scholarly journals Phase 2 trial of combination thalidomide plus temozolomide in patients with metastatic malignant melanoma: Southwest Oncology Group S0508

Cancer ◽  
2010 ◽  
Vol 116 (2) ◽  
pp. 424-431 ◽  
Author(s):  
Joseph I. Clark ◽  
James Moon ◽  
Laura F. Hutchins ◽  
Jeffrey A. Sosman ◽  
W. Martin Kast ◽  
...  
Blood ◽  
2003 ◽  
Vol 102 (5) ◽  
pp. 1606-1612 ◽  
Author(s):  
Oliver W. Press ◽  
Joseph M. Unger ◽  
Rita M. Braziel ◽  
David G. Maloney ◽  
Thomas P. Miller ◽  
...  

AbstractAdvanced follicular lymphoma is incurable with conventional chemotherapy and radiotherapy. The Southwest Oncology Group (SWOG) conducted a phase 2 trial (S9911) of a novel regimen consisting of 6 cycles of CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) chemotherapy followed 4 to 8 weeks later by tositumomab/iodine I 131 tositumomab (anti-CD20 antibody) in 90 eligible patients with previously untreated, advanced stage follicular lymphoma. Treatment was well tolerated. Reversible myelosuppression was the main adverse event and was more severe during CHOP chemotherapy than following radioimmunotherapy. The overall response rate to the entire treatment regimen was 90%, including 67% complete remissions (CRs plus unconfirmed CRs [CRu's]) and 23% partial remissions (PRs). Twenty-seven (57%) of the 47 fully evaluable patients who achieved less than a CR with CHOP improved their remission status after tositumomab/iodine I 131 tositumomab. With a median follow-up of 2.3 years, the 2-year progression-free survival (PFS) was estimated to be 81%, with a 2-year overall survival of 97%. This study has established the feasibility, tolerability, and efficacy of this regimen for patients with advanced follicular lymphoma. This novel treatment appears promising compared with the SWOG's historical experience using CHOP alone and is currently being compared with CHOP plus rituximab in a randomized phase 3 trial (S0016).


1984 ◽  
Vol 2 (4) ◽  
pp. 316-319 ◽  
Author(s):  
J M Quagliana ◽  
R L Stephens ◽  
L H Baker ◽  
J J Costanzi

A phase II study using vindesine (3 mg/m2 by slow intravenous push at seven to 14 day intervals) was carried out in 42 patients with metastatic melanoma. There was one complete remission (2.5%) of greater than 12 months duration; seven partial remissions (17.5%) of two, three, three, four, five, six and eight months duration; 11 with no change (27.5%) of one to 10 months duration; and 21 (52.5%) patients with increasing disease. Toxicity included neutropenia, neurotoxicity, phlebitis and cellulitis at the site of injection, alopecia, fever and chills, myalgias, and gastrointestinal toxicity. It was concluded that vindesine does have activity in some patients with metastatic malignant melanoma. Further studies in previously untreated patients are warranted.


2007 ◽  
Vol 14 (8) ◽  
pp. 2367-2376 ◽  
Author(s):  
Kimberly A. Varker ◽  
Jennifer E. Biber ◽  
Cheryl Kefauver ◽  
Rhonda Jensen ◽  
Amy Lehman ◽  
...  

Cancer ◽  
2013 ◽  
Vol 120 (3) ◽  
pp. 344-351 ◽  
Author(s):  
Jubilee Brown ◽  
William E. Brady ◽  
Julian Schink ◽  
Linda Van Le ◽  
Mario Leitao ◽  
...  

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