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Poster Display session 3

3611 - Phase II trial of SM 88 in Non-Metastatic Biochemical Recurrent Prostate Cancer.

Date

30 Sep 2019

Session

Poster Display session 3

Topics

Tumour Site

Prostate Cancer

Presenters

Benjamin Gartrell

Citation

Annals of Oncology (2019) 30 (suppl_5): v325-v355. 10.1093/annonc/mdz248

Authors

B. Gartrell1, G. Del Priore2, A. Retter3, W. Chen4, G.H. Sokol5, A. Vandell6, M. Roach7, H.I. Scher8

Author affiliations

  • 1 Oncology, Montefiore Medical Center, 10461 - New York/US
  • 2 Cmo, Tyme Inc, 10004 - New York/US
  • 3 Oncology, Eastchester Cancer Care Center, 10469 - New York/US
  • 4 Oncology, Vitatex, 11794 - Stony Brook/US
  • 5 Oncology, Florida Cancer Specialist, 34667 - Florida/US
  • 6 Clinical Research, Tyme Inc., 10004 - New York/US
  • 7 Radiation Oncology/urology, UCSF, 94143 - San Francisco/US
  • 8 Medicine, Memorial Sloan-Kettering Cancer Center, 10065 - New York/US

Resources

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Abstract 3611

Background

Androgen deprivation therapy (ADT) is standard treatment for rising PSA with/without circulating tumor cells (CTCs) but adverse events (AEs) limit patient acceptance. We report results of SM-88 (D,L-alpha-metyrosine; racemetyrosine [USAN]) in combination with a CYP3A4 inducer, mTOR inhibitor and catalyst that does not lower testosterone (T).

Methods

Phase 2 with a rising PSA (per PCWG3), no disease on imaging and detectable CTCs.

Results

From Sept 2016-April 2019, 35 subjects consented; 23 evaluable (completed >1 cycle); 60.9% were post RT. Mean age 70.6; BMI 28.9; 21.7% black. Mean T rose (319.1 to 346.0 ng/dL p = 0.08) over 12 weeks. Subjects did not report side effects commonly associated with hormone suppression. Assessments of EORTC measured domains sexual health, overall health, and quality of life remained stable, with depression, hot flushes, and enlarged breast reported as “Not at all” (remained at 1). There was no detectable worsening in any domain of EORTC QLQ-C30 or QLQ-PR25. No clinically significant changes were seen in weight, hct, glu, urinary N telopeptide, MAP (in normotensives and hypertensives), heart rate, Ca ++, LDH, bsAlkPhos, triglycerides, albumin, or QTc. NLR decreased at the end of cycle 1 in 75% of those with radiographic and/or PSA progression vs 53% of those who did not. 15/23 (65.2%) subjects reported experiencing an AE. 1 unrelated Grade 3; 18/35 (51.4%) at least possibly related to drug. No AEs were related to T levels. There were no skeletal or cardiovascular events. From initial diagnosis of PSA rise 100% (23/23) remained metastases free. PSA declined (4% 1/23) stabilized (83% 19/23) or rose (13% 3/23). 56.5% (13/23) subjects experienced an improvement in median PSA DT. Median DT time improved from 6.2 to 8.0 months for all subjects completing 3 cycles of therapy. CTCs were > 5 in 100% at baseline. After 12 weeks, there was a 65.3% (-100% to -8.8%) median CTC decrease from baseline (n = 18), with all subjects having CTC counts below baseline and 2 undetectable.

Conclusions

SM-88 may delay the start of HT and be useful when normal T is preferred. QOL was maintained without ADT AEs. Favorable effects on PSA and CTCs kinetics were observed consistent with a favorable treatment effect. Trials to confirm these benefits are planned.

Clinical trial identification

NCT02796898.

Editorial acknowledgement

Legal entity responsible for the study

Tyme Inc.

Funding

Tyme Inc.

Disclosure

G. Del Priore: Leadership role, Shareholder / Stockholder / Stock options, Full / Part-time employment, Officer / Board of Directors: Tyme Inc. G.H. Sokol: Advisory / Consultancy: Tyme Inc. A. Vandell: Full / Part-time employment: Tyme Inc. All other authors have declared no conflicts of interest.

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