Standard diametric versus volumetric early tumor shrinkage as a predictor of survival in metastatic colorectal cancer: subgroup findings of the randomized, open-label phase III trial FIRE-3 / AIO KRK-0306.


Journal

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

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 16 05 2022
accepted: 24 07 2022
revised: 16 05 2022
pubmed: 18 8 2022
medline: 3 2 2023
entrez: 17 8 2022
Statut: ppublish

Résumé

Early tumor shrinkage (ETS) quantifies the objective response at the first assessment during systemic treatment. In metastatic colorectal cancer (mCRC), ETS gains relevance as an early available surrogate for patient survival. The aim of this study was to increase the predictive accuracy of ETS by using semi-automated volumetry instead of standard diametric measurements. Diametric and volumetric ETS were retrospectively calculated in 253 mCRC patients who received 5-fluorouracil, leucovorin, and irinotecan (FOLFIRI) combined with either cetuximab or bevacizumab. The association of diametric and volumetric ETS with overall survival (OS) and progression-free survival (PFS) was compared. Continuous diametric and volumetric ETS predicted survival similarly regarding concordance indices (p > .05). In receiver operating characteristics, a volumetric threshold of 45% optimally identified short-term survivors. For patients with volumetric ETS ≥ 45% (vs < 45%), median OS was longer (32.5 vs 19.0 months, p < .001) and the risk of death reduced for the first and second year (hazard ratio [HR] = 0.25, p < .001, and HR = 0.39, p < .001). Patients with ETS ≥ 45% had a reduced risk of progressive disease only for the first 6 months (HR = 0.26, p < .001). These survival times and risks were comparable to those of diametric ETS ≥ 20% (vs < 20%). The accuracy of ETS in predicting survival was not increased by volumetric instead of diametric measurements. Continuous diametric and volumetric ETS similarly predicted survival, regardless of whether patients received cetuximab or bevacizumab. A volumetric ETS threshold of 45% and a diametric ETS threshold of 20% equally identified short-term survivors. • ETS based on volumetric measurements did not predict survival more accurately than ETS based on standard diametric measurements. • Continuous diametric and volumetric ETS predicted survival similarly in patients receiving FOLFIRI with cetuximab or bevacizumab. • A volumetric ETS threshold of 45% and a diametric ETS threshold of 20% equally identified short-term survivors.

Identifiants

pubmed: 35976398
doi: 10.1007/s00330-022-09053-2
pii: 10.1007/s00330-022-09053-2
pmc: PMC9889429
doi:

Substances chimiques

Bevacizumab 2S9ZZM9Q9V
Camptothecin XT3Z54Z28A
Cetuximab PQX0D8J21J
Fluorouracil U3P01618RT

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1174-1184

Informations de copyright

© 2022. The Author(s).

