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转移性黑色素瘤的全身化疗。

Systemic chemotherapy for metastatic melanoma.

作者信息

Mc Clay E F, Mastrangelo M J

机构信息

Division of Medical Oncology, Jefferson Medical College, Philadelphia.

出版信息

Semin Oncol. 1988 Dec;15(6):569-77.

PMID:2462747
Abstract

The treatment of patients with metastatic melanoma remains a difficult problem. It is clear that more effective agents need to be developed. No single agent in conventional doses has been shown to be more effective than DTIC alone. The results obtained with detrorubicin in untreated patients are encouraging, but need further confirmation. If confirmed, combination regimens incorporating detrorubicin should be studied. Further experience is needed with high-dose cisplatin before it can be recommended for broader clinical use. Recent experience with the 4 drug combination of DTIC, BCNU, cisplatin, and tamoxifen is encouraging. The objective response rate is approximately 50% and patients with visceral disease have demonstrated regressions. CRs are not uncommon with occasional patients exhibiting durable remissions for as long as 3 years. An added benefit is that this regimen is well tolerated by most patients making it technically easy to administer. Finally, the role of interferon needs further study. The response rate to interferon alfa-2a is reasonably well defined at about 20%. Combinations of chemotherapeutic agents and interferons have only begun to be evaluated but the preliminary data are interesting.

摘要

转移性黑色素瘤患者的治疗仍然是一个难题。显然,需要研发更有效的药物。常规剂量下,没有单一药物被证明比达卡巴嗪(DTIC)更有效。在未经治疗的患者中使用去甲柔红霉素所获得的结果令人鼓舞,但需要进一步证实。如果得到证实,应研究包含去甲柔红霉素的联合治疗方案。在高剂量顺铂被推荐用于更广泛的临床应用之前,还需要更多的经验。近期使用达卡巴嗪、卡莫司汀(BCNU)、顺铂和他莫昔芬的四联药物组合的经验令人鼓舞。客观缓解率约为50%,内脏疾病患者已出现病情缓解。完全缓解(CR)并不罕见,偶尔有患者可表现出长达3年的持久缓解。另一个好处是,大多数患者对该方案耐受性良好,使其在技术上易于给药。最后,干扰素的作用需要进一步研究。对α-2a干扰素的缓解率已得到较为明确的界定,约为20%。化疗药物与干扰素的联合应用才刚刚开始评估,但初步数据很有意思。

相似文献

1
Systemic chemotherapy for metastatic melanoma.转移性黑色素瘤的全身化疗。
Semin Oncol. 1988 Dec;15(6):569-77.
2
Systemic therapy in melanoma.黑色素瘤的全身治疗
Semin Surg Oncol. 1998 Jun;14(4):319-27. doi: 10.1002/(sici)1098-2388(199806)14:4<319::aid-ssu8>3.0.co;2-5.
3
Current therapy for malignant melanoma.恶性黑色素瘤的当前治疗方法。
Semin Oncol. 1989 Feb;16(1 Suppl 1):34-44.
4
The treatment of metastatic melanoma with chemotherapy and biologics.采用化疗和生物制剂治疗转移性黑色素瘤。
Curr Opin Oncol. 1997 Mar;9(2):205-13. doi: 10.1097/00001622-199703000-00016.
5
[Chemo-/immunotherapy in advanced malignant melanoma: carboplatin and DTIC or cisplatin, dtic, bcnu and tamoxifen followed by immunotherapy with interleukin 2 and interferon alpha-2a].[晚期恶性黑色素瘤的化疗/免疫疗法:卡铂与达卡巴嗪联合或顺铂、达卡巴嗪、卡莫司汀及他莫昔芬,随后采用白细胞介素2和干扰素α-2a进行免疫治疗]
Med Klin (Munich). 1996 Apr 12;91 Suppl 3:44-9.
6
The treatment of disseminated malignant melanoma with special reference to the role of interferons, vinca alkaloids and tamoxifen.播散性恶性黑色素瘤的治疗,特别提及干扰素、长春花生物碱和他莫昔芬的作用。
Cancer Treat Rev. 1997 Jan;23(1):17-34. doi: 10.1016/s0305-7372(97)90018-9.
7
Dacarbazine-based chemotherapy for metastatic melanoma: thirty-year experience overview.基于达卡巴嗪的转移性黑色素瘤化疗:三十年经验概述。
J Exp Clin Cancer Res. 2000 Mar;19(1):21-34.
8
Interferon alfa-2a and interleukin-2 with or without cisplatin in metastatic melanoma: a randomized trial of the European Organization for Research and Treatment of Cancer Melanoma Cooperative Group.
J Clin Oncol. 1997 Jul;15(7):2579-88. doi: 10.1200/JCO.1997.15.7.2579.
9
Multicenter randomized trial of dacarbazine alone or in combination with two different doses and schedules of interferon alfa-2a in the treatment of advanced melanoma.达卡巴嗪单药或联合两种不同剂量及给药方案的α-2a干扰素治疗晚期黑色素瘤的多中心随机试验
J Clin Oncol. 1994 Apr;12(4):806-11. doi: 10.1200/JCO.1994.12.4.806.
10
Rationale for intergroup trial E-3695 comparing concurrent biochemotherapy with cisplatin, vinblastine, and DTIC alone in patients with metastatic melanoma.比较顺铂、长春碱和达卡巴嗪联合生物化疗与单独使用这些药物治疗转移性黑色素瘤患者的E-3695组间试验原理
Cancer J Sci Am. 2000 Feb;6 Suppl 1:S15-20.

