Show simple item record

Volumetric 18F‐FDG‐PET parameters as predictors of locoregional failure in low‐risk HPV‐related oropharyngeal cancer after definitive chemoradiation therapy

dc.contributor.authorChotchutipan, Thong
dc.contributor.authorRosen, Benjamin S.
dc.contributor.authorHawkins, Peter G.
dc.contributor.authorLee, Jae Y.
dc.contributor.authorSaripalli, Anjali L.
dc.contributor.authorThakkar, Dharmesh
dc.contributor.authorEisbruch, Avraham
dc.contributor.authorEl Naqa, Issam
dc.contributor.authorMierzwa, Michelle L.
dc.date.accessioned2019-02-12T20:23:44Z
dc.date.available2020-04-01T15:06:24Zen
dc.date.issued2019-02
dc.identifier.citationChotchutipan, Thong; Rosen, Benjamin S.; Hawkins, Peter G.; Lee, Jae Y.; Saripalli, Anjali L.; Thakkar, Dharmesh; Eisbruch, Avraham; El Naqa, Issam; Mierzwa, Michelle L. (2019). "Volumetric 18F‐FDG‐PET parameters as predictors of locoregional failure in low‐risk HPV‐related oropharyngeal cancer after definitive chemoradiation therapy." Head & Neck 41(2): 366-373.
dc.identifier.issn1043-3074
dc.identifier.issn1097-0347
dc.identifier.urihttps://hdl.handle.net/2027.42/147800
dc.description.abstractBackgroundWe sought to investigate the prognostic value of volumetric positron emission tomography (PET) parameters in patients with human papillomavirus (HPV)‐related oropharyngeal squamous cell carcinoma (OPSCC) and a ≤10 pack‐year smoking history treated with chemoradiation.MethodsA total of 142 patients were included. Maximum standardized uptake value, metabolic tumor volume, and total lesion glycolysis (TLG) of the primary tumor, involved regional lymph nodes, and total lesion were calculated. Cox proportional hazard modeling was used to evaluate associations of clinical and PET parameters with locoregional failure‐free survival (LRFFS), distant metastasis‐free survival (DMFS), and overall survival (OS).ResultsOn univariate analysis, volumetric PET parameters were significantly associated with all endpoints, and 8th edition American Joint Committee on Cancer/Union Internationale Contre le Cancer staging was significantly associated with DMFS and OS. On multivariate analysis, total lesion TLG was significantly associated with LRFFS, while staging was most significantly prognostic for DMFS and OS.ConclusionVolumetric PET parameters are uniquely prognostic of LRFFS in low‐risk HPV‐related OPSCC and may be useful for directing de‐intensification strategies.
dc.publisherJohn Wiley & Sons, Inc.
dc.subject.otherOPSCC
dc.subject.otherTNM staging
dc.subject.otherFDG‐PET
dc.subject.otherlocal control
dc.subject.otherradiation oncology
dc.titleVolumetric 18F‐FDG‐PET parameters as predictors of locoregional failure in low‐risk HPV‐related oropharyngeal cancer after definitive chemoradiation therapy
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelOtolaryngology
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/147800/1/hed25505_am.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/147800/2/hed25505.pdf
dc.identifier.doi10.1002/hed.25505
dc.identifier.sourceHead & Neck
dc.identifier.citedreferenceMoeller BJ, Rana V, Cannon BA, et al. Prospective risk‐adjusted [18F]Fluorodeoxyglucose positron emission tomography and computed tomography assessment of radiation response in head and neck cancer. J Clin Oncol. 2009; 27 ( 15 ): 2509 ‐ 2515.
dc.identifier.citedreferenceStock GT, Bonadio R, de Castro GJ. De‐escalation treatment of human papillomavirus‐positive oropharyngeal squamous cell carcinoma: an evidence‐based review for the locally advanced disease. Curr Opin Oncol. 2018; 30: 146 ‐ 151.
dc.identifier.citedreferenceMasterson L, Moualed D, Liu ZW, et al. De‐escalation treatment protocols for human papillomavirus‐associated oropharyngeal squamous cell carcinoma: a systematic review and meta‐analysis of current clinical trials. Eur J Cancer. 2014; 50 ( 15 ): 2636 ‐ 2648.
