Journal of the National Cancer Center (Sep 2024)

Association of overall survival benefit of radiotherapy with progression-free survival after chemotherapy for diffuse large B-cell lymphoma: A systematic review and meta-analysis

  • Jingnan Wang,
  • Xin Liu,
  • Yunpeng Wu,
  • Qiuzi Zhong,
  • Tao Wu,
  • Yong Yang,
  • Bo Chen,
  • Hao Jing,
  • Yuan Tang,
  • Jing Jin,
  • Yueping Liu,
  • Yongwen Song,
  • Hui Fang,
  • Ningning Lu,
  • Ning Li,
  • Yirui Zhai,
  • Wenwen Zhang,
  • Min Deng,
  • Shulian Wang,
  • Fan Chen,
  • Lin Yin,
  • Chen Hu,
  • Shunan Qi,
  • Yexiong Li

Journal volume & issue
Vol. 4, no. 3
pp. 249 – 259

Abstract

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Objective: To evaluate whether improved progression-free survival (PFS) from radiotherapy (RT) translates into an overall survival (OS) benefit for diffuse large B-cell lymphoma (DLBCL). Methods: A systematic literature search identified randomized controlled trials (RCTs) and retrospective studies that compared combined-modality therapy (CMT) with chemotherapy (CT) alone. Weighted regression analyses were used to estimate the correlation between OS and PFS benefits. Cohen's kappa statistic assessed the consistency between DLBCL risk-models and PFS patterns. Furthermore, the benefit trend of RT was analyzed by fitting a linear regression model to the pooled hazard ratio (HR) according to the PFS patterns. Results: For both 7 RCTs and 52 retrospective studies, correlations were found between PFS HR (HRPFS) and OS HR (HROS) at trial level (r = 0.639–0.876), and between PFS and OS rates at treatment-arm level, regardless of CT regimens (r = 0.882–0.964). Incorporating RT into CT increased about 18% of PFS, and revealed a different OS benefit profile. Patients were stratified into four CT-generated PFS patterns (>80%, >60–80%, >40–60%, and ≤40%), which was consistent with risk-stratified subgroups (kappa > 0.6). Absolute gain in OS from RT ranged from ≤5% at PFS >80% to about 21% at PFS ≤40%, with pooled HROS from 0.70 (95% CI, 0.51–0.97) to 0.48 (95% CI, 0.36–0.63) after rituximab-based CT. The OS benefit of RT was predominant in intermediate- and high-risk patients with PFS ≤ 80%. Conclusion: We demonstrated a varied OS benefit profile of RT to inform treatment decisions and clinical trial design.

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