Kaitlyn D’Onofrio

Lung Cancers Today

The Food and Drug Administration (FDA) has granted approval for <a href="https://www.docwirenews.com/docwire-pick/hem-onc-picks/fda-keytruda-firstline-head-neck-cancer/">Keytruda</a>® (<a href="https://www.docwirenews.com/conference-coverage/asco-2019/maintenance-pembrolizumab-first-line-chemotherapy/">pembrolizumab</a>) to treat metastatic small cell lung cancer (SCLC).
<a href="https://www.docwirenews.com/docwire-pick/hem-onc-picks/fda-approves-firstline-keytruda-inlyta-combo-kidney-cancer/">Pembrolizumab</a> was approved as a third-line therapy for SCLC patients who still present disease progression despite current or past platinum-based chemo and at least one other prior line of therapy, according to the FDA.
Keytruda is manufactured by Merck.
https://twitter.com/FDAHealthNews/status/1143107015247425537
“KEYTRUDA is already an established treatment option for non-small cell lung cancer, and today’s approval in small cell lung cancer demonstrates our commitment to bringing forward new treatment options for patients with advanced, difficult-to-treat cancers,” said Jonathan Cheng, MD, vice president, oncology clinical research, Merck Research Laboratories, in a press release. “We look forward to continuing to advance important clinical research in small cell lung cancer.”
“Small cell lung cancer, which accounts for 10 to 15% of all lung cancers, is often diagnosed at an advanced stage where the prognosis is very poor and there have historically been limited treatment options,” said Patrick Ott, MD, PhD, clinical director, Center for Immuno-Oncology, Dana-Farber Cancer Institute. “The approval of KEYTRUDA in small cell lung cancer provides an additional treatment option for patients based on the clinical response rates from KEYNOTE-158 and KEYNOTE-028.”
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On June 17th, 2019, the <a href="https://twitter.com/US_FDA?ref_src=twsrc%5Etfw">@US_FDA</a> approved pembrolizumab for patients with metastatic <a href="https://twitter.com/hashtag/SCLC?src=hash&amp;ref_src=twsrc%5Etfw">#SCLC</a> "with disease progression on or after platinum-based chemotherapy &amp; at least one other prior line of therapy." <a href="https://twitter.com/hashtag/LCSM?src=hash&amp;ref_src=twsrc%5Etfw">#LCSM</a> 
Read about the decision: <a href="https://t.co/B9JBQmDJfX">https://t.co/B9JBQmDJfX</a>
— IASLC (@IASLC) <a href="https://twitter.com/IASLC/status/1143172246913069056?ref_src=twsrc%5Etfw">June 24, 2019</a>
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<h2>Two Studies Evaluate Pembrolizumab</h2>
The FDA’s latest approval follows the results of two trials—<a href="https://www.ncbi.nlm.nih.gov/pubmed/30943124">KEYNOTE-158</a> and <a href="https://www.ncbi.nlm.nih.gov/pubmed/30557521">KEYNOTE-028</a>.
KEYNOTE-158 was a phase II study investigating the use of pembrolizumab in patients with previously treated advanced cervical cancer. A total of 98 patients (mean age, 46 years; range, 24–75 years) were treated with pembrolizumab 200 mg every three weeks for two years, if they presented progression or intolerable toxicity, or until a patient or physician decided to stop treatment. For the first year of treatment, patients underwent tumor imaging every nine weeks, and subsequently every 12 weeks. The primary outcome was objective response rate (ORR) per the Response Evaluation Criteria in Solid Tumors (version 1.1), and the secondary outcome was safety. Patients were followed for a median 10.2 months (range, 0.6–22.7 months).
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FDA approves pembrolizumab for metastatic SCLC <a href="https://twitter.com/Merck?ref_src=twsrc%5Etfw">@Merck</a>; <a href="https://twitter.com/Amgen?ref_src=twsrc%5Etfw">@Amgen</a> and @Allergan's Kanjinti, Herceptin biosimilar – <a href="https://twitter.com/FDAOncology?ref_src=twsrc%5Etfw">@FDAOncology</a> <a href="https://t.co/TTjIqxjdHl">https://t.co/TTjIqxjdHl</a> <a href="https://t.co/hwPrfYen9J">pic.twitter.com/hwPrfYen9J</a>
— The Cancer Letter (@TheCancerLetter) <a href="https://twitter.com/TheCancerLetter/status/1143576867297005568?ref_src=twsrc%5Etfw">June 25, 2019</a>
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There were 12 responses—three complete and nine partial; ORR was 12.2% (95% confidence interval [CI] 6.5–20.4%). All 12 of the patients with responses had PD-L1-positive tumors for an ORR of 14.6% (95% CI 7.8–24.2%), of which 14.3% (95% CI 7.4–24.1%) were in patients who had received at least one line of chemotherapy for recurrent or metastatic disease. Adverse events occurred in 65.3% of patients, the most prevalent of which included hypothyroidism (10.2%), decreased appetite (9.2%), and fatigue (9.2%).
