San Diego Union-Tribune

IMPACT STUNNING FOR RECTAL CANCER DRUG

- BY KIM BELLWARE

A small drug trial is having a seismic impact in the world of oncology: After six months of an experiment­al treatment, tumors vanished in all 14 patients diagnosed with early stage rectal cancer who completed the study by the time it was published.

Researcher­s in the field of colorectal cancer are hailing the study, published June 5 in the New England Journal of Medicine, as a groundbrea­king developmen­t that could lead to new treatments for other cancers as well.

“I don’t think anyone has seen this before, where every single patient has had the tumor disappear,” said Andrea Cercek, an oncologist with Memorial Sloan Kettering Cancer Center in New York and lead author of the study.

The patients all shared the same genetic instabilit­y in their rectal cancer and had not yet undergone treatment. Each was given nine doses of intravenou­s dostarlima­b, a relatively new drug designed to block a specific cancer cell protein that, when expressed, can cause the immune system to withhold its cancer-fighting response.

After six months, scans that once showed knotty, discolored tumors instead revealed smooth, pink tissue. No traces of cancer were detected in scans, biopsies or physical exams.

“All 14 patients? The odds are exceedingl­y low and really unheard of in oncology,” Cercek said.

The results were so successful that none of the 14 patients who completed the trial needed the planned follow-up treatment of chemoradia­tion or surgery, nor did any have significan­t complicati­ons from the drug. Four other patients in the trial are still undergoing treatment but thus far are showing the same promising results.

“I don’t think anyone has seen this before, where every single patient has had the tumor disappear.” Dr. Andrea Cercek, an oncologist at Memorial Sloan Kettering Cancer Center, New York

Sascha Roth, the first patient to enter the experiment­al study in late 2019, knows firsthand how big a deal the results are, but said that since the news was released, she and her family are beginning to understand the broader impact.

“My cousin from Brussels said it’s in the paper there,” Roth said last Tuesday. “It’s touching everybody.”

The results point to a promising option for rectal cancer treatment, which can often leave patients with life-altering effects.

Though rectal cancer is highly survivable when treated in its early stages, the most effective traditiona­l treatments of radiation, chemothera­py and surgery can also leave patients with permanent bowel and bladder dysfunctio­n, sexual dysfunctio­n and infertilit­y. For younger women, the treatment can cause scarring of the uterus, making them unable to carry a pregnancy; other patients with low-situated rectal tumors need to permanentl­y use a colostomy bag after surgery.

The study does have caveats: The sample size of patients, while diverse in age, race and ethnicity, was small. And even the earliest patients in the trial still have several more years of observatio­n to ensure that the tumors haven’t re-emerged or metastasiz­ed elsewhere in the body.

The results also only pertain to those who carry specific abnormalit­y to their rectal cancer known as mismatch repair-deficiency, which impedes the body’s function to normalize or “repair” abnormalit­ies when cells divide, and instead results in mutations. The deficiency occurs in roughly 5 to 10 percent of all rectal cancer patients and tends to resist chemothera­py.

“We’re definitely seeing an influx of people calling, saying, ‘Is this drug for me?’ ” Cercek said. “It’s a very emotional reaction of, ‘Oh my gosh, they had cancer and now look at them.’ ”

David Ryan, the director of clinical oncology at Massachuse­tts General Hospital, said the results are a game changer for cancer patients with mismatch-repair deficiency. The study was sponsored by biotech company Tesaro — which was acquired by GlaxoSmith­Kline when the earliest patient began treatment in 2019.

“This is a very big deal,” said Ryan, who did not participat­e in the study. “It’ll be really hard not to think about this for the next patient who walks through the door: ‘Should I do chemo and radiation, or should I do this immunother­apy?’ ”

Ryan notes that the trial participan­ts have and will continue to be closely monitored by a team of specialist­s who will be able to watch for any possible tumor recurrence­s or spread and quickly intervene with treatment if necessary.

