AI Article Synopsis

  • The International Prognostic Score (IPS) is a key tool for predicting outcomes in Hodgkin's lymphoma, based on historic data, but hasn't been validated for more recently treated patients where outcomes have improved.
  • The study reviewed data from 740 patients diagnosed with advanced-stage Hodgkin's lymphoma, finding 5-year freedom from progression (FFP) at 78% and overall survival (OS) at 90%.
  • Results show that while the IPS still predicts FFP and OS, the outcomes for patients have significantly improved, indicating the need to consider these advancements before evaluating new treatments against historical data.*

Article Abstract

Purpose: The International Prognostic Score (IPS) is the most widely used risk stratification index for Hodgkin's lymphoma (HL). It is based on patients treated before 1992 and predicts 5-year freedom from progression (FFP) and overall survival (OS) ranging from 42% to 84% and 56% to 89%, respectively. The IPS has not been validated in a recently treated population in which outcomes have improved compared with historic results.

Patients And Methods: By using the British Columbia Cancer Agency Lymphoid Cancer Database, we identified all patients age ≥ 16 years newly diagnosed with advanced-stage HL (stage III to IV, or stage I to II with "B" symptoms or bulky disease ≥ 10 cm) from 1980 to 2010, treated with curative intent with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) or an ABVD-equivalent regimen with complete clinical information.

Results: In all, 740 patients were identified. Five-year FFP and OS were 78% and 90%, respectively. The IPS was prognostic for both FFP (P < .001) and OS (P < .001), with 5-year FFP ranging from 62% to 88% and 5-year OS ranging from 67% to 98%. Analysis limited to patients age 16 to 65 years (n = 686) demonstrated a narrower range of outcomes, with 5-year FFP ranging from 70% to 88% and 5-year OS ranging from 73% to 98%.

Conclusion: The IPS remains prognostic for advanced-stage HL, but the range of outcomes has narrowed considerably. This improvement in outcome with ABVD should be acknowledged before consideration of alternate initial therapies and when comparing results from current trials with those of historic controls.

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Source
http://dx.doi.org/10.1200/JCO.2011.41.0910DOI Listing

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