Radiotherapy in pediatric medulloblastoma: Quality assessment of Pediatric Oncology Group Trial 9031

被引:35
|
作者
Miralbell, R [1 ]
Fitzgerald, TJ
Laurie, F
Kessel, S
Glicksman, A
Friedman, HS
Urie, M
Kepner, JL
Zhou, TN
Chen, ZJ
Barnes, P
Kun, L
Tarbell, NJ
机构
[1] Univ Hosp Geneva, Div Radiooncol, Dept Radiat Oncol, CH-1211 Geneva 14, Switzerland
[2] Qual Assurance Review Comm, Providence, RI USA
[3] Duke Univ, South Hosp, Pediat Neurooncol Div, Durham, NC USA
[4] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[5] Childrens Oncol Grp, Operat Ctr, Arcadia, CA USA
[6] Stanford Univ, Dept Radiol, Stanford, CA 94305 USA
[7] St Jude Childrens Hosp, Dept Radiat Oncol, Memphis, TN 38105 USA
[8] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
关键词
medulloblastoma; quality assurance; Pediatric Oncology Group; radiotherapy;
D O I
10.1016/j.ijrobp.2005.11.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the potential influence of radiotherapy quality on survival in high-risk pediatric medulloblastoma patients. Methods and Materials: Trial 9031 of the Pediatric Oncology Group (POG) aimed to study the relative benefit of cisplatin and etoposide randomization of high-risk patients with medulloblastoma to preradiotherapy vs. postradiotherapy treatment. Two-hundred and ten patients were treated according to protocol guidelines and were eligible for the present analysis. Treatment volume (whole brain, spine, posterior fossa, and primary tumor bed) and dose prescription deviations were assessed for each patient. An analysis of first site of failure was undertaken. Event-free and overall survival rates were calculated. A log-rank test was used to determine the significance of potential survival differences between patients with and without major deviations in the radiotherapy procedure. Results: Of 160 patients who were fully evaluable for all treatment quality parameters, 91 (57%) had 1 or more major deviations in their treatment schedule. Major deviations by treatment site were brain (26%), spinal (7%), posterior fossa (40%), and primary tumor bed (17%). Major treatment volume or total dose deviations did not significantly influence overall and event-free survival. Conclusions: Despite major treatment deviations in more than half of fully evaluable patients, underdosage or treatment volume misses were not associated with a worse event-free or overall survival. (c) 2006 Elsevier Inc.
引用
收藏
页码:1325 / 1330
页数:6
相关论文
共 50 条
  • [21] THE CHANGING-ROLE OF RADIOTHERAPY IN PEDIATRIC ONCOLOGY
    BARRETT, A
    [J]. CANCER SURVEYS, 1984, 3 (04) : 633 - 648
  • [22] Medulloblastoma: The 35 Years Experience of a Pediatric Oncology Clinic in Turkey
    Kizmazoglu, D.
    Sivis, Z.
    Kamer, S.
    Gunes, B.
    Ozcan, E.
    Turker, M.
    Atabay, B.
    Oniz, H.
    [J]. PEDIATRIC BLOOD & CANCER, 2020, 67 : S252 - S252
  • [23] MANAGEMENT OF MEDULLOBLASTOMA PATIENTS IN PRAGUE PEDIATRIC HEMATOLOGY AND ONCOLOGY CENTER
    Sumerauer, David
    Cyprova, Sona
    Zapotocky, Michal
    Zamecnik, Josef
    Kyncl, Martin
    Malinova, Bela
    Ondrova, Barbora
    Tichy, Michal
    Stary, Jan
    [J]. NEURO-ONCOLOGY, 2017, 19 : 46 - 46
  • [24] Pediatric Patients with High Risk Medulloblastoma: Experience in an Oncology Unit
    Cores, M.
    Novas, F. N.
    Nana, M.
    Urbieta, M.
    Garcia Lombardi, M.
