You are here: Home: PCU 3 | 2006: Paul F Schellhammer, MD

Schellhammer, MD

Tracks 1-9
Track 1 Introduction
Track 2 A clinical investigator’s experience with the diagnosis and treatment of prostate cancer
Track 3 Differences in reaction to prostate cancer versus other chronic diseases
Track 4 Coping with the fear and uncertainty associated with prostate cancer
Track 5 Translating personal experience with prostate cancer to patient care
Track 6 Clinical benefit of docetaxel in prostate cancer
Track 7 Barriers and initiatives to increase clinical trial participation
Track 8 Use of PSA doubling time to identify candidates for clinical trials
Track 9 Selection of hormonal therapy when sexual functioning is not a patient concern

Select Excerpts from the Interview

Track 2

- DR LOVE: You were diagnosed with prostate cancer in 1999, and since then you have spoken with us several times about your experience. Can you review the clinical course of your disease and update us on your current situation?

- DR SCHELLHAMMER: Since age 50, my PSA has regularly been tested and the scores were quite stable with a PSA level of 2-3 ng/mL. Although at the time I was happy with those scores, I know from the information we have now that a 50-year-old with a PSA score of two to three is at increased risk. My PSA went up after 1999, and in 2000 I underwent a radical prostatectomy.

I was found to have organ-confined but high-grade disease. Three expert pathologists examined my tissue, and based on their variable readings, the sum of the Gleason scores interpreted ranged from a seven to a nine. It was quite different, depending on the pathologist who looked at the tissue.

Within a year I had a PSA rise. I received androgen deprivation for six months with salvage radiation therapy, did well for almost three years with an undetectable PSA level, and then most recently the PSA level has started to rise. Obviously, I’ve been looking for the next step.

- DR LOVE: How recently was it that it your PSA level started to rise?

- DR SCHELLHAMMER: It started going up about six months ago and has risen at a pace that is somewhere between a three- and six-month doubling time. Rather than wait and observe, I wanted to do something proactive. I was interested in clinical trials and also felt an obligation to my patients for whom I had repeatedly urged participation in trials.

Not many trials are available for rising PSA levels in hormone-naïve circumstances, but an ECOG trial is using a breast cancer drug, lapatinib, for patients with a rising PSA and a doubling time of less than 12 months. So I’ve initiated that trial and I’m about two months into it. We’ll have to see what it does with regard to the PSA kinetics.

Track 4

- DR LOVE: You and urologic oncologist Paul Lange wrote a book recently — A View from the Other Side. How did this come about?

- DR SCHELLHAMMER: We were both diagnosed with the disease, and we were able to spend many hours together during our summer vacation talking about how to advise patients about prostate cancer and about the issues we personally were facing, such as selection of our own therapies, dealing with the issues of rising PSA levels, the issues of hormone therapy, the changes in quality of life, the issues of complementary medicine and fear. It seemed reasonable to get together and take a dual approach to these issues.

- DR LOVE: What are some of the main ideas that you wanted to communicate?

- DR SCHELLHAMMER: I don’t think we appreciate as much as we should the fear factor for patients diagnosed with this disease. The uncertainty about which treatment may be best leaves patients hanging as to how they should proceed. We should listen more carefully to our patients, for example, regarding their use of complementary medicines and how they would like to integrate them into their treatment.

By ignoring this issue, I believe we sometimes allow patients to use supplements and vitamins to excess or in an inappropriate way. I consider it better to guide than to ignore, and I believe it is important to appreciate the overall issues surrounding quality of life, which is inevitably reduced by primary and secondary therapy.

- DR LOVE: Over these last few years when you’ve encountered difficult times and challenges, how did you cope?

- DR SCHELLHAMMER: It’s always helpful to consider other patients, such as those with virulent benign disease or those with other cancers with a poor prognosis, and put into perspective the fact that a patient with prostate cancer can expect a longer life span than can be expected with most maladies.

In addition, not only are good therapies currently available, but therapies may also come up in the future. As someone once said, a cure for prostate cancer is not insurance against any other bullet that might be headed your way, so you can’t look at this disease as the only impediment to good living.

Track 5

- DR LOVE: Any specific insights you have gained about taking care of patients with prostate cancer or lessons that you have learned that you think are relevant to physicians?

- DR SCHELLHAMMER: I realize that offering a number of positive possibilities without specific direction to one therapy is the best way to advise. It helps to offer a number of good therapies, explain them to the patient and allow the patient to decide in a reasonable period of time what he is most comfortable with.

I have no doubt that if my own experience is brought up or is eventually talked about and I give him the monograph we’ve written, this provides a bond that tells the patient I know somewhat where I am coming from — from a scientific and from an emotional standpoint.

- DR LOVE: What are some of the directions in clinical research that you feel the most optimistic about in prostate cancer?

- DR SCHELLHAMMER: I hope that in the next five years the so-called fourth modality of therapy, immunotherapy, might find a role and complement our current options of surgery, chemotherapy and radiation therapy that we’ve used for so long and with good or reasonable success.

Better information about when to begin androgen deprivation and whether intermittent schedules remain positive with no downsides would also be helpful. In addition, the use of chemotherapy at earlier stages of disease may show promise in the near future, particularly as adjuvant therapy for patients with high risk factors such as PSA doubling time, time to recurrence and Gleason score.

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Michael J Zelefsky, MD
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Mario A Eisenberger, MD
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Paul F Schellhammer, MD
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