Is the Sipuleucel-T Saga Poised for a New Chapter?

Publication
Article
Oncology Live®Vol. 20/No.3
Volume 20
Issue 3

Advocates for sipuleucel-T point out that the public has become more aware of and interested in immunotherapy now, and they believe the product has the potential to benefit a larger group of patients.

Raoul S. Concepcion, MD, FACS

Nearly a decade ago, sipuleucel-T (Provenge) became the first FDA-approved personalized cancer vaccine, a harbinger of the current era of immunotherapy. After the autologous cellular vaccine gained approval in April 2010, its entry into the clinic was accompanied by expectations that it would see significant uptake by men with asymptomatic or minimally symptomatic metastatic castration-resistant prostate cancer (mCRPC).

The trajectory of this groundbreaking therapy, however, has been far different from the rapid adoption now underway with checkpoint blockade immunotherapy. Sipuleucel-T did find a place in the prostate cancer toolkit, particularly among urologists, but it was not widely adopted. Although it extends survival and is well tolerated, a combination of factors has led to limited use of the therapy, according to experts. These factors include a delayed initial approval, incomplete understanding of the new therapeutic mechanism, a lack of biomarkers to measure efficacy, cost barriers, the complexity of administration, and the subsequent approval of competing drugs. It was dogged by controversy and its manufacturer, Dendreon, declared bankruptcy and changed ownership 3 times.1

Yet advocates for sipuleucel-T point out that the public has become more aware of and interested in immunotherapy now, and they believe the product has the potential to benefit a larger group of patients. Dendreon last year began a new effort to expand its market by launching ProVent (NCT03686683), a phase III randomized trial testing the effectiveness of sipuleucel-T versus active surveillance in decreasing histologic progression of low-grade prostate cancer (Figure).2

ProVent “has a lot of potential, depending on how quickly it can accrue. Obviously, that is a very, very big space. There’s lots of interest in newly diagnosed, low-grade prostate cancer patients on active surveillance,” said Raoul S. Concepcion, MD, director of The Comprehensive Prostate Center and clinical associate professor at Vanderbilt University School of Medicine, both in Nashville, Tennessee. He has served as a physician adviser to Dendreon.

Impact on PSA

Several other trials are testing combinations or sequencing of sipuleucel-T with radiotherapy, checkpoint inhibitors, and other therapies. “It will maintain itself as a go-to medication for metastatic castrate-resistant prostate cancer, but the future is in combination therapy— learning how to mix it not only with chemotherapy, but with androgen-receptor pathway blockers or with other immunotherapeutic agents that might enhance the overall response to sipuleucel- T,” said Leonard G. Gomella, MD, director of the Kimmel Cancer Center Network at Thomas Jefferson University Hospital in Philadelphia.Sipuleucel-T treatment begins with leukapheresis, typically at a physician’s office or blood-collection center. The harvested white blood cells, most importantly dendritic antigen-presenting cells, are sent to a manufacturing facility. They are incubated with a recombinant fusion protein consisting of prostatic acid phosphatase (PAP), an antigen that is highly expressed in most prostate cancer cells, and granulocyte-macrophage colony-stimulating factor.

Three or 4 days after the initial blood draw, the activated cells are reinfused into the patient, activating an immune system response against PAP-expressing prostate cancer cells. The procedure is conducted 3 times over a period of 6 weeks.3

Attitudes toward sipuleucel-T have been heavily shaped by the fact that the therapy has not demonstrated significant impacts on lowering PSA levels and on slowing disease progression in radiographic imaging studies. The first phase III trial, D9901 (N = 127), did not achieve a statistically significant improvement in the primary endpoint of median time to progression; PSA progression was not included in the primary endpoint.4 The study was not powered for overall survival (OS), but investigators were surprised to find the sipuleucel-T group had a median survival advantage of 4.5 months over the placebo group (25.9 vs 21.4 months; log-rank P = .01). The estimated survival rate at 36 months was 34% for sipuleucel-T and 11% for placebo (P = .005).