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Malignant melanoma metastasis in the gallbladder. A case report of an unusual metastatic site.恶性黑色素瘤转移至胆囊。一例罕见转移部位的病例报告。
Int J Surg Case Rep. 2020;75:372-375. doi: 10.1016/j.ijscr.2020.09.116. Epub 2020 Sep 19.
2
Tanapoxvirus lacking the 15L gene inhibits melanoma cell growth in vitro by inducing interferon-λ1 release.缺失15L基因的塔纳痘病毒通过诱导干扰素-λ1释放来抑制黑色素瘤细胞的体外生长。
Virus Genes. 2017 Jun;53(3):477-482. doi: 10.1007/s11262-017-1434-2. Epub 2017 Feb 10.
3
Sequential administration of varying doses of dacarbazine and fotemustine in advanced malignant melanoma.
在晚期恶性黑色素瘤中序贯给予不同剂量的达卡巴嗪和福莫司汀。
Br J Cancer. 1993 Jun;67(6):1356-60. doi: 10.1038/bjc.1993.251.
4
Combination of highly purified human leukocyte interferon alpha and 13-cis-retinoic acid for the treatment of metastatic melanoma.高纯度人白细胞干扰素α与13-顺式维甲酸联合用于治疗转移性黑色素瘤。
Cancer Immunol Immunother. 1995 Mar;40(3):157-64. doi: 10.1007/BF01517347.
5
Intermittent interferon and polychemotherapy in metastatic melanoma.转移性黑色素瘤的间歇性干扰素与多药化疗
J Cancer Res Clin Oncol. 1995;121(3):175-80. doi: 10.1007/BF01198100.
6
A phase II trial of piroxantrone in disseminated malignant melanoma. A Southwest Oncology Group study.吡柔比星治疗播散性恶性黑色素瘤的II期试验。一项西南肿瘤协作组的研究。
Invest New Drugs. 1995;13(1):83-7. doi: 10.1007/BF02614226.
7
Dacarbazine (DTIC) and human recombinant interferon alpha 2a (Roferon) in the treatment of disseminated malignant melanoma.达卡巴嗪(DTIC)和重组人干扰素α2a(罗扰素)治疗播散性恶性黑色素瘤
Br J Cancer. 1990 Dec;62(6):1006-7. doi: 10.1038/bjc.1990.427.
8
A randomised phase II study of carmustine alone or in combination with tumour necrosis factor in patients with advanced melanoma.一项关于卡莫司汀单独使用或与肿瘤坏死因子联合用于晚期黑色素瘤患者的随机II期研究。
Cancer Chemother Pharmacol. 1992;30(1):73-6. doi: 10.1007/BF00686489.