Brief, intense radiation and hormone therapy for very high-risk prostate cancer

As we’ve seen, brachy boost therapy seems to have the best oncological results for men with very high-risk prostate cancer. … READ MORE …

One large “zap” for painful bone metastases is enough

In 2011, the American Society for Radiation Oncology (ASTRO) issued a consensus statement as part of its “Choosing Wisely” campaign that found that 30 Gy in 10 fractions (treatments), 20 Gy in 5 fractions, and 8 Gy in 1 fraction all gave equivalent pain relief. … READ MORE …

Is ADT still needed for high-risk patients receiving brachy boost therapy?

Brachy boost therapy (external beam plus a brachytherapy boost to the prostate) is arguably the gold standard treatment for high-risk patients, reporting the best oncological outcomes of any therapy. While long-term adjuvant ADT has proven to be beneficial in prolonging survival in high-risk patients when used in conjunction with dose-escalated external beam radiation therapy (DART 01/05 GICOR), there has never been a randomized trial to determine if there is any benefit to ADT when used with brachy boost therapy .

All we have to go by are several single- or multi-institutional studies and one large database analysis. Almost all of the studies so far show no effect to short-term adjuvant ADT (i.e., 4 months of ADT, starting 2 months prior and running concurrent with the radiation therapy)

Two of the studies used a boost of low-dose-rate brachytherapy, predominantly using Pd-103 seeds. Dattoli et al.  found there was no significant difference in 16-year PSA progression-free survival (PSA-PFS) whether 4 months of ADT were added or not. D’Amico et al. also found no significant difference in 8-year prostate cancer-specific mortality (PCSM) with the addition of ADT. However, they felt that it was “approaching significance” (p = 0.08) and might become statistically significant with longer follow-up. In contrast to the Dattoli study, the D’Amico study did not treat the pelvic lymph nodes.

A recent analysis of the large National Cancer Database by Yang et al. did not detect any benefit to adding ADT on 8-year overall survival (OS). However, the database lacks specific information about type of brachytherapy, radiation doses, duration of ADT, and whole-pelvic treatment,

Several studies that used high-dose-rate brachytherapy as a boost also looked at this issue retrospectively. Demanes et al. was the earliest of those studies. They found no difference in 10-year PSA-PFS in their 113 high-risk patients treated between 1991 and 1998. Several subsequent studies confirmed those findings. Galalae et al. concatenated the databases from three institutions: Kiel University, the University of Washington in Seattle, and William Beaumont Hospital. Short-term adjuvant ADT failed to demonstrate improved 10-year PSA-PFS in the 359 high-risk patients treated between 1986 and 2000. And the lack of effect was demonstrated at all three institutions. Kotecha et al. also failed to find any differential improvement in 5-year PSA-PFS among 61 high-risk patients treated with HDR brachy boost at Memorial Sloan-Kettering Cancer Center between 1998 and 2009.

There has been one “outlier” study. Schiffmann et al. reported on 211 consecutive high-risk patients treated at the University Medical Center Hamburg-Eppendorf from 1999 to 2009. After 10 years, the biochemical recurrence-free survival rate was 50 percent with the adjuvant ADT but only 39 percent without it — a very statistically significant difference. However, even the “improved” outcome seems low compared to the ASCENDE-RT trial, in which everyone got early neoadjuvant and adjuvant ADT. In that trial, the 9-year PSA-PFS for high-risk patients receiving the trimodality therapy was 83 percent. Another multi-institutional study of HDR-brachy boost therapy reported 10-year PSA-PFS of 85 percent with ADT and 81 percent without ADT in high-risk patients. It is plausible that the patients in the Hamburg study had more advanced disease and had more undetected micrometastases compared to the other studies.

The following table summarizes the treatments given in the aforementioned studies, and whether there was a statistically significant improvement (p < 0.05).

Short-term vs. long-term adjuvant ADT

ADT is believed to have two effects when used in conjunction with radiation. Used before radiation begins (neoadjuvant use) and during radiation treatments (concurrent use), it radio-sensitizes the cancer. Laboratory findings suggest that it interferes with cancer cell repair of the induced DNA double-strand breaks. After radiation (adjuvant use), ADT is believed to “clean up” any remaining local micrometastases that survived. The death of cancer cells from both the radiation and the ADT dumps antigens into the serum that may activate T-cells. Those T-cells may hunt out and destroy small amounts of cancer cells nearby (the bystander effect) or systemically (the abscopal effect).

