Patterns of failure after immunotherapy with checkpoint inhibitors predict durable progression-free survival after local therapy for metastatic melanoma.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
24 07 2019
Historique:
received: 03 04 2019
accepted: 09 07 2019
entrez: 26 7 2019
pubmed: 26 7 2019
medline: 25 6 2020
Statut: epublish

Résumé

Checkpoint inhibitors (CPI) have revolutionized the treatment of metastatic melanoma, but most patients treated with CPI eventually develop progressive disease. Local therapy including surgery, ablation or stereotactic body radiotherapy (SBRT) may be useful to manage limited progression, but criteria for patient selection have not been established. Previous work has suggested progression-free survival (PFS) after local therapy is associated with patterns of immunotherapy failure, but this has not been studied in patients treated with CPI. We analyzed clinical data from patients with metastatic melanoma who were treated with antibodies against CTLA-4, PD-1 or PD-L1, either as single-agent or combination therapy, and identified those who had disease progression in 1 to 3 sites managed with local therapy. Patterns of CPI failure were designated by independent radiological review as growth of established metastases or appearance of new metastases. Local therapy for diagnosis, palliation or CNS metastases was excluded. Four hundred twenty-eight patients with metastatic melanoma received treatment with CPI from 2007 to 2018. Seventy-seven have ongoing complete responses while 69 died within 6 months of starting CPI; of the remaining 282 patients, 52 (18%) were treated with local therapy meeting our inclusion criteria. Local therapy to achieve no evidence of disease (NED) was associated with three-year progression-free survival (PFS) of 31% and five-year disease-specific survival (DSS) of 60%. Stratified by patterns of failure, patients with progression in established tumors had three-year PFS of 70%, while those with new metastases had three-year PFS of 6% (P = 0.001). Five-year DSS after local therapy was 93% versus 31%, respectively (P = 0.046). Local therapy for oligoprogression after CPI can result in durable PFS in selected patients. We observed that patterns of failure seen during or after CPI treatment are strongly associated with PFS after local therapy, and may represent a useful criterion for patient selection. This experience suggests there may be an increased role for local therapy in patients being treated with immunotherapy.

Sections du résumé

BACKGROUND
Checkpoint inhibitors (CPI) have revolutionized the treatment of metastatic melanoma, but most patients treated with CPI eventually develop progressive disease. Local therapy including surgery, ablation or stereotactic body radiotherapy (SBRT) may be useful to manage limited progression, but criteria for patient selection have not been established. Previous work has suggested progression-free survival (PFS) after local therapy is associated with patterns of immunotherapy failure, but this has not been studied in patients treated with CPI.
METHODS
We analyzed clinical data from patients with metastatic melanoma who were treated with antibodies against CTLA-4, PD-1 or PD-L1, either as single-agent or combination therapy, and identified those who had disease progression in 1 to 3 sites managed with local therapy. Patterns of CPI failure were designated by independent radiological review as growth of established metastases or appearance of new metastases. Local therapy for diagnosis, palliation or CNS metastases was excluded.
RESULTS
Four hundred twenty-eight patients with metastatic melanoma received treatment with CPI from 2007 to 2018. Seventy-seven have ongoing complete responses while 69 died within 6 months of starting CPI; of the remaining 282 patients, 52 (18%) were treated with local therapy meeting our inclusion criteria. Local therapy to achieve no evidence of disease (NED) was associated with three-year progression-free survival (PFS) of 31% and five-year disease-specific survival (DSS) of 60%. Stratified by patterns of failure, patients with progression in established tumors had three-year PFS of 70%, while those with new metastases had three-year PFS of 6% (P = 0.001). Five-year DSS after local therapy was 93% versus 31%, respectively (P = 0.046).
CONCLUSIONS
Local therapy for oligoprogression after CPI can result in durable PFS in selected patients. We observed that patterns of failure seen during or after CPI treatment are strongly associated with PFS after local therapy, and may represent a useful criterion for patient selection. This experience suggests there may be an increased role for local therapy in patients being treated with immunotherapy.

