Real-world recurrence-free and distant metastasis-free survival in early-stage melanoma: concordance with KEYNOTE-716 trial estimates

Real-world evidence is increasingly used to support treatment effectiveness in oncology research, but endpoint validation in early stage melanoma is limited. This study evaluated the concordance between real-world recurrence-free survival (rwRFS) and distant metastasis-free survival (rwDMFS) with KEYNOTE-716 trial control arm estimates. This was a retrospective observational cohort study using electronic health record data from US community oncology practices within The US Oncology Network. Eligible patients were diagnosed with stage IIB-IIC cutaneous melanoma between 1 January 2018 and 5 December 2023 and had not initiated adjuvant therapy 12 weeks postresection with clear margins. Trial eligibility criteria were applied to define a real-world cohort aligned with that of KEYNOTE-716. Available baseline characteristics were balanced between the two populations using a matching-adjusted indirect comparison. Hazard ratios, confidence intervals (CIs), and P-values were calculated for rwRFS and rwDMFS with the KEYNOTE-716 control arm as the reference. After applying eligibility criteria, 75 patients were included in the real-world cohort. Adjusted hazard ratios for rwRFS and rwDMFS were: 1.17 (95% CI: 0.71-1.94; P = 0.527) and 0.83 (95% CI: 0.51-1.37; P = 0.462), respectively. Sensitivity analyses that censored real-world patients at the time of immunotherapy treatment gave adjusted hazard ratios of 0.98 (95% CI: 0.59-1.64; P = 0.938) for rwRFS, and 0.70 (95% CI: 0.41-1.17; P = 0.171) for rwDMFS. rwRFS and rwDMFS were concordant with estimates from the KEYNOTE-716 control arm. Results of real-world endpoints can reliably reflect clinical trial outcomes when key study design elements are aligned. These findings increase confidence in the validity of real-world outcomes for early stage melanoma.

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Publication Details

Journal
Melanoma Research
Published
2026-04-28
DOI
https://doi.org/10.1097/cmr.0000000000001101
Primary Topic
Cutaneous Melanoma Detection and Management
Type
article
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article

Real-world recurrence-free and distant metastasis-free survival in early-stage melanoma: concordance with KEYNOTE-716 trial estimates

Zhaohui Su, Carole Berini, Kaushal Desai, Malcolm Charles et al.
Melanoma Research
Cutaneous Melanoma Detection and Management
article

Real-world recurrence-free and distant metastasis-free survival in early-stage melanoma: concordance with KEYNOTE-716 trial estimates

Zhaohui Su, Carole Berini, Kaushal Desai, Malcolm Charles, Paul Conkling, Jessica K. Paulus, Shan Jiang
article en

Abstract

Real-world evidence is increasingly used to support treatment effectiveness in oncology research, but endpoint validation in early stage melanoma is limited. This study evaluated the concordance between real-world recurrence-free survival (rwRFS) and distant metastasis-free survival (rwDMFS) with KEYNOTE-716 trial control arm estimates. This was a retrospective observational cohort study using electronic health record data from US community oncology practices within The US Oncology Network. Eligible patients were diagnosed with stage IIB-IIC cutaneous melanoma between 1 January 2018 and 5 December 2023 and had not initiated adjuvant therapy 12 weeks postresection with clear margins. Trial eligibility criteria were applied to define a real-world cohort aligned with that of KEYNOTE-716. Available baseline characteristics were balanced between the two populations using a matching-adjusted indirect comparison. Hazard ratios, confidence intervals (CIs), and P-values were calculated for rwRFS and rwDMFS with the KEYNOTE-716 control arm as the reference. After applying eligibility criteria, 75 patients were included in the real-world cohort. Adjusted hazard ratios for rwRFS and rwDMFS were: 1.17 (95% CI: 0.71-1.94; P = 0.527) and 0.83 (95% CI: 0.51-1.37; P = 0.462), respectively. Sensitivity analyses that censored real-world patients at the time of immunotherapy treatment gave adjusted hazard ratios of 0.98 (95% CI: 0.59-1.64; P = 0.938) for rwRFS, and 0.70 (95% CI: 0.41-1.17; P = 0.171) for rwDMFS. rwRFS and rwDMFS were concordant with estimates from the KEYNOTE-716 control arm. Results of real-world endpoints can reliably reflect clinical trial outcomes when key study design elements are aligned. These findings increase confidence in the validity of real-world outcomes for early stage melanoma.

Melanoma Research
Merck & Co., Inc., Rahway, NJ, USA (United States) (US), AIR Worldwide (United States) (US)
Openalex Percentile: Top 7%
Cutaneous Melanoma Detection and Management
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