dc.identifier.citedreferenceChera BS, Amdur RJ, Tepper J, et al. Phase 2 trial of de‐intensified chemoradiation therapy for favorable‐risk human papillomavirus‐associated oropharyngeal squamous cell carcinoma. Int J Radiat Oncol Biol Phys. 2015; 93 ( 5 ): 976 ‐ 985.
dc.identifier.citedreferenceChera BS, Amdur RJ, Tepper JE, et al. Mature results of a prospective study of deintensified chemoradiotherapy for low‐risk human papillomavirus‐associated oropharyngeal squamous cell carcinoma. Cancer. 2018; 124 ( 11 ): 2347 ‐ 2354.
dc.identifier.citedreferenceMarur S, Li S, Cmelak AJ, et al. E1308: phase II trial of induction chemotherapy followed by reduced‐dose radiation and weekly Cetuximab in patients with HPV‐associated resectable squamous cell carcinoma of the oropharynx‐ ECOG‐ACRIN Cancer Research Group. J Clin Oncol. 2017; 35 ( 5 ): 490 ‐ 497.
dc.identifier.citedreferenceChen AM, Felix C, Wang PC, et al. Reduced‐dose radiotherapy for human papillomavirus‐associated squamous‐cell carcinoma of the oropharynx: a single‐arm, phase 2 study. Lancet Oncol. 2017; 18 ( 6 ): 803 ‐ 811.
dc.identifier.citedreferenceAmin M, Edge S, Greene F, et al. AJCC Cancer Staging Manual. 8th ed. New York, NY: Springer; 2017.
dc.identifier.citedreferenceO’Sullivan B, Huang SH, Su J, et al. Development and validation of a staging system for HPV‐related oropharyngeal cancer by the International Collaboration on Oropharyngeal cancer Network for Staging (ICON‐S): a multicentre cohort study. Lancet Oncol. 2016; 17 ( 4 ): 440 ‐ 451.
dc.identifier.citedreferenceHuang SH, Xu W, Waldron J, et al. Refining American Joint Committee on Cancer/Union for International Cancer Control TNM stage and prognostic groups for human papillomavirus‐related oropharyngeal carcinomas. J Clin Oncol. 2015; 33 ( 8 ): 836 ‐ 845.
dc.identifier.citedreferenceTrosman SJ, Koyfman SA, Ward MC, et al. Effect of human papillomavirus on patterns of distant metastatic failure in oropharyngeal squamous cell carcinoma treated with chemoradiotherapy. JAMA Otolaryngol Head Neck Surg. 2015; 141 ( 5 ): 457 ‐ 462.
dc.identifier.citedreferenceO’Sullivan B, Huang SH, Perez‐Ordonez B, et al. Outcomes of HPV‐related oropharyngeal cancer patients treated by radiotherapy alone using altered fractionation. Radiother Oncol. 2012; 103 ( 1 ): 49 ‐ 56.
dc.identifier.citedreferenceCacicedo J, Navarro A, Del Hoyo O, et al. Role of fluorine‐18 fluorodeoxyglucose PET/CT in head and neck oncology: the point of view of the radiation oncologist. Br J Radiol. 2016; 89 ( 1067 ): 20160217.
dc.identifier.citedreferenceLa TH, Filion EJ, Turnbull BB, et al. Metabolic tumor volume predicts for recurrence and death in head‐and‐neck cancer. Int J Radiat Oncol Biol Phys. 2009; 74 ( 5 ): 1335 ‐ 1341.
dc.identifier.citedreferenceTang C, Murphy JD, Khong B, et al. Validation that metabolic tumor volume predicts outcome in head‐and‐neck cancer. Int J Radiat Oncol Biol Phys. 2012; 83 ( 5 ): 1514 ‐ 1520.
dc.identifier.citedreferenceMena E, Taghipour M, Sheikhbahaei S, et al. Value of intratumoral metabolic heterogeneity and quantitative 18F‐FDG PET/CT parameters to predict prognosis in patients with HPV‐positive primary oropharyngeal squamous cell carcinoma. Clin Nucl Med. 2017; 42 ( 5 ): e227 ‐ e234.
dc.identifier.citedreferenceLim R, Eaton A, Lee NY, et al. 18F‐FDG PET/CT metabolic tumor volume and total lesion glycolysis predict outcome in oropharyngeal squamous cell carcinoma. J Nucl Med. 2012; 53 ( 10 ): 1506 ‐ 1513.