The data were pooled with findings from another phase III trial, D9902A, and the integrated results showed a similar median survival benefit of 4.3 months (HR, 1.50; 95% CI, 1.10-2.05; log rank P = .011).5 Yet the failure to meet the original endpoint and the lack of evidence of direct antitumor effect, along with other concerns, sowed skepticism among some members of the FDA advisory committee reviewing the data. In 2007, the agency rejected sipuleucel-T and asked for more data.6

Gomella said immunotherapy was still new and the FDA wanted more robust evidence that it was effective. At the time, “immunotherapy in prostate cancer was heresy,” he said. “Whoever thought that prostate cancer would respond to an immune agent? There was a lot of hesitation.” With patients desperate for effective prostate cancer treatments, the decision led to accusations that the FDA was too risk-averse, a protest outside the agency’s offices, and a lawsuit seeking to force approval of the therapy.7

Dendreon followed up with the pivotal IMPACT trial, in which 512 patients were assigned in a 2:1 ratio to receive either sipuleucel-T (n = 341) or placebo (n = 171), with a primary endpoint of OS.8 In the sipuleucel-T group, there was a relative reduction of 22% in the risk of death as compared with the placebo group (HR, 0.78; 95% CI, 0.61-0.98; P = .03). This represented a 4.1-month improvement in median survival (25.8 vs 21.7 months), confirming the findings of the previous studies.

Marketplace Challenges

The 36-month survival probability in IMPACT was 31.7% in the sipuleucel-T group versus 23.0% in the placebo group. The median time to objective disease progression did not differ significantly between the study groups (14.6 vs 14.4 weeks, respectively). Among patients with PSA assessments after baseline, reductions of at least 50% on 2 visits at least 4 weeks apart were observed in 8 of 311 patients (2.6%) in the sipuleucel- T group, compared with 2 of 153 patients (1.3%) in the placebo group. Adverse events (AEs), all-grade and grades 3 to 5, were comparable between the 2 treatment groups; all-grade AEs more frequently reported in the sipuleucel-T patients included chills, fever, and headache.The FDA approved sipuleucel-T in April 2010, providing the first alternative to the chemotherapy docetaxel (Taxotere) for patients with asymptomatic or minimally symptomatic mCRPC. The decision was hailed by patients and advocacy groups, but the new therapy did not fare well in the marketplace, earning Dendreon a little more than half of the expected product revenues in 2011. It did not become available in other countries. Physicians at some US medical centers declined to use sipuleucel- T because of doubts that it worked, while fearing angry responses from patients who demanded it.9

At the same time, other patients who would benefit from sipuleucel-T could not always be convinced to take the therapy. “The hard part was, we didn’t know if it worked in patients or not because there was no objective decrease in PSA and there was no objective decrease in lymph nodes. Bone scans are always tough to evaluate in patients. So there was really nothing objective from a patient [or] a provider point of view to tell us if this drug or worked or not,” said Sandy Srinivas, MD, a professor of medicine (oncology) at Stanford University Medical Center and member of the National Comprehensive Cancer Network guidelines panel for prostate cancer.

“Patients are used to PSA. It was a total change in our approach and in our ability to convince patients that you have to take this drug: ‘It may not drop your PSA, it may not make your bone scans get better, but it will make you live a little bit longer, by about 4 months.’ That was a little bit of a tough sell,” Srinivas said.

It is possible that sipuleucel-T would eventually have an observable effect on tumor progression, but trial investigators may have felt compelled to switch therapies before that point because their patients’ PSA levels were rising, Gomella said. “The patient gets nervous, the doctor gets nervous, and they might not have given the drug enough of a chance to really have an impact before they moved to the next treatment,” he said.

Uncertainty about the therapy’s mechanism stoked an unusual controversy. In 2012, a paper in the Journal of the National Cancer Institute hypothesized that sipuleucel-T appeared to extend survival only because older men (aged ≥65 years) in the control group had worse OS outcomes versus younger participants, due perhaps to differences in the harvested cells used in the placebo group (two-thirds of cells were frozen and not reinfused).10 Dendreon and the IMPACT investigators rejected the claims.

Another obstacle to adoption has been what Concepcion called the “cost density” of sipuleucel- T, which runs about $100,000. “At that time, very few drugs were in that stratosphere of costs, especially given the contracted nature of the administration,” Concepcion said.

That administration is also complex, which put some doctors off the therapy, said Gurkamal Chatta, MD, clinical chief of genitourinary medicine at Roswell Park Comprehensive Cancer Center in Buffalo, New York.

“There are multiple layers to coordinating everything. You have to arrange for the leukapheresis, then you have to get the patient to come in to receive the product. It’s really 6 trips rather than 3 trips,” he said. “At least in our area, the leukapheresis doesn’t really happen at our place; it happens at the local Red Cross facility. Then, this is a slightly older population. They may or may not be able to be pheresed easily; they may need a central line. It just becomes complicated. It’s not the friendliest therapy logistically.”