Références

Van Cutsem E, Köhne CH, Hitre E et al (2009) Cetuximab and chemotherapy as initial treatment for metastatic colorectal cancer. N Engl J Med 360:1408–1417
doi: 10.1056/NEJMoa0805019
Hurwitz H, Fehrenbacher L, Novotny W et al (2004) Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med 350:2335–2342
doi: 10.1056/NEJMoa032691
Douillard JY, Oliner KS, Siena S et al (2013) Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med 369:1023–1034
doi: 10.1056/NEJMoa1305275
Heinemann V, Stintzing S, Modest DP, Giessen-Jung C, Michl M, Mansmann UR (2015) Early tumour shrinkage (ETS) and depth of response (DpR) in the treatment of patients with metastatic colorectal cancer (mCRC). Eur J Cancer 51:1927–1936
doi: 10.1016/j.ejca.2015.06.116
Venook AP, Tabernero J (2015) Progression-free survival: helpful biomarker or clinically meaningless end point? J Clin Oncol 33:4–6
doi: 10.1200/JCO.2014.57.9557
De Roock W, Piessevaux H, De Schutter J et al (2008) KRAS wild-type state predicts survival and is associated to early radiological response in metastatic colorectal cancer treated with cetuximab. Ann Oncol 19:508–515
doi: 10.1093/annonc/mdm496
Piessevaux H, Buyse M, De Roock W et al (2009) Radiological tumor size decrease at week 6 is a potent predictor of outcome in chemorefractory metastatic colorectal cancer treated with cetuximab (BOND trial). Ann Oncol 20:1375–1382
doi: 10.1093/annonc/mdp011
Suzuki C, Blomqvist L, Sundin A et al (2012) The initial change in tumor size predicts response and survival in patients with metastatic colorectal cancer treated with combination chemotherapy. Ann Oncol 23:948–954
doi: 10.1093/annonc/mdr350
Piessevaux H, Buyse M, Schlichting M et al (2013) Use of early tumor shrinkage to predict long-term outcome in metastatic colorectal cancer treated with cetuximab. J Clin Oncol 31:3764–3775
doi: 10.1200/JCO.2012.42.8532
Giessen C, Laubender RP, Fischer von Weikersthal L et al (2013) Early tumor shrinkage in metastatic colorectal cancer: retrospective analysis from an irinotecan-based randomized first-line trial. Cancer Sci 104:718–724
doi: 10.1111/cas.12148
Stintzing S, Modest DP, Rossius L et al (2016) FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab for metastatic colorectal cancer (FIRE-3): a post-hoc analysis of tumour dynamics in the final RAS wild-type subgroup of this randomised open-label phase 3 trial. Lancet Oncol 17:1426–1434
doi: 10.1016/S1470-2045(16)30269-8
Cremolini C, Loupakis F, Antoniotti C et al (2015) Early tumor shrinkage and depth of response predict long-term outcome in metastatic colorectal cancer patients treated with first-line chemotherapy plus bevacizumab: results from phase III TRIBE trial by the Gruppo Oncologico del Nord Ovest. Ann Oncol 26:1188–1194
doi: 10.1093/annonc/mdv112
Petrelli F, Pietrantonio F, Cremolini C et al (2015) Early tumour shrinkage as a prognostic factor and surrogate end-point in colorectal cancer: a systematic review and pooled-analysis. Eur J Cancer 51:800–807
doi: 10.1016/j.ejca.2015.02.011
Aprile G, Fontanella C, Bonotto M et al (2015) Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials. Oncotarget 6:28716–28730
doi: 10.18632/oncotarget.4747
Rothe JH, Grieser C, Lehmkuhl L et al (2013) Size determination and response assessment of liver metastases with computed tomography--comparison of RECIST and volumetric algorithms. Eur J Radiol 82:1831–1839
doi: 10.1016/j.ejrad.2012.05.018
Wulff AM, Fabel M, Freitag-Wolf S et al (2013) Volumetric response classification in metastatic solid tumors on MSCT: initial results in a whole-body setting. Eur J Radiol 82:e567–e573
doi: 10.1016/j.ejrad.2013.05.030
Van Hoe L, Van Cutsem E, Vergote I et al (1997) Size quantification of liver metastases in patients undergoing cancer treatment: reproducibility of one-, two-, and three-dimensional measurements determined with spiral CT. Radiology 202:671–675
doi: 10.1148/radiology.202.3.9051014
Zhao B, Oxnard GR, Moskowitz CS et al (2010) A pilot study of volume measurement as a method of tumor response evaluation to aid biomarker development. Clin Cancer Res 16:4647–4653
doi: 10.1158/1078-0432.CCR-10-0125
Sun C, Guo S, Zhang H et al (2017) Automatic segmentation of liver tumors from multiphase contrast-enhanced CT images based on FCNs. Artif Intell Med 83:58–66
doi: 10.1016/j.artmed.2017.03.008
Heinemann V, Fischer von Weikersthal L, Decker T et al (2014) FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol 15:1065–1075
doi: 10.1016/S1470-2045(14)70330-4
Van Cutsem E, Cervantes A, Adam R et al (2016) ESMO consensus guidelines for the management of patients with metastatic colorectal cancer. Ann Oncol 27:1386–1422
doi: 10.1093/annonc/mdw235
Stintzing S, Modest DP, Fischer von Weikersthal L et al (2014) Independent radiological evaluation of objective response, early tumor shrinkage, and depth of response in FIRE-3 (AIO KRK-0306) in the final RAS evaluable population. Ann Oncol 25:v1–v41
doi: 10.1093/annonc/mdu438.9
Winter KS, Hofmann FO, Thierfelder KM et al (2018) Towards volumetric thresholds in RECIST 1.1: therapeutic response assessment in hepatic metastases. Eur Radiol 28:4839–4848
doi: 10.1007/s00330-018-5424-0
Kang L, Chen W, Petrick NA, Gallas BD (2015) Comparing two correlated C indices with right-censored survival outcome: a one-shot nonparametric approach. Stat Med 34:685–703
doi: 10.1002/sim.6370
Youden WJ (1950) Index for rating diagnostic tests. Cancer 3:32–35
doi: 10.1002/1097-0142(1950)3:1<32::AID-CNCR2820030106>3.0.CO;2-3
Core Team R (2016) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna
Mansmann UR, Laubender RP, Sartorius U, Giessen CA, Graser A, Heinemann V (2012) Improved early prediction of individual prognosis for patients with mCRC: joint modeling of tumor shrinkage with volume data for PFS and OS. J Clin Oncol 30:Abstr 3603
doi: 10.1200/jco.2012.30.15_suppl.3603
Froelich MF, Heinemann V, Sommer WH et al (2018) CT attenuation of liver metastases before targeted therapy is a prognostic factor of overall survival in colorectal cancer patients. Results from the randomised, open-label FIRE-3/AIO KRK0306 trial. Eur Radiol. https://doi.org/10.1007/s00330-018-5454-7
Sunakawa Y, Ichikawa W, Tsuji A et al (2017) Prognostic impact of primary tumor location on clinical outcomes of metastatic colorectal cancer treated with cetuximab plus oxaliplatin-based chemotherapy: a subgroup analysis of the JACCRO CC-05/06 trials. Clin Colorectal Cancer 16:e171–e180
doi: 10.1016/j.clcc.2016.09.010
Tsuji A, Ohori H, Yamaguchi T et al (2021) The randomized phase II study of FOLFOXIRI plus cetuximab versus FOLFOXIRI plus bevacizumab as the first-line treatment in metastatic colorectal cancer with RAS wild-type tumors: the DEEPER trial (JACCRO CC-13). J Clin Oncol 39:3501–3501
doi: 10.1200/JCO.2021.39.15_suppl.3501
Colloca GA, Venturino A, Guarneri D (2019) Early tumor shrinkage after first-line medical treatment of metastatic colorectal cancer: a meta-analysis. Int J Clin Oncol 24:231–240
doi: 10.1007/s10147-019-01405-1
Palmieri LJ, Fihri A, Doat S et al (2019) Tumor-size responses to first-line is a predictor of overall survival in metastatic colorectal cancer. Eur Radiol 29:3871–3880
doi: 10.1007/s00330-018-5967-0
Moehler M, Folprecht G, Heinemann V et al (2022) Survival after secondary liver resection in metastatic colorectal cancer: comparing data of three prospective randomized European trials (LICC, CELIM, FIRE-3). Int J Cancer 150:1341–1349
doi: 10.1002/ijc.33881
Taieb J, Rivera F, Siena S et al (2018) Exploratory analyses assessing the impact of early tumour shrinkage and depth of response on survival outcomes in patients with RAS wild-type metastatic colorectal cancer receiving treatment in three randomised panitumumab trials. J Cancer Res Clin Oncol 144:321–335
doi: 10.1007/s00432-017-2534-z

