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Erschienen in: Die Onkologie 5/2021

01.03.2021 | Solide Tumoren | Leitthema

Fortschrittliche radiologische Diagnostik bei soliden Tumoren im Kindes- und Jugendalter

Staging, Risikostratifizierung und Responsebeurteilung

verfasst von: Prof. Dr. Jürgen Frank Schäfer, Jochen Herrmann, Birgit Kammer, Friederike Koerber, Ilias Tsiflikas, Thekla von Kalle, Hans-Joachim Mentzel

Erschienen in: Die Onkologie | Ausgabe 5/2021

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Zusammenfassung

Hintergrund

Das Spektrum solider Tumore bei Kindern und Jugendlichen unterscheidet sich ebenso wie bestimmte Therapieformen (z. B. Knochenmarktransplantationen) von denen des Erwachsenen. Darüber hinaus werden fast alle Patienten in Studien nationaler und internationaler onkologischer Gesellschaften eingeschlossen und in kinderonkologischen Zentren behandelt. Die pädiatrische Radiologie übernimmt hierbei essenzielle Aufgaben, insbesondere bei der therapeutischen Risikostratifizierung und der Therapiekontrolle.

Material und Methoden

Auf der Basis selektiver Literaturrecherche in der Datenbank PubMed, der Leitlinien und Studienprotokollen der nationalen und internationalen Fachgesellschaften wurden die bildgebenden Standards sowie die neuesten Entwicklungen für ausgewählte solide Tumorentitäten beschrieben. Im Einzelnen werden von den in kinderonkologischen Zentren tätigen Autoren embryonale Tumoren, Lymphome. Hirntumoren sowie Tumorprädispositionssyndrome erörtert.

Schlussfolgerung

In der Bildgebung solider Tumore sind sowohl die Durchführung als auch die Beurteilung der Bilddaten bereits relativ standardisiert. Erfahrene Untersucher in zertifizierten Zentren sollten in erster Linie hieran beteiligt sein. Insbesondere die weiteren Innovationen in funktioneller Bildgebung lassen hoffen, dass zukünftig bildgebende Biomarker als Zielparameter in Therapiestudien verwendet werden können.
Literatur
1.
Zurück zum Zitat Mensah J, Jürgens H, Eggert A, Wesselmann S (2017) Zertifizierung Kinderonkologischer Zentren. Forum 32:177–178 Mensah J, Jürgens H, Eggert A, Wesselmann S (2017) Zertifizierung Kinderonkologischer Zentren. Forum 32:177–178
2.
Zurück zum Zitat Gröbner SN, Worst BC, Weischenfeldt J et al (2018) The landscape of genomic alterations across childhood cancers. Nature 555(7696):321–327PubMed Gröbner SN, Worst BC, Weischenfeldt J et al (2018) The landscape of genomic alterations across childhood cancers. Nature 555(7696):321–327PubMed
3.
Zurück zum Zitat Zhang J, Walsh MF, Wu G et al (2015) Germline mutations in predisposition genes in pediatric cancer. N Engl J Med 373(24):2336–2346PubMedPubMedCentral Zhang J, Walsh MF, Wu G et al (2015) Germline mutations in predisposition genes in pediatric cancer. N Engl J Med 373(24):2336–2346PubMedPubMedCentral
4.
Zurück zum Zitat Gatidis S, Bender B, Reimold M, Schäfer JF (2017) PET/MRI in children. Eur J Radiol 94:A64–A70PubMed Gatidis S, Bender B, Reimold M, Schäfer JF (2017) PET/MRI in children. Eur J Radiol 94:A64–A70PubMed
5.
Zurück zum Zitat Brodeur GM, Pritchard J, Berthold F et al (1993) Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 11(8):1466–1477PubMed Brodeur GM, Pritchard J, Berthold F et al (1993) Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 11(8):1466–1477PubMed
6.
Zurück zum Zitat Monclair T, Brodeur GM, Ambros PF et al (2009) The international neuroblastoma risk group (INRG) staging system: an INRG task force report. J Clin Oncol 27(2):298–303PubMedPubMedCentral Monclair T, Brodeur GM, Ambros PF et al (2009) The international neuroblastoma risk group (INRG) staging system: an INRG task force report. J Clin Oncol 27(2):298–303PubMedPubMedCentral
7.
Zurück zum Zitat Cohn SL, Pearson AD, London WB et al (2009) The international neuroblastoma risk group (INRG) classification system: an INRG task force report. J Clin Oncol 27(2):289–297PubMedPubMedCentral Cohn SL, Pearson AD, London WB et al (2009) The international neuroblastoma risk group (INRG) classification system: an INRG task force report. J Clin Oncol 27(2):289–297PubMedPubMedCentral
8.
