Contrast enhancement early after renal malignancy cryoablation: imaging findings associated with benignity.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 09 11 2022
accepted: 15 04 2023
revised: 16 03 2023
medline: 27 11 2023
pubmed: 5 7 2023
entrez: 5 7 2023
Statut: ppublish

Résumé

Contrast enhancement by MRI done early after cryoablation for renal malignancies may suggest residual tumor (RT). However, we have observed MRI enhancement within 48 h of cryoablation in patients who had no contrast enhancement 6 weeks later. Our purpose was to identify features of 48-h contrast enhancement in patients without RT. This single-center retrospective study included consecutive patients who underwent percutaneous cryoablation of renal malignancies in 2013-2020, exhibited cryoablation-zone MRI contrast enhancement 48 h later, and had available 6-week MRI scans. Persistent or growing CE at 6 weeks vs. 48 h was classified as RT. A washout index was calculated for each 48-h MRI, and its performance for predicting RT was assessed by receiver operating characteristic curve analysis. We included 60 patients with 72 cryoablation procedures and 83 cryoablation zones exhibiting 48-h contrast enhancement; mean age was 66 ± 17 years. Clear-cell renal cell carcinoma accounted for 95% of tumors. Of the 83 48-h enhancement zones, RT was observed in eight while 75 were benign. The 48-h enhancement was consistently visible at the arterial phase. Washout was significantly associated with RT (p < 0.001) and gradually increasing contrast enhancement with benignity (p < 0.009). A washout index below  - 1.1 predicted RT with 88% sensitivity and 84% specificity. MRI contrast enhancement 48 h after cryoablation of renal malignancies was usually benign. Washout was associated with residual tumor, with a washout index value below  - 1.1 exhibiting good performance in predicting residual tumor. These findings may help to guide decisions about repeat cryoablation. Magnetic resonance imaging contrast enhancement 48 h after cryoablation of renal malignancies rarely indicates residual tumor, which is characterized by washout with a washout index lower than  - 1.1. • Contrast enhancement at the arterial phase of magnetic resonance imaging done 48 h after cryoablation of a renal malignancy is usually benign. • Residual tumor manifesting as contrast enhancement at the arterial phase is characterized by subsequent marked washout. • A washout index below  - 1.1 has 88% sensitivity and 84% specificity for residual tumor.

Identifiants

pubmed: 37405502
doi: 10.1007/s00330-023-09814-7
pii: 10.1007/s00330-023-09814-7
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8703-8714

Informations de copyright

© 2023. The Author(s), under exclusive licence to European Society of Radiology.

