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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1986 1
1987 5
1988 18
1989 31
1990 13
1991 15
1992 14
1993 21
1994 15
1995 26
1996 19
1997 19
1998 20
1999 20
2000 29
2001 22
2002 34
2003 27
2004 37
2005 29
2006 27
2007 32
2008 26
2009 28
2010 27
2011 39
2012 36
2013 52
2014 77
2015 79
2016 85
2017 88
2018 110
2019 113
2020 118
2021 140
2022 121
2023 125
2024 120
2025 17

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1,684 results

Results by year

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Page 1
Dedifferentiated liposarcoma.
Nascimento AG. Nascimento AG. Semin Diagn Pathol. 2001 Nov;18(4):263-6. Semin Diagn Pathol. 2001. PMID: 11757866 Review.
Dedifferentiated liposarcoma is a high-grade nonlipogenic sarcoma that arises in a background of a preexisting well-differentiated liposarcoma. The phenomenon of dedifferentiation is time dependent, and primary or de novo tumors exceed secondary neoplasms in a ratio of 9:1 …
Dedifferentiated liposarcoma is a high-grade nonlipogenic sarcoma that arises in a background of a preexisting well-differentiated li …
Clinical genomic profiling in the management of patients with soft tissue and bone sarcoma.
Gounder MM, Agaram NP, Trabucco SE, Robinson V, Ferraro RA, Millis SZ, Krishnan A, Lee J, Attia S, Abida W, Drilon A, Chi P, Angelo SP, Dickson MA, Keohan ML, Kelly CM, Agulnik M, Chawla SP, Choy E, Chugh R, Meyer CF, Myer PA, Moore JL, Okimoto RA, Pollock RE, Ravi V, Singh AS, Somaiah N, Wagner AJ, Healey JH, Frampton GM, Venstrom JM, Ross JS, Ladanyi M, Singer S, Brennan MF, Schwartz GK, Lazar AJ, Thomas DM, Maki RG, Tap WD, Ali SM, Jin DX. Gounder MM, et al. Nat Commun. 2022 Jun 15;13(1):3406. doi: 10.1038/s41467-022-30496-0. Nat Commun. 2022. PMID: 35705558 Free PMC article.
There are more than 70 distinct sarcomas, and this diversity complicates the development of precision-based therapeutics for these cancers. Prospective comprehensive genomic profiling could overcome this challenge by providing insight into sarcomas' molecular driver …
There are more than 70 distinct sarcomas, and this diversity complicates the development of precision-based therapeutics for these ca …
Sarcoma chemotherapy.
Walczak BE, Irwin RB. Walczak BE, et al. J Am Acad Orthop Surg. 2013 Aug;21(8):480-91. doi: 10.5435/JAAOS-21-08-480. J Am Acad Orthop Surg. 2013. PMID: 23908254 Review.
Sarcomas are a rare, heterogeneous group of malignant tumors of the bone or soft tissue. ...
Sarcomas are a rare, heterogeneous group of malignant tumors of the bone or soft tissue. ...
Neoplastic Pericardial Disease.
Maleszewski JJ, Anavekar NS. Maleszewski JJ, et al. Cardiol Clin. 2017 Nov;35(4):589-600. doi: 10.1016/j.ccl.2017.07.011. Epub 2017 Sep 6. Cardiol Clin. 2017. PMID: 29025549 Review.
Ewing sarcoma.
Eaton BR, Claude L, Indelicato DJ, Vatner R, Yeh B, Schwarz R, Laack N. Eaton BR, et al. Pediatr Blood Cancer. 2021 May;68 Suppl 2:e28355. doi: 10.1002/pbc.28355. Pediatr Blood Cancer. 2021. PMID: 33818887 Review.
Ewing sarcoma is a rare tumor that requires complex multidisciplinary management. This report describes the general management and standard radiotherapy guidelines in both North America (Children's Oncology Group) and Europe (International Society of Pediatric Oncology). . …
