2001
DOI: 10.1016/s0360-3016(01)01798-9
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Response-adapted radiotherapy in the treatment of pediatric Hodgkin’s disease: an interim report at 5 years of the German GPOH-HD 95 trial

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Cited by 86 publications
(52 citation statements)
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“…In contrast, GPOH-HD95 did not support the safe omission of radiation therapy in intermediate and high-risk groups following a complete response to chemotherapy, while CCG 5942 was not able to demonstrate a benefit in these patients. Randomization, risk stratification, chemotherapy, response criteria, and the lack of functional imaging make it hard to directly compare the results of these two studies, however the opposing results indicate that there is still much to be determined regarding the optimal use of risk adaptive strategy in pediatric Hodgkin lymphoma treatment [25][26][27]. As outlined by these and other studies, this strategy is not limited to low risk pediatric Hodgkin lymphoma patients.…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, GPOH-HD95 did not support the safe omission of radiation therapy in intermediate and high-risk groups following a complete response to chemotherapy, while CCG 5942 was not able to demonstrate a benefit in these patients. Randomization, risk stratification, chemotherapy, response criteria, and the lack of functional imaging make it hard to directly compare the results of these two studies, however the opposing results indicate that there is still much to be determined regarding the optimal use of risk adaptive strategy in pediatric Hodgkin lymphoma treatment [25][26][27]. As outlined by these and other studies, this strategy is not limited to low risk pediatric Hodgkin lymphoma patients.…”
Section: Discussionmentioning
confidence: 99%
“…Following two cycles of chemotherapy, 27% of lowrisk patients achieved a CR, defi ned as complete absence of measurable disease. There was no statistically significant difference in EFS or OS at median follow-up of 38 months between low-risk patients who received or did not receive IFRT [13]. A smaller series using two courses of COPP and two courses of ABVD also validated the elimination of radiation in a group of children with stage I and II disease with no bulky disease [30].…”
Section: Table1 Combination Chemotherapy Regimensmentioning
confidence: 87%
“…Additional prognostic factors commonly used to stratify patients into risk categories in recent pediatric and adolescent trials include bulky disease and the number of involved lymph node regions, although precise defi nitions vary among trials. The rapidity of response to initial chemotherapy has been demonstrated to have prognostic signifi cance, leading to the use of "response-directed" therapy that limits total therapy for patients with rapid response and, in some cases, escalates therapy for patients with a slow response [13,17]. Until recently, early response was determined by the percentage reduction in the volume of pretreatment disease, based on CT scan evaluation.…”
Section: Staging and Risk Assessmentmentioning
confidence: 99%
“…After 1989, the nodular sclerosis subtype became predominant (55%), but the rate is still lower than that 1978-1980 1981-1983 1984-1988 1989-1998 1999- NOS not otherwise specified Table 4 Therapeutic results of treatment for childhood HL according to periods 1978-1980 1981-1983 1984-1988 1989-1998 1999 Fig. 3 Overall survival and relapse-free survival according to stages reported in developed countries (more than 70%) [16,18,23,24]. A predominance of the mixed cellularity type has been reported in many other developing countries [2,4,5,7].…”
Section: Discussionmentioning
confidence: 99%