PMID- 9741068 OWN - NLM STAT- MEDLINE DCOM- 19981207 LR - 20131121 IS - 1057-9249 (Print) IS - 1057-9249 (Linking) VI - 7 IP - 4 DP - 1998 Jul-Aug TI - A controlled trial of fluoxetine and desipramine in depressed women with advanced cancer. PG - 291-300 AB - BACKGROUND: This study was conducted to determine the efficacy and tolerability of fluoxetine and desipramine in treating depressive symptoms in women with cancer. METHOD: In this prospective, 6-week, double-blind, placebo-controlled trial, we compared fluoxetine with desipramine in treating depressive symptoms in 40 women diagnosed with cancer. Scales used to measure efficacy and tolerability were the Hamilton Depression Rating Scale (HAM-D), the Hamilton Anxiety Rating Scale (HAM-A), the Clinical and Patient's Global Impression (CGI and PGI) scales, the Functional Living Index for Cancer (FLIC), the Memorial Pain Assessment Card (MPAC), and the SF-36 Health Survey. RESULTS: Fluoxetine and desipramine treatments improved depression and anxiety symptoms. There was a trend towards significance in improvement of FLIC scores (as evidenced by greater numerical improvements with fluoxetine treatment). Fluoxetine treatment alone was associated with statistically significant improvements in MPAC Mood scale scores. Both treatments showed statistically significant improvements in the quality of life SF-36 scores in Role Emotional, Social Functioning, Mental Health, and Vitality. CONCLUSIONS: Both fluoxetine and desipramine were effective and well-tolerated in improving depressive symptoms and quality of life in women with advanced cancer. Fluoxetine may offer greater benefit to these patients, as evidenced by greater improvements in fluoxetine-treated patients on several quality of life measures. Our results, while meaningful, should be confirmed in a larger patients sample. However, experience from studies of antidepressant use in patients with advanced cancer has shown that intercurrent disease and treatment variables make it difficult to conduct large studies. FAU - Holland, J C AU - Holland JC AD - Department of Psychiatry and Behavioral Sciences, Memorial Sloan-Kettering Cancer Center, New York, NY, USA. FAU - Romano, S J AU - Romano SJ FAU - Heiligenstein, J H AU - Heiligenstein JH FAU - Tepner, R G AU - Tepner RG FAU - Wilson, M G AU - Wilson MG LA - eng PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - England TA - Psychooncology JT - Psycho-oncology JID - 9214524 RN - 0 (Antidepressive Agents, Second-Generation) RN - 0 (Antidepressive Agents, Tricyclic) RN - 01K63SUP8D (Fluoxetine) RN - TG537D343B (Desipramine) SB - IM MH - Antidepressive Agents, Second-Generation/*administration & dosage MH - Antidepressive Agents, Tricyclic/*administration & dosage MH - Depressive Disorder/*drug therapy/etiology MH - Desipramine/*administration & dosage MH - Double-Blind Method MH - Drug Therapy, Combination MH - Female MH - Fluoxetine/*administration & dosage MH - Humans MH - Middle Aged MH - Neoplasms/complications/*psychology MH - Prospective Studies MH - Quality of Life MH - Treatment Outcome EDAT- 1998/09/19 00:00 MHDA- 1998/09/19 00:01 CRDT- 1998/09/19 00:00 PHST- 1998/09/19 00:00 [pubmed] PHST- 1998/09/19 00:01 [medline] PHST- 1998/09/19 00:00 [entrez] AID - 10.1002/(SICI)1099-1611(199807/08)7:4<291::AID-PON361>3.0.CO;2-U [doi] PST - ppublish SO - Psychooncology. 1998 Jul-Aug;7(4):291-300. doi: 10.1002/(SICI)1099-1611(199807/08)7:4<291::AID-PON361>3.0.CO;2-U.