Khan Khurum H, Goody Rebecca B, Hameed Hassan, Jalil Awais, Coyle Vicky M, McAleer James J A
Royal Marsden Hospital, London, UK.
Tumori. 2012 Sep-Oct;98(5):575-80. doi: 10.1177/030089161209800506.
. The incidence of malignant melanoma has risen steadily over recent decades. NCI data from 2005-2007 have suggested that 1.93% of individuals born today in the US will develop melanoma at some stage. Approximately 15% of patients with MM either present with metastatic disease or develop metastases during the course of their illness. Unfortunately, metastatic MM remains a challenge with limited treatment options, and median overall survival is 6-9 months.
We reviewed our data for the treatment of metastatic MM over a period of four years. Data from all patients with metastatic MM treated with systemic therapy without clinical trials from 2006 to 2009 were reviewed. Response rate was determined as per RECIST criteria.
Sixty four patients were treated with one or more lines of cytotoxic therapy. Median age was 62 years (range, 23-82) with 53% males. Primary site of the disease was the skin in 75%, mucosal in 12.5%, ocular in 9.4% and nodal with an occult primary in 3.1%. Visceral metastases were present in 75% of patients at the start of treatment, including pulmonary (39.6%) and hepatic (34.4%). All patients were screened for brain metastases, which were present in 26.5% of patients. ECOG performance status was 0 in 7.8%, 1 in 68.7%, 2 in 9.4% and undocumented in the remaining 14%. Patients without brain metastases received single agent DTIC as first line; those with brain metastases received temozolomide. Response rate was 7% for DTIC and 28% for temozolomide, with median progression-free survival of 2.4 and 3.2 months, respectively. Seven patients who received DTIC are alive on follow-up, 2 have ongoing stable disease post-DTIC at 41 months and 18 months. Second line therapy with vinblastine was given to 21 patients (32%), with a response rate of 9.5% and median progression-free survival of 3.4 months. Median overall survival from initiation of therapy was 7.7 months for DTIC and 3.6 months for patients with brain metastases receiving temozolomide. A performance status of 2 was associated with shorter median overall survival (2.0 months).
. Our results are comparable to published data. Malignant melanoma is a disease with rising incidence and limited treatment options. These patients are best treated in the context of clinical trials as new targeted therapies are promising as future strategies.
近几十年来,恶性黑色素瘤的发病率一直在稳步上升。美国国立癌症研究所2005 - 2007年的数据表明,如今在美国出生的人中有1.93%在某个阶段会患上黑色素瘤。大约15%的黑色素瘤患者在疾病过程中要么初诊时就有转移性疾病,要么会发生转移。不幸的是,转移性黑色素瘤仍然是一个挑战,治疗选择有限,总体中位生存期为6 - 9个月。
我们回顾了四年期间转移性黑色素瘤的治疗数据。对2006年至2009年接受全身治疗且未参加临床试验的所有转移性黑色素瘤患者的数据进行了回顾。根据RECIST标准确定缓解率。
64例患者接受了一种或多种细胞毒性治疗方案。中位年龄为62岁(范围23 - 82岁),男性占53%。疾病的原发部位皮肤占75%,黏膜占12.5%,眼部占9.4%,隐匿原发灶的淋巴结占3.1%。75%的患者在治疗开始时存在内脏转移,包括肺部(39.6%)和肝脏(34.4%)。所有患者均接受了脑转移筛查,26.5%的患者存在脑转移。东部肿瘤协作组(ECOG)体能状态评分为0的占7.8%,评分为1的占68.7%,评分为2的占9.4%,其余14%未记录。无脑转移的患者一线接受单药达卡巴嗪(DTIC)治疗;有脑转移的患者接受替莫唑胺治疗。DTIC的缓解率为7%,替莫唑胺为28%,无进展生存期的中位值分别为2.4个月和3.2个月。7例接受DTIC治疗的患者在随访中存活,2例在接受DTIC治疗后分别在41个月和18个月病情持续稳定。21例患者(32%)接受了长春花碱二线治疗,缓解率为9.5%,无进展生存期的中位值为3.4个月。从治疗开始计算,DTIC治疗患者的总体中位生存期为7.7个月,接受替莫唑胺治疗的脑转移患者为3.6个月。体能状态评分为2与较短的总体中位生存期(2.0个月)相关。
我们的结果与已发表的数据相当。恶性黑色素瘤是一种发病率不断上升且治疗选择有限的疾病。随着新的靶向治疗有望成为未来的治疗策略,这些患者最好在临床试验的背景下接受治疗。