KEYNOTE-028 evaluated patients with PD-L1-positive advanced solid tumors. The nonrandomized, phase Ib trial included 475 patients who received pembrolizumab 10 mg/kg every two weeks for two years or until progression or toxicity. The primary endpoint in this trial was also ORR, with secondary outcomes including safety, progression-free survival (PFS), and overall survival (OS).
<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
On June 17, 2019, <a href="https://twitter.com/US_FDA?ref_src=twsrc%5Etfw">@US_FDA</a> granted accelerated approval to pembrolizumab (KEYTRUDA) for patients with metastatic small cell <a href="https://twitter.com/hashtag/lungcancer?src=hash&amp;ref_src=twsrc%5Etfw">#lungcancer</a> (SCLC) with disease progression on or after platinum-based chemotherapy and at least one other prior line of therapy.<a href="https://t.co/XO5jkxY2CY">https://t.co/XO5jkxY2CY</a>
— Lung Cancer Europe (@LungCancerEu) <a href="https://twitter.com/LungCancerEu/status/1141724022574604289?ref_src=twsrc%5Etfw">June 20, 2019</a>
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Outcomes varied significantly based on cancer type. ORRs ranged from 0% (95% CI 0.0–14.2%) in pancreatic cancer to 33% (95% CI 15.6–55.3%) in SCLC. Similarly, median PFS varied from 1.7 months (95% CI 1.5–2.9 months) in pancreatic cancer to 6.8 months (95% CI 1.9–14.1 months) in thyroid cancer, and median OS was 3.9 months (95% CI 2.8–5.5 months) in vulvar tumors versus 21.1 months (95% CI 9.1–22.4 months) in carcinoid tumors. Safety outcomes were consistent with previous pembrolizumab studies.
<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
FDA Approves Pembrolizumab for Metastatic Small Cell Lung Cancer | American Pharmaceutical Review – The Review of American Pharmaceutical Business &amp; Technology <a href="https://t.co/oXjjVAGdvQ">https://t.co/oXjjVAGdvQ</a> via <a href="https://twitter.com/American?ref_src=twsrc%5Etfw">@American</a> Pharmaceutical Review
— DR.ARUN ACHUTHAN (@DOCTORHELLOW8YM) <a href="https://twitter.com/DOCTORHELLOW8YM/status/1141558671316590593?ref_src=twsrc%5Etfw">June 20, 2019</a>
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The Food and Drug Administration (FDA) has granted approval for <a href="https://www.docwirenews.com/docwire-pick/hem-onc-picks/fda-keytruda-firstline-head-neck-cancer/">Keytruda</a>® (<a href="https://www.docwirenews.com/conference-coverage/asco-2019/maintenance-pembrolizumab-first-line-chemotherapy/">pembrolizumab</a>) to treat metastatic small cell lung cancer (SCLC).<a href="https://www.docwirenews.com/docwire-pick/hem-onc-picks/fda-approves-firstline-keytruda-inlyta-combo-kidney-cancer/">Pembrolizumab</a> was approved as a third-line therapy for SCLC patients who still present disease progression despite current or past platinum-based chemo and at least one other prior line of therapy, according to the FDA.Keytruda is manufactured by Merck.https://twitter.com/FDAHealthNews/status/1143107015247425537“KEYTRUDA is already an established treatment option for non-small cell lung cancer, and today’s approval in small cell lung cancer demonstrates our commitment to bringing forward new treatment options for patients with advanced, difficult-to-treat cancers,” said Jonathan Cheng, MD, vice president, oncology clinical research, Merck Research Laboratories, in a press release. “We look forward to continuing to advance important clinical research in small cell lung cancer.”“Small cell lung cancer, which accounts for 10 to 15% of all lung cancers, is often diagnosed at an advanced stage where the prognosis is very poor and there have historically been limited treatment options,” said Patrick Ott, MD, PhD, clinical director, Center for Immuno-Oncology, Dana-Farber Cancer Institute. “The approval of KEYTRUDA in small cell lung cancer provides an additional treatment option for patients based on the clinical response rates from KEYNOTE-158 and KEYNOTE-028.”<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
On June 17th, 2019, the <a href="https://twitter.com/US_FDA?ref_src=twsrc%5Etfw">@US_FDA</a> approved pembrolizumab for patients with metastatic <a href="https://twitter.com/hashtag/SCLC?src=hash&amp;ref_src=twsrc%5Etfw">#SCLC</a> "with disease progression on or after platinum-based chemotherapy &amp; at least one other prior line of therapy." <a href="https://twitter.com/hashtag/LCSM?src=hash&amp;ref_src=twsrc%5Etfw">#LCSM</a> 