Auteurs

Felix O Hofmann (FO)

Department of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany. Felix.Hofmann@med.uni-muenchen.de.
Department of General, Visceral and Transplantation Surgery, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany. Felix.Hofmann@med.uni-muenchen.de.
German Cancer Consortium (DKTK), partner site Munich, and German Cancer Research Centre (DKFZ), Heidelberg, Germany. Felix.Hofmann@med.uni-muenchen.de.

Volker Heinemann (V)

German Cancer Consortium (DKTK), partner site Munich, and German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Department of Medicine III, Comprehensive Cancer Center Munich, University Hospital Grosshadern, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.

Melvin D'Anastasi (M)

Department of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.
Mater Dei Hospital, University of Malta, Triq tal-Qroqq, Msida, MSD2090, Malta.

Alena B Gesenhues (AB)

Department of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.

Nina Hesse (N)

Department of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.

Ludwig Fischer von Weikersthal (LF)

Klinikum St. Marien Amberg, Amberg, Germany.

Thomas Decker (T)

Onkologische Praxis, Ravensburg, Germany.

Alexander Kiani (A)

Department of Medicine IV, Klinikum Bayreuth GmbH, Bayreuth, Germany.
Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), Erlangen, Germany.

Markus Moehler (M)

Department of Internal Medicine I, University Medical Center Mainz, Mainz, Germany.

Florian Kaiser (F)

VK&K Studien GbR, Landshut, Germany.

Tobias Heintges (T)

Rheinlandklinikum Neuss, Lukaskrankenhaus, Neuss, Germany.

Christoph Kahl (C)

Department of Hematology, Oncology and Palliative Care, Klinikum Magdeburg gGmbH, Magdeburg, Germany.

Frank Kullmann (F)

Department of Internal Medicine I, Hospital Weiden, Weiden, Germany.

Werner Scheithauer (W)

Department of Internal Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Hartmut Link (H)

Department of Medicine I, Westpfalz-Klinikum GmbH, Kaiserslautern, Germany.

Dominik P Modest (DP)

Medical Department of Hematology, Oncology and Cancer Immunology (CCM), Charité-Universitätsmedizin Berlin, Berlin, Germany.

Sebastian Stintzing (S)

Medical Department of Hematology, Oncology and Cancer Immunology (CCM), Charité-Universitätsmedizin Berlin, Berlin, Germany.

Julian W Holch (JW)

German Cancer Consortium (DKTK), partner site Munich, and German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Department of Medicine III, Comprehensive Cancer Center Munich, University Hospital Grosshadern, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.

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