Your browser doesn't support javascript.
loading
Bridging therapeutic opportunities: a survey by the Italian molecular tumor board workgroup of Alliance Against Cancer.
Ciliberto, Gennaro; Canfora, Marco; Terrenato, Irene; Agnoletto, Chiara; Agustoni, Francesco; Amoroso, Loredana; Baldassarre, Gustavo; Curigliano, Giuseppe; Delmonte, Angelo; De Luca, Antonella; Fiorentino, Michelangelo; Gregorc, Vanesa; Ibrahim, Toni; Lazzari, Chiara; Mastronuzzi, Angela; Pronzato, Paolo; Santoro, Armando; Scambia, Giovanni; Tommasi, Stefania; Vingiani, Andrea; Giacomini, Patrizio; De Maria, Ruggero.
Afiliação
  • Ciliberto G; IRCCS Istituto Nazionale Tumori Regina Elena, Rome, Italy.
  • Canfora M; IRCCS Istituto Nazionale Tumori Regina Elena, Rome, Italy.
  • Terrenato I; IRCCS Istituto Nazionale Tumori Regina Elena, Rome, Italy.
  • Agnoletto C; ROV, Istituto Oncologico Veneto IOV-IRCCS, Padua, Italy.
  • Agustoni F; Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Amoroso L; IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Baldassarre G; Centro Di Riferimento Oncologico Di Aviano IRCCS, Aviano, Italy.
  • Curigliano G; Istituto Europeo Di Oncologia IRCCS, Milan, Italy.
  • Delmonte A; Dipartimento Di Oncologia Ed Emato-Oncologia, Università La Statale Di Milano, Milan, Italy.
  • De Luca A; Istituto Romagnolo Per Lo Studio Dei Tumori "Dino Amadori" - IRST IRCCS, Meldola, Italy.
  • Fiorentino M; Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, Italy.
  • Gregorc V; IRCCS Policlinico Sant' Orsola-Malpighi, Bologna, Italy.
  • Ibrahim T; Istituto Di Candiolo - FPO (Fondazione del Piemonte Per L'Oncologia) IRCCS, Candiolo, Italy.
  • Lazzari C; IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
  • Mastronuzzi A; IRCCS Ospedale San Raffaele, Milan, Italy.
  • Pronzato P; IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy.
  • Santoro A; IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Scambia G; IRCCS Humanitas Research Hospital-Humanitas Cancer Center, Rozzano, Milan, Italy.
  • Tommasi S; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Vingiani A; Dipartimento Di Ostetricia E Ginecologia, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Giacomini P; Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • De Maria R; IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
J Exp Clin Cancer Res ; 41(1): 305, 2022 Oct 17.
Article em En | MEDLINE | ID: mdl-36245005
ABSTRACT

BACKGROUND:

Molecular tumor boards (MTBs) match molecular alterations with targeted anticancer drugs upon failure of the available therapeutic options. Special and local needs are most likely to emerge through the comparative analysis of MTB networks, but these are rarely reported. This manuscript summarizes the state-of-art of 16 active Italian MTBs, as it emerges from an online survey curated by Alliance Against Cancer (ACC). MAIN TEXT Most MTBs (13/16) are exclusively supported through local Institutional grants and meet regularly. All but one adopts a fully virtual or a mixed face-to-face/virtual calling/attendance meeting model. It appears that the ACC MTB initiative is shaping a hub-and-spoke virtual MTB network reminiscent of non-redundant, cost-effective healthcare organization models. Unfortunately, public awareness of MTB opportunities presently remains insufficient. Only one center has a website. Dedicated e-mail addresses are for the exclusive use of the MTB staff. More than half of ACC members consider a miscellanea of most or all solid and hematological malignancies, and more than one-third consider neoplasms arising at any anatomical location. The average number of Staff Members in MTBs is 9. More than 10 staff members simultaneously attend MTB meetings in 13 MTBs. A medical oncologist is invariably present and is in charge of introducing the clinical case either with (45%) or without previous discussion in organ-specific multidisciplinary Boards. All but two MTBs take charge of not only patients with no standard-of-care (SoC) therapy option, but also cases receiving NGS profiling in SoC settings, implying a larger number of yearly cases. All MTBs run targeted NGS panels. Three run whole-exome and/or RNAseq approaches. ESCAT-ESMO and/or Onco-KB levels of evidence are similarly used for diagnostic reporting. Most MTBs (11) provide a written diagnostic report within 15 days. Conclusions are invariably communicated to the patient by the medical oncologist.

CONCLUSIONS:

MTB networking is crucial not only for molecular diagnosis and therapy assignment, but also for healthcare governance. Survey results show that MTBs review therapeutic opportunities at the crossover between standard-of-care with off-label, the former task being much beyond their scope. Societal and scientific implications of this beyond-the-scope MTB function may be relevant for healthcare in Italy and abroad.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Qualitative_research Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Qualitative_research Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article