Zurück zum Zitat Sea S (2019) S1-Leitlinie 025-008 Neuroblastom aktueller Stand: 06/2019 LL Neuroblastom (AWMF-Register Nr. 025/008 Klasse: S) Sea S (2019) S1-Leitlinie 025-008 Neuroblastom aktueller Stand: 06/2019 LL Neuroblastom (AWMF-Register Nr. 025/008 Klasse: S)
9.
Zurück zum Zitat Gassenmaier S, Tsiflikas I, Maennlin S, Urla C, Warmann SW, Schaefer JF (2020) Retrospective accuracy analysis of MRI based lesion size measurement in neuroblastic tumors: which sequence should we choose? BMC Med Imaging 20(1):105PubMedPubMedCentral Gassenmaier S, Tsiflikas I, Maennlin S, Urla C, Warmann SW, Schaefer JF (2020) Retrospective accuracy analysis of MRI based lesion size measurement in neuroblastic tumors: which sequence should we choose? BMC Med Imaging 20(1):105PubMedPubMedCentral
10.
Zurück zum Zitat Gahr N, Darge K, Hahn G, Kreher BW, von Buiren M, Uhl M (2011) Diffusion-weighted MRI for differentiation of neuroblastoma and ganglioneuroblastoma/ganglioneuroma. Eur J Radiol 79(3):443–446PubMed Gahr N, Darge K, Hahn G, Kreher BW, von Buiren M, Uhl M (2011) Diffusion-weighted MRI for differentiation of neuroblastoma and ganglioneuroblastoma/ganglioneuroma. Eur J Radiol 79(3):443–446PubMed
11.
Zurück zum Zitat Peschmann AL, Beer M, Ammann B et al (2019) Quantitative DWI predicts event-free survival in children with neuroblastic tumours: preliminary findings from a retrospective cohort study. Eur Radiol Exp 3(1):6PubMedPubMedCentral Peschmann AL, Beer M, Ammann B et al (2019) Quantitative DWI predicts event-free survival in children with neuroblastic tumours: preliminary findings from a retrospective cohort study. Eur Radiol Exp 3(1):6PubMedPubMedCentral
12.
Zurück zum Zitat Brisse HJ, McCarville MB, Granata C et al (2011) Guidelines for imaging and staging of neuroblastic tumors: consensus report from the international neuroblastoma risk group project. Radiology 261(1):243–257PubMed Brisse HJ, McCarville MB, Granata C et al (2011) Guidelines for imaging and staging of neuroblastic tumors: consensus report from the international neuroblastoma risk group project. Radiology 261(1):243–257PubMed
13.
Zurück zum Zitat Kembhavi SA, Rangarajan V, Shah S et al (2014) Prospective observational study on diagnostic accuracy of whole-body MRI in solid small round cell tumours. Clin Radiol 69(9):900–908PubMed Kembhavi SA, Rangarajan V, Shah S et al (2014) Prospective observational study on diagnostic accuracy of whole-body MRI in solid small round cell tumours. Clin Radiol 69(9):900–908PubMed
14.
Zurück zum Zitat Schaefer JF, Berthold LD, Hahn G et al (2019) Whole-body MRI in children and adolescents—S1 guideline. RoFo 191(7):618–625PubMed Schaefer JF, Berthold LD, Hahn G et al (2019) Whole-body MRI in children and adolescents—S1 guideline. RoFo 191(7):618–625PubMed
15.
Zurück zum Zitat Franzius C, Schmidt M, Hero B, Pfluger T, Hahn K (2008) Procedure guidelines for MIBG-scintigraphy in children. Nuklearmedizin 47(3):132–138PubMed Franzius C, Schmidt M, Hero B, Pfluger T, Hahn K (2008) Procedure guidelines for MIBG-scintigraphy in children. Nuklearmedizin 47(3):132–138PubMed
16.
Zurück zum Zitat Li C, Zhang J, Chen S et al (2018) Prognostic value of metabolic indices and bone marrow uptake pattern on preoperative 18F-FDG PET/CT in pediatric patients with neuroblastoma. Eur J Nucl Med Mol Imaging 45(2):306–315PubMed Li C, Zhang J, Chen S et al (2018) Prognostic value of metabolic indices and bone marrow uptake pattern on preoperative 18F-FDG PET/CT in pediatric patients with neuroblastoma. Eur J Nucl Med Mol Imaging 45(2):306–315PubMed
17.
Zurück zum Zitat Bar-Sever Z, Biassoni L, Shulkin B et al (2018) Guidelines on nuclear medicine imaging in neuroblastoma. Eur J Nucl Med Mol Imaging 45(11):2009–2024PubMed Bar-Sever Z, Biassoni L, Shulkin B et al (2018) Guidelines on nuclear medicine imaging in neuroblastoma. Eur J Nucl Med Mol Imaging 45(11):2009–2024PubMed
18.