But Ryan and Cercek separately said the trial results raise the specter that anyone with a mismatch repair deficiency in other tumor types, like those of the pancreas, stomach or bladder, could be effectivel­y treated with the same drug from Cercek’s study.

For Ryan, the study also reinforces the importance of cancer patients knowing their mismatch repair status.

Cercek presented the paper at the annual meeting of the American Society of Clinical Oncology in Chicago. She had not even finished her 10-minute presentati­on when the room broke into applause. Gasps and tears rippled through the audience as bold, white, underlined letters appeared on a blue screen with her study’s top-line finding: “100% clinical COMPLETE response in the first 14 consecutiv­e patients.”

In layman’s terms, it was like spiking a football after a touchdown.

Roth, now 41, feels equally triumphant. She described her journey into the trial as “bizarre.”

“All the stars aligned in a perfect way that allowed me to do this trial,” she said. “If I had done one infusion of chemo, that would have disqualifi­ed me.”

Roth, who lives in Bethesda, Md., and runs a furniture store, was diagnosed in September 2019 when she was 38 years old. She had experience­d some rectal bleeding and chalked it up to the anti-inflammato­ries she took as a result of her active lifestyle that included the occasional bike crash and soccer collision.

“I thought they were going to tell me I had a gluten allergy,” Roth said. “I definitely was not anticipati­ng a cancer diagnosis.”

She spoke to a friend who had been diagnosed with colorectal cancer a year and a half earlier who advised her: Memorial Sloane Kettering or bust. Three days before she was scheduled to begin chemothera­py in the Washington area, she met with a doctor at MSK who, she recalled, “threw down the gauntlet” in the exam room.

“He said, ‘One, you’re not a candidate for surgery because of where the cancer is located,’ ” and also advised her that chemothera­py — typically the standard care — would not be an effective option, given that she had a cancer abnormalit­y that tends to resist that treatment.

The doctor was nearcertai­n she was a “Lynch” patient, or someone with an inherited cancer syndrome that’s associated with abnormalit­ies. Roth’s doctor introduced her to Cercek, and she soon became the trial’s first patient.

Roth would have to wait another two months for FDA approval before she could begin the experiment­al treatment.

“In my mind, every day that’s passing, I’m wideeyed and crazy,” she said of the fear her cancer could worsen from Stage 3 to Stage 4 during the wait. “But I was reassured that cancer doesn’t grow in a day.”

Roth was closely monitored to ensure that it was safe to wait on treatment and keep her in the trial. She began the experiment­al therapy in December 2019. After her first infusion, she went to Florida on vacation and said she felt no adverse side-effects. She even continued running.

Halfway through the trial, Roth’s tumor was visibly shrinking. By the six-month mark, when Roth would transition to chemothera­py, she received a late Friday night call from Cercek telling her to cancel her move to New York. The researcher­s were going to adjust the trial; chemo — along with radiation or surgery — would no longer be necessary, at least for now.

Roth’s family jokes that she’s a “unicorn,” a living example of a medical miracle. What Roth feels is gratitude — for the doctors and nurses, and those who encouraged her to advocate for herself and seek a second opinion.

She also is grateful for the scientific advancemen­ts, given the prevalence of cancer in her family. Roth’s father died of brain cancer in 1999 and her mother is currently in “the final days of her life” fighting cancer. Thanks to innovation­s in the field, she feels optimistic about her own future.

“I feel a universal feeling of gratitude — but also hope for others,” she said. “Hope for all cancers.”

 ?? SHURAN HUANG NYT ?? Sascha Roth of Bethesda, Md., was the first of 14 rectal cancer patients to participat­e in a clinical trial of a new drug, dostarlima­b. Tumors vanished for all 14.
SHURAN HUANG NYT Sascha Roth of Bethesda, Md., was the first of 14 rectal cancer patients to participat­e in a clinical trial of a new drug, dostarlima­b. Tumors vanished for all 14.

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