Correlation of Morphological Appearance of Peritoneal Lesions at Laparotomy and Disease at Pathological Assessment in Patients Undergoing Cytoreductive Surgery for Peritoneal Malignancy: Results of Phase I of the PRECINCT Study in 707 Patients.

Cytoreductive surgery Morphology of peritoneal lesions Peritoneal cancer index Peritoneal metastases Peritoneal surface malignancy Surgical PCI

Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
26 Aug 2024
Historique:
received: 23 01 2024
accepted: 01 08 2024
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 26 8 2024
Statut: aheadofprint

Résumé

The PRECINCT (Pattern of peritoneal dissemination and REsponse to systemic Chemotherapy IN Common and uncommon peritoneal Tumors) is a prospective, multicenter, observational study. This report from phase I of PRECINCT outlines variations in recording the surgical peritoneal cancer index (sPCI) at experienced peritoneal malignancy centers and the incidence of pathologically confirmed disease in morphologically different peritoneal lesions (PL). The sPCI was recorded in a prespecified format that included the morphological appearance of PL. Six prespecified morphological terms were provided. The surgical and pathological findings were compared. From September 2020 to December 2021, 707 patients were enrolled at 10 centers. The morphological details are routinely recorded at two centers, structure bearing the largest nodule, and exact size of the largest tumor deposit in each region at four centers each. The most common morphological terms used were normal peritoneum in 3091 (45.3%), tumor nodules in 2607 (38.2%) and confluent disease in 786 (11.5%) regions. The incidence of pathologically confirmed disease was significantly higher in 'tumor nodules' with a lesion score of 2/3 compared with a lesion score of 1 (63.1% vs. 31.5%; p < 0.001). In patients receiving neoadjuvant chemotherapy, the incidence of pathologically confirmed disease did not differ significantly from those undergoing upfront surgery [751 (47.7%) and 532 (51.4%) respectively; p = 0.069]. The sPCI was recorded with heterogeneity at different centers. The incidence of pathologically confirmed disease was 49.2% in 'tumor nodules'. Frozen section could be used more liberally for these lesions to aid clinical decisions. A large-scale study involving pictorial depiction of different morphological appearances and correlation with pathological findings is indicated.

Sections du résumé

BACKGROUND BACKGROUND
The PRECINCT (Pattern of peritoneal dissemination and REsponse to systemic Chemotherapy IN Common and uncommon peritoneal Tumors) is a prospective, multicenter, observational study. This report from phase I of PRECINCT outlines variations in recording the surgical peritoneal cancer index (sPCI) at experienced peritoneal malignancy centers and the incidence of pathologically confirmed disease in morphologically different peritoneal lesions (PL).
METHODS METHODS
The sPCI was recorded in a prespecified format that included the morphological appearance of PL. Six prespecified morphological terms were provided. The surgical and pathological findings were compared.
RESULTS RESULTS
From September 2020 to December 2021, 707 patients were enrolled at 10 centers. The morphological details are routinely recorded at two centers, structure bearing the largest nodule, and exact size of the largest tumor deposit in each region at four centers each. The most common morphological terms used were normal peritoneum in 3091 (45.3%), tumor nodules in 2607 (38.2%) and confluent disease in 786 (11.5%) regions. The incidence of pathologically confirmed disease was significantly higher in 'tumor nodules' with a lesion score of 2/3 compared with a lesion score of 1 (63.1% vs. 31.5%; p < 0.001). In patients receiving neoadjuvant chemotherapy, the incidence of pathologically confirmed disease did not differ significantly from those undergoing upfront surgery [751 (47.7%) and 532 (51.4%) respectively; p = 0.069].
CONCLUSIONS CONCLUSIONS
The sPCI was recorded with heterogeneity at different centers. The incidence of pathologically confirmed disease was 49.2% in 'tumor nodules'. Frozen section could be used more liberally for these lesions to aid clinical decisions. A large-scale study involving pictorial depiction of different morphological appearances and correlation with pathological findings is indicated.