    [J]. PEDIATRIC BLOOD & CANCER, 2019, 66 : S173 - S173
  • [25] A PHASE-I TRIAL OF FAZARABINE IN REFRACTORY PEDIATRIC SOLID TUMORS - A PEDIATRIC-ONCOLOGY-GROUP STUDY
    BERNSTEIN, ML
    WHITEHEAD, VM
    GRIER, H
    DUBOWY, R
    LAND, V
    DEVINE, S
    MURPHY, S
    KUNG, F
    [J]. INVESTIGATIONAL NEW DRUGS, 1993, 11 (04) : 309 - 312
  • [26] GUIDELINES FOR RESPONSE ASSESSMENT IN MEDULLOBLASTOMA AND OTHER LEPTOMENINGEAL SEEDING TUMORS: A REPORT FROM THE RESPONSE ASSESSMENT IN PEDIATRIC NEURO-ONCOLOGY (RAPNO) WORKING GROUP
    Warren, Katherine
    Harreld, Julie
    Chamberlain, Marc
    Vezina, Gilbert
    Warmuth-Metz, Monika
    von Hoff, Katja
    Packer, Roger
    Brandes, Alba A.
    Reiss, Moshe
    Goldman, Stewart
    Fisher, Michael
    Poussaint, Tina Young
    Pollack, Ian
    Prados, Michael
    Wen, Patrick
    Chang, Susan
    Dufour, Christelle
    Zurakowski, David
    Kortman, Rolf-Dieter
    Kieran, Mark
    [J]. NEURO-ONCOLOGY, 2016, 18 : 148 - 149
  • [27] Survival impact of postoperative radiotherapy timing in pediatric and adolescent medulloblastoma
    Chin, Alexander L.
    Moding, Everett J.
    Donaldson, Sarah S.
    Gibbs, Iris C.
    Soltys, Scott G.
    Hiniker, Susan M.
    Pollom, Erqi L.
    [J]. NEURO-ONCOLOGY, 2018, 20 (08) : 1133 - 1141
  • [28] Long Term Clinical Outcomes of Proton Radiotherapy for Pediatric Medulloblastoma
    Baliga, S.
    Bajaj, B.
    Gallotto, S.
    Lewy, J.
    Weyman, E. A.
    Lawell, M. P.
    Yeap, B. Y.
    Ebb, D. H.
    Huang, M.
    Perry, A.
    MacDonald, S.
    Jones, R. M.
    Tarbell, N. J.
    Yock, T. I.
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2020, 108 (03): : S126 - S127
  • [29] RE-EVALUATING THE SEQUENCING OF RADIOTHERAPY AND CHEMOTHERAPY IN PEDIATRIC MEDULLOBLASTOMA
    Hess, Clayton
    Yeap, Beow
    Sahasakmontri, Jay
    Lawell, Miranda
    Weyman, Elizabeth
    Gallotto, Sara
    Bajaj, Benjamin
    Sieger, Kira
    MacDonald, Shannon
    Marcus, Karen
    Kieran, Mark
    Huang, Mary
    Tarbell, Nancy
    Ebb, David
    Yock, Torunn
    [J]. NEURO-ONCOLOGY, 2018, 20 : 226 - 227
  • [30] RESPONSE ASSESSMENT IN PEDIATRIC INTRACRANIAL EPENDYMOMA: RECOMMENDATIONS FROM THE RESPONSE ASSESSMENT IN PEDIATRIC NEURO-ONCOLOGY (RAPNO) WORKING GROUP
    Lindsay, Holly
    Massimino, Maura
    Avula, Shivaram
    Stivaros, Stavros
    Grundy, Richard
    Metrock, Katie
    Bhatia, Aashim
    Fernandez-Teijeiro, Ana
    Chiapparini, Luisa
    Bennett, Jeffrey
    Wright, Karen
    Hoffman, Lindsey
    Smith, Amy
    Pajtler, Kristian
    Poussaint, Tina Young
    Warren, Katherine
    Foreman, Nicholas
    Mirsky, David
    [J]. NEURO-ONCOLOGY, 2022, 24 : 38 - 38