Detailed Information on Publication Record
2016
Prognostic value of medulloblastoma extent of resection after accounting for molecular subgroup: a retrospective integrated clinical and molecular analysis
THOMPSON, Eric M., Thomas HIELSCHER, Eric BOUFFET, Marc REMKE, Betty LUU et. al.Basic information
Original name
Prognostic value of medulloblastoma extent of resection after accounting for molecular subgroup: a retrospective integrated clinical and molecular analysis
Authors
THOMPSON, Eric M. (124 Canada), Thomas HIELSCHER (276 Germany), Eric BOUFFET (124 Canada), Marc REMKE (124 Canada), Betty LUU (124 Canada), Sridharan GURURANGAN (840 United States of America), Roger E. MCLENDON (840 United States of America), Darell D. BIGNER (840 United States of America), Eric S. LIPP (840 United States of America), Sebastien PERREAULT (840 United States of America), Yoon-Jae CHO (840 United States of America), Gerald GRANT (840 United States of America), Seung-Ki KIM (410 Republic of Korea), Ji Yeoun LEE (410 Republic of Korea), Amulya A Nageswara RAO (840 United States of America), Caterina GIANNINI (840 United States of America), Kay Ka Wai LI (156 China), Ho-Keung NG (156 China), Yu YAO (156 China), Toshihiro KUMABE (392 Japan), Teiji TOMINAGA (392 Japan), Wieslawa A. GRAJKOWSKA (616 Poland), Marta PEREK-POLNIK (616 Poland), David C. Y. LOW (702 Singapore), Wan Tew SEOW (702 Singapore), Kenneth T. E. CHANG (702 Singapore), Jaume MORA (724 Spain), Ian F. POLLACK (840 United States of America), Ronald L. HAMILTON (840 United States of America), Sarah LEARY (840 United States of America), Andrew S. MOORE (36 Australia), Wendy J. INGRAM (36 Australia), Andrew R. HALLAHAN (36 Australia), Anne JOUVET (250 France), Michelle FÈVRE-MONTANGE (250 France), Alexandre VASILJEVIC (250 France), Cecile FAURE-CONTER (250 France), Tomoko SHOFUDA (392 Japan), Naoki KAGAWA (392 Japan), Naoya HASHIMOTO (392 Japan), Nada JABADO (124 Canada), Alexander G. WEIL (124 Canada), Tenzin GAYDEN (124 Canada), Takafumi WATAYA (392 Japan), Tarek SHALABY (756 Switzerland), Michael GROTZER (756 Switzerland), Karel ZITTERBART (203 Czech Republic, belonging to the institution), Jaroslav ŠTĚRBA (203 Czech Republic, guarantor, belonging to the institution), Leoš KŘEN (203 Czech Republic, belonging to the institution), Tibor HORTOBÁGYI (348 Hungary), Almos KLEKNER (348 Hungary), Bognár LÁSZLÓ (348 Hungary), Tímea PÓCZA (348 Hungary), Peter HAUSER (348 Hungary), Ulrich SCHÜLLER (276 Germany), Shin JUNG (410 Republic of Korea), Woo-Youl JANG (410 Republic of Korea), Pim J. FRENCH (528 Netherlands), Johan M. KROS (528 Netherlands), Marie-Lise C. van VEELEN (528 Netherlands), Luca MASSIMI (380 Italy), Jeffrey R. LEONARD (840 United States of America), Joshua B. RUBIN (840 United States of America), Rajeev VIBHAKAR (840 United States of America), Lola B. CHAMBLESS (840 United States of America), Michael K. COOPER (840 United States of America), Reid C. THOMPSON (840 United States of America), Claudia C. FARIA (620 Portugal), Alice CARVALHO (620 Portugal), Sofia NUNES (620 Portugal), José PIMENTEL (620 Portugal), Xing FAN (840 United States of America), Karin M. MURASZKO (840 United States of America), Enrique LÓPEZ-AGUILAR (484 Mexico), David LYDEN (840 United States of America), Livia GARZIA (124 Canada), David J. H. SHIH (124 Canada), Noriyuki KIJIMA (124 Canada), Christian SCHNEIDER (124 Canada), Jennifer ADAMSKI (124 Canada), Paul A. NORTHCOTT (276 Germany), Marcel KOOL (276 Germany), David T.W. JONES (276 Germany), Jennifer A. CHAN (124 Canada), Ana NIKOLIC (124 Canada), Maria Luisa GARRE (380 Italy), Erwin G. Van MEIR (840 United States of America), Satoru OSUKA (840 United States of America), Jeffrey J. OLSON (840 United States of America), Arman JAHANGIRI (840 United States of America), Brandyn A. CASTRO (840 United States of America), Nalin GUPTA (840 United States of America), William A. WEISS (840 United States of America), Iska MOXON-EMRE (124 Canada), Donald J. MABBOTT (124 Canada), Alvaro LASSALETTA (124 Canada), Cynthia E. HAWKINS (124 Canada), Uri TABORI (124 Canada), James DRAKE (124 Canada), Abhaya KULKARNI (124 Canada), Peter DIRKS (124 Canada), James T. RUTKA (124 Canada), Andrey KORSHUNOV (276 Germany), Stefan M. PFISTER (276 Germany), Roger J. PACKER (840 United States of America), Vijay RAMASWAMY (124 Canada) and Michael D. TAYLOR (124 Canada)
Edition
