Prognostic and predictive role of elevated lactate dehydrogenase in patients with melanoma treated with immunotherapy and BRAF inhibitors: a systematic review and meta-analysis

被引:70
作者
Petrelli, Fausto [1 ]
Ardito, Raffaele [3 ]
Merelli, Barbara [4 ]
Lonati, Veronica [1 ]
Cabiddu, Mary [1 ]
Seghezzi, Silvia [2 ]
Barni, Sandro [1 ]
Ghidini, Antonio [5 ]
机构
[1] ASST Bergamo Ovest, Oncol Unit, Treviglio, BG, Italy
[2] ASST Bergamo Ovest, Nucl Med Unit, Treviglio, BG, Italy
[3] IRCCS Ctr Riferimento Oncol Basilicata CROB, Oncol Day Hosp, Vulture, PZ, Italy
[4] ASST Papa Giovanni XXIII, Oncol Unit, Bergamo, Italy
[5] Casa Cura Igea, Oncol Unit, Milan, Italy
关键词
BRAF inhibitors; immunotherapy; lactate dehydrogenase; melanoma; meta-analysis; prognosis; INVESTIGATOR-CHOICE CHEMOTHERAPY; TRAMETINIB COMBINATION TREATMENT; AMERICAN JOINT COMMITTEE; EXPANDED ACCESS PROGRAM; LONG-TERM SURVIVAL; STAGE IV MELANOMA; METASTATIC MELANOMA; POOLED ANALYSIS; OPEN-LABEL; COMBINED NIVOLUMAB;
D O I
10.1097/CMR.0000000000000520
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Levels of serum lactate dehydrogenase (LDH) are a recognized prognostic factor in malignant melanoma (MM). It is relevant to confirm its prognostic role in patients treated with targeted therapies [BRAF inhibitors (BRAFi) and MEK inhibitors (MEKi)] and immunotherapy (IT). Furthermore, its role as a predictive marker in patients treated with these drugs had still not been investigated. We performed an electronic search for studies reporting information on overall survival (OS) or progression-free survival (PFS) according to LDH levels and on their predictive effect in patients treated with targeted therapies (BRAFi and MEKi) and IT. Data were pooled using hazard ratios (HRs) for OS and HRs for PFS according to a fixed-effect or a random-effect model. For predictive analysys, effect of new agents versus standard therapy was evaluated in LDH high population. A total of 71 publications were retrieved for a total of 16 159 patients. Overall, elevated LDH levels were associated with an HR for OS of 1.72 [95% confidence interval (CI): 1.6-1.85; P<0.0001]. Similarly, HR for PFS was 1.83 (95% CI: 1.53-2.2; P<0.0001). In the LDH elevated subgroup, new agents improved OS significantly (HR: 0.71; 95% CI: 0.62-0.82; P<0.0001) and PFS (HR: 0.63; 95% CI: 0.55-0.72; P<0.0001). In advanced MM treated with IT or BRAFi +/- MEKi, elevated LDH level at baseline represents a poor prognostic factor. However, patients with increased LDH levels and treated with these drugs gain significant benefits in terms of PFS and OS.
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页码:1 / 12
页数:12
相关论文
共 89 条
[1]   Outcomes of Patients With Metastatic Melanoma Treated With Immunotherapy Prior to or After BRAF Inhibitors [J].
Ackerman, Allison ;
Klein, Oliver ;
McDermott, David F. ;
Wang, Wei ;
Ibrahim, Nageatte ;
Lawrence, Donald P. ;
Gunturi, Anasuya ;
Flaherty, Keith T. ;
Hodi, F. Stephen ;
Kefford, Richard ;
Menzies, Alexander M. ;
Atkins, Michael B. ;
Long, Georgina V. ;
Sullivan, Ryan J. .
CANCER, 2014, 120 (11) :1695-1701
[2]   Ipilimumab in the real world: the UK expanded access programme experience in previously treated advanced melanoma patients [J].