Identifiants

pubmed: 31340861
doi: 10.1186/s40425-019-0672-3
pii: 10.1186/s40425-019-0672-3
pmc: PMC6657062
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
CD274 protein, human 0
CTLA-4 Antigen 0
CTLA4 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

196

Subventions

Organisme : NCI NIH HHS
ID : K12 CA215110
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Références

J Clin Oncol. 1999 Jul;17(7):2105-16
pubmed: 10561265
Semin Radiat Oncol. 2006 Apr;16(2):131-5
pubmed: 16564448
Clin Cancer Res. 2009 Dec 1;15(23):7412-20
pubmed: 19934295
N Engl J Med. 2010 Aug 19;363(8):711-23
pubmed: 20525992
Clin Cancer Res. 2011 Jul 1;17(13):4550-7
pubmed: 21498393
N Engl J Med. 2011 Jun 2;364(22):2119-27
pubmed: 21631324
N Engl J Med. 2011 Jun 30;364(26):2517-26
pubmed: 21639810
Clin Cancer Res. 2012 Apr 1;18(7):2039-47
pubmed: 22271879
Ann Surg Oncol. 2012 Aug;19(8):2547-55
pubmed: 22648554
J Neurosurg. 2012 Aug;117(2):227-33
pubmed: 22702482
Nat Genet. 2012 Sep;44(9):1006-14
pubmed: 22842228
Ann Surg Oncol. 2013 Sep;20(9):3106-11
pubmed: 23681603
N Engl J Med. 2013 Jul 11;369(2):122-33
pubmed: 23724867
Ann Surg Oncol. 2013 Oct;20(11):3618-25
pubmed: 23838913
N Engl J Med. 1990 Feb 22;322(8):494-500
pubmed: 2405271
N Engl J Med. 2015 Jul 2;373(1):23-34
pubmed: 26027431
J Clin Oncol. 2016 Jul 10;34(20):2389-97
pubmed: 27217459
Ann Surg Oncol. 2017 Jan;24(1):135-141
pubmed: 27638681
Lancet Oncol. 2016 Dec;17(12):1672-1682
pubmed: 27789196
J Clin Oncol. 2017 Jan 10;35(2):226-235
pubmed: 28056206
N Engl J Med. 2017 Oct 5;377(14):1345-1356
pubmed: 28889792
JAMA Oncol. 2018 Jan 11;4(1):e173501
pubmed: 28973074
Ann Surg Oncol. 2017 Dec;24(13):3991-4000
pubmed: 29019177
CA Cancer J Clin. 2017 Nov;67(6):472-492
pubmed: 29028110
J Clin Oncol. 2019 Jan 1;37(1):52-60
pubmed: 30407895
J Surg Oncol. 2019 Jan;119(2):249-261
pubmed: 30561079
N Engl J Med. 1988 Dec 22;319(25):1676-80
pubmed: 3264384
Surgery. 1993 Apr;113(4):389-94
pubmed: 8456394
Cancer J Sci Am. 1998 Mar-Apr;4(2):86-93
pubmed: 9532410

Auteurs

Nicholas D Klemen (ND)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA.

Melinda Wang (M)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA.

Paul L Feingold (PL)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA.

Kirsten Cooper (K)

Department of Radiology, Yale School of Medicine, New Haven, CT, USA.

Sabrina N Pavri (SN)

Orlando Health Aesthetic and Reconstructive Surgery Institute, Orlando, FL, USA.

Dale Han (D)

Division of Surgical Oncology, Oregon Health and Science University, Portland, OR, USA.

Frank C Detterbeck (FC)

Section of Thoracic Surgery, Yale School of Medicine, New Haven, CT, USA.

Daniel J Boffa (DJ)

Section of Thoracic Surgery, Yale School of Medicine, New Haven, CT, USA.

Sajid A Khan (SA)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA.

Kelly Olino (K)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA.

James Clune (J)

Section of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, USA.

Stephan Ariyan (S)

Section of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, USA.

Ronald R Salem (RR)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA.

Sarah A Weiss (SA)

Section of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.

Harriet M Kluger (HM)

Section of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.

Mario Sznol (M)

Section of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.

Charles Cha (C)

Section of Surgical Oncology, Yale School of Medicine, 20 Park Street, New Haven, CT, 06519, USA. charles.cha@yale.edu.

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