On the other hand, Concepcion said 5 or 6 weeks is a relatively short treatment period, and he noted that giving sipuleucel-T does not require a full infusion center with a hood, making it easier to administer than chemotherapy.

The Hunt for Biomarkers

Two additional issues were that Dendreon had limited manufacturing capacity in the first year after approval, and the Centers for Medicare and Medicaid Services opened a national coverage analysis that delayed Medicare coverage of the therapy until late 2011.11 The complexity, cost, and uncertainty about reimbursement deterred doctors from prescribing sipuleucel-T and hurt Dendreon’s bottom line, leading to a bankruptcy declaration in 2014. The company was sold 3 times in 3 years, mostly recently to Nanjing Cenbest, a Chinese department store chain that has expanded into healthcare.Sipuleucel-T’s surprising OS benefit was both the key to its eventual approval and a complicating factor in the trial designs. One of the “major selling points” for trial patients was the availability of sipuleucel-T as a salvage therapy for those in the control arm, Gomella said. When those patients’ cancer progressed, they had the option of having their cryopreserved blood cells activated with the fusion protein and reinfused, extending their survival but muddying the trial results.

“The IMPACT trial was its own worst enemy, in a way, and actually probably underrepresented the survival advantage from sipuleucel-T,” said Gomella, who coauthored an analysis of the salvage therapy. “This was not the cleanest trial in the world, because the placebo arm was not a pure placebo arm. If you started to look at the net benefit, if you took the sipuleucel-T salvage arm out, you actually saw much, much better survival in the treatment arm.”

About two-thirds (165 of 249) of the control patients received the frozen product, APC8015F. After adjusting for independent predictors of postprogression survival, a statistical analysis showed them trending toward improved survival (HR, 0.78; 95% CI, 0.54-1.11; P = .17).12 Estimated median OS benefit for sipuleucel-T versus control adjusted for APC8015F treatment was 8.1 months, if APC8015F was equally effective as sipuleucel-T.

“Theoretically, it was a doubling of the survival, which is pretty impressive,” Gomella said.

Another posthoc analysis of the IMPACT data showed greater survival benefit in patients who had lower PSA when they received sipuleucel-T.13 When the trial results were subdivided by baseline PSA into quartiles, patients in the lowest baseline PSA quartile (≤22.1 ng/mL) showed an estimated median survival time of 41.3 months, versus 18.4 months in the highest quartile (>134.1 ng/mL). In the control arm, the estimated median survival times were 28.3 months versus 15.6 months for patients in the lowest versus highest baseline PSA quartile.

“You need to treat people who have maybe intermediate- to low-risk disease, where the PSA is not taking off but is gradually going up, where essentially you give the immune system a chance to ‘harness’ the cancer,” Chatta said. “If somebody doesn’t have superaggressive disease, you could give them Provenge, you’re done in 6 weeks, and if you get reasonable control—the scan stays stable, the PSA isn’t going up that fast—you can buy some time before you commit them to essentially lifelong therapy on a daily basis either with abiraterone [Zytiga] or enzalutamide [Xtandi].” The other therapies available for these patients are docetaxel and radium-223 (Xofigo).

Further data have come from PROCEED, a phase IV registry study that Dendreon set up. A significant finding was the greater benefit for African American men with mCRPC. A multivariate analysis matching 420 Caucasian patients with 210 African American patients by baseline PSA found OS was 39.5 months for the latter group versus 28.1 months for the former (P <.001; HR, 0.665; 95% CI, 0.530-0.835).14 Younger age, lower PSA or alkaline phosphatase, and higher hemoglobin levels were independently associated with longer OS, as was no prior chemotherapy.

Sequencing has been the subject of numerous studies, but actionable findings have been scarce. The phase II STAND trial found that patients with biochemically recurrent disease (BRPC) had greater peripheral T-cell PA2024-specific immune responses when receiving sipuleucel-T prior to starting androgen-deprivation therapy (ADT), compared with those who had the immunotherapy after starting ADT.15 However, there was no difference in time to next intervention or to metastasis. Other studies found that the timing of sipuleucel-T administration when combined with abiraterone and prednisone, or with enzalutamide, did not affect response.