Zurück zum Zitat Arumugam S, Manning-Cork NJ, Gains JE, Boterberg T, Gaze MN (2019) The evidence for external beam radiotherapy in high-risk neuroblastoma of childhood: a systematic review. Clin Oncol (R Coll Radiol) 31(3):182–190 Arumugam S, Manning-Cork NJ, Gains JE, Boterberg T, Gaze MN (2019) The evidence for external beam radiotherapy in high-risk neuroblastoma of childhood: a systematic review. Clin Oncol (R Coll Radiol) 31(3):182–190
19.
Zurück zum Zitat Simon T, Hero B, Bongartz R, Schmidt M, Müller RP, Berthold F (2006) Intensified external-beam radiation therapy improves the outcome of stage 4 neuroblastoma in children >1 year with residual local disease. Strahlenther Onkol 182(7):389–394PubMed Simon T, Hero B, Bongartz R, Schmidt M, Müller RP, Berthold F (2006) Intensified external-beam radiation therapy improves the outcome of stage 4 neuroblastoma in children >1 year with residual local disease. Strahlenther Onkol 182(7):389–394PubMed
20.
Zurück zum Zitat Matthay KK, Villablanca JG, Seeger RC et al (1999) Treatment of high-risk neuroblastoma with intensive chemotherapy, radiotherapy, autologous bone marrow transplantation, and 13-cis-retinoic acid. Children’s cancer group. N Engl J Med 341(16):1165–1173PubMed Matthay KK, Villablanca JG, Seeger RC et al (1999) Treatment of high-risk neuroblastoma with intensive chemotherapy, radiotherapy, autologous bone marrow transplantation, and 13-cis-retinoic acid. Children’s cancer group. N Engl J Med 341(16):1165–1173PubMed
21.
Zurück zum Zitat Benz-Bohm G, Hero B, Gossmann A, Simon T, Körber F, Berthold F (2010) Focal nodular hyperplasia of the liver in longterm survivors of neuroblastoma: how much diagnostic imaging is necessary? Eur J Radiol 74(3):e1–5PubMed Benz-Bohm G, Hero B, Gossmann A, Simon T, Körber F, Berthold F (2010) Focal nodular hyperplasia of the liver in longterm survivors of neuroblastoma: how much diagnostic imaging is necessary? Eur J Radiol 74(3):e1–5PubMed
22.
Zurück zum Zitat Irtan S, Ehrlich PF, Pritchard-Jones K (2016) Wilms tumor: “state-of-the-art” update, 2016. Semin Pediatr Surg 25(5):250–256PubMed Irtan S, Ehrlich PF, Pritchard-Jones K (2016) Wilms tumor: “state-of-the-art” update, 2016. Semin Pediatr Surg 25(5):250–256PubMed
23.
Zurück zum Zitat van den Heuvel-Eibrink MM, Hol JA, Pritchard-Jones K et al (2017) Position paper: rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol. Nat Rev Urol 14(12):743–752PubMed van den Heuvel-Eibrink MM, Hol JA, Pritchard-Jones K et al (2017) Position paper: rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol. Nat Rev Urol 14(12):743–752PubMed
24.
Zurück zum Zitat Vujanic GM, Gessler M, Ooms A et al (2018) The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol. Nat Rev Urol 15(11):693–701PubMedPubMedCentral Vujanic GM, Gessler M, Ooms A et al (2018) The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol. Nat Rev Urol 15(11):693–701PubMedPubMedCentral
25.
Zurück zum Zitat AWMF (Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften e.V) (2016) S1-Leitlinie 025/004: Nephroblastom (Wilms-Tumor) AWMF (Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften e.V) (2016) S1-Leitlinie 025/004: Nephroblastom (Wilms-Tumor)
26.
Zurück zum Zitat Watson T, Oostveen M, Rogers H, Pritchard-Jones K, Olsen Ø (2020) The role of imaging in the initial investigation of paediatric renal tumours. Lancet Child Adolesc Health 4(3):232–241PubMed Watson T, Oostveen M, Rogers H, Pritchard-Jones K, Olsen Ø (2020) The role of imaging in the initial investigation of paediatric renal tumours. Lancet Child Adolesc Health 4(3):232–241PubMed
27.
Zurück zum Zitat Schenk JP, Graf N, Günther P et al (2008) Role of MRI in the management of patients with nephroblastoma. Eur Radiol 18(4):683–691PubMed Schenk JP, Graf N, Günther P et al (2008) Role of MRI in the management of patients with nephroblastoma. Eur Radiol 18(4):683–691PubMed
28.