The bulk of the above retrospective studies suggest that the radio-sensitizing effect is unnecessary with the very high radiation doses given with brachy boost therapy. However, what remains to be shown is whether long-term ADT might confer any additional benefit. The DART 01/05 GICOR trial proved that there was a significant benefit to 28 months of ADT compared to 4 months in high-risk patients treated with dose-escalated EBRT. It is possible that while short-term ADT may have no benefit, long-term ADT might. On the other hand, the very high rates of cancer control (around 80 to 85 percent) using brachy boost therapy may be as high as we can reasonably hope for, given that there will always be some patients with undetected,occult micrometastases.

Better patient selection

High-risk patients are usually given a bone scan and CT to help rule out distant metastases. Bone scans are non-specific to prostate cancer and are not very sensitive when the PSA is below 20 ng/ml. CT scans detect metastases larger than about 1.2 cm, but most metastases are smaller than that. The newly-approved Axumin PET scan, and the experimental PSMA-based PET scans now in clinical trials may be able to detect those distant metastases earlier in recurrent patients. However, there are currently no PET scans approved for high-risk patients outside of clinical trials. (They are only approved for recurrent and advanced cancer patients.) In the future, those high-risk men in whom metastases have been detected via PET scans may be better candidates for systemic therapies, while those in whom no metastases have been detected may be better candidates for brachy boost therapy. It may be economically justifiable to use PET scans for this purpose. Perhaps we will see another 5 to 10 percent increase in cancer control rates, even without ADT, with better patient selection.

Dose escalation

At the high biologically effective doses (BEDs) used in all the brachy boost studies, there does not seem to be a significant interaction between dose used and whether ADT was effective. The Dattoli study had the lowest BED, but no benefit to added ADT, while the Galalae study had the highest BED, but also no benefit to added ADT. The Hamburg study had high BED but did demonstrate a benefit to added ADT. All of the brachy boost studies seem to have adequate radiation doses.

Whole pelvic radiation

It is possible that pelvic lymph nodes are best treated with a combination of radiation and ADT.  Bittner et al. looked at 186 high-risk patients treated with the brachy boost therapy. The 10-year PSA-PFS was:

  • 94 percent if they received both whole pelvic radiation and ADT
  • 82 percent if the received whole pelvic radiation without ADT
  • 90 percent if they received ADT without whole pelvic radiation
  • 75 percent if they received neither ADT nor whole pelvic radiation

ADT seemed to have a bigger effect than whole pelvic radiation. This may be because the whole pelvic radiation dose is inadequate. The doses given to the pelvic lymph nodes are quite a bit lower (about 50 Gy in 28 fractions) than the dose to the prostate. If Dr. King is right that prostate cancer is inherently radio-resistant and requires a higher lethal dose (about 79.2 Gy/44 fx) to be effective, even when the cancer is only in the prostate bed (see this link), it is possible that pelvic lymph nodes require a higher dose as well. Because of the potential bowel toxicity of escalated pelvic doses, adjuvant ADT may be necessary to achieve effective cell kill rates without dose-limiting toxicity. We saw in a recent analysis that, in the salvage situation among patients with Gleason scores of 8 to 10, whole pelvic radiation and ADT both had significant benefits. Whether whole pelvic radiation is effective in high-risk patients treated with brachy boost therapy and ADT is the subject of a major ongoing randomized clinical trial (RTOG 0934).

Retrospective vs prospective trials

All of the published studies so far have been retrospective, and are therefore subject to selection bias: those who received the ADT had more progressed disease than those who received the brachy boost without ADT. Therefore, it will always be impossible to convincingly resolve this issue without a prospective, randomized clinical trial.

Patient decisions

Until we have definitive results from randomized clinical trials, the decision over whether to add ADT to brachy boost therapy will be challenging. Many patients are persuaded by the extra insurance ADT provides, and that only a short course seems to be necessary. Others are so ADT-averse that even a short course is unthinkable, especially with no concrete evidence of efficacy.

