TY - JOUR
T1 - Nivolumab for advanced melanoma
T2 - Pretreatment prognostic factors and early outcome markers during therapy
AU - Nakamura, Yoshio
AU - Kitano, Shigehisa
AU - Takahashi, Akira
AU - Tsutsumida, Arata
AU - Namikawa, Kenjiro
AU - Tanese, Keiji
AU - Abe, Takayuki
AU - Funakoshi, Takeru
AU - Yamamoto, Noboru
AU - Amagai, Masayuki
AU - Yamazaki, Naoya
PY - 2016
Y1 - 2016
N2 - Background: An anti-programmed cell death protein 1 monoclonal antibody, nivolumab, is one of the most effective drugs for advanced melanoma. Tumor cellderived or immune cell-derived markers and clinical predictors such as serum lactate dehydrogenase (LDH) and cutaneous adverse events, have already been described as prognostic factors for advanced melanoma treated with nivolumab. We sought to identify further clinical predictors that can be determined in routine clinical practice. Methods: We retrospectively analyzed clinical findings of 98 consecutive patients with unresectable stage III or IV melanoma treated with nivolumab, at the National Cancer Center Hospital or at Keio University Hospital, in Tokyo, Japan, between July 2014 and July 2016. These patients had been administered nivolumab at a dose of 2mg/kg every 3 weeks. Results: As for pretreatment prognostic factors, ECOG performance status (PS) ≥1, maximum tumor diameters of = 30mm, elevated LDH and elevated C-reactive protein were significantly associated with poor overall survival (OS) (hazard ratio [HR] 0.29 [P < 0.001], HR 0.40 [p = 0.003], HR 0.29 [P < 0.001], HR 0.42 [P = 0.004], respectively) on univariate analysis. Among these factors, PS and LDH were identified as independent variables by multivariate analysis. As for early markers examined during therapy, patients with absolute lymphocyte count (ALC) = 1000/μl (Week3: HR 0.40 [P = 0.004], Week6: HR 0.33 [P = 0.001]) and absolute neutrophil count (ANC) < 4000/μl (Week3: HR 0.46 [P = 0.014], Week6: HR 0.51 [P = 0.046]) had significantly better OS. Conclusion: ALC≥1000/μl and ANC < 4000/μl during treatment appear to be early markers associated with OS. Nivolumab might have minimal efficacy in patients with a massive tumor burden.
AB - Background: An anti-programmed cell death protein 1 monoclonal antibody, nivolumab, is one of the most effective drugs for advanced melanoma. Tumor cellderived or immune cell-derived markers and clinical predictors such as serum lactate dehydrogenase (LDH) and cutaneous adverse events, have already been described as prognostic factors for advanced melanoma treated with nivolumab. We sought to identify further clinical predictors that can be determined in routine clinical practice. Methods: We retrospectively analyzed clinical findings of 98 consecutive patients with unresectable stage III or IV melanoma treated with nivolumab, at the National Cancer Center Hospital or at Keio University Hospital, in Tokyo, Japan, between July 2014 and July 2016. These patients had been administered nivolumab at a dose of 2mg/kg every 3 weeks. Results: As for pretreatment prognostic factors, ECOG performance status (PS) ≥1, maximum tumor diameters of = 30mm, elevated LDH and elevated C-reactive protein were significantly associated with poor overall survival (OS) (hazard ratio [HR] 0.29 [P < 0.001], HR 0.40 [p = 0.003], HR 0.29 [P < 0.001], HR 0.42 [P = 0.004], respectively) on univariate analysis. Among these factors, PS and LDH were identified as independent variables by multivariate analysis. As for early markers examined during therapy, patients with absolute lymphocyte count (ALC) = 1000/μl (Week3: HR 0.40 [P = 0.004], Week6: HR 0.33 [P = 0.001]) and absolute neutrophil count (ANC) < 4000/μl (Week3: HR 0.46 [P = 0.014], Week6: HR 0.51 [P = 0.046]) had significantly better OS. Conclusion: ALC≥1000/μl and ANC < 4000/μl during treatment appear to be early markers associated with OS. Nivolumab might have minimal efficacy in patients with a massive tumor burden.
KW - Absolute lymphocyte count
KW - Absolute neutrophil count
KW - Early markers for outcome
KW - Metastatic melanoma
KW - Nivolumab
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U2 - 10.18632/oncotarget.12677
DO - 10.18632/oncotarget.12677
M3 - Article
C2 - 27764805
AN - SCOPUS:84998546948
SN - 1949-2553
VL - 7
SP - 77404
EP - 77415
JO - Oncotarget
JF - Oncotarget
IS - 47
ER -