Zurück zum Zitat McDonald K, Duffy P, Chowdhury T, McHugh K (2013) Added value of abdominal cross-sectional imaging (CT or MRI) in staging of Wilms’ tumours. Clin Radiol 68(1):16–20PubMed McDonald K, Duffy P, Chowdhury T, McHugh K (2013) Added value of abdominal cross-sectional imaging (CT or MRI) in staging of Wilms’ tumours. Clin Radiol 68(1):16–20PubMed
29.
Zurück zum Zitat Fuchs J, Warmann SW, Szavay P et al (2005) Three-dimensional visualization and virtual simulation of resections in pediatric solid tumors. J Pediatr Surg 40(2):364–370PubMed Fuchs J, Warmann SW, Szavay P et al (2005) Three-dimensional visualization and virtual simulation of resections in pediatric solid tumors. J Pediatr Surg 40(2):364–370PubMed
30.
Zurück zum Zitat Warmann SW, Fuchs J (2019) Technical aspects of nephron-sparing surgery (NSS) in children with bilateral centrally located renal tumors. Semin Pediatr Surg 28(6):150865PubMed Warmann SW, Fuchs J (2019) Technical aspects of nephron-sparing surgery (NSS) in children with bilateral centrally located renal tumors. Semin Pediatr Surg 28(6):150865PubMed
31.
Zurück zum Zitat Schenk JP, Schrader C, Zieger B et al (2006) Reference radiology in nephroblastoma: accuracy and relevance for preoperative chemotherapy. RoFo 178(1):38–45PubMed Schenk JP, Schrader C, Zieger B et al (2006) Reference radiology in nephroblastoma: accuracy and relevance for preoperative chemotherapy. RoFo 178(1):38–45PubMed
32.
Zurück zum Zitat Littooij AS, Nikkels PG, Hulsbergen-van de Kaa CA, van de Ven CP, van den Heuvel-Eibrink MM, Olsen ØE (2017) Apparent diffusion coefficient as it relates to histopathology findings in post-chemotherapy nephroblastoma: a feasibility study. Pediatr Radiol 47(12):1608–1614PubMedPubMedCentral Littooij AS, Nikkels PG, Hulsbergen-van de Kaa CA, van de Ven CP, van den Heuvel-Eibrink MM, Olsen ØE (2017) Apparent diffusion coefficient as it relates to histopathology findings in post-chemotherapy nephroblastoma: a feasibility study. Pediatr Radiol 47(12):1608–1614PubMedPubMedCentral
33.
Zurück zum Zitat Hötker AM, Lollert A, Mazaheri Y et al (2020) Diffusion-weighted MRI in the assessment of nephroblastoma: results of a multi-center trial. Abdom Radiol 45(10):3202–3212 Hötker AM, Lollert A, Mazaheri Y et al (2020) Diffusion-weighted MRI in the assessment of nephroblastoma: results of a multi-center trial. Abdom Radiol 45(10):3202–3212
34.
Zurück zum Zitat Müller S, Farag I, Weickert J et al (2019) Benchmarking Wilms’ tumor in multisequence MRI data: why does current clinical practice fail? Which popular segmentation algorithms perform well? J Med Imaging 6(3):34001 Müller S, Farag I, Weickert J et al (2019) Benchmarking Wilms’ tumor in multisequence MRI data: why does current clinical practice fail? Which popular segmentation algorithms perform well? J Med Imaging 6(3):34001
35.
Zurück zum Zitat Perilongo G, Maibach R, Shafford E et al (2009) Cisplatin versus cisplatin plus doxorubicin for standard-risk hepatoblastoma. N Engl J Med 361(17):1662–1670PubMed Perilongo G, Maibach R, Shafford E et al (2009) Cisplatin versus cisplatin plus doxorubicin for standard-risk hepatoblastoma. N Engl J Med 361(17):1662–1670PubMed
36.
Zurück zum Zitat Häberle B, Maxwell R, Schweinitz DV, Schmid I (2019) High dose chemotherapy with autologous stem cell transplantation in hepatoblastoma does not improve outcome. Results of the GPOH study HB99. Klin Padiatr 231(6):283–290PubMed Häberle B, Maxwell R, Schweinitz DV, Schmid I (2019) High dose chemotherapy with autologous stem cell transplantation in hepatoblastoma does not improve outcome. Results of the GPOH study HB99. Klin Padiatr 231(6):283–290PubMed
37.
Zurück zum Zitat Zsiros J, Brugieres L, Brock P et al (2013) Dose-dense cisplatin-based chemotherapy and surgery for children with high-risk hepatoblastoma (SIOPEL-4): a prospective, single-arm, feasibility study. Lancet Oncol 14(9):834–842PubMedPubMedCentral Zsiros J, Brugieres L, Brock P et al (2013) Dose-dense cisplatin-based chemotherapy and surgery for children with high-risk hepatoblastoma (SIOPEL-4): a prospective, single-arm, feasibility study. Lancet Oncol 14(9):834–842PubMedPubMedCentral
38.
