Literature DB >> 1561807

Active immunotherapy with viral lysates of micrometastases following surgical removal of high risk melanoma.

P Hersey1.   

Abstract

Patients who develop lymph node metastases from melanoma are known to be at risk of developing further recurrences from melanoma following surgical removal of lymph node metastases. The purpose of the present study was to examine whether immunization over a 2 year period with a vaccine made from vaccinia viral lysates of an allogeneic melanoma cell (VMCL), following surgical removal of lymph node metastases, would help prevent the development of distant metastases and improve survival from the disease. Eighty patients treated with VMCL alone and followed for a minimum of 5.5 years had improved survival compared to a historical control group of 151 patients and a concurrent non-randomized group of 55 patients. Similarly, the survival of 102 patients treated with VMCL + low dose cyclophosphamide for a minimum of 3.5 years was superior to that of the historical control group but not to that of the VMCL alone treated group. Improvement in survival was still evident when this was measured from the date of removal of the primary tumor. Analysis of subsets of patients showed that VMCL treatment appeared to benefit patients irrespective of the number of lymph nodes involved and whether surgery was carried out near to (synchronous metastases) or some time after removal of the primary (delayed metastases). Analysis of the effect of treatment on duration to development of distant metastases suggested that there was a lower proportion of metastases during treatment with VMCL compared to the historical control groups. Treatment with VMCL also appeared to be associated with a lower incidence of cutaneous metastases but a higher proportion of visceral (including liver) metastases. Treatment was not associated with prolongation of survival after development of distant metastases. The results from this prolonged follow-up provide further support for an apparent survival benefit from immunotherapy with VMCL and suggest that the duration to and site of distant metastases is altered by this treatment. A randomized control (Phase III) study based on these results is in progress.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1561807     DOI: 10.1007/bf02071529

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


  26 in total

Review 1.  Virus augmentation of the antigenicity of tumor cell extracts.

Authors:  F C Austin; C W Boone
Journal:  Adv Cancer Res       Date:  1979       Impact factor: 6.242

2.  Western blot analysis of antigens on melanoma cells recognized by cytotoxic T cells.

Authors:  P Hersey; M MacDonald; H Werkman
Journal:  J Natl Cancer Inst       Date:  1988-08-03       Impact factor: 13.506

3.  Non-randomized controls in cancer clinical trials.

Authors:  E A Gehan; E J Freireich
Journal:  N Engl J Med       Date:  1974-01-24       Impact factor: 91.245

4.  Surgical adjuvant therapy of malignant melanoma with corynebacterium parvum.

Authors:  E Y Hilal; C M Pinsky; Y Hirshaut; H J Wanebo; J A Hansen; D W Braun; J G Fortner; H F Oettgen
Journal:  Cancer       Date:  1981-07-15       Impact factor: 6.860

5.  Tumor-specific T-cell clones recognize different protein determinants of autologous human malignant melanoma cells.

Authors:  M Notter; V Schirrmacher
Journal:  Int J Cancer       Date:  1990-05-15       Impact factor: 7.396

6.  Randomized versus historical controls for clinical trials.

Authors:  H Sacks; T C Chalmers; H Smith
Journal:  Am J Med       Date:  1982-02       Impact factor: 4.965

7.  Regulation of cellular immune response against autologous human melanoma. II. Mechanism of induction and specificity of suppression.

Authors:  B Mukherji; A L Nashed; A Guha; M T Ergin
Journal:  J Immunol       Date:  1986-03-01       Impact factor: 5.422

8.  Phase II study of vaccinia melanoma cell lysates (VMCL) as adjuvant to surgical treatment of stage II melanoma. II. Effects on cell mediated cytotoxicity and leucocyte dependent antibody activity: immunological effects of VMCL in melanoma patients.

Authors:  P Hersey; A Edwards; G D'Alessandro; M MacDonald
Journal:  Cancer Immunol Immunother       Date:  1986       Impact factor: 6.968

9.  Inflammatory cell infiltrates in human melanoma at different stages of tumor progression.

Authors:  E B Bröcker; G Zwadlo; B Holzmann; E Macher; C Sorg
Journal:  Int J Cancer       Date:  1988-04-15       Impact factor: 7.396

Review 10.  Current status and future prospects for adjuvant therapy of melanoma.

Authors:  P Hersey; C M Balch
Journal:  Aust N Z J Surg       Date:  1984-08
View more
  5 in total

Review 1.  Melanoma vaccines. Current status and future prospects.

Authors:  P Hersey
Journal:  Drugs       Date:  1994-03       Impact factor: 9.546

Review 2.  Recent advances in the treatment of malignant melanoma with gene therapy.

Authors:  E M Hersh; A T Stopeck
Journal:  Mol Med       Date:  1997-10       Impact factor: 6.354

3.  Clinical features of malignant melanoma of the finger and therapeutic efficacies of different treatments.

Authors:  Zuozhang Yang; Lin Xie; Yunchao Huang; Hongpu Sun; Tao Yuan; Xiang Ma; Congguo Jing; Pengjie Liu
Journal:  Oncol Lett       Date:  2011-06-10       Impact factor: 2.967

4.  Favorable clinical responses in subsets of patients from a randomized, multi-institutional melanoma vaccine trial.

Authors:  M K Wallack; M Sivanandham; B Whooley; K Ditaranto; A A Bartolucci
Journal:  Ann Surg Oncol       Date:  1996-03       Impact factor: 5.344

5.  Prolonged repeated vaccine immuno-chemotherapy induces long-term clinical responses and survival for advanced metastatic melanoma.

Authors:  Brendon J Coventry; Carrie A Lilly; Peter Hersey; Antonio Michele; Richard J Bright
Journal:  J Immunother Cancer       Date:  2014-04-15       Impact factor: 13.751

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.