Références

Pierorazio PM, Johnson MH, Patel HD et al (2016) Management of renal masses and localized renal cancer: systematic review and meta-analysis. J Urol 196(4):989–999. https://doi.org/10.1016/j.juro.2016.04.081
doi: 10.1016/j.juro.2016.04.081 pubmed: 27157369 pmcid: 5593254
Leveillee RJ, Castle SM, Gorbatiy V et al (2013) Oncologic outcomes using real-time peripheral thermometry-guided radiofrequency ablation of small renal masses. J Endourol 27(4):480–489. https://doi.org/10.1089/end.2012.0305
doi: 10.1089/end.2012.0305 pubmed: 23098088
Ramirez D, Ma YB, Bedir S, Antonelli JA, Cadeddu JA, Gahan JC (2014) Laparoscopic radiofrequency ablation of small renal tumors: long-term oncologic outcomes. J Endourol 28(3):330–334. https://doi.org/10.1089/end.2013.0542
doi: 10.1089/end.2013.0542 pubmed: 24156661
Atwell TD, Schmit GD, Boorjian SA et al (2013) Percutaneous ablation of renal masses measuring 3.0 cm and smaller: comparative local control and complications after radiofrequency ablation and cryoablation. AJR Am J Roentgenol 200(2):461–466. https://doi.org/10.2214/AJR.12.8618
El Dib R, Touma NJ, Kapoor A (2012) Cryoablation vs radiofrequency ablation for the treatment of renal cell carcinoma: a meta-analysis of case series studies: CRYOABLATION VS RADIOFREQUENCY ABLATION IN RCC. BJU Int 110(4):510–516. https://doi.org/10.1111/j.1464-410X.2011.10885.x
doi: 10.1111/j.1464-410X.2011.10885.x pubmed: 22304329
Campbell SC, Clark PE, Chang SS, Karam JA, Souter L, Uzzo RG (2021) Renal mass and localized renal cancer: evaluation, management, and follow-up: AUA Guideline: Part I. J Urol 206(2):199–208. https://doi.org/10.1097/JU.0000000000001911
doi: 10.1097/JU.0000000000001911 pubmed: 34115547
Bhagavatula SK, Tuncali K, Shyn PB, Levesque VM, Chang SL, Silverman SG (2020) Percutaneous CT- and MRI-guided cryoablation of cT1 renal cell carcinoma: intermediate- to long-term outcomes in 307 patients. Radiology 296(3):687–695. https://doi.org/10.1148/radiol.2020200149
doi: 10.1148/radiol.2020200149 pubmed: 32633677
Correas JM, Delavaud C, Gregory J et al (2017) Ablative therapies for renal tumors: patient selection, treatment planning, and follow-up. Semin Ultrasound CT MRI 38(1):78–95. https://doi.org/10.1053/j.sult.2016.11.009
doi: 10.1053/j.sult.2016.11.009
Stewart SB, Thompson RH, Psutka SP et al (2014) Evaluation of the National Comprehensive Cancer Network and American Urological Association Renal Cell Carcinoma Surveillance Guidelines. J Clin Oncol 32(36):4059–4065. https://doi.org/10.1200/JCO.2014.56.5416
doi: 10.1200/JCO.2014.56.5416 pubmed: 25403213 pmcid: 4265116
Wood EL, Adibi M, Qiao W et al (2018) Local tumor bed recurrence following partial nephrectomy in patients with small renal masses. J Urol 199(2):393–400. https://doi.org/10.1016/j.juro.2017.09.072
doi: 10.1016/j.juro.2017.09.072 pubmed: 28941919
Cheong BYC, Wilson JM, Preventza OA, Muthupillai R (2022) Gadolinium-based contrast agents: updates and answers to typical questions regarding gadolinium use. Tex Heart Inst J 49(3):e217680. https://doi.org/10.14503/THIJ-21-7680
Brenner DJ, Hall EJ (2007) Computed tomography — an increasing source of radiation exposure. N Engl J Med 357(22):2277–2284. https://doi.org/10.1056/NEJMra072149
doi: 10.1056/NEJMra072149 pubmed: 18046031
Breen DJ, Rutherford EE, Stedman B et al (2007) Management of renal tumors by image-guided radiofrequency ablation: experience in 105 tumors. Cardiovasc Intervent Radiol 30(5):936–942. https://doi.org/10.1007/s00270-007-9090-x
doi: 10.1007/s00270-007-9090-x pubmed: 17573550 pmcid: 2700242
Gervais DA, Arellano RS, McGovern FJ, McDougal WS, Mueller PR (2005) Radiofrequency ablation of renal cell carcinoma: part 2, lessons learned with ablation of 100 tumors. AJR Am J Roentgenol 185(1):72–80. https://doi.org/10.2214/ajr.185.1.01850072
doi: 10.2214/ajr.185.1.01850072 pubmed: 15972401
Porter CA, Woodrum DA, Callstrom MR et al (2010) MRI after technically successful renal cryoablation: early contrast enhancement as a common finding. AJR Am J Roentgenol 194(3):790–793. https://doi.org/10.2214/AJR.09.2518
doi: 10.2214/AJR.09.2518 pubmed: 20173161
Kawamoto S, Permpongkosol S, Bluemke DA, Fishman EK, Solomon SB (2007) Sequential changes after radiofrequency ablation and cryoablation of renal neoplasms: role of CT and MR imaging. Radiographics 27(2):343–355. https://doi.org/10.1148/rg.272065119
doi: 10.1148/rg.272065119 pubmed: 17374857
Bodmer D (2002) Understanding familial and non-familial renal cell cancer. Hum Mol Genet 11(20):2489–2498. https://doi.org/10.1093/hmg/11.20.2489