Identifiants

pubmed: 39187665
doi: 10.1245/s10434-024-16035-9
pii: 10.1245/s10434-024-16035-9
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

Références

Jacquet P, Sugarbaker PH. Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis. Cancer Treat Res. 1996;82:359–74. https://doi.org/10.1007/978-1-4613-1247-5_23 .
doi: 10.1007/978-1-4613-1247-5_23 pubmed: 8849962
Foster JM, Zhang C, Rehman S, Sharma P, Alexander HR. The contemporary management of peritoneal metastasis: a journey from the cold past of treatment futility to a warm present and a bright future. CA Cancer J Clin. 2023;73:49–71. https://doi.org/10.3322/caac.21749 .
doi: 10.3322/caac.21749 pubmed: 35969103
Faron M, Macovei R, Goéré D, Honoré C, Benhaim L, Elias D. Linear Relationship of Peritoneal Cancer Index and Survival in Patients with Peritoneal Metastases from Colorectal Cancer. Ann Surg Oncol. 2016;23(1):114–9. https://doi.org/10.1245/s10434-015-4627-8 .
doi: 10.1245/s10434-015-4627-8 pubmed: 26014158
Kusamura S, Torres Mesa PA, Cabras A, Baratti D, Deraco M. The Role of Ki-67 and Pre-cytoreduction Parameters in Selecting Diffuse Malignant Peritoneal Mesothelioma (DMPM) Patients for Cytoreductive Surgery (CRS) and Hyperthermic Intraperitoneal Chemotherapy (HIPEC). Ann Surg Oncol. 2016;23(5):1468–73. https://doi.org/10.1245/s10434-015-4962-9 .
doi: 10.1245/s10434-015-4962-9 pubmed: 26572754
Chia CS, You B, Decullier E, Vaudoyer D, Lorimier G, Abboud K, Bereder JM, Arvieux C, Boschetti G, Glehen O; BIG RENAPE Group. Patients with Peritoneal Carcinomatosis from Gastric Cancer Treated with Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy: Is Cure a Possibility? Ann Surg Oncol. 2016 Jun;23(6):1971-9. https://doi.org/10.1245/s10434-015-5081-3 .
Jónsdóttir B, Lomnytska M, Poromaa IS, et al. The Peritoneal Cancer Index is a Strong Predictor of Incomplete Cytoreductive Surgery in Ovarian Cancer. Ann Surg Oncol. 2021;28:244–51. https://doi.org/10.1245/s10434-020-08649-6 .
doi: 10.1245/s10434-020-08649-6 pubmed: 32472412
Demey K, Wolthuis A, de Buck van Overstraeten A, Fieuws S, Vandecaveye V, Van Cutsem E, D'Hoore A. External Validation of the Prognostic Nomogram (COMPASS) for Patients with Peritoneal Carcinomatosis of Colorectal Cancer. Ann Surg Oncol. 2017 Nov;24(12):3604-3608. https://doi.org/10.1245/s10434-017-6042-9 .
Enblad M, Ghanipour L, Cashin PH. Prognostic scores for colorectal cancer with peritoneal metastases treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy. Int J Hyperthermia. 2018;34(8):1390–5. https://doi.org/10.1080/02656736.2018.1464668 .
doi: 10.1080/02656736.2018.1464668 pubmed: 29695209
Quénet F, Elias D, Roca L, Goéré D, Ghouti L, Pocard M, Facy O, et al. Cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy versus cytoreductive surgery alone for colorectal peritoneal metastases (PRODIGE 7): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol. 2021;22(2):256–66. https://doi.org/10.1016/S1470-2045(20)30599-4 .
doi: 10.1016/S1470-2045(20)30599-4 pubmed: 33476595
