.
Thirty newly diagnosed patients with bulky (> or = 10 cm) advanced-stage aggressive NHL were treated with a four-cycle high-dose CHOP regimen (22 patients at maximum-tolerated dose [MTD]: cyclophosphamide 4 g/m2, doxorubicin 70 mg/m2, vincristine 2 mg, and prednisone 100 mg orally for 5 days). All patients had chest/abdominal/pelvic CT scans and 10-mCi Ga scans at baseline and following two and four cycles of therapy. Scans were reviewed in a blinded manner for CT-documented rates of response and sizes of residual masses and Ga avidity of residual masses. The results of early (post-cycle 2) and final (post-cycle 4) restaging were subsequently associated with clinical outcome.
CT-documented rates of response and residual mass sizes were indistinguishable in complete responders who remained continuously disease-free (CR-Cont), complete responders who subsequently relapsed (CR-Rel), and partial responders who then progressed (PR/Prog). In marked contrast, early restaging (post-cycle 2) Ga scans accurately delineated these three categories of patients: CR-Cont 90% Ga-negative (18 of 20 patients) versus CR-Rel 25% Ga-negative (one of four patients) versus PR/Prog 0% Ga-negative (zero of six patients) (P = .000014). At a median follow-up duration of 31 months (range, 21 to 46), 94% of patients who had negative early restaging Ga scans remain free from progression (FFP), whereas only 18% of patients who had positive early restaging Ga scans remain FFP (P = .000007). Early restaging Ga scans were more predictive for FFP than final restaging Ga scans because patients who required four full cycles of therapy to become Ga-negative were more likely to develop recurrent disease.
Early restaging Ga scans delineate patients who are likely to have prolonged disease-free survival from those who fail to respond to intensive induction therapy. Patients whose tumors remain Ga-positive midway through high-dose CHOP therapy have a poor outcome and may be candidates for alternative treatment.
本前瞻性研究评估了早期再分期镓(Ga)扫描和计算机断层扫描(CT)对接受大剂量环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗的预后不良侵袭性非霍奇金淋巴瘤(NHL)患者的预测价值。
30例新诊断的晚期侵袭性大肿块(≥10 cm)NHL患者接受了四个周期的大剂量CHOP方案治疗(22例患者接受最大耐受剂量[MTD]:环磷酰胺4 g/m²、阿霉素70 mg/m²、长春新碱2 mg,泼尼松100 mg口服5天)。所有患者在基线时以及治疗两个周期和四个周期后均进行了胸部/腹部/盆腔CT扫描和10 mCi的Ga扫描。以盲法对扫描结果进行评估,以确定CT记录的缓解率、残留肿块大小以及残留肿块的Ga摄取情况。早期(第2周期后)和最终(第4周期后)再分期的结果随后与临床结局相关联。
在持续无病(CR-Cont)的完全缓解者、随后复发的完全缓解者(CR-Rel)以及随后病情进展的部分缓解者(PR/Prog)中,CT记录的缓解率和残留肿块大小没有差异。形成鲜明对比的是,早期再分期(第2周期后)的Ga扫描准确地区分了这三类患者:CR-Cont患者中90%的Ga扫描为阴性(20例患者中的18例),CR-Rel患者中25%的Ga扫描为阴性(4例患者中的1例),PR/Prog患者中0%的Ga扫描为阴性(6例患者中的0例)(P = 0.000014)。在中位随访时间31个月(范围21至46个月)时,早期再分期Ga扫描为阴性的患者中有94%无疾病进展(FFP),而早期再分期Ga扫描为阳性的患者中只有18%保持FFP(P = 0.000007)。早期再分期Ga扫描对FFP的预测性比最终再分期Ga扫描更强,因为需要四个完整周期治疗才能使Ga扫描转为阴性的患者更有可能发生疾病复发。
早期再分期Ga扫描区分了可能有较长无病生存期的患者和对强化诱导治疗无反应的患者。在大剂量CHOP治疗中途肿瘤仍为Ga阳性的患者预后不良,可能是替代治疗的候选者。