UT Southwestern Medical Center, Dallas, TX
Rohit R Badia , Rashed Ghandour , Jeffrey Howard , Joseph G Cheaib , Ragheed Saoud , Scott E. Eggener , Nirmish Singla , Phillip M. Pierorazio , Aditya Bagrodia
Background: Organ confined (stage IA/IB) testicular cancer has a high cure rate regardless of initial treatment modality, making it important to weigh the toxicities of treatment against potential benefits. While many clinicians routinely obtain serum tumor markers (STMs) prior to radical orchiectomy, their role in predicting recurrence in stage IA and IB testicular cancer has not been studied. Methods: A multi-institutional database of stage I testicular cancer patients diagnosed between 2006 and 2018 was created. Univariate and multivariate regression models were created to understand which factors predict recurrence. Recurrence analyses using Kaplan-Meier curves for elevated and normal pre-orchiectomy STMs were also generated. Results: 150 patients met the study criteria, of whom 16 (11%) relapsed (Table). 9 (56%) patients with recurrence had elevated pre-orchiectomy STMs, and 7 (44%) had normal pre-orchiectomy STMs. Similarly, 75 patients (56%) without relapse had elevated pre-orchiectomy STMs. Of 9 patients with elevated pre-orchiectomy STMs, 6 (67%) had normal STMs at recurrence; of 7 with normal pre-orchiectomy STMs, 4 patients (57%) had elevated STMs at recurrence. On Kaplan-Meier analysis, no association between level of pre-orchiectomy STMs and recurrence free survival was observed. Conclusions: Pre-orchiectomy STMs were not independently associated with recurrence in stage I testis cancer. Interestingly, there was also no association between positivity of pre-orchiectomy STMs and whether or not STMs were elevated at recurrence. These findings support the continued use of standard-of-care imaging and STMs in surveillance of stage IA/IB testicular cancer patients regardless of pre-orchiectomy STMs.
Pre-Orchiectomy STMs | Recurrence STMs | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Race | Age at Orchiectomy | Time to Recurrence (months) | Histology | Pathologic T Stage | Tumor Size (mm) | Primary treatment | Normal or Elevated? | AFP | β-hCG | LDH | Normal or Elevated? | AFP | β-hCG | LDH |
White | 20 | 27 | Mixed | T1 | 60 | Surveillance | ↑ | 2 | 2095 | 202 | ↔ | 6.3 | 1 | 168 |
White | 25 | 5 | Mixed | T1 | 24 | Surveillance | ↔ | 1 | 9.4 | 100 | ↑ | 61.5 | 49.4 | 165 |
White | 16 | 50 | Pure embryonal | T1 | - | Surveillance | ↑ | 11 | 3 | 302 | ↔ | 1.1 | 1 | 230 |
Hispanic | 32 | 37 | Pure teratoma | T1 | 90 | Surveillance | ↔ | 1 | 2.2 | 137 | ↑ | 83.6 | 1 | 154 |
White | 16 | 3 | Pure embryonal | T1 | 20 | Surveillance | ↔ | 1 | 1 | 120 | ↔ | 1.3 | 1 | 125 |
White | 35 | 17 | Mixed | T1 | 40 | Surveillance | ↑ | 20 | 86 | - | ↔ | 2.9 | 0.1 | - |
White | 34 | 15 | Seminoma | T1 | 45 | Surveillance | ↔ | 2.1 | 2 | 146 | ↑ | 2.1 | 2 | 235 |
White | 36 | 22 | Seminoma | T1 | 62 | Chemotherapy | ↑ | 3 | 2 | 445 | ↑ | 4 | 2 | 261 |
White | 33 | 11 | Mixed | T1 | 25 | Surveillance | ↔ | 3.8 | 2 | - | ↔ | 6.6 | 2 | 157 |
White | 29 | 7 | Mixed | T1 | 15 | Surveillance | ↑ | 72 | 4 | 185 | ↑ | 208 | 36 | 230 |
White | 35 | 4 | Mixed | T1 | 22 | Surveillance | ↔ | 2 | 2 | 217 | ↑ | 2.3 | 2 | 283 |
Hispanic | 32 | 7 | Seminoma | T1 | 77 | Surveillance | ↔ | 9 | 2 | 216 | ↔ | 7 | 2 | 205 |
White | 48 | 38 | Seminoma | T1 | 46 | Surveillance | ↑ | 3 | 33.9 | - | ↔ | 2.6 | 2 | 198 |
Hispanic | 41 | 16 | Seminoma | T2 | 52 | Surveillance | ↑ | 3 | 2 | 275 | ↔ | 4 | 3 | 227 |
Hispanic | 17 | 4 | Yolk sac | T2 | 70 | Surveillance | ↑ | 22 | 2 | 275 | ↑ | 18 | 2 | 244 |
White | 24 | 3 | Mixed | T2 | 11 | RPLND | ↑ | 2 | 2 | 255 | ↔ | 2.1 | 2 | 181 |
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