Yonemura Y, Prabhu A, Sako S, Ishibashi H, Mizumoto A, Takao N, Ichinose M, Motoi S, Liu Y, Nishihara K, et al. Long Term Survival after Cytoreductive Surgery Combined with Perioperative Chemotherapy in Gastric Cancer Patients with Peritoneal Metastasis. Cancers. 2020;12(1):116. https://doi.org/10.3390/cancers12010116 .
doi: 10.3390/cancers12010116 pubmed: 31906405 pmcid: 7016959
Bhatt A, Kammar P, Mehta S, Damodaran D, Zaveri S, Patel MD, Sinukumar S, et al. Chasing Rainbows? the Possibility of “Cure” in Patients with Colorectal Peritoneal Metastases Undergoing Cytoreductive Surgery and HIPEC: a Retrospective Study by INDEPSO. Indian J Surg Oncol. 2019;10(Suppl 1):49–56. https://doi.org/10.1007/s13193-019-00879-9 .
doi: 10.1007/s13193-019-00879-9 pubmed: 30886494 pmcid: 6397129
Salo SAS, Lantto E, Robinson E, Myllärniemi M, Laaksonen S, Salo JA, Rantanen T, Ilonen I. Prognostic role of radiological peritoneal cancer index in malignant peritoneal mesothelioma: national cohort study. Sci Rep. 2020;10(1):13257. https://doi.org/10.1038/s41598-020-70044-8 .
doi: 10.1038/s41598-020-70044-8 pubmed: 32764701 pmcid: 7411064
Avesani G, Arshad M, Lu H, Fotopoulou C, Cannone F, Melotti R, Aboagye E, Rockall A. Radiological assessment of Peritoneal Cancer Index on preoperative CT in ovarian cancer is related to surgical outcome and survival. Radiol Med. 2020;125(8):770–6. https://doi.org/10.1007/s11547-020-01170-6 .
doi: 10.1007/s11547-020-01170-6 pubmed: 32239470
Bhatt A, Yonemura Y, Mehta S, Benzerdjeb N, Kammar P, Parikh L, et al. The Pathologic Peritoneal Cancer Index (PCI) Strongly Differs From the Surgical PCI in Peritoneal Metastases Arising From Various Primary Tumors. Ann Surg Oncol. 2020;27(8):2985–96. https://doi.org/10.1245/s10434-020-08234-x .
doi: 10.1245/s10434-020-08234-x pubmed: 32040698
de Boer NL, Brandt-Kerkhof ARM, Madsen EVE, Doukas M, Verhoef C, Burger JWA. The Accuracy of the Surgical Peritoneal Cancer Index in Patients with Peritoneal Metastases of Colorectal Cancer. Dig Surg. 2021;38(3):205–11. https://doi.org/10.1159/000513353 .
doi: 10.1159/000513353 pubmed: 33657551
Hynninen J, Lavonius M, Oksa S, Grénman S, Carpén O, Auranen A. Is perioperative visual estimation of intra-abdominal tumor spread reliable in ovarian cancer surgery after neoadjuvant chemotherapy? Gynecol Oncol. 2013;128(2):229–32. https://doi.org/10.1016/j.ygyno.2012.11.007 .
doi: 10.1016/j.ygyno.2012.11.007 pubmed: 23142076
Costantini B, Rosati A, Vargiu V, Gallitelli V, Di Ilio C, Moroni R, et al. Visual Peritoneal Evaluation of Residual Disease After Neoadjuvant Chemotherapy in Advanced Ovarian Cancer Patients: The VIPER Study. Ann Surg Oncol. 2023;30(4):2319–28. https://doi.org/10.1245/s10434-022-12861-x .
doi: 10.1245/s10434-022-12861-x pubmed: 36745255
Bhatt A, Rousset P, Baratti D, et al. Patterns of peritoneal dissemination and response to systemic chemotherapy in common and rare peritoneal tumours treated by cytoreductive surgery: study protocol of a prospective, multicentre, observational study BMJ Open 2021;11:e046819.  https://doi.org/10.1136/bmjopen-2020-046819
Bhatt A, Yonemura Y, Benzerdjeb N, Mehta S, Mishra S, Parikh L, et al. Pathological assessment of cytoreductive surgery specimens and its unexplored prognostic potential-a prospective multi-centric study. Eur J Surg Oncol. 2019;45(12):2398–404. https://doi.org/10.1016/j.ejso.2019.07.019 .