The search for biomarkers has also yielded few clinically useful data. Prostatectomy specimens from patients who received presurgical sipuleucel-T showed significant increases in several types of infiltrating T cells, compared with specimens from those who did not receive the therapy, but downstaging of tumors was not observed.16 A small study of men with BRPC showed slowing of PSA doubling time after treatment with sipuleucel-T but no declines in absolute PSA levels.17 Chatta and others said the lack of methods for measuring the product’s intermediate effects has hampered research.

“We really have no biomarkers to guide us. That’s been a shame, because it’s hard to incorporate this product into earlier stages of disease. If somebody says, it’s going to make you live longer the earlier you take it, but it’s going to take you 20 years to find out, who cares?” Chatta said.

Ongoing Studies

One study suggests that cytotoxic T lymphocytes (CTLs) could serve as a useful biomarker. Investigators testing samples taken during previous combination trials found that 26 weeks after administration of sipuleucel-T, OS correlated with the magnitude of PAP (Pearson R, 0.52; P = .013) or PA2024 (Pearson R, 0.67; P = .0006) CTL activity.18The ProVent trial launched last year takes a different tack, using standard needle biopsies to measure histopathologic disease progression in men on active surveillance. The phase III trial will be conducted at approximately 50 sites across the United States with a targeted enrollment of 450 participants. They are being randomized 2:1 to receive sipuleucel-T or placebo.

The primary endpoint is histological upgrade from International Society of Urological Pathology Grade Group 1 to Grade Group 2 or higher, or Grade Group 2 upgraded to Grade Group 3 or higher. Secondary endpoints include the number of study participants with subsequent prostate cancer treatment (for example, surgery, radiation, or hormone therapy), the percentage of participants with a negative biopsy, and safety. Exploratory objectives will evaluate the association of immunologic responses with efficacy and patient quality-of-life outcomes.

Immunotherapy combinations are also beginning to get attention. In a recent, small phase I trial, 9 men with mCRPC received sipuleucel-T followed by escalating doses of ipilimumab (Yervoy).19 The combination was well tolerated. Statistically significant increases in serum immunoglobulin G (IgG) and IgG-IgM levels specific for PAP and PA2024 were observed after administration of sipuleucel-T, and levels increased further with use of ipilimumab. A phase II trial combining sipuleucel-T with immediate versus delayed ipilimumab remains active (NCT01804465).

Other current trials combine sipuleucel-T with atezolizumab (Tecentriq) in patients with asymptomatic or minimally symptomatic mCRPC (NCT03024216) and with stereotactic ablative body radiation (NCT01818986).