Lancet Oncology, New York, Elsevier Science INC, 2016, 1470-2045
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 33.900
RIV identification code
RIV/00216224:14110/16:00092577
Organization unit
Faculty of Medicine
UT WoS
000373497600049
Keywords in English
POSTERIOR-FOSSA TUMORS; CHILDRENS CANCER GROUP; RISK MEDULLOBLASTOMA; RADIATION-THERAPY; ADJUVANT CHEMOTHERAPY; RANDOMIZED-TRIAL; PHASE-III; ONCOLOGY; CHILDHOOD; PATTERNS
Tags
Tags
International impact, Reviewed
Změněno: 10/1/2017 11:26, Ing. Mgr. Věra Pospíšilíková
Abstract
V originále
Background Patients with incomplete surgical resection of medulloblastoma are controversially regarded as having a marker of high-risk disease, which leads to patients undergoing aggressive surgical resections, so-called second-look surgeries, and intensified chemoradiotherapy. All previous studies assessing the clinical importance of extent of resection have not accounted for molecular subgroup. We analysed the prognostic value of extent of resection in a subgroup-specific manner. Methods We retrospectively identified patients who had a histological diagnosis of medulloblastoma and complete data about extent of resection and survival from centres participating in the Medulloblastoma Advanced Genomics International Consortium. We collected from resections done between April, 1997, and February, 2013, at 35 international institutions. We established medulloblastoma subgroup affiliation by gene expression profiling on frozen or formalin-fixed paraffin-embedded tissues. We classified extent of resection on the basis of postoperative imaging as gross total resection (no residual tumour), near-total resection (< 1.5 cm(2) tumour remaining), or sub-total resection (>= 1.5 cm(2) tumour remaining). We did multivariable analyses of overall survival and progression-free survival using the variables molecular subgroup (WNT, SHH, group 4, and group 3), age (< 3 vs >= 3 years old), metastatic status (metastases vs no metastases), geographical location of therapy (North America/Australia vs rest of the world), receipt of chemotherapy (yes vs no) and receipt of craniospinal irradiation (< 30 Gy or > 30 Gy vs no craniospinal irradiation). The primary analysis outcome was the effect of extent of resection by molecular subgroup and the effects of other clinical variables on overall and progression-free survival. Findings We included 787 patients with medulloblastoma (86 with WNT tumours, 242 with SHH tumours, 163 with group 3 tumours, and 296 with group 4 tumours) in our multivariable Cox models of progression-free and overall survival. We found that the prognostic benefit of increased extent of resection for patients with medulloblastoma is attenuated after molecular subgroup affiliation is taken into account. We identified a progression-free survival benefit for gross total resection over sub-total resection (hazard ratio [HR] 1.45, 95% CI 1.07-1.96, p=0.16) but no overall survival benefit (HR 1.23, 0.87-1.72, p=0.24). We saw no progression-free survival or overall survival benefit for gross total resection compared with near-total resection (HR 1.05, 0.71-1.53, p=0.8158 for progression-free survival and HR 1.14, 0.75-1.72, p=0.55 for overall survival). No significant survival benefit existed for greater extent of resection for patients with WNT, SHH, or group 3 tumours (HR 1.03, 0.67-1.58, p=0.89 for sub-total resection vs gross total resection). For patients with group 4 tumours, gross total resection conferred a benefit to progression-free survival compared with sub-total resection (HR 1.97, 1.22-3.17, p= 0.0056), especially for those with metastatic disease (HR 2.22, 1.00-4.93, p= 0.050). However, gross total resection had no effect on overall survival compared with sub-total resection in patients with group 4 tumours (HR 1.67, 0.93-2.99, p= 0.084). Interpretation The prognostic benefit of increased extent of resection for patients with medulloblastoma is attenuated after molecular subgroup affiliation is taken into account. Although maximum safe surgical resection should remain the standard of care, surgical removal of small residual portions of medulloblastoma is not recommended when the likelihood of neurological morbidity is high because there is no definitive benefit to gross total resection compared with near-total resection.
Links
EE2.3.20.0183, research and development project |
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