Zurück zum Zitat Towbin AJ, Meyers RL, Woodley H et al (2018) 2017 PRETEXT: radiologic staging system for primary hepatic malignancies of childhood revised for the paediatric hepatic international tumour trial (PHITT). Pediatr Radiol 48(4):536–554PubMed Towbin AJ, Meyers RL, Woodley H et al (2018) 2017 PRETEXT: radiologic staging system for primary hepatic malignancies of childhood revised for the paediatric hepatic international tumour trial (PHITT). Pediatr Radiol 48(4):536–554PubMed
40.
Zurück zum Zitat Meyers RL, Maibach R, Hiyama E et al (2017) Risk-stratified staging in paediatric hepatoblastoma: a unified analysis from the children’s hepatic tumors international collaboration. Lancet Oncol 18(1):122–131PubMed Meyers RL, Maibach R, Hiyama E et al (2017) Risk-stratified staging in paediatric hepatoblastoma: a unified analysis from the children’s hepatic tumors international collaboration. Lancet Oncol 18(1):122–131PubMed
41.
Zurück zum Zitat Meyer JS, Siegel MJ, Farooqui SO, Jaramillo D, Fletcher BD, Hoffer FA (2005) Which MRI sequence of the spine best reveals bone-marrow metastases of neuroblastoma? Pediatr Radiol 35(8):778–785PubMed Meyer JS, Siegel MJ, Farooqui SO, Jaramillo D, Fletcher BD, Hoffer FA (2005) Which MRI sequence of the spine best reveals bone-marrow metastases of neuroblastoma? Pediatr Radiol 35(8):778–785PubMed
43.
Zurück zum Zitat Inarejos Clemente EJ, Navallas M, Barber Martínez de la Torre I et al (2020) MRI of rhabdomyosarcoma and other soft-tissue sarcomas in children. Radiographics 40(3):791–814PubMed Inarejos Clemente EJ, Navallas M, Barber Martínez de la Torre I et al (2020) MRI of rhabdomyosarcoma and other soft-tissue sarcomas in children. Radiographics 40(3):791–814PubMed
44.
Zurück zum Zitat Vaarwerk B, van der Lee JH, Breunis WB et al (2018) Prognostic relevance of early radiologic response to induction chemotherapy in pediatric rhabdomyosarcoma: a report from the international society of pediatric oncology malignant Mesenchymal tumor 95 study. Cancer 124(5):1016–1024PubMed Vaarwerk B, van der Lee JH, Breunis WB et al (2018) Prognostic relevance of early radiologic response to induction chemotherapy in pediatric rhabdomyosarcoma: a report from the international society of pediatric oncology malignant Mesenchymal tumor 95 study. Cancer 124(5):1016–1024PubMed
45.
Zurück zum Zitat Schoot RA, McHugh K, van Rijn RR et al (2013) Response assessment in pediatric rhabdomyosarcoma: can response evaluation criteria in solid tumors replace three-dimensional volume assessments? Radiology 269(3):870–878PubMed Schoot RA, McHugh K, van Rijn RR et al (2013) Response assessment in pediatric rhabdomyosarcoma: can response evaluation criteria in solid tumors replace three-dimensional volume assessments? Radiology 269(3):870–878PubMed
46.
Zurück zum Zitat Scheer M, Dantonello T, Brossart P et al (2018) Importance of whole-body imaging with complete coverage of hands and feet in alveolar rhabdomyosarcoma staging. Pediatr Radiol 48(5):648–657PubMed Scheer M, Dantonello T, Brossart P et al (2018) Importance of whole-body imaging with complete coverage of hands and feet in alveolar rhabdomyosarcoma staging. Pediatr Radiol 48(5):648–657PubMed
47.
Zurück zum Zitat García-Figueiras R, Baleato-González S, Luna A et al (2020) Assessing immunotherapy with functional and molecular imaging and radiomics. Radiographics 40(7):1987–2010PubMed García-Figueiras R, Baleato-González S, Luna A et al (2020) Assessing immunotherapy with functional and molecular imaging and radiomics. Radiographics 40(7):1987–2010PubMed
48.
Zurück zum Zitat Siegel RL, Miller KD, Jemal A (2015) Cancer statistics, 2015. CA A Cancer J Clin 65(1):5–29 Siegel RL, Miller KD, Jemal A (2015) Cancer statistics, 2015. CA A Cancer J Clin 65(1):5–29
49.
Zurück zum Zitat Cheson BD, Fisher RI, Barrington SF et al (2014) Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol 32(27):3059–3068PubMedPubMedCentral Cheson BD, Fisher RI, Barrington SF et al (2014) Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol 32(27):3059–3068PubMedPubMedCentral
50.
