Pellegrino B, Terrier-Lacombe M J, Oberlin O, Leblanc T, Perel Y, Bertrand Y, Beard C, Edan C, Schmitt C, Plantaz D, Pacquement H, Vannier J P, Lambilliote C, Couillault G, Babin-Boilletot A, Thuret I, Demeocq F, Leverger G, Delsol G, Landman-Parker J
Departments of Pediatric Hematology/Oncology of Hôpital, Armand Trousseau, Paris, France.
J Clin Oncol. 2003 Aug 1;21(15):2948-52. doi: 10.1200/JCO.2003.01.079.
To clarify treatment strategy for lymphocyte-predominant Hodgkin's lymphoma (LPHL), the French Society of Pediatric Oncology initiated a prospective, nonrandomized study in 1988. Patients received either standard treatment for Hodgkin's lymphoma or were not treated beyond initial adenectomy.
From 1988 to 1998, 27 patients were available for study. Twenty-four patients were male, and median age was 10 years (range, 4 to 16 years). Twenty-two, two, and three patients had stage I, II, and III disease, respectively. Thirteen patients (stage I, n = 11; stage III, n = 2) received no further treatment after initial surgical adenectomy (SA). Fourteen patients received combined treatment (CT; n = 10), involved-field radiotherapy alone (n = 1), or chemotherapy alone (n = 3). The two groups were comparable for clinical status, treatment, and follow-up.
Twenty-three of 27 patients achieved complete remission (CR). With a median follow-up time of 70 months (range, 32 to 214 months), overall survival to date is 100%, and overall event-free survival (EFS) is 69% +/- 10% (SA, 42% +/- 16%; CT, 90% +/- 8.6%; P <.04). If we considered only the patients in CR after initial surgery (n = 12), EFS was no longer significantly different between the two groups. Patients with residual mass after initial surgery (n = 15) had worse EFS if they did not receive complementary treatment (P <.05).
Although based on a small number of patients, our study showed that (1). no further therapy is a valid therapeutic approach in LPHL patient in CR after initial lymph node resection, and (2). complementary treatment diminishes relapse frequency but has no impact on survival.
为明确淋巴细胞为主型霍奇金淋巴瘤(LPHL)的治疗策略,法国儿科肿瘤学会于1988年启动了一项前瞻性、非随机研究。患者接受霍奇金淋巴瘤的标准治疗,或仅在初次淋巴结切除术后不再接受进一步治疗。
1988年至1998年,有27例患者可供研究。24例为男性,中位年龄为10岁(范围4至16岁)。分别有22例、2例和3例患者处于Ⅰ期、Ⅱ期和Ⅲ期疾病。13例患者(Ⅰ期,n = 11;Ⅲ期,n = 2)在初次手术淋巴结切除(SA)后未接受进一步治疗。14例患者接受了联合治疗(CT;n = 10)、单纯受累野放疗(n = 1)或单纯化疗(n = 3)。两组在临床状态、治疗和随访方面具有可比性。
27例患者中有23例实现完全缓解(CR)。中位随访时间为70个月(范围32至214个月),迄今为止总生存率为100%,总无事件生存率(EFS)为69%±10%(SA组,42%±16%;CT组,90%±8.6%;P <.04)。如果仅考虑初次手术后达到CR的患者(n = 12),两组之间的EFS不再有显著差异。初次手术后有残留肿块的患者(n = 15)如果未接受辅助治疗,其EFS较差(P <.05)。
尽管基于少数患者,但我们的研究表明,(1)对于初次淋巴结切除术后达到CR的LPHL患者,不再进行进一步治疗是一种有效的治疗方法;(2)辅助治疗可降低复发频率,但对生存率无影响。