中华放射肿瘤学杂志
中華放射腫瘤學雜誌
중화방사종류학잡지
CHINESE JOURNAL OF RADIATION ONCOLOGY
2014年
3期
187-190
,共4页
房辉%张希梅%金晶%王维虎%宋永文%刘跃平%王淑莲%任骅%余子豪
房輝%張希梅%金晶%王維虎%宋永文%劉躍平%王淑蓮%任驊%餘子豪
방휘%장희매%금정%왕유호%송영문%류약평%왕숙련%임화%여자호
淋巴瘤,间变大细胞%淋巴瘤,青少年%淋巴瘤,儿童%化学疗法%放射疗法%预后
淋巴瘤,間變大細胞%淋巴瘤,青少年%淋巴瘤,兒童%化學療法%放射療法%預後
림파류,간변대세포%림파류,청소년%림파류,인동%화학요법%방사요법%예후
Lymphoma,anaplastic large cell%Lymphoma,adolescent%Lymphoma,childhood%Chemotherapy%Radiotherapy%Prognosis
目的 分析青少年儿童原发系统性间变大细胞淋巴瘤(ALCL)患者接受CHOP方案化疗±受累野放疗的疗效.方法 回顾分析本院1998-2010年收治的28例青少年、儿童ALCL患者资料.Ⅰ、Ⅱ期12例中单纯化疗2例、综合治疗10例,Ⅲ、Ⅳ期16例中单纯化疗14例、综合治疗2例.CHOP方案15例、CHOP联合其他高强度化疗13例.化疗周期数3~17个(中位数6个).放疗多为受累野照射,剂量39.6~ 50.0 Gy(中位数45 Gy).结果 全组患者首程疗后达CR者25例(89%),3例病变进展.中位随访时间45.3个月.全组5年无事件生存率为80%,5年OS为93%.疗终达CR者5年OS为100%,而未达CR者无5年OS(P=0.000).≥2个结外器官受侵者5年无事件生存率为38%,而<2个结外器官受侵者的为85% (P =0.010).结论 青少年、儿童原发系统性ALCL按成人方案治疗效果满意,但还需要长期随访.
目的 分析青少年兒童原髮繫統性間變大細胞淋巴瘤(ALCL)患者接受CHOP方案化療±受纍野放療的療效.方法 迴顧分析本院1998-2010年收治的28例青少年、兒童ALCL患者資料.Ⅰ、Ⅱ期12例中單純化療2例、綜閤治療10例,Ⅲ、Ⅳ期16例中單純化療14例、綜閤治療2例.CHOP方案15例、CHOP聯閤其他高彊度化療13例.化療週期數3~17箇(中位數6箇).放療多為受纍野照射,劑量39.6~ 50.0 Gy(中位數45 Gy).結果 全組患者首程療後達CR者25例(89%),3例病變進展.中位隨訪時間45.3箇月.全組5年無事件生存率為80%,5年OS為93%.療終達CR者5年OS為100%,而未達CR者無5年OS(P=0.000).≥2箇結外器官受侵者5年無事件生存率為38%,而<2箇結外器官受侵者的為85% (P =0.010).結論 青少年、兒童原髮繫統性ALCL按成人方案治療效果滿意,但還需要長期隨訪.
목적 분석청소년인동원발계통성간변대세포림파류(ALCL)환자접수CHOP방안화료±수루야방료적료효.방법 회고분석본원1998-2010년수치적28례청소년、인동ALCL환자자료.Ⅰ、Ⅱ기12례중단순화료2례、종합치료10례,Ⅲ、Ⅳ기16례중단순화료14례、종합치료2례.CHOP방안15례、CHOP연합기타고강도화료13례.화료주기수3~17개(중위수6개).방료다위수루야조사,제량39.6~ 50.0 Gy(중위수45 Gy).결과 전조환자수정료후체CR자25례(89%),3례병변진전.중위수방시간45.3개월.전조5년무사건생존솔위80%,5년OS위93%.료종체CR자5년OS위100%,이미체CR자무5년OS(P=0.000).≥2개결외기관수침자5년무사건생존솔위38%,이<2개결외기관수침자적위85% (P =0.010).결론 청소년、인동원발계통성ALCL안성인방안치료효과만의,단환수요장기수방.
Objective To investigate the long-term efficacy of CHOP (cyclophosphamide,doxorubicin,vincristine,and prednisone)-based chemotherapy alone or combined with regional radiotherapy for adolescent/childhood primary systemic anaplastic large-cell lymphoma (ALCL).Methods A retrospective analysis was performed on the medical records of 28 patients not older than 21 years with a confirmed diagnosis of primary systemic ALCL,who were admitted to our hospital from January 1998 to December 2010.Of 12 stage Ⅰ / Ⅱ patients,2 received chemotherapy alone,and 10 received chemotherapy and radiotherapy;of 16 stage Ⅲ/Ⅳ patients,14 received chemotherapy alone,and 2 received chemotherapy and radiotherapy.CHOP regimen was adopted in 15 patients,and CHOP regimen combined with other highintensity regimens was adopted in 13 patients.There were 3-17 chemotherapy cycles (median:6 cycles).Radiotherapy was performed mainly by involved field radiation,with a dose of 39.6-50.0 Gy (median:45 Gy).Results After the first course of treatment,25 (89%) of all patients achieved a complete remission (CR),and 3 patients experienced disease progression.With a median follow-up of 45.3 months,the 5-year event-free survival (EFS) and overall survival (OS) for all patients were 80% and 93%,respectively.The 5-year OS was 100% for patients achieving a CR after treatment,versus 0% for those not achieving a CR (P =0.000).The 5-year EFS was 38 % for patients with involvement of ≥ 2 extranodal organs,versus 85 % for those with involvement of < 2 extranodal organs (P =0.010).Conclusions CHOP chemotherapy combined with regional radiotherapy (for patients with localized disease) is an effective treatment for adolescent/childhood primary systemic ALCL,but long-term follow-up is needed to investigate treatmentrelated toxicities.