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Reduced-Dose Schedule of Cabazitaxel Viable for Seniors With mCRPC - MedPage Today, November 1, 2023

CaptnMojoe profile image
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Modified dosing schedule from phase III randomized CABASTY trial for Jetvana (+ G-CSF) for older patients out of non-chemo treatment options.

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Reduced-Dose Schedule of Cabazitaxel Viable for Seniors With mCRPC - Grade 3 or higher neutropenia, neutropenic complications reduced by 12-fold, by Mike Bassett, Staff Writer, MedPage Today November 1, 2023.

A reduced-dose schedule of cabazitaxel (Jevtana) plus prophylactic granulocyte colony-stimulating factor (G-CSF) should be offered to older men with metastatic castration-resistant prostate cancer (mCRPC), according to results from the phase III randomized CABASTY trial.

Rates of grade 3 or higher neutropenia or neutropenic complications were about 12 times lower with biweekly cabazitaxel 16 mg/m2 plus G-CSF compared with the standard regimen of triweekly cabazitaxel 25 mg/m2 plus G-CSF (5.1% vs 62.5%; OR 0.03, 95% CI 0.01-0.08, P<0.001), reported Stephane Oudard, MD, PhD, of Georges Pompidou Hospital in Paris, and colleagues.

Among the 196 patients ages 65 and older, grade 3 or higher adverse events (AEs) in general were also more common with triweekly dosing compared with biweekly dosing (72.9% vs 56.1%), they noted in JAMA Oncology.

Despite providing a survival advantage, standard regimens of taxanes, such as docetaxel and cabazitaxel, have been associated with more grade 3 or higher AEs -- including neutropenia -- in patients ages 75 and older compared with younger patients.

Thus "these data may be practice changing, especially in patients 65 years or older with metastatic CRPC who are often denied chemotherapy in daily clinical routines," Oudard and colleagues concluded.

In a commentary accompanying the study, Alicia Morgans, MD, MPH, of Dana-Farber Cancer Institute and Harvard Medical School in Boston, noted that "more than simply providing a treatment option" for older men, "this study reminds the community of clinicians caring for patients with prostate cancer that we must engage in studies to define options for treatment that extend the benefit of therapies evaluated in registration trials to the more vulnerable and frail populations."

Despite the results suggesting "a way in which we can safely and effectively treat the frail older adult population with cabazitaxel, it does come at the expense of more frequent dosing," she added.

"Approaches to treatment that increase the number of clinic and laboratory visits may pose challenges for some of the patients they are meant to support," she wrote. Further work is needed to design trials "that not only meet patient needs in terms of cancer control, but also optimize accessibility and reduce burdens."

For the CABASTY trial, Oudard and team enrolled 196 heavily pretreated patients with mCRPC from France (18 centers) and Germany (seven centers) from May 2017 through January 2021. Median age was 74.6, and 92.3% had an Eastern Cooperative Oncology Group performance status score of 0 or 1. All patients had received previous docetaxel, and 48.1% had received at least three lines of hormone therapy.

Median follow-up was 31.3 months, and relative dose intensities were comparable between groups (median 92.7% in the triweekly group vs 92.8% in the biweekly group).

Median radiographic progression-free survival was similar between the triweekly and biweekly groups (10.25 vs 7.82 months, P=0.89), as was median overall survival (14.1 months in both arms, P=0.39).

Treatment was prematurely discontinued in 70.8% of patients in the triweekly group, mainly due to AEs, and 89.8% in the biweekly group, mainly due to disease progression.

The incidence of serious AEs of any grade was comparable between the groups (43.8% in the triweekly group and 45.9% in the biweekly group), as was the percentage of patients with AEs leading to permanent discontinuation (33.3% vs 31.6%, respectively).

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CABASTY Trial Abstract is here:

JAMA Oncology - Original Investigation - Biweekly vs Triweekly Cabazitaxel in Older Patients With Metastatic Castration-Resistant Prostate CancerThe CABASTY Phase 3 Randomized Clinical Trial, October 26, 2023.

jamanetwork.com/journals/ja...

Alicia Morgans commentary (Abstact only) is here:

JAMA Oncology - Invited Commentary - Expanding Treatment Options for Older Adults With Prostate Cancer, Alicia Morgans, MD, MPH, October 26, 2023.

jamanetwork.com/journals/ja...

Link to MedPage Today article is here:

medpagetoday.com/hematology...

Let's hope none of us ever needs this,

Mojoe

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j-o-h-n profile image
j-o-h-n

Greeting Cap,

Would you be kind enough to fill in your bio, e.g. "age, location, Prostate Medical procedure(s), PSA and your Gleason scores, Medical treatment facilities, and Doctor(s) names). All information is voluntary but can be helpful to you and to us. THANK YOU!

Good Luck, Good Health and Good Humor.

j-o-h-n Friday 11/03/2023 6:20 PM DST Billy's gone

TeleGuy profile image
TeleGuy

This is strange to me. It’s not really a reduced dose, it’s just a changed frequency. Both approaches are close to 8 mg/m2 but the biweekly dosing did much better with SEs.

NPfisherman profile image
NPfisherman

Cujoe,

Like you, I hope people don't need this tx. As I learned in school, the higher dosing increases risks for SE's, and behold....it does... no surprise...

After Checkmate 650, people should realize that while immunotherapy is not highly effective against PCa, that science is changing so rapidly. Checkmate 650 showed that immunotherapy was effective in 25% of chemo naive PCa patients, but only effective at 10% for those that had chemo.

Immunotherapy is the future... why decrease your chances of success if not necessary??

DD