Read about the decision: <a href="https://t.co/B9JBQmDJfX">https://t.co/B9JBQmDJfX</a>
— IASLC (@IASLC) <a href="https://twitter.com/IASLC/status/1143172246913069056?ref_src=twsrc%5Etfw">June 24, 2019</a>
</blockquote><script async src="https://platform.twitter.com/widgets.js" charset="utf-8"></script><h2>Two Studies Evaluate Pembrolizumab</h2>The FDA’s latest approval follows the results of two trials—<a href="https://www.ncbi.nlm.nih.gov/pubmed/30943124">KEYNOTE-158</a> and <a href="https://www.ncbi.nlm.nih.gov/pubmed/30557521">KEYNOTE-028</a>.KEYNOTE-158 was a phase II study investigating the use of pembrolizumab in patients with previously treated advanced cervical cancer. A total of 98 patients (mean age, 46 years; range, 24–75 years) were treated with pembrolizumab 200 mg every three weeks for two years, if they presented progression or intolerable toxicity, or until a patient or physician decided to stop treatment. For the first year of treatment, patients underwent tumor imaging every nine weeks, and subsequently every 12 weeks. The primary outcome was objective response rate (ORR) per the Response Evaluation Criteria in Solid Tumors (version 1.1), and the secondary outcome was safety. Patients were followed for a median 10.2 months (range, 0.6–22.7 months).<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
FDA approves pembrolizumab for metastatic SCLC <a href="https://twitter.com/Merck?ref_src=twsrc%5Etfw">@Merck</a>; <a href="https://twitter.com/Amgen?ref_src=twsrc%5Etfw">@Amgen</a> and @Allergan's Kanjinti, Herceptin biosimilar – <a href="https://twitter.com/FDAOncology?ref_src=twsrc%5Etfw">@FDAOncology</a> <a href="https://t.co/TTjIqxjdHl">https://t.co/TTjIqxjdHl</a> <a href="https://t.co/hwPrfYen9J">pic.twitter.com/hwPrfYen9J</a>
— The Cancer Letter (@TheCancerLetter) <a href="https://twitter.com/TheCancerLetter/status/1143576867297005568?ref_src=twsrc%5Etfw">June 25, 2019</a>
</blockquote><script async src="https://platform.twitter.com/widgets.js" charset="utf-8"></script>There were 12 responses—three complete and nine partial; ORR was 12.2% (95% confidence interval [CI] 6.5–20.4%). All 12 of the patients with responses had PD-L1-positive tumors for an ORR of 14.6% (95% CI 7.8–24.2%), of which 14.3% (95% CI 7.4–24.1%) were in patients who had received at least one line of chemotherapy for recurrent or metastatic disease. Adverse events occurred in 65.3% of patients, the most prevalent of which included hypothyroidism (10.2%), decreased appetite (9.2%), and fatigue (9.2%).KEYNOTE-028 evaluated patients with PD-L1-positive advanced solid tumors. The nonrandomized, phase Ib trial included 475 patients who received pembrolizumab 10 mg/kg every two weeks for two years or until progression or toxicity. The primary endpoint in this trial was also ORR, with secondary outcomes including safety, progression-free survival (PFS), and overall survival (OS).<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
On June 17, 2019, <a href="https://twitter.com/US_FDA?ref_src=twsrc%5Etfw">@US_FDA</a> granted accelerated approval to pembrolizumab (KEYTRUDA) for patients with metastatic small cell <a href="https://twitter.com/hashtag/lungcancer?src=hash&amp;ref_src=twsrc%5Etfw">#lungcancer</a> (SCLC) with disease progression on or after platinum-based chemotherapy and at least one other prior line of therapy.<a href="https://t.co/XO5jkxY2CY">https://t.co/XO5jkxY2CY</a>
— Lung Cancer Europe (@LungCancerEu) <a href="https://twitter.com/LungCancerEu/status/1141724022574604289?ref_src=twsrc%5Etfw">June 20, 2019</a>
</blockquote><script async src="https://platform.twitter.com/widgets.js" charset="utf-8"></script>Outcomes varied significantly based on cancer type. ORRs ranged from 0% (95% CI 0.0–14.2%) in pancreatic cancer to 33% (95% CI 15.6–55.3%) in SCLC. Similarly, median PFS varied from 1.7 months (95% CI 1.5–2.9 months) in pancreatic cancer to 6.8 months (95% CI 1.9–14.1 months) in thyroid cancer, and median OS was 3.9 months (95% CI 2.8–5.5 months) in vulvar tumors versus 21.1 months (95% CI 9.1–22.4 months) in carcinoid tumors. Safety outcomes were consistent with previous pembrