Randomized Controlled Trial of Interval-Compressed Chemotherapy for the Treatment of Localized Ewing Sarcoma: A Report From the Children's Oncology Group

被引:500
作者
Womer, Richard B. [1 ,2 ]
West, Daniel C. [3 ]
Krailo, Mark D. [4 ]
Dickman, Paul S. [5 ]
Pawel, Bruce R. [2 ]
Grier, Holcombe E. [6 ]
Marcus, Karen [6 ]
Sailer, Scott [7 ]
Healey, John H. [8 ]
Dormans, John P. [2 ]
Weiss, Aaron R. [9 ]
机构
[1] Childrens Hosp Philadelphia, Div Oncol, Philadelphia, PA 19104 USA
[2] Univ Penn, Philadelphia, PA 19104 USA
[3] Univ Calif San Francisco, San Francisco, CA 94143 USA
[4] Childrens Oncol Grp, Arcadia, CA USA
[5] Phoenix Childrens Hosp, Phoenix, AZ USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
[7] Univ N Carolina, Chapel Hill, NC USA
[8] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[9] Univ Med & Dent New Jersey, Robert Wood Johnson Univ Hosp, New Brunswick, NJ USA
关键词
COLONY-STIMULATING FACTOR; DOXORUBICIN DOSE INTENSITY; STANDARD CHEMOTHERAPY; HISTORICAL CONTROLS; MULTIMODAL THERAPY; PEDIATRIC-PATIENTS; INTERGROUP; CANCER; BONE; MANAGEMENT;
D O I
10.1200/JCO.2011.41.5703
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Chemotherapy with alternating vincristine-doxorubicin-cyclophosphamide and ifosfamide-etoposide cycles and primary tumor treatment with surgery and/or radiation therapy constitute the usual approach to localized Ewing sarcoma in North America. We tested whether chemotherapy intensification through interval compression could improve outcome. Patients and Methods This was a prospective, randomized controlled trial for patients younger than 50 years old with newly diagnosed localized extradural Ewing sarcoma. Patients assigned to standard and intensified treatment were to begin chemotherapy cycles every 21 and 14 days, respectively, provided an absolute neutrophil count greater than 750 x 10(6)/L and a platelet count greater than 75 x 10(9)/L. Patients received vincristine (2 mg/m(2)), doxorubicin (75 mg/m(2)), and cyclophosphamide (1.2 g/m(2)) alternating with ifosfamide (9 g/m(2)) and etoposide (500 mg/m(2)) for 14 cycles, with filgrastim (5 mg/kg per day; maximum, 300 mg) between cycles. Primary tumor treatment (surgery, radiation, or both) was to begin at week 13 (after four cycles in the standard arm and six cycles in the intensified arm). The primary end point was event-free survival (EFS). The study is registered at ClinicalTrials.gov (identifier: NCT00006734). Results Five hundred eighty-seven patients were enrolled and randomly assigned, and 568 patients were eligible, with 284 patients in each regimen. For all cycles, the median cycle interval for standard treatment was 21 days (mean, 22.45 days); for intensified treatment, the median interval was 15 days (mean, 17.29 days). EFS at a median of 5 years was 65% in the standard arm and 73% in the intensified arm (P = .048). The toxicity of the regimens was similar. Conclusion For localized Ewing sarcoma, chemotherapy administered every 2 weeks is more effective than chemotherapy administered every 3 weeks, with no increase in toxicity.
引用
收藏
页码:4148 / 4154
页数:7
相关论文
共 25 条
  • [1] Bishop M.M., 1975, DISCRETE MULTIVARIAT
  • [2] Pegfilgrastim for Prevention of Chemotherapy-Associated Neutropenia in Pediatric Patients With Solid Tumors
    Borinstein, Scott C.
    Pollard, Jessica
    Winter, Laura
    Hawkins, Douglas S.
    [J]. PEDIATRIC BLOOD & CANCER, 2009, 53 (03) : 375 - 378
  • [3] MULTIMODAL THERAPY FOR THE MANAGEMENT OF NONPELVIC, LOCALIZED EWINGS-SARCOMA OF BONE - INTERGROUP STUDY IESS-II
    BURGERT, EO
    NESBIT, ME
    GARNSEY, LA
    GEHAN, EA
    HERRMANN, J
    VIETTI, TJ
    CANGIR, A
    TEFFT, M
    EVANS, R
    THOMAS, P
    ASKIN, FB
    KISSANE, JM
    PRITCHARD, DJ
    NEFF, J
    MAKLEY, JT
    GILULA, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (09) : 1514 - 1524
  • [4] Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: First report of intergroup trial C9741/cancer and leukemia group B trial 9741
    Citron, ML
    Berry, DA
    Cirrincione, C
    Hudis, C
    Winer, EP
    Gradishar, WJ
    Davidson, NE
    Martino, S
    Livingston, R
    Ingle, JN
    Perez, EA
    Carpenter, J
    Hurd, D
    Holland, JF
    Smith, BL
    Sartor, CI
    Leung, EH
    Abrams, J
    Schilsky, RL
    Muss, HB
    Norton, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) : 1431 - 1439
  • [5] A SIMULATED STUDY OF HISTORICAL CONTROLS USING REAL DATA
    FAREWELL, VT
    DANGIO, GJ
    [J]. BIOMETRICS, 1981, 37 (01) : 169 - 176
  • [6] FAREWELL VT, 1982, PEDIATRICS, V70, P145
  • [7] A proportional hazards model for the subdistribution of a competing risk
    Fine, JP
    Gray, RJ
    [J]. JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1999, 94 (446) : 496 - 509
  • [8] Foote M, 1999, BIOPHARMACEUTICALS I
  • [9] Granowetter L, 2001, MED PEDIATR ONCOL, V37, P172
  • [10] Dose-Intensified Compared With Standard Chemotherapy for Nonmetastatic Ewing Sarcoma Family of Tumors: A Children's Oncology Group Study
    Granowetter, Linda
    Womer, Richard
    Devidas, Meenakshi
    Krailo, Mark
    Wang, Chenguang
    Bernstein, Mark
    Marina, Neyssa
    Leavey, Patrick
    Gebhardt, Mark
    Healey, John
    Shamberger, Robert Cooper
    Goorin, Allen
    Miser, James
    Meyer, James
    Arndt, Carola A. S.
    Sailer, Scott
    Marcus, Karen
    Perlman, Elizabeth
    Dickman, Paul
    Grier, Holcombe E.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15) : 2536 - 2541