Ewing sarcoma is a rare tumor that requires complex multidisciplinary management. This report describes the general management and st …
Pseudoendocrine Sarcoma.
Torres-Mora J, Trejo-Lopez J, Erickson LA. Torres-Mora J, et al. Mayo Clin Proc. 2024 Oct;99(10):1676-1677. doi: 10.1016/j.mayocp.2024.08.004. Mayo Clin Proc. 2024. PMID: 39362706 No abstract available.
Pembrolizumab in advanced soft-tissue sarcoma and bone sarcoma (SARC028): a multicentre, two-cohort, single-arm, open-label, phase 2 trial.
Tawbi HA, Burgess M, Bolejack V, Van Tine BA, Schuetze SM, Hu J, D'Angelo S, Attia S, Riedel RF, Priebat DA, Movva S, Davis LE, Okuno SH, Reed DR, Crowley J, Butterfield LH, Salazar R, Rodriguez-Canales J, Lazar AJ, Wistuba II, Baker LH, Maki RG, Reinke D, Patel S. Tawbi HA, et al. Lancet Oncol. 2017 Nov;18(11):1493-1501. doi: 10.1016/S1470-2045(17)30624-1. Epub 2017 Oct 4. Lancet Oncol. 2017. PMID: 28988646 Free PMC article. Clinical Trial.
We assessed pembrolizumab, an anti-PD-1 antibody, for safety and activity in patients with advanced soft-tissue sarcoma or bone sarcoma. METHODS: In this two-cohort, single-arm, open-label, phase 2 study, we enrolled patients with soft-tissue sarcoma or bone …
We assessed pembrolizumab, an anti-PD-1 antibody, for safety and activity in patients with advanced soft-tissue sarcoma or bone sa …
Postoperative Imaging of Sarcomas.
Tavare AN, Robinson P, Altoos R, LiMarzi GM, Scherer KF, Kransdorf MJ, Bancroft LW. Tavare AN, et al. AJR Am J Roentgenol. 2018 Sep;211(3):506-518. doi: 10.2214/AJR.18.19954. Epub 2018 Jun 21. AJR Am J Roentgenol. 2018. PMID: 29927329 Review.
OBJECTIVE: The purpose of this article is to assist radiologists in developing an organized, systematic approach to imaging interpretation in the care of patients who have been surgically treated for sarcoma. CONCLUSION: Postoperative imaging interpretation of sarcoma …
OBJECTIVE: The purpose of this article is to assist radiologists in developing an organized, systematic approach to imaging interpretation i …
Myxoid Liposarcoma: How to Stage and Follow.
Ho TP. Ho TP. Curr Treat Options Oncol. 2023 Apr;24(4):292-299. doi: 10.1007/s11864-023-01064-5. Epub 2023 Mar 3. Curr Treat Options Oncol. 2023. PMID: 36867390 Review.
Myxoid liposarcoma (MLPS) is a rare soft tissue sarcoma, with propensity to metastasize to locations such as soft tissue and bone. Thus, whole-body MRI should be a consideration as part of staging for patients with a new diagnosis of MLPS since PET and CT may not identify …
Myxoid liposarcoma (MLPS) is a rare soft tissue sarcoma, with propensity to metastasize to locations such as soft tissue and bone. Th …
Multiply recurrent retroperitoneal liposarcoma.
Bagaria SP, Gabriel E, Mann GN. Bagaria SP, et al. J Surg Oncol. 2018 Jan;117(1):62-68. doi: 10.1002/jso.24929. Epub 2017 Dec 19. J Surg Oncol. 2018. PMID: 29266232 Review.
Retroperitoneal liposarcomas (RPLPS) are rare tumors that represent at least 50% of all retroperitoneal sarcomas. Surgical resection remains the standard of care. Unfortunately, many RPLPS patients will develop a local recurrence and subsequently die in the absence of dist …
Retroperitoneal liposarcomas (RPLPS) are rare tumors that represent at least 50% of all retroperitoneal sarcomas. Surgical resection …
1,684 results