doi: 10.1093/hmg/11.20.2489 pubmed: 12351585
Georgiades CS, Rodriguez R (2014) Efficacy and safety of percutaneous cryoablation for stage 1A/B renal cell carcinoma: results of a prospective, single-arm, 5-year study. Cardiovasc Intervent Radiol 37(6):1494–1499. https://doi.org/10.1007/s00270-013-0831-8
doi: 10.1007/s00270-013-0831-8 pubmed: 24385225
Ho VB, Allen SF, Hood MN, Choyke PL (2002) Renal masses: quantitative assessment of enhancement with dynamic MR imaging. Radiology 224(3):695–700. https://doi.org/10.1148/radiol.2243011048
doi: 10.1148/radiol.2243011048 pubmed: 12202701
Al Salmi IS, Halperin J, Al-Douri F, Leung V, Patlas M, Alabousi A (2019) Validation of region of interest measurements for the objective assessment of post-contrast enhancement of renal lesions on MRI. Br J Radiol 92(1103):20190507. https://doi.org/10.1259/bjr.20190507
doi: 10.1259/bjr.20190507 pubmed: 31365281 pmcid: 6849669
Hecht EM, Israel GM, Krinsky GA et al (2004) Renal masses: quantitative analysis of enhancement with signal intensity measurements versus qualitative analysis of enhancement with image subtraction for diagnosing malignancy at MR imaging. Radiology 232(2):373–378. https://doi.org/10.1148/radiol.2322031209
doi: 10.1148/radiol.2322031209 pubmed: 15215544
Cornelis F, Tricaud E, Lasserre AS et al (2014) Routinely performed multiparametric magnetic resonance imaging helps to differentiate common subtypes of renal tumours. Eur Radiol 24(5):1068–1080. https://doi.org/10.1007/s00330-014-3107-z
doi: 10.1007/s00330-014-3107-z pubmed: 24557052
Ganguli S, Brennan DD, Faintuch S, Rayan ME, Goldberg SN (2008) Immediate renal tumor involution after radiofrequency thermal ablation. J Vasc Interv Radiol 19(3):412–418. https://doi.org/10.1016/j.jvir.2007.10.024
doi: 10.1016/j.jvir.2007.10.024 pubmed: 18295702
Fraisse G, Colleter L, Peyronnet B et al (2019) Peri-operative and local control outcomes of robot-assisted partial nephrectomy vs percutaneous cryoablation for renal masses: comparison after matching on radiological stage and renal score. BJU Int 123(4):632–638. https://doi.org/10.1111/bju.14530
doi: 10.1111/bju.14530 pubmed: 30153399
Yamanaka T, Yamakado K, Yamada T et al (2015) CT-guided percutaneous cryoablation in renal cell carcinoma: factors affecting local tumor control. J Vasc Interv Radiol 26(8):1147–1153. https://doi.org/10.1016/j.jvir.2015.04.031
doi: 10.1016/j.jvir.2015.04.031 pubmed: 26123809
Ge BH, Guzzo TJ, Nadolski GJ et al (2016) Percutaneous renal cryoablation: short-axis ice-ball margin as a predictor of outcome. J Vasc Interv Radiol 27(3):403–409. https://doi.org/10.1016/j.jvir.2015.11.035
doi: 10.1016/j.jvir.2015.11.035 pubmed: 26755344
Canter D, Kutikov A, Manley B et al (2011) Utility of the R.E.N.A.L. Nephrometry scoring system in objectifying treatment decision-making of the enhancing renal mass. Urology 78(5):1089–1094. https://doi.org/10.1016/j.urology.2011.04.035
Kunkle DA, Uzzo RG (2008) Cryoablation or radiofrequency ablation of the small renal mass: a meta-analysis. Cancer 113(10):2671–2680. https://doi.org/10.1002/cncr.23896
doi: 10.1002/cncr.23896 pubmed: 18816624
Zargar H, Atwell TD, Cadeddu JA et al (2016) Cryoablation for small renal masses: selection criteria, complications, and functional and oncologic results. Eur Urol 69(1):116–128. https://doi.org/10.1016/j.eururo.2015.03.027
doi: 10.1016/j.eururo.2015.03.027 pubmed: 25819723
Zondervan PJ, Buijs M, De Bruin DM, van Delden OM, Van Lienden KP (2019) Available ablation energies to treat cT1 renal cell cancer: emerging technologies. World J Urol 37(3):445–455. https://doi.org/10.1007/s00345-018-2546-6
doi: 10.1007/s00345-018-2546-6 pubmed: 30448873
Beksac AT, Rivera-Sanfeliz G, Dufour CA et al (2017) Impact of tumor histology and grade on treatment success of percutaneous renal cryoablation. World J Urol 35(4):633–640. https://doi.org/10.1007/s00345-016-1911-6
doi: 10.1007/s00345-016-1911-6 pubmed: 27484204
Kim EH, Tanagho YS, Bhayani SB, Saad NE, Benway BM, Figenshau RS (2013) Percutaneous cryoablation of renal masses: Washington University experience of treating 129 tumours: Percutaneous cryoablation of renal masses. BJU Int 111(6):872–879. https://doi.org/10.1111/j.1464-410X.2012.11432.x
doi: 10.1111/j.1464-410X.2012.11432.x pubmed: 23145500
Lee HJ, Chung HJ, Wang HK et al (2016) Evolutionary magnetic resonance appearance of renal cell carcinoma after percutaneous cryoablation. Br J Radiol 89(1065):20160151. https://doi.org/10.1259/bjr.20160151
doi: 10.1259/bjr.20160151 pubmed: 27401340 pmcid: 5124922