The decision over whether to include the whole pelvic area in the external beam radiation field may be an easier decision. High-risk patients have a significant probability that there are small metastases harbored in pelvic lymph nodes. Recent studies have shown the treatment field must be wider than was previously thought. For some patients with anatomical abnormalities, low visceral fat, and a history of bowel disease, this too may present a challenging decision.

Editorial note: This commentary was written by Allen Edel for The “New” Prostate Cancer InfoLink.

No need to endure 38 to 44 treatments with IMRT anymore

There have been several hypofractionation trials maturing in the last couple of years. With minor exceptions, they all tell the same story: external beam radiation therapy (EBRT) can be completed in less time without loss of efficacy or increase in toxicity. … READ MORE …

Baseline data from the ProtecT trial … with outcomes still to come

Many readers of this blog will be interested to look through the data on the preliminary study design and diagnostic and baseline results of the randomized, phase III ProtecT trial that have just been reported in The Lancet Oncology. … READ MORE …

Delaying onset of erectile dysfunction when receiving radiation therapy

Daily treatment with sildenafil citrate (Viagra) seems to have been able to help maintain erectile function for up to 2 years among men receiving such adjuvant treatment during and after radiotherapy for localized prostate cancer. … READ MORE …

Is combination EBRT + LDR-BT worth the risk for most patients?

Long-term data from the Radiaton Treatment Oncology Group (RTOG) 00-19 Phase II trial of external beam radiation therapy (EBRT) + low-dose-rate permanent implant brachytherapy (LDR-BT) has suggested that this type of radiation treatment is probably no more effective than either EBRT or LDR-BT alone … but does have a greater risk for long-term side effects. … READ MORE …

Prostate cancer-specific mortality after biochemical recurrence in a cohort of US veterans

A study reported this week in the Archives of Internal Medicine addresses the impact of biochemical recurrence on risk for prostate cancer-specific mortality (PCSM) among a cohort of more than 1,000 US veterans initially diagnosed and treated between 1991 and 1995. … READ MORE …

Timing of salvage hormone therapy when radiotherapy has failed

The question of when one should initiate hormone therapy in a man who has a rising PSA after radiation therapy has long been a topic of controversy. And a reanalysis of data from RTOG 85-31 has not helped to give us a definitive answer. … READ MORE …

Prostate cancer news reports: Tuesday, March 30, 2010

Today’s news reports address:

  • Diabetes and prostate cancer risk among Japanese men
  • The accuracy of T2w ecMRI in detection of prostate cancer
  • Escalated dose radiation therapy and treatment of localized prostate cancer
  • Erectile dysfunction and penile rehabilitation post-surgery … READ MORE …

Prostate cancer news reports: Sunday, January 17, 2010

In today’s news reports we address recent publications on:

  • The GEMCaP biomarkers and prediction of prostate cancer recurrence post-surgery
  • Biopsy Gleason score under-staging and active surveillance
  • The value of exercise during radiotherapy
  • Impact of type of surgery on post-surgical continence at 1 year … READ MORE …

Prostate cancer news reports: Monday, October 12, 2009

In today’s news reports we note items on:

  • DNA histone levels and adverse prognosis
  • Outcomes to active surveillance vs EBRT
  • The use of radiation therapy as first-line treatment over time
  • Prostate cancer-specific mortality, brachytherapy, and EBRT … READ MORE …

What cost prostate cancer treatment?

Many readers will be interested in the article titled “Debate surrounds new prostate-cancer treatment” that appeared today in the Philadelphia Inquirer on the topic of prostate cancer treatment costs. … READ MORE …

Prostate cancer news reports: Sunday, July 12, 2009

This weekend’s news reports deal with:

  • A new epidemiological database for prostate cancer research
  • Phase II trial results for the “vaccine” PSA: 154-163 (155L)
  • The degree to which adding hormone therapy to radiotherapy affects outcomes in patients with localized prostate cancer
  • The possibility that zoledronic acid could be used just once a year to prevent bone loss and related events in men having androgen deprivation therapy … READ MORE …

Palliative prostate-specific radiotherapy in men with advanced prostate cancer

It is still not unusual, in large parts of the world, for patients to be diagnosed with prostate cancer and treated with hormone therapy as a first-line treatment or following a period of active surveillance or monitoring — for all sorts of reasons. … READ MORE …