dc.identifier.citedreferenceRomesser PB, Lim R, Spratt DE, et al. The relative prognostic utility of standardized uptake value, gross tumor volume, and metabolic tumor volume in oropharyngeal cancer patients treated with platinum based concurrent chemoradiation with a pre‐treatment [(18)F] fluorodeoxyglucose positron emission tomography scan. Oral Oncol. 2014; 50 ( 9 ): 802 ‐ 808.
dc.identifier.citedreferenceKim JW, Oh JS, Roh JL, et al. Prognostic significance of standardized uptake value and metabolic tumour volume on (1)(8)F‐FDG PET/CT in oropharyngeal squamous cell carcinoma. Eur J Nucl Med Mol Imaging. 2015; 42 ( 9 ): 1353 ‐ 1361.
dc.identifier.citedreferencePak K, Cheon GJ, Nam HY, et al. Prognostic value of metabolic tumor volume and total lesion glycolysis in head and neck cancer: a systematic review and meta‐analysis. J Nucl Med. 2014; 55 ( 6 ): 884 ‐ 890.
dc.identifier.citedreferenceAlluri KC, Tahari AK, Wahl RL, Koch W, Chung CH, Subramaniam RM. Prognostic value of FDG PET metabolic tumor volume in human papillomavirus‐positive stage III and IV oropharyngeal squamous cell carcinoma. AJR Am J Roentgenol. 2014; 203 ( 4 ): 897 ‐ 903.
dc.identifier.citedreferenceMoon SH, Choi JY, Lee HJ, et al. Prognostic value of 18F‐FDG PET/CT in patients with squamous cell carcinoma of the tonsil: comparisons of volume‐based metabolic parameters. Head Neck. 2013; 35 ( 1 ): 15 ‐ 22.
dc.identifier.citedreferenceKikuchi M, Koyasu S, Shinohara S, et al. Prognostic value of pretreatment 18F‐fluorodeoxyglucose positron emission tomography/CT volume‐based parameters in patients with oropharyngeal squamous cell carcinoma with known p16 and p53 status. Head Neck. 2015; 37 ( 10 ): 1524 ‐ 1531.
dc.identifier.citedreferenceCheng NM, Chang JT, Huang CG, et al. Prognostic value of pretreatment (1)(8)F‐FDG PET/CT and human papillomavirus type 16 testing in locally advanced oropharyngeal squamous cell carcinoma. Eur J Nucl Med Mol Imaging. 2012; 39 ( 11 ): 1673 ‐ 1684.
dc.identifier.citedreferencePollom EL, Song J, Durkee BY, et al. Prognostic value of midtreatment FDG‐PET in oropharyngeal cancer. Head Neck. 2016; 38 ( 10 ): 1472 ‐ 1478.
dc.identifier.citedreferenceSchwartz DL, Harris J, Yao M, et al. Metabolic tumor volume as a prognostic imaging‐based biomarker for head‐and‐neck cancer: pilot results from Radiation Therapy Oncology Group protocol 0522. Int J Radiat Oncol Biol Phys. 2015; 91 ( 4 ): 721 ‐ 729.
dc.identifier.citedreferenceVainshtein JM, Spector ME, Ibrahim M, et al. Matted nodes: high distant‐metastasis risk and a potential indication for intensification of systemic therapy in human papillomavirus‐related oropharyngeal cancer. Head Neck. 2016; 38 ( Suppl 1 ): E805 ‐ E814.
dc.identifier.citedreferenceHarrell FE Jr, Califf RM, Pryor DB, Lee KL, Rosati RA. Evaluating the yield of medical tests. JAMA. 1982; 247 ( 18 ): 2543 ‐ 2546.
dc.identifier.citedreferenceDahlstrom KR, Calzada G, Hanby JD, et al. An evolution in demographics, treatment, and outcomes of oropharyngeal cancer at a major cancer center: a staging system in need of repair. Cancer. 2013; 119 ( 1 ): 81 ‐ 89.
dc.identifier.citedreferenceAng KK, Harris J, Wheeler R, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med. 2010; 363 ( 1 ): 24 ‐ 35.
dc.identifier.citedreferenceRamaekers BL, Joore MA, Grutters JP, et al. The impact of late treatment‐toxicity on generic health‐related quality of life in head and neck cancer patients after radiotherapy. Oral Oncol. 2011; 47 ( 8 ): 768 ‐ 774.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.