Initial dose intensity has limited impact on the outcome of ABVD chemotherapy for advanced Hodgkin lymphoma (HL): data from UKLG LY09 (ISRCTN97144519).
dc.contributor.author | Owadally, W S | |
dc.contributor.author | Sydes, M R | |
dc.contributor.author | Radford, John A | |
dc.contributor.author | Hancock, B W | |
dc.contributor.author | Cullen, M H | |
dc.contributor.author | Stenning, S P | |
dc.contributor.author | Johnson, P W M | |
dc.date.accessioned | 2010-08-04T10:15:30Z | |
dc.date.available | 2010-08-04T10:15:30Z | |
dc.date.issued | 2010-03 | |
dc.identifier.citation | Initial dose intensity has limited impact on the outcome of ABVD chemotherapy for advanced Hodgkin lymphoma (HL): data from UKLG LY09 (ISRCTN97144519). 2010, 21 (3):568-73 Ann Oncol | en |
dc.identifier.issn | 1569-8041 | |
dc.identifier.pmid | 19684105 | |
dc.identifier.doi | 10.1093/annonc/mdp331 | |
dc.identifier.uri | http://hdl.handle.net/10541/109033 | |
dc.description.abstract | BACKGROUND: This analysis was undertaken to assess the relationship between the dose intensity (DI) of initial chemotherapy and outcome in a large cohort of patients with advanced Hodgkin lymphoma treated in a randomised controlled trial, in which detailed dose data were collected prospectively. PATIENTS AND METHODS: Three-hundred and eighty patients randomly assigned to receive standard doxorubicin, bleomycin, vinblastine and dacarbazine who underwent at least two cycles of treatment were studied. With a median follow-up of 6.9 years, progression-free survival (PFS) from the end of cycle 2 was analysed according to DI during those cycles. RESULTS: During the first two cycles, 25% of patients received >97% of planned DI, 37% received between 86% and 97% and 38% received <86%. DI during the first two cycles was correlated with DI during the remainder of the course, but there was no evidence that early DI influenced PFS (hazard ratio 0.87, 95% confidence interval 0.67-1.11; P = 0.265). Multivariate analysis also failed to confirm the influence of early DI on PFS or overall survival. CONCLUSIONS: At the range of DI delivered in a multicentre trial using conventional therapy, there is no clear evidence that early DI influences outcome. This should be tested in a prospective study. | |
dc.language.iso | en | en |
dc.subject | Cancer Staging | en |
dc.subject.mesh | Adult | |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject.mesh | Bleomycin | |
dc.subject.mesh | Dacarbazine | |
dc.subject.mesh | Dose-Response Relationship, Drug | |
dc.subject.mesh | Doxorubicin | |
dc.subject.mesh | Hodgkin Disease | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Neoplasm Staging | |
dc.subject.mesh | Prospective Studies | |
dc.subject.mesh | Survival Rate | |
dc.subject.mesh | Treatment Outcome | |
dc.subject.mesh | Vinblastine | |
dc.title | Initial dose intensity has limited impact on the outcome of ABVD chemotherapy for advanced Hodgkin lymphoma (HL): data from UKLG LY09 (ISRCTN97144519). | en |
dc.type | Article | en |
dc.contributor.department | Cancer Sciences Division, Cancer Research UK Clinical Centre, Southampton, UK. | en |
dc.identifier.journal | Annals of Oncology | en |
html.description.abstract | BACKGROUND: This analysis was undertaken to assess the relationship between the dose intensity (DI) of initial chemotherapy and outcome in a large cohort of patients with advanced Hodgkin lymphoma treated in a randomised controlled trial, in which detailed dose data were collected prospectively. PATIENTS AND METHODS: Three-hundred and eighty patients randomly assigned to receive standard doxorubicin, bleomycin, vinblastine and dacarbazine who underwent at least two cycles of treatment were studied. With a median follow-up of 6.9 years, progression-free survival (PFS) from the end of cycle 2 was analysed according to DI during those cycles. RESULTS: During the first two cycles, 25% of patients received >97% of planned DI, 37% received between 86% and 97% and 38% received <86%. DI during the first two cycles was correlated with DI during the remainder of the course, but there was no evidence that early DI influenced PFS (hazard ratio 0.87, 95% confidence interval 0.67-1.11; P = 0.265). Multivariate analysis also failed to confirm the influence of early DI on PFS or overall survival. CONCLUSIONS: At the range of DI delivered in a multicentre trial using conventional therapy, there is no clear evidence that early DI influences outcome. This should be tested in a prospective study. |