Zurück zum Zitat Rosolen A, Perkins SL, Pinkerton CR et al (2015) Revised international pediatric non-Hodgkin lymphoma staging system. J Clin Oncol 33(18):2112–2118PubMedPubMedCentral Rosolen A, Perkins SL, Pinkerton CR et al (2015) Revised international pediatric non-Hodgkin lymphoma staging system. J Clin Oncol 33(18):2112–2118PubMedPubMedCentral
51.
Zurück zum Zitat Zwarthoed C, El-Galaly TC, Canepari M et al (2017) Prognostic value of bone marrow tracer uptake pattern in baseline PET scans in Hodgkin lymphoma: results from an international collaborative study. J Nucl Med 58(8):1249–1254PubMed Zwarthoed C, El-Galaly TC, Canepari M et al (2017) Prognostic value of bone marrow tracer uptake pattern in baseline PET scans in Hodgkin lymphoma: results from an international collaborative study. J Nucl Med 58(8):1249–1254PubMed
52.
Zurück zum Zitat Yağci-Küpeli B, Koçyiğit-Deveci E, Adamhasan F, Küpeli S (2019) The value of 18F-FDG PET/CT in detecting bone marrow involvement in childhood cancers. J Pediatr Hematol Oncol 41(6):438–441PubMed Yağci-Küpeli B, Koçyiğit-Deveci E, Adamhasan F, Küpeli S (2019) The value of 18F-FDG PET/CT in detecting bone marrow involvement in childhood cancers. J Pediatr Hematol Oncol 41(6):438–441PubMed
53.
Zurück zum Zitat Bakhshi S, Bhethanabhotla S, Kumar R et al (2017) Posttreatment PET/CT rather than interim PET/CT using Deauville criteria predicts outcome in pediatric Hodgkin lymphoma: a prospective study comparing PET/CT with conventional imaging. J Nucl Med 58(4):577–583PubMed Bakhshi S, Bhethanabhotla S, Kumar R et al (2017) Posttreatment PET/CT rather than interim PET/CT using Deauville criteria predicts outcome in pediatric Hodgkin lymphoma: a prospective study comparing PET/CT with conventional imaging. J Nucl Med 58(4):577–583PubMed
54.
Zurück zum Zitat Furth C, Amthauer H, Hautzel H et al (2011) Evaluation of interim PET response criteria in paediatric Hodgkin’s lymphoma—results for dedicated assessment criteria in a blinded dual-centre read. Ann Oncol 22(5):1198–1203PubMed Furth C, Amthauer H, Hautzel H et al (2011) Evaluation of interim PET response criteria in paediatric Hodgkin’s lymphoma—results for dedicated assessment criteria in a blinded dual-centre read. Ann Oncol 22(5):1198–1203PubMed
55.
Zurück zum Zitat Gatidis S, Schmidt H, Gucke B et al (2016) Comprehensive oncologic imaging in infants and preschool children with substantially reduced radiation exposure using combined simultaneous (1)(8)F-fluorodeoxyglucose positron emission tomography/magnetic resonance imaging: a direct comparison to (1)(8)F-fluorodeoxyglucose positron emission tomography/computed tomography. Invest Radiol 51(1):7–14PubMed Gatidis S, Schmidt H, Gucke B et al (2016) Comprehensive oncologic imaging in infants and preschool children with substantially reduced radiation exposure using combined simultaneous (1)(8)F-fluorodeoxyglucose positron emission tomography/magnetic resonance imaging: a direct comparison to (1)(8)F-fluorodeoxyglucose positron emission tomography/computed tomography. Invest Radiol 51(1):7–14PubMed
56.
Zurück zum Zitat Schafer JF, Gatidis S, Schmidt H et al (2014) Simultaneous whole-body PET/MR imaging in comparison to PET/CT in pediatric oncology: initial results. Radiology 273(1):220–231PubMed Schafer JF, Gatidis S, Schmidt H et al (2014) Simultaneous whole-body PET/MR imaging in comparison to PET/CT in pediatric oncology: initial results. Radiology 273(1):220–231PubMed
57.
Zurück zum Zitat Chawla SC, Federman N, Zhang D et al (2010) Estimated cumulative radiation dose from PET/CT in children with malignancies: a 5-year retrospective review. Pediatr Radiol 40(5):681–686PubMed Chawla SC, Federman N, Zhang D et al (2010) Estimated cumulative radiation dose from PET/CT in children with malignancies: a 5-year retrospective review. Pediatr Radiol 40(5):681–686PubMed
58.