doi: 10.1016/j.ejso.2019.07.019 pubmed: 31337527
Villeneuve L, Thivolet A, Bakrin N, et al. A new Internet tool to report peritoneal malignancy extent. peritoneal malignancy stage evaluation (promise) application. Eur J Surg Oncol 2016;42:877–82. https://doi.org/10.1016/j.ejso.2016.03.015
Villeneuve L, Passot G, Glehen O, et al. The RENAPE observational registry: rationale and framework of the rare peritoneal tumors French patient registry. Orphanet J Rare Dis. 2017;12:37. https://doi.org/10.1186/s13023-017-0571-y .
doi: 10.1186/s13023-017-0571-y pubmed: 28212684 pmcid: 5316145
Bhatt A, Rousset P, Benzerdjeb N, et al. Prospective correlation of the radiological, surgical and pathological findings in patients undergoing cytoreductive surgery for colorectal peritoneal metastases: implications for the preoperative estimation of the peritoneal cancer index. Colorectal Dis. 2020;22:2123–32. https://doi.org/10.1111/codi.15368 .
doi: 10.1111/codi.15368 pubmed: 32940414
Schnelldorfer T, Castro J, Goldar-Najafi A, Liu L. Development of a Deep Learning System for Intra-Operative Identification of Cancer Metastases. Ann Surg. Epub 5 Apr 2024. https://doi.org/10.1097/SLA.0000000000006294 .
Boussedra S, Benoit L, Koual M, Bentivegna E, Nguyen-Xuan HT, Bats AS, et al. Fluorescence guided surgery to improve peritoneal cytoreduction in epithelial ovarian cancer: A systematic review of available data. Eur J Surg Oncol. 2022;48(6):1217–23. https://doi.org/10.1016/j.ejso.2022.02.022 .
doi: 10.1016/j.ejso.2022.02.022 pubmed: 35227555
El-Swaify ST, Laban M, Ali SH, et al. Can fluorescence-guided surgery improve optimal surgical treatment for ovarian cancer? A systematic scoping review of clinical studies. Int J Gynecol Cancer. 2023;33:549–61.
doi: 10.1136/ijgc-2022-003846 pubmed: 36707085
Paumgartner G, Probst P, Kraines R, Leevy CM. Kinetics of indocyanine green removal from the blood. Ann N Y Acad Sci. 1970170:134–147
Yonemura Y, Canbay E, Ishibashi H, Nishino E, Endou Y, Sako S, et al. 5-Aminolevulinic Acid Fluorescence in Detection of Peritoneal Metastases. Asian Pac J Cancer Prev. 2016;17(4):2271–5. https://doi.org/10.7314/apjcp.2016.17.4.2271 .
doi: 10.7314/apjcp.2016.17.4.2271 pubmed: 27221929
Hentzen JEKR, de Jongh SJ, Hemmer PHJ, van der Plas WY, van Dam GM, Kruijff S. Molecular fluorescence-guided surgery of peritoneal carcinomatosis of colorectal origin: a narrative review. J Surg Oncol. 2018;118(2):332–43. https://doi.org/10.1002/jso.25106 .
doi: 10.1002/jso.25106 pubmed: 29938400 pmcid: 6174973
Yonemura Y, Kawamura T, Bandou E, et al. The natural history of free cancer cells in the peritoneal cavity. In: S Gonzalez-Moreno, editor., et al., Advances in peritoneal surface oncology. Berlin: Springer-Verlag, Berlin Heidelberg; 2007. p. 11–23.
doi: 10.1007/978-3-540-30760-0_2
Deraco M, Kusamura S, Corbellini C, Guaglio M, Paviglianiti C, Baratti D. Treatment principles for peritoneal surface malignancies. Minerva Chir. 2016;71(2):124–45.
pubmed: 26847729

