Molecular profiling identifies targeted therapy opportunities in pediatric solid cancer

被引:31
|
作者
Church, Alanna J. [1 ,2 ]
Corson, Laura B. [3 ,4 ,31 ]
Kao, Pei-Chi [1 ]
Imamovic-Tuco, Alma [3 ,4 ]
Reidy, Deirdre [3 ,32 ]
Doan, Duong [3 ,33 ]
Kang, Wenjun [5 ]
Pinto, Navin [6 ,7 ]
Maese, Luke [8 ,9 ]
Laetsch, Theodore W. [10 ,11 ,12 ]
Kim, AeRang [13 ,14 ]
Colace, Susan I. [15 ,16 ]
Macy, Margaret E. [17 ,18 ]
Applebaum, Mark A. [5 ,19 ]
Bagatell, Rochelle [11 ,12 ]
Sabnis, Amit J. [20 ]
Weiser, Daniel A. [21 ,22 ]
Glade-Bender, Julia L. [2 ,23 ,24 ]
Homans, Alan C. [25 ,26 ]
Hipps, John [27 ,28 ]
Harris, Haley [1 ]
Manning, Danielle [29 ]
Al-Ibraheemi, Alyaa [1 ,2 ]
Li, Yvonne [2 ,3 ,4 ]
Gupta, Hersh [2 ,3 ,4 ]
Cherniack, Andrew D. [2 ,3 ,4 ]
Lo, Ying-Chun [1 ,29 ,34 ]
Strand, Gianna R. [3 ,35 ]
Lee, Lobin A. [3 ,36 ]
Pinches, R. Seth [1 ,37 ]
Lazo De La Vega, Lorena [3 ]
Harden, Maegan V. [4 ]
Lennon, Niall J. [4 ]
Choi, Seong [5 ]
Comeau, Hannah [3 ]
Harris, Marian H. [1 ,2 ]
Forrest, Suzanne J. [2 ,3 ]
Clinton, Catherine M. [1 ,3 ]
Crompton, Brian D. [2 ,3 ]
Kamihara, Junne [2 ,3 ]
MacConaill, Laura E. [2 ,29 ]
Volchenboum, Samuel L. [5 ]
Lindeman, Neal I. [2 ,29 ]
Van Allen, Eliezer [2 ,4 ,30 ]
DuBois, Steven G. [2 ,3 ]
London, Wendy B. [1 ,2 ]
Janeway, Katherine A. [2 ,3 ]
机构
[1] Boston Childrens Hosp, Boston, MA USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Dana Farber Boston Childrens Canc & Blood Disorde, Boston, MA USA
[4] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[5] Univ Chicago, Chicago, IL 60637 USA
[6] Seattle Childrens Hosp, Seattle, WA USA
[7] Univ Washington, Seattle, WA 98195 USA
[8] Primary Childrens Med Ctr, Salt Lake City, UT USA
[9] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[10] Univ Texas Southwestern Med Ctr, Dallas, TX USA
[11] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[12] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[13] Childrens Natl Hosp, Washington, DC USA
[14] George Washington Univ, Sch Med & Hlth Sci, Washington, DC 20052 USA
[15] Nationwide Childrens Hosp, Columbus, OH USA
[16] Ohio State Univ, Coll Med, Columbus, OH 43210 USA
[17] Childrens Hosp Colorado, Aurora, CO USA
[18] Univ Colorado, Sch Med, Aurora, CO USA
[19] Comer Childrens Hosp, Chicago, IL USA
[20] Univ Calif San Francisco, Benioff Childrens Hosp, San Francisco, CA 94143 USA
[21] Childrens Hosp Montefiore, New York, NY USA
[22] Albert Einstein Coll Med, New York, NY USA
[23] Columbia Univ, Irving Med Ctr, New York, NY USA
[24] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[25] Univ Vermont, Med Ctr, Burlington, VT USA
[26] Univ Vermont, Burlington, VT USA
[27] Univ N Carolina, Med Ctr, Chapel Hill, NC 27515 USA
[28] Univ N Carolina, Chapel Hill Sch Med, Chapel Hill, NC 27515 USA
[29] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[30] Dana Farber Canc Inst, Boston, MA 02115 USA
[31] Sema4, Stamford, CT USA
[32] Univ Connecticut, Sch Med, Farmington, CT USA
[33] Univ Massachusetts, Sch Med, Worcester, MA USA
[34] Mayo Clin, Rochester, MN USA
[35] Loyola Univ, Chicago, IL 60611 USA
[36] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[37] Philadelphia Coll Osteopath Med, Philadelphia, PA USA
关键词
MISMATCH REPAIR DEFICIENCY; TUMORS; ASSOCIATION; COMBINATION; INHIBITORS; GUIDELINE; MUTATIONS; VARIANTS; FUSION;
D O I
10.1038/s41591-022-01856-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An interim report from the GAIN/iCat2 study shows that molecular profiling of pediatric solid malignancies clarifies diagnostic classifications and provides opportunities for matched targeted therapy. To evaluate the clinical impact of molecular tumor profiling (MTP) with targeted sequencing panel tests, pediatric patients with extracranial solid tumors were enrolled in a prospective observational cohort study at 12 institutions. In the 345-patient analytical population, median age at diagnosis was 12 years (range 0-27.5); 298 patients (86%) had 1 or more alterations with potential for impact on care. Genomic alterations with diagnostic, prognostic or therapeutic significance were present in 61, 16 and 65% of patients, respectively. After return of the results, impact on care included 17 patients with a clarified diagnostic classification and 240 patients with an MTP result that could be used to select molecularly targeted therapy matched to identified alterations (MTT). Of the 29 patients who received MTT, 24% had an objective response or experienced durable clinical benefit; all but 1 of these patients received targeted therapy matched to a gene fusion. Of the diagnostic variants identified in 209 patients, 77% were gene fusions. MTP with targeted panel tests that includes fusion detection has a substantial clinical impact for young patients with solid tumors.
引用
收藏
页码:1581 / +
页数:24
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