Zurück zum Zitat Schäfer JF, Granata C, von Kalle T et al (2020) Whole-body magnetic resonance imaging in pediatric oncology—recommendations by the oncology task force of the ESPR. Pediatr Radiol 50(8):1162–1174PubMedPubMedCentral Schäfer JF, Granata C, von Kalle T et al (2020) Whole-body magnetic resonance imaging in pediatric oncology—recommendations by the oncology task force of the ESPR. Pediatr Radiol 50(8):1162–1174PubMedPubMedCentral
59.
Zurück zum Zitat Latifoltojar A, Punwani S, Lopes A et al (2019) Whole-body MRI for staging and interim response monitoring in paediatric and adolescent Hodgkin’s lymphoma: a comparison with multi-modality reference standard including (18)F-FDG-PET-CT. Eur Radiol 29(1):202–212PubMed Latifoltojar A, Punwani S, Lopes A et al (2019) Whole-body MRI for staging and interim response monitoring in paediatric and adolescent Hodgkin’s lymphoma: a comparison with multi-modality reference standard including (18)F-FDG-PET-CT. Eur Radiol 29(1):202–212PubMed
60.
Zurück zum Zitat Littooij AS, Kwee TC, Barber I et al (2014) Whole-body MRI for initial staging of paediatric lymphoma: prospective comparison to an FDG-PET/CT-based reference standard. Eur Radiol 24(5):1153–1165PubMed Littooij AS, Kwee TC, Barber I et al (2014) Whole-body MRI for initial staging of paediatric lymphoma: prospective comparison to an FDG-PET/CT-based reference standard. Eur Radiol 24(5):1153–1165PubMed
61.
Zurück zum Zitat Punwani S, Taylor SA, Bainbridge A et al (2010) Pediatric and adolescent lymphoma: comparison of whole-body STIR half-Fourier RARE MR imaging with an enhanced PET/CT reference for initial staging. Radiology 255(1):182–190PubMed Punwani S, Taylor SA, Bainbridge A et al (2010) Pediatric and adolescent lymphoma: comparison of whole-body STIR half-Fourier RARE MR imaging with an enhanced PET/CT reference for initial staging. Radiology 255(1):182–190PubMed
62.
Zurück zum Zitat Klenk C, Gawande R, Uslu L et al (2014) Ionising radiation-free whole-body MRI versus (18)F-fluorodeoxyglucose PET/CT scans for children and young adults with cancer: a prospective, non-randomised, single-centre study. Lancet Oncol 15(3):275–285PubMed Klenk C, Gawande R, Uslu L et al (2014) Ionising radiation-free whole-body MRI versus (18)F-fluorodeoxyglucose PET/CT scans for children and young adults with cancer: a prospective, non-randomised, single-centre study. Lancet Oncol 15(3):275–285PubMed
63.
Zurück zum Zitat Gatidis S, Gueckel B, Reimold M, Pfannenberg C, Tsiflikas I, Schaefer JF (2017) 18F-FDG-PET/MRI for primary staging and therapy response assessment in pediatric oncology: when do we need it and is it sufficient? Gatidis S, Gueckel B, Reimold M, Pfannenberg C, Tsiflikas I, Schaefer JF (2017) 18F-FDG-PET/MRI for primary staging and therapy response assessment in pediatric oncology: when do we need it and is it sufficient?
64.
Zurück zum Zitat Voss SD, Cairo MS (2019) Surveillance imaging in pediatric lymphoma. Pediatr Radiol 49(11):1565–1573PubMed Voss SD, Cairo MS (2019) Surveillance imaging in pediatric lymphoma. Pediatr Radiol 49(11):1565–1573PubMed
65.
Zurück zum Zitat Louis DN, Perry A, Reifenberger G et al (2016) The 2016 world health organization classification of tumors of the central nervous system: a summary. Acta Neuropathol 131(6):803–820 Louis DN, Perry A, Reifenberger G et al (2016) The 2016 world health organization classification of tumors of the central nervous system: a summary. Acta Neuropathol 131(6):803–820
66.
Zurück zum Zitat Almansory KO, Fraioli F (2019) Combined PET/MRI in brain glioma imaging. Br J Hosp Med (Lond) 80(7):380–386 Almansory KO, Fraioli F (2019) Combined PET/MRI in brain glioma imaging. Br J Hosp Med (Lond) 80(7):380–386
67.
Zurück zum Zitat Fangusaro J, Witt O, Hernáiz Driever P et al (2020) Response assessment in paediatric low-grade glioma: recommendations from the response assessment in pediatric neuro-oncology (RAPNO) working group. Lancet Oncol 21(6):e305–e16PubMed Fangusaro J, Witt O, Hernáiz Driever P et al (2020) Response assessment in paediatric low-grade glioma: recommendations from the response assessment in pediatric neuro-oncology (RAPNO) working group. Lancet Oncol 21(6):e305–e16PubMed
68.
