Literature DB >> 1642409

Treatment of stage IV malignant melanoma with dacarbazine, carmustine, cisplatin, and tamoxifen regimens: a University of South Florida and H. Lee Moffitt Melanoma Center Study.

H I Saba1, C W Cruse, K E Wells, C J Klein, D S Reintgen.   

Abstract

Fourteen consecutive patients with stage IV metastatic melanoma with measurable disease were treated between January 1989 and August 1990 with combination chemotherapy. The chemotherapy regimen (DBPT) included dacarbazine (DTIC) 200 mg/m2/i.v. on days 1 through 3, carmustine (BCNU) 150 mg/m2/i.v. on day 1, cisplatin 25 mg/m2/i.v. on days 1 through 3, and tamoxifen citrate 10 mg p.o. twice daily. This cycle was repeated every 4 weeks. BCNU was given every other cycle. A total of six cycles of chemotherapy were delivered. Patients were then restaged to assess the response. Six concurrent patients during the study period did not elect to undergo chemotherapeutic approach and served as control subjects. When evaluated at 300 days of follow-up, 4 patients had response (3 complete response and 1 partial response), 3 had stable disease, and 7 showed progression. At 300 days of evaluation after chemotherapy, survival appeared significantly increased between treated and nontreated groups, that is, 48% in the chemotherapy group versus 27% in the control group (p = 0.03). Actuarial survival was significantly increased between those who responded to chemotherapy versus the nonresponders. At 300 days follow-up, survival was at 83% in the responders and 22% in nonresponders (p = 0.0002). This study shows that in stage IV disease, systemic chemotherapy appears to make a difference in survival. Attempts to discover better chemotherapy regimens to improve response in patients with stage IV malignant melanoma should continue to be rewarded.

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Year:  1992        PMID: 1642409     DOI: 10.1097/00000637-199201000-00017

Source DB:  PubMed          Journal:  Ann Plast Surg        ISSN: 0148-7043            Impact factor:   1.539


  6 in total

Review 1.  Primary malignant melanoma of the esophagus: long-term survival following pre- and postoperative adjuvant hormone/chemotherapy.

Authors:  Hirokazu Uetsuka; Yoshio Naomoto; Toshiya Fujiwara; Yasuhiro Shirakawa; Hirofumi Noguchi; Tomoki Yamatsuji; Minoru Haisa; Junji Matsuoka; Mehmet Gunduz; Kaiyo Takubo; Noriaki Tanaka
Journal:  Dig Dis Sci       Date:  2004-10       Impact factor: 3.199

Review 2.  Current status of primary malignant melanoma of the esophagus: clinical features, pathology, management and prognosis.

Authors:  Yoshimi Iwanuma; Natsumi Tomita; Takayuki Amano; Fuyumi Isayama; Masahiko Tsurumaru; Takuo Hayashi; Yoshiaki Kajiyama
Journal:  J Gastroenterol       Date:  2011-11-03       Impact factor: 7.527

Review 3.  The history and future of chemotherapy for melanoma.

Authors:  Arvin S Yang; Paul B Chapman
Journal:  Hematol Oncol Clin North Am       Date:  2009-06       Impact factor: 3.722

4.  Solitary pulmonary metastasis from primary melanoma of the oesophagus 5 years after resection of the primary tumor.

Authors:  Gianlorenzo Dionigi; Francesca Rovera; Luigi Boni; Andrea Imperatori; Renzo Dionigi
Journal:  World J Surg Oncol       Date:  2006-04-13       Impact factor: 2.754

5.  The effect of tamoxifen and cisplatin on the disease-free and overall survival of patients with high risk malignant melanoma.

Authors:  E F McClay; M E McClay; L Monroe; P L Baron; D J Cole; P H O'Brien; J S Metcalf; J C Maize
Journal:  Br J Cancer       Date:  2000-07       Impact factor: 7.640

6.  Drug-selected population in melanoma A2058 cells as melanoma stem-like cells retained angiogenic features - the potential roles of heparan-sulfate binding ANGPTL4 protein.

Authors:  Chia-Yu Shih; Yu-Che Cheng; ChiaoHui Hsieh; TingTing Tseng; ShihSheng Jiang; Shao-Chen Lee
Journal:  Aging (Albany NY)       Date:  2020-11-10       Impact factor: 5.682

  6 in total

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