References

  1. Liu A. Dendreon changes hands—again&mdash;in $868M deal that keeps seller Sanpower in the game. FiercePharma website. fiercepharma.com/pharma/dendreon-resold-by-sanpower-868m-deal-it-undesirable. Published August 3, 2018. Accessed January 25, 2019.
  2. Fitzhugh M. Dendreon seeks expanded role for Provenge in new early stage prostate cancer trial. Dendreon website [reprinted from BioWorld. 2018;29(98)]. dendreon.com/Portals/12/dendreon-pharmaceuticals-bioworld-reprint.pdf. Accessed January 8, 2019.
  3. Questions and answers—Provenge. US FDA website. fda.gov/biologicsbloodvaccines/cellulargenetherapyproducts/approvedproducts/ucm210037.htm. Updated March 16, 2018. Accessed January 25, 2019.
  4. Small EJ, Schellhammer PF, Higano CS, et al. Placebo-controlled phase III trial of immunologic therapy with sipuleucel-T (APC8015) in patients with metastatic, asymptomatic hormone refractory prostate cancer. J Clin Oncol. 2006; 2006;24(19):3089-3094. doi: 10.1200/JCO.2005.04.5252.
  5. Higano CS, Schellhammer PF, Small EJ, et al. Integrated data from 2 randomized double-blind, placebo-controlled, phase 3 trials of active cellular immunotherapy with sipuleucel-T in advanced prostate cancer. Cancer. 2009;115(16):3670-3679. doi: 10.1002/cncr.24429.
  6. Dendreon receives complete response letter from FDA for Provenge BLA [news release]. Seattle, WA: Dendreon Corporation; May 9, 2007. fiercebiotech.com/biotech/press-release-dendreon-receives-complete-response-letter-from-fda-for-provenge-bla. Accessed January 25, 2019.
  7. Bates B. Tempers flare over fate of prostate cancer drug. MDedge/Family Practice News website. mdedge.com/familymedicine/article/26994/mens-health/tempers-flare-over-fate-prostate-cancer-drug. Published October 15, 2007. Accessed January 25, 2019.
  8. Kantoff PW, Higano CS, Shore ND, et al; IMPACT Study Investigators. Sipuleucel-T immunotherapy for castration-resistant prostate cancer. N Engl J Med. 2010;363(5):411-422. doi: 10.1056/NEJMoa1001294.
  9. Begley S. Insight: new doubts about prostate-cancer vaccine Provenge. Reuters website. reuters.com/article/us-provenge/insight-new-doubts-about-prostate-cancer-vaccine-provenge-idUSBRE82T07420120330. Published March 30, 2012. Accessed January 8, 2019.
  10. Huber ML, Haynes L, Parker C, Iversen P. Interdisciplinary critique of sipuleucel-T as immunotherapy in castration-resistant prostate cancer. J Natl Cancer Inst. 2012;104(4):273-279. doi: 10.1093/jnci/djr514.
  11. Jaros&#322;awski S, Toumi M. Sipuleucel-T (Provenge®): autopsy of an innovative paradigm change in cancer treatment: why a single-product biotech company failed to capitalize on its breakthrough invention. BioDrugs. 2015;29(5):301—307. doi: 10.1007/s40259-015-0140-7.
  12. George DJ, Nabhan C, DeVries T, et al. Survival outcomes of sipuleucel-T phase III studies: impact of control-arm cross-over to salvage immunotherapy. Cancer Immunol Res. 2015;3(9):1063-1069. doi: 10.1158/2326-6066.CIR-15-0006.
  13. Schellhammer PF, Chodak G, Whitmore JB, et al. Lower baseline prostate-specific antigen is associated with a great overall survival benefit from sipuleucel-T in the Immunotherapy for Prostate Adenocarcinoma Treatment (IMPACT) trial. Urology. 2013;81(6):1297-1302. doi: 10.1016/j.urology.2013.01.061.
  14. Sartor AO, Armstrong A, Ahaghotu C, et al. PD24-12 Overall survival analysis of African American and Caucasian patients receiving sipuleucel-T: preliminary data from the PROCEED registry. J Urol. 2017;197(4S):e456-e457. doi: 10.1016/j.juro.2017.02.1089.
  15. Antonarakis ES, Kibel AS, Yu EY, et al; STAND Investigators. Sequencing of sipuleucel-T and androgen deprivation therapy in men with hormone-sensitive biochemically recurrent prostate cancer: a phase II randomized trial. Clin Cancer Res. 2017;23(10):2451-2459. doi: 10.1158/1078-0432.CCR-16-1780.
  16. Fong L, Carroll P, Weinberg V, et al. Activated lymphocyte recruitment into the tumor microenvironment following preoperative sipuleucel-T for localized prostate cancer [published correction appears in J Natl Cancer Inst. 2014;106(11);dju372]. J Natl Cancer Inst. 2014;106(11);dju268. doi: 10.1093/jnci/dju268.
  17. Beinart G, Rini BI, Weinberg V, Small EJ. Antigen-presenting cells 8015 (Provenge) in patients with androgen-dependent, biochemically relapsed prostate cancer. Clin Prostate Cancer. 2005;4(1):55-60. doi: 10.3816/CGC.2005.n.013.
  18. Antonarakis ES, Small EJ, Petrylak DP, et al. Antigen-specific CD8 lytic phenotype induced by sipuleucel-T in hormone-sensitive or castration-resistant prostate cancer and association with overall survival. Clin Cancer Res. 2018;24(19):4662-4671. doi: 10.1158/1078-0432.CCR-18-0638.
  19. Scholz M, Yep S, Chancey M, et al. Phase I clinical trial of sipuleucel-T combined with escalating doses of ipilimumab in progressive metastatic castrate-resistant prostate cancer. Immunotargets Ther. 2017;6:11-16. doi: 10.2147/ITT.S122497.
Related Videos
Minesh Mehta, MD
Ruben Olivares, MD
Phillip J. Koo, MD
Daniel Spratt, MD
Daniel Spratt, MD
Philip J. Koo, MD
Anthony D'Amico MD, PhD
Mary Ellen Taplin, MD
Emmanuel Antonarakis, MD
Mary-Ellen Taplin, MD