Auteurs

Aditi Bhatt (A)

Department of Surgical Oncology, Zydus Hospital, Ahmedabad, India.

Laurent Villeneuve (L)

Department of Clinical Research, Centre-Hospitalier Lyon-sud, Lyon, France.

Armando Sardi (A)

Department of Surgical Oncology, Mercy Medical Centre, Baltimore, MD, USA.

Amine Souadka (A)

Department of Surgical Oncology, National Cancer Institute, Rabat, Morocco.

Alison Buseck (A)

Department of Surgical Oncology, Mercy Medical Centre, Baltimore, MD, USA.

Brendan J Moran (BJ)

Department of Surgical Oncology, Peritoneal Malignancy Institute, Basingstoke, UK.

Basma El Khannousi (BE)

Department of Pathology, National Cancer Institute, Rabat, Morocco.

Carlos Gonzalez de Pedro (CG)

Department of Surgical Oncology, Hospital Universitario Virgen del Rocio, Sevilla, Spain.

Dario Baratti (D)

Department of Surgical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Danielle Biacchi (D)

Department of Surgical Oncology, Sapienza University of Rome, Rome, Italy.

David Morris (D)

Department of Surgical Oncology, St. George Hospital, Sydney, NSW, Australia.

Daniel Labow (D)

Department of Surgical Oncology, Mount Sinai Hospital, New York, NY, USA.

Edward A Levine (EA)

Section of Surgical Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Faheez Mohamed (F)

Department of Surgical Oncology, Peritoneal Malignancy Institute, Basingstoke, UK.

Gbadebo Adeleke (G)

Department of Pathology, Peritoneal Malignancy Institute, Basingstoke, UK.

Gaurav Goswami (G)

Department of Radiology, Zydus Hospital, Ahmedabad, India.

Isabelle Bonnefoy (I)

Department of Clinical Research, Centre-Hospitalier Lyon-sud, Lyon, France.

Katherine Cummins Perry (KC)

Section of Surgical Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Konstantinos I Votanopoulos (KI)

Section of Surgical Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Loma Parikh (L)

Department of Pathology, Zydus Hospital, Ahmedabad, India.

Marcello Deraco (M)

Department of Surgical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Mohammad Alyami (M)

Department of Surgical Oncology, King Khaled Hospital, Najran, Saudi Arabia.

Noah Cohen (N)

Department of Surgical Oncology, Mount Sinai Hospital, New York, NY, USA.

Nazim Benzerdjeb (N)

Department of Pathology, Centre Hospitalier Lyon-sud, Lyon, France.

Nehal Shah (N)

Department of Pathology, National Cancer Institute, Rabat, Morocco.

Nezha El Bahaoui (NE)

Department of Surgical Oncology, National Cancer Institute, Rabat, Morocco.

Nazanin Khajoueinejad (N)

Department of Surgical Oncology, Mount Sinai Hospital, New York, NY, USA.

Pascal Rousset (P)

Department of Radiology, Centre Hospitalier Lyon-sud, Lyon, France.

Perry Shen (P)

Section of Surgical Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Shoma Barat (S)

Department of Surgical Oncology, St. George Hospital, Sydney, NSW, Australia.

Sophia Stanford (S)

Department of Clinical Research, Peritoneal Malignancy Institute, Basingstoke, UK.

Selma Khouchoua (S)

Department of Radiology, National Cancer Institute, Rabat, Morocco.

Samantha Troob (S)

Department of Surgical Oncology, Mount Sinai Hospital, New York, NY, USA.

Sakina Shaikh (S)

Department of Surgical Oncology, Zydus Hospital, Ahmedabad, India.

Umut Sarpel (U)

Department of Surgical Oncology, Mount Sinai Hospital, New York, NY, USA.

Vadim Gushchin (V)

Department of Surgical Oncology, Mercy Medical Centre, Baltimore, MD, USA.

Vasanth Mark Samuel (VM)

Department of Surgical Oncology, Peritoneal Malignancy Institute, Basingstoke, UK.

Vahan Kepenekian (V)

Department of Surgical Oncology, Centre Hospitalier Lyon-sud, Lyon, Pierre Bénite, France.

Paolo Sammartino (P)

Department of Surgical Oncology, Sapienza University of Rome, Rome, Italy.

Olivier Glehen (O)

Department of Surgical Oncology, Centre Hospitalier Lyon-sud, Lyon, Pierre Bénite, France. olivier.glehen@chu-lyon.fr.

Classifications MeSH