Auteurs

Téodor Grand (T)

AP-HP, Hôpital Necker Enfants Malades, Service d'Imagerie Adulte, F-75015, Paris, France. teodor.grand@aphp.fr.
Adult Radiology Department, Necker University Hospital, 149 Rue de Sèvres, 75015, Paris, France. teodor.grand@aphp.fr.

Christophe Delavaud (C)

AP-HP, Hôpital Necker Enfants Malades, Service d'Imagerie Adulte, F-75015, Paris, France.

Charles Dariane (C)

AP-HP, Hôpital Européen Georges Pompidou, Service d'urologie, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.

Toulsie Ramtohul (T)

Institut Curie, Service de Radiologie, PSL Research University, F-75005, Paris, France.

Sylvain Guinebert (S)

AP-HP, Hôpital Necker Enfants Malades, Service d'Imagerie Adulte, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.

Olivier Hélénon (O)

AP-HP, Hôpital Necker Enfants Malades, Service d'Imagerie Adulte, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.

Arnaud Mejean (A)

AP-HP, Hôpital Européen Georges Pompidou, Service d'urologie, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.

Marc-Olivier Timsit (MO)

AP-HP, Hôpital Européen Georges Pompidou, Service d'urologie, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.

Jean-Michel Correas (JM)

AP-HP, Hôpital Necker Enfants Malades, Service d'Imagerie Adulte, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.
Sorbonne Université, CNRS, INSERM Laboratoire d'Imagerie Biomédicale, Paris, France.

Sylvain Bodard (S)

AP-HP, Hôpital Necker Enfants Malades, Service d'Imagerie Adulte, F-75015, Paris, France.
Université de Paris Cité, F-75006, Paris, France.
Sorbonne Université, CNRS, INSERM Laboratoire d'Imagerie Biomédicale, Paris, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH