Evaluation of Intratumoral Response Heterogeneity in Metastatic Colorectal Cancer and Its Impact on Patient Overall Survival: Findings from 10,551 Patients in the ARCAD Database.

cancer trials tumor measurement-based endpoints

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
15 Aug 2023
Historique:
received: 16 06 2023
revised: 30 07 2023
accepted: 09 08 2023
medline: 26 8 2023
pubmed: 26 8 2023
entrez: 26 8 2023
Statut: epublish

Résumé

Metastatic colorectal cancer (mCRC) is a heterogeneous disease that can evoke discordant responses to therapy among different lesions in individual patients. The Response Evaluation Criteria in Solid Tumors (RECIST) criteria do not take into consideration response heterogeneity. We explored and developed lesion-based measurement response criteria to evaluate their prognostic effect on overall survival (OS). Patients enrolled in 17 first-line clinical trials, who had mCRC with ≥ 2 lesions at baseline, and a restaging scan by 12 weeks were included. For each patient, lesions were categorized as a progressing lesion (PL: > 20% increase in the longest diameter (LD)), responding lesion (RL: > 30% decrease in LD), or stable lesion (SL: neither PL nor RL) based on the 12-week scan. Lesion-based response criteria were defined for each patient as follows: PL only, SL only, RL only, and varied responses (mixture of RL, SL, and PL). Lesion-based response criteria and OS were correlated using stratified multivariable Cox models. The concordance between OS and classifications was measured using the C statistic. Among 10,551 patients with mCRC from 17 first-line studies, varied responses were noted in 51.6% of patients, among whom, 3.3% had RL/PL at 12 weeks. Among patients with RL/SL, 52% had stable disease (SD) by RECIST 1.1, and they had a longer OS (median OS (mOS) = 19.9 months) than those with SL only (mOS = 16.8 months, HR (95% CI) = 0.81 (0.76, 0.85), Varied responses at first restaging are common among patients receiving first-line therapy for mCRC. Our lesion-based measurement criteria allowed for better mortality discrimination, which could potentially be informative for treatment decision-making and influence patient outcomes.

Identifiants

pubmed: 37627145
pii: cancers15164117
doi: 10.3390/cancers15164117
pmc: PMC10452983
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Références

Sci Transl Med. 2011 Sep 7;3(99):99ra86
pubmed: 21900593
Eur J Cancer. 2009 Jan;45(2):228-47
pubmed: 19097774
Cancer. 1981 Jan 1;47(1):207-14
pubmed: 7459811
Insights Imaging. 2012 Dec;3(6):573-89
pubmed: 23093486
Clin Cancer Res. 2008 Feb 1;14(3):772-81
pubmed: 18245538
Eur J Cancer. 2013 Jul;49(11):2486-93
pubmed: 23692811
J Clin Oncol. 2008 May 10;26(14):2311-9
pubmed: 18390971
N Engl J Med. 2007 Nov 15;357(20):2040-8
pubmed: 18003960
J Clin Oncol. 2010 Feb 1;28(4):527-30
pubmed: 19841311
Stat Med. 1996 Feb 28;15(4):361-87
pubmed: 8668867
N Engl J Med. 2019 Oct 24;381(17):1632-1643
pubmed: 31566309
J Natl Cancer Inst. 2000 Feb 2;92(3):205-16
pubmed: 10655437
N Engl J Med. 2013 Sep 12;369(11):1023-34
pubmed: 24024839
J Gastrointest Oncol. 2016 Aug;7(4):499-505
pubmed: 27563438
Biochim Biophys Acta. 2010 Jan;1805(1):105-17
pubmed: 19931353
J Clin Oncol. 2007 May 1;25(13):1753-9
pubmed: 17470865
Clin Chem. 2013 Jan;59(1):38-40
pubmed: 23143327
Biochem Biophys Res Commun. 2015 Feb 27;458(1):52-6
pubmed: 25623536
Immunol Rev. 1995 Jun;145:91-122
pubmed: 7590832
Lancet Oncol. 2017 Mar;18(3):e143-e152
pubmed: 28271869
Nature. 2012 Jun 28;486(7404):532-6
pubmed: 22722830
J Natl Cancer Inst. 2008 May 21;100(10):698-711
pubmed: 18477802
Clin Cancer Res. 2013 Jul 15;19(14):3936-43
pubmed: 23743568
Nat Commun. 2016 Dec 08;7:13665
pubmed: 27929064
N Engl J Med. 2004 Jul 22;351(4):337-45
pubmed: 15269313
Lancet Oncol. 2013 Jan;14(1):29-37
pubmed: 23168366
Gastroenterology. 2015 Jan;148(1):77-87.e2
pubmed: 25280443

Auteurs

Fang-Shu Ou (FS)

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.

Daniel H Ahn (DH)

Division of Medical Oncology, Mayo Clinic, Phoenix, AZ 85259, USA.

Jesse G Dixon (JG)

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.

Axel Grothey (A)

West Cancer Center, University of Tennessee, Memphis, TN 38104, USA.

Yiyue Lou (Y)

Vertex Pharmaceuticals, Boston, MA 02210, USA.

Pashtoon M Kasi (PM)

Division of Hematology and Oncology, University of Iowa, Iowa City, IA 52242, USA.

Joleen M Hubbard (JM)

Department of Oncology, Mayo Clinic, Rochester, MN 55905, USA.

Eric Van Cutsem (E)

Department of Gastroenterology/Digestive Oncology, University Hospitals Gasthuisberg Leuven and KU Leuven, 3000 Leuven, Belgium.

Leonard B Saltz (LB)

Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Hans-Joachim Schmoll (HJ)

Department of Internal Medicine, Clinic for Internal Medicine IV, Martin-Luther-University Halle/Saale, 06120 Halle, Germany.

Richard M Goldberg (RM)

West Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.

Alan P Venook (AP)

Department of Medicine, The University of California San Francisco, San Francisco, CA 94143, USA.

Paulo Hoff (P)

Department of Clinical Oncology, University of Sao Paulo, Sao Paulo 05508-010, Brazil.

Jean-Yves Douillard (JY)

Department of Medical Oncology, University of Nantes Medical School, 44035 Nantes, France.

J Randolph Hecht (JR)

Ronald Reagan UCLA Medical Center, Los Angeles, CA 90095, USA.

Herbert Hurwitz (H)

Duke Cancer Institute, Duke University, Durham, NC 27710, USA.

Cornelis J A Punt (CJA)

Julius Center, University Medical Centre Utrecht, Utrecht University, 3584 CG Utrecht, The Netherlands.

Miriam Koopman (M)

Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Carsten Bokemeyer (C)

Department of Oncology, Hematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.

Charles S Fuchs (CS)

Yale Cancer Center, New Haven, CT 06510, USA.

Eduardo Diaz-Rubio (E)

Department of Oncology, Hospital Clínico San Carlos, 28040 Madrid, Spain.

Niall C Tebbutt (NC)

Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia.

Chiara Cremolini (C)

Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, 56126 Pisa, Italy.

Fairooz F Kabbinavar (FF)

Cardiff Oncology, San Diego, CA 92121, USA.

Tanios Bekaii-Saab (T)

Division of Medical Oncology, Mayo Clinic, Phoenix, AZ 85259, USA.

Benoist Chibaudel (B)

Department of Medical Oncology, Franco-British Institute, 92300 Levallois-Perret, France.

Takayuki Yoshino (T)

Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba 277-8577, Japan.

John Zalcberg (J)

School of Public Health and Preventative Medicine, Monash University, Melbourne, VIC 3004, Australia.

Richard A Adams (RA)

Centre for Trials Research, Cardiff University, Cardiff CF14 4YS, UK.
Velindre Cancer Center, Velindre NHS Trust, Cardiff CF14 2TL, UK.

Aimery de Gramont (A)

Department of Medical Oncology, Franco-British Institute, 92300 Levallois-Perret, France.

Qian Shi (Q)

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.

Classifications MeSH