Age-related Toxicity in Patients With Rhabdomyosarcoma: A Report From the Children's Oncology Group

被引:0
作者
Altaf, Sadaf [1 ]
Enders, Felicity [2 ]
Lyden, Elizabeth [3 ]
Donaldson, Sarah S. [4 ]
Rodeberg, David [5 ]
Arndt, Carola [1 ]
机构
[1] Mayo Clin, Dept Pediat & Adolescent Med, Rochester, MN 55901 USA
[2] Mayo Clin, Dept Stat & Informat, Rochester, MN 55901 USA
[3] Univ Nebraska Med Ctr, Omaha, NE USA
[4] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[5] E Carolina Univ, Div Pediat Surg, Greenville, NC USA
基金
美国国家卫生研究院;
关键词
rhabdomyosarcoma; age; toxicity; chemotherapy; neurotoxicity; mucositis; neutropenia; CHILDHOOD-CANCER; RISK-FACTORS; CHEMOTHERAPY; VINCRISTINE; DACTINOMYCIN; ADOLESCENTS; YOUNGER; EVENTS; SEX;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
On the Fourth Intergroup Rhabdomyosarcoma study, older children experienced excessive neurotoxicity, whereas younger children had increased myelosuppression. The purpose of this study was to determine whether the same pattern of toxicity was seen on the successor study when use of growth factor was required and dosing of chemotherapy was different by performing a retrospective cohort analysis on patients treated on Children's Oncology Group protocol D9803. Toxicity data were analyzed by stratifying children into 4 age groups. The frequency of grade 3/4 neurotoxicity, myelosuppression, infection, and mucositis was predicted for each age group. The cumulative doses of vincristine and cyclophosphamide administered were measured as percent of protocol-prescribed dose. Adolescents (aged 15+) were more likely to experience neurotoxicity compared with younger patients (odds ratio, 3.6; P < 0.0001). There was no difference in myelosuppression, infection, or mucositis. The mean percent protocol-prescribed doses administered for vincristine and cyclophosphamide did not differ much by age group. Adolescents experienced more neurotoxicity with vincristine compared with younger patients. No differences in other toxicities were observed between age groups. As adolescents received at least 85% of protocol-prescribed doses of vincristine, it is difficult to attribute the poorer survival in this age group to inadequate protocol-delivered therapy.
引用
收藏
页码:599 / 604
页数:6
相关论文
共 18 条
  • [1] Age is a risk factor for chemotherapy-induced hepatopathy with vincristine, dactinomycin, and cyclophosphamide
    Arndt, C
    Hawkins, D
    Anderson, JR
    Breitfeld, P
    Womer, R
    Meyer, W
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (10) : 1894 - 1901
  • [2] Vincristine, Actinomycin, and Cyclophosphamide Compared With Vincristine, Actinomycin, and Cyclophosphamide Alternating With Vincristine, Topotecan, and Cyclophosphamide for Intermediate-Risk Rhabdomyosarcoma: Children's Oncology Group Study D9803
    Arndt, Carola A. S.
    Stoner, Julie A.
    Hawkins, Douglas S.
    Rodeberg, David A.
    Hayes-Jordan, Andrea A.
    Paidas, Charles N.
    Parham, David M.
    Teot, Lisa A.
    Wharam, Moody D.
    Breneman, John C.
    Donaldson, Sarah S.
    Anderson, James R.
    Meyer, William H.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (31) : 5182 - 5188
  • [3] Risk Assessment of Drug Interaction Potential and Concomitant Dosing Pattern on Targeted Toxicities in Pediatric Cancer Patients
    Barrett, Jeffrey S.
    Patel, Dimple
    Dombrowsky, Erin
    Bajaj, Gaurav
    Skolnik, Jeffrey M.
    [J]. AAPS JOURNAL, 2013, 15 (03): : 775 - 786
  • [4] Benefits and Adverse Events in Younger Versus Older Patients Receiving Neoadjuvant Chemotherapy for Osteosarcoma: Findings From a Meta-Analysis
    Collins, Marnie
    Wilhelm, Miriam
    Conyers, Rachel
    Herschtal, Alan
    Whelan, Jeremy
    Bielack, Stefan
    Kager, Leo
    Kuehne, Thomas
    Sydes, Matthew
    Gelderblom, Hans
    Ferrari, Stefano
    Picci, Piero
    Smeland, Sigbjorn
    Eriksson, Mikael
    Petrilli, Antonio Sergio
    Bleyer, Archie
    Thomas, David M.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (18) : 2303 - 2312
  • [5] Increased Risk of Vincristine Neurotoxicity Associated With Low CYP3A5 Expression Genotype in Children With Acute Lymphoblastic Leukemia
    Egbelakin, Akinbode
    Ferguson, Michael J.
    MacGill, Emily A.
    Lehmann, Amalia S.
    Topletz, Ariel R.
    Quinney, Sara K.
    Li, Lang
    McCammack, Kevin C.
    Hall, Stephen D.
    Renbarger, Jamie L.
    [J]. PEDIATRIC BLOOD & CANCER, 2011, 56 (03) : 361 - 367
  • [6] Frost BM, 2003, ACTA PAEDIATR, V92, P551, DOI 10.1080/08035320310000000
  • [7] Patterns of chemotherapy-induced toxicities in younger children and adolescents with rhabdomyosarcoma
    Gupta, Abha A.
    Anderson, James R.
    Pappo, Alberto S.
    Spunt, Sheri L.
    Dasgupta, Roshni
    Indelicato, Daniel J.
    Hawkins, Douglas S.
    [J]. CANCER, 2012, 118 (04) : 1130 - 1137
  • [8] The ontogeny of drug metabolism enzymes and implications for adverse drug events
    Hines, Ronald N.
    [J]. PHARMACOLOGY & THERAPEUTICS, 2008, 118 (02) : 250 - 267
  • [9] Age is an independent prognostic factor in rhabdomyosarcoma: A report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group
    Joshi, D
    Anderson, JR
    Paidas, C
    Breneman, J
    Parham, DM
    Crist, W
    [J]. PEDIATRIC BLOOD & CANCER, 2004, 42 (01) : 64 - 73
  • [10] Dactinomycin and Vincristine Toxicity in the Treatment of Childhood Cancer: A Retrospective Study From the Children's Oncology Group
    Langholz, Bryan
    Skolnik, Jeffrey M.
    Barrett, Jeffrey S.
    Renbarger, Jamie
    Seibel, Nita L.
    Zajicek, Anne
    Arndt, Carola A. S.
    [J]. PEDIATRIC BLOOD & CANCER, 2011, 57 (02) : 252 - 257