Zurück zum Zitat Lequin M, Hendrikse J (2017) Advanced MR imaging in pediatric brain tumors, clinical applications. Neuroimaging Clin N Am 27(1):167–190PubMed Lequin M, Hendrikse J (2017) Advanced MR imaging in pediatric brain tumors, clinical applications. Neuroimaging Clin N Am 27(1):167–190PubMed
70.
Zurück zum Zitat Kikuchi K, Hiwatashi A, Togao O et al (2019) Intravoxel incoherent motion MR imaging of pediatric Intracranial tumors: correlation with histology and diagnostic utility. AJNR Am J Neuroradiol 40(5):878–884PubMedPubMedCentral Kikuchi K, Hiwatashi A, Togao O et al (2019) Intravoxel incoherent motion MR imaging of pediatric Intracranial tumors: correlation with histology and diagnostic utility. AJNR Am J Neuroradiol 40(5):878–884PubMedPubMedCentral
71.
Zurück zum Zitat Manias KA, Gill SK, MacPherson L et al (2019) Diagnostic accuracy and added value of qualitative radiological review of (1)H-magnetic resonance spectroscopy in evaluation of childhood brain tumors. Neurooncol Pract 6(6):428–437PubMedPubMedCentral Manias KA, Gill SK, MacPherson L et al (2019) Diagnostic accuracy and added value of qualitative radiological review of (1)H-magnetic resonance spectroscopy in evaluation of childhood brain tumors. Neurooncol Pract 6(6):428–437PubMedPubMedCentral
72.
Zurück zum Zitat Greer MC (2018) Imaging of cancer predisposition syndromes. Pediatr Radiol 48(9):1364–1375PubMed Greer MC (2018) Imaging of cancer predisposition syndromes. Pediatr Radiol 48(9):1364–1375PubMed
73.
Zurück zum Zitat Greer MC, Voss SD, States LJ (2017) Pediatric cancer predisposition imaging: focus on whole-body MRI. Clin Cancer Res 23(11):e6–e13PubMed Greer MC, Voss SD, States LJ (2017) Pediatric cancer predisposition imaging: focus on whole-body MRI. Clin Cancer Res 23(11):e6–e13PubMed
74.
Zurück zum Zitat Kratz CP, Achatz MI, Brugières L et al (2017) Cancer screening recommendations for individuals with Li-Fraumeni syndrome. Clin Cancer Res 23(11):e38–e45PubMed Kratz CP, Achatz MI, Brugières L et al (2017) Cancer screening recommendations for individuals with Li-Fraumeni syndrome. Clin Cancer Res 23(11):e38–e45PubMed
75.
Zurück zum Zitat Ballinger ML, Best A, Mai PL et al (2017) Baseline surveillance in Li-Fraumeni syndrome using whole-body magnetic resonance imaging: a meta-analysis. JAMA Oncol 3(12):1634–1639PubMedPubMedCentral Ballinger ML, Best A, Mai PL et al (2017) Baseline surveillance in Li-Fraumeni syndrome using whole-body magnetic resonance imaging: a meta-analysis. JAMA Oncol 3(12):1634–1639PubMedPubMedCentral
76.
Zurück zum Zitat Ahlawat S, Blakeley JO, Langmead S, Belzberg AJ, Fayad LM (2020) Current status and recommendations for imaging in neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. Skelet Radiol 49(2):199–219 Ahlawat S, Blakeley JO, Langmead S, Belzberg AJ, Fayad LM (2020) Current status and recommendations for imaging in neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. Skelet Radiol 49(2):199–219
77.
Zurück zum Zitat Grasparil AD 2nd, Gottumukkala RV, Greer MC, Gee MS (2020) Whole-body MRI surveillance of cancer predisposition syndromes: current best practice guidelines for use, performance, and interpretation. AJR Am J Roentgenol 215(4):1002–1011PubMed Grasparil AD 2nd, Gottumukkala RV, Greer MC, Gee MS (2020) Whole-body MRI surveillance of cancer predisposition syndromes: current best practice guidelines for use, performance, and interpretation. AJR Am J Roentgenol 215(4):1002–1011PubMed
Metadaten
Titel
Fortschrittliche radiologische Diagnostik bei soliden Tumoren im Kindes- und Jugendalter
Staging, Risikostratifizierung und Responsebeurteilung
verfasst von
Prof. Dr. Jürgen Frank Schäfer
Jochen Herrmann
Birgit Kammer
Friederike Koerber
Ilias Tsiflikas
Thekla von Kalle
Hans-Joachim Mentzel
Publikationsdatum
01.03.2021
Verlag
Springer Medizin
Erschienen in
Die Onkologie / Ausgabe 5/2021
Print ISSN: 2731-7226
Elektronische ISSN: 2731-7234
DOI
https://doi.org/10.1007/s00761-021-00910-1

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