Ahmad, Saif S. ;
Qian, Wendi ;
Ellis, Sarah ;
Mason, Elaine ;
Khattak, Muhammad A. ;
Gupta, Avinash ;
Shaw, Heather ;
Quinton, Amy ;
Kovarikova, Jarmila ;
Thillai, Kiruthikah ;
Rao, Ankit ;
Board, Ruth ;
Nobes, Jenny ;
Dalgleish, Angus ;
Grumett, Simon ;
Maraveyas, Anthony ;
Danson, Sarah ;
Talbot, Toby ;
Harries, Mark ;
Marples, Maria ;
Plummer, Ruth ;
Kumar, Satish ;
Nathan, Paul ;
Middleton, Mark R. ;
Larkin, James ;
Lorigan, Paul ;
Wheater, Matthew ;
Ottensmeier, Christian H. ;
Corrie, Pippa G. .
MELANOMA RESEARCH, 2015, 25 (05) :432-442
[3]  
[Anonymous], 1997, J Clin Oncol, V15, P594
[4]  
[Anonymous], ONCOIMMUNOL
[5]  
[Anonymous], PATHOL ONCOL RES
[6]  
[Anonymous], 2016, NEWCASTLE OTTAWA SCA
[7]  
[Anonymous], ANN ONCOL
[8]   Safety of vemurafenib in patients with BRAF V600 mutated metastatic melanoma: the Spanish experience [J].
Arance, A. M. ;
Berrocal, A. ;
Lopez-Martin, J. A. ;
de la Cruz-Merino, L. ;
Soriano, V. ;
Martin Algarra, S. ;
Alonso, L. ;
Cerezuela, P. ;
La Orden, B. ;
Espinosa, E. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2016, 18 (11) :1147-1157
[9]   Ipilimumab 10 mg/kg versus ipilimumab 3 mg/kg in patients with unresectable or metastatic melanoma: a randomised, double-blind, multicentre, phase 3 trial [J].
Ascierto, Paolo A. ;
Del Vecchio, Michele ;
Robert, Caroline ;
Mackiewicz, Andrzej ;
Chiarion-Sileni, Vanna ;
Arance, Ana ;
Lebbe, Celeste ;
Bastholt, Lars ;
Hamid, Omid ;
Rutkowski, Piotr ;
McNeil, Catriona ;
Garbe, Claus ;
Loquai, Carmen ;
Dreno, Brigitte ;
Thomas, Luc ;
Grob, Jean-Jacques ;
Liszkay, Gabriella ;
Nyakas, Marta ;
Gutzmer, Ralf ;
Pikiel, Joanna ;
Grange, Florent ;
Hoeller, Christoph ;
Ferraresi, Virginia ;
Smylie, Michael ;
Schadendorf, Dirk ;
Mortier, Laurent ;
Svane, Inge Marie ;
Hennicken, Delphine ;
Qureshi, Anila ;
Maio, Michele .
LANCET ONCOLOGY, 2017, 18 (05) :611-622
[10]   Cobimetinib combined with vemurafenib in advanced BRAFV600-mutant melanoma (coBRIM): updated efficacy results from a randomised, double-blind, phase 3 trial [J].
Ascierto, Paolo A. ;
McArthur, Grant A. ;
Dreno, Brigitte ;
Atkinson, Victoria ;
Liszkay, Gabrielle ;
Di Giacomo, Anna Maria ;
Mandala, Mario ;
Demidov, Lev ;
Stroyakovskiy, Daniil ;
Thomas, Luc ;
de la Cruz-Merino, Luis ;
Dutriaux, Caroline ;
Garbe, Claus ;
Yan, Yibing ;
Wongchenko, Matthew ;
Chang, Ilsung ;
Hsu, Jessie J. ;
Koralek, Daniel O. ;
Rooney, Isabelle ;
Ribas, Antoni ;
Larkin, James .
LANCET ONCOLOGY, 2016, 17 (09) :1248-1260