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Efficacy of immune checkpoint inhibitors for the treatment of advanced melanoma in patients with concomitant chronic lymphocytic leukemia.
Cass, S H; Tobin, J W D; Seo, Y D; Gener-Ricos, G; Keung, E Z; Burton, E M; Davies, M A; McQuade, J L; Lazar, A J; Mason, R; Millward, M; Sandhu, S; Khoo, C; Warburton, L; Guerra, V; Haydon, A; Dearden, H; Menzies, A M; Carlino, M S; Smith, J L; Mollee, P; Burgess, M; Mapp, S; Keane, C; Atkinson, V; Parikh, S A; Markovic, S N; Ding, W; Call, T G; Hampel, P J; Long, G V; Wargo, J A; Ferrajoli, A.
Afiliação
  • Cass SH; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Tobin JWD; Haematology Department, Princess Alexandra Hospital, Woolloongabba; University of Queensland, Brisbane, Australia.
  • Seo YD; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Gener-Ricos G; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston.
  • Keung EZ; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Burton EM; Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
  • Davies MA; Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
  • McQuade JL; Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
  • Lazar AJ; Departments of Pathology and Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Mason R; Gold Coast University Hospital, Southport.
  • Millward M; University of Western Australia, Perth.
  • Sandhu S; Peter Macallum Cancer Centre, Melbourne.
  • Khoo C; Peter Macallum Cancer Centre, Melbourne.
  • Warburton L; Fiona Stanley Hospital, Perth; Edith Cowan University, Joondalup; Future Health Research and Innovation Fund/Raine Clinician Research Fellowship.
  • Guerra V; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston.
  • Haydon A; Alfred Hospital, Melbourne.
  • Dearden H; Melanoma Institute Australia, The University of Sydney, Sydney.
  • Menzies AM; Melanoma Institute Australia, The University of Sydney, Sydney; Faculty of Medicine and Health, The University of Sydney, Sydney; The University of Sydney Charles Perkins Centre, Sydney; The University of Sydney Royal North Shore and Mater Hospitals, Sydney.
  • Carlino MS; Melanoma Institute Australia, The University of Sydney, Sydney; Westmead Hospital, Sydney, Australia.
  • Smith JL; Westmead Hospital, Sydney, Australia.
  • Mollee P; Haematology Department, Princess Alexandra Hospital, Woolloongabba; University of Queensland, Brisbane, Australia.
  • Burgess M; Haematology Department, Princess Alexandra Hospital, Woolloongabba; University of Queensland, Brisbane, Australia.
  • Mapp S; Haematology Department, Princess Alexandra Hospital, Woolloongabba; University of Queensland, Brisbane, Australia.
  • Keane C; Haematology Department, Princess Alexandra Hospital, Woolloongabba; University of Queensland, Brisbane, Australia.
  • Atkinson V; Haematology Department, Princess Alexandra Hospital, Woolloongabba; University of Queensland, Brisbane, Australia.
  • Parikh SA; Mayo Clinic, Rochester, USA.
  • Markovic SN; Mayo Clinic, Rochester, USA.
  • Ding W; Mayo Clinic, Rochester, USA.
  • Call TG; Mayo Clinic, Rochester, USA.
  • Hampel PJ; Mayo Clinic, Rochester, USA.
  • Long GV; Melanoma Institute Australia, The University of Sydney, Sydney; Faculty of Medicine and Health, The University of Sydney, Sydney; The University of Sydney Charles Perkins Centre, Sydney; The University of Sydney Royal North Shore and Mater Hospitals, Sydney.
  • Wargo JA; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA. Electronic address: jwargo@mdanderson.org.
  • Ferrajoli A; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston.
Ann Oncol ; 34(9): 796-805, 2023 09.
Article em En | MEDLINE | ID: mdl-37414216
ABSTRACT

BACKGROUND:

Immune checkpoint inhibitors (ICIs) have revolutionized the management of advanced melanoma (AM). However, data on ICI effectiveness have largely been restricted to clinical trials, thereby excluding patients with co-existing malignancies. Chronic lymphocytic leukemia (CLL) is the most prevalent adult leukemia and is associated with increased risk of melanoma. CLL alters systemic immunity and can induce T-cell exhaustion, which may limit the efficacy of ICIs in patients with CLL. We, therefore, sought to examine the efficacy of ICI in patients with these co-occurring diagnoses. PATIENTS AND

METHODS:

In this international multicenter study, a retrospective review of clinical databases identified patients with concomitant diagnoses of CLL and AM treated with ICI (US-MD Anderson Cancer Center, N = 24; US-Mayo Clinic, N = 15; AUS, N = 19). Objective response rates (ORRs), assessed by RECIST v1.1, and survival outcomes [overall survival (OS) and progression-free survival (PFS)] among patients with CLL and AM were assessed. Clinical factors associated with improved ORR and survival were explored. Additionally, ORR and survival outcomes were compared between the Australian CLL/AM cohort and a control cohort of 148 Australian patients with AM alone.

RESULTS:

Between 1997 and 2020, 58 patients with concomitant CLL and AM were treated with ICI. ORRs were comparable between AUS-CLL/AM and AM control cohorts (53% versus 48%, P = 0.81). PFS and OS from ICI initiation were also comparable between cohorts. Among CLL/AM patients, a majority were untreated for their CLL (64%) at the time of ICI. Patients with prior history of chemoimmunotherapy treatment for CLL (19%) had significantly reduced ORRs, PFS, and OS.

CONCLUSIONS:

Our case series of patients with concomitant CLL and melanoma demonstrate frequent, durable clinical responses to ICI. However, those with prior chemoimmunotherapy treatment for CLL had significantly worse outcomes. We found that CLL disease course is largely unchanged by treatment with ICI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Melanoma Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans País/Região como assunto: Oceania Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Melanoma Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans País/Região como assunto: Oceania Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos