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1. 复旦大学附属肿瘤医院骨软组织外科,复旦大学上海医学院肿瘤学系,上海 200032
2. 复旦大学附属肿瘤医院消化肿瘤内科,复旦大学上海医学院肿瘤学系,上海 200032
3. 复旦大学附属肿瘤医院头颈及神经内分泌肿瘤内科,复旦大学上海医学院肿瘤学系,上海 200032
Received:01 November 2022,
Revised:2022-12-12,
Published:30 December 2022
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Xinyi LIN, Wei SUN, Tu HU, et al. Multivariable prognostic analyses of Chinese acral and cutaneous melanoma after surgical treatment for the past five years in a single cancer center[J]. China Oncology, 2022, 32(12): 1158-1167.
Xinyi LIN, Wei SUN, Tu HU, et al. Multivariable prognostic analyses of Chinese acral and cutaneous melanoma after surgical treatment for the past five years in a single cancer center[J]. China Oncology, 2022, 32(12): 1158-1167. DOI: 10.19401/j.cnki.1007-3639.2022.12.003.
背景与目的:
中国及亚洲部分国家和地区的恶性黑色素瘤(malignant melanoma,MM)患者的预后显著低于欧美人群,主要是因为肢端型黑色素瘤(acral melanoma,AM)无论是在生物学行为、临床特征、预后以及药物的疗效(主要是免疫治疗)上都差于皮肤型黑色素瘤(cutaneous melanoma,CM)。近5年在MM外科治疗和药物辅助治疗选择方面发生了一定的变化。本文回顾性分析近5年单中心经手术治疗的AM及CM患者的生存变化和相关的独立预后因素。
方法:
对2017—2021年在复旦大学肿瘤医院黑色素瘤诊治中心接受外科治疗的MM患者进行回顾性研究。通过病史回顾和随访收集患者完整的基本信息、原发灶特点、淋巴灶转移特征和生存状态,剔除黏膜型、原发不明、随访时间短于6个月的病例。通过生存分析和多因素分析,探讨患者生存的差异和相关预后因素。
结果:
本研究共入组585例黑色素瘤患者,其中AM 397例,CM 188例。中位年龄59(19~89)岁,女性占54%。AM和CM在性别、年龄、原发灶位置、基因突变分布和辅助治疗等方面存在差异,但在Breslow深度、溃疡、淋巴结转移等肿瘤负荷因素上差异无统计学意义。中位随访时间为24个月,中位无疾病生存期为36个月,1、2年无复发生存期(relapse-free survival,RFS)分别为75.6%和61.2%。但两亚型的预后差异无统计学意义。AM中RFS的独立风险因素包括:原发灶溃疡(HR=2.265,95% CI:1.257~4.080),
NRAS
基因突变(HR=1.816,95% CI:1.211~2.725),较晚的N分期(N
1
、N
2
、N
3
相较N
0
的HR分别为1.850、4.085、4.191);保护因素为女性(HR=0.636,95% CI:0.433~0.933)和上肢原发灶(HR=0.259,95% CI:0.105~0.639)。CM中RFS的独立风险因素包括:原发灶溃疡(HR=4.073,95% CI:1.718~9.654),较晚的N分期(其中N
3
期的HR=5.482,95% CI:2.385~12.601)。
结论:
预后分析发现,原发灶的肿瘤负荷仍旧与CM和AM患者的预后密切相关,而
NRAS
基因的突变状态则提示AM预后更差。
Background and purpose:
The prognosis of malignant melanoma (MM) in China and Asia is significantly worse than that of European and American populations
mainly because acral melanoma (AM) is inferior to cutaneous melanoma (CM) in terms of biological behavior
clinical features
prognosis
and efficacy of drugs (mainly immunotherapy). Certain changes have occurred in the last 5 years in the choice of surgical and drug-adjuvant treatment for MM. This study retrospectively analyzed the survival outcomes of Chinese CM and AM patients after surgical treatment in a single cancer center for the past five years.
Methods:
Data of melanoma patients undergoing surgical treatment were retrospectively collected from 2017 to 2021 in Fudan University Shanghai Cancer Center. The basic clinical characteristics
pathological features
lymph node tumor burden and survival information were carefully collected from medical document. Patients with mucosal subtype
unknown primary sites
or follow-up less than 6 months were excluded. Survival analysis and multivariable Cox regression analysis were performed to explore prognosis and associated risk factors.
Results:
Totally 585 patients were enrolled
including 397 AM and 188 CM patients. The median age was 59 (19-89) years
and 54% were female. AM and CM patients differed in gender
age
primary tumor location
gene mutation distribution and adjuvant therapy
but not in tumor burden associated factors including the Breslow thickness
ulceration and lymph node involvment. The median follow-up time was 24 months
and the median relapse-free survival (mRFS) was 36 months
with 1-year and 2-year RFS of 75.6% and 61.2%
respectively. However
there was no statistically significant difference in prognosis between the two subtypes. Primary ulceration (HR=2.265
95% CI: 1.257-4.080)
NRAS
mutation (HR=1.816
95% CI: 1.211-2.725) and advanced N stage (HR of N
1
N
2
and N
3
versus N
0
were 1.850
4.085 and 4.191
respectively) were independent prognostic risk factors for RFS in AM; while the protective factors were female (HR=0.636
95% CI: 0.433-0.933) and upper extremity primary lesions (HR=0.259
95% CI: 0.105-0.639). Independent risk factors for RFS in CM included primary ulceration (HR=4.073
95% CI: 1.718-9.654)
and later N stage (HR=5.482
95% CI: 2.385-12.601 for N
3
stage).
Conclusion:
High tumor burden of primay lesion still deteriorates overall outcomes for both AM and CM
while harboring
NRAS
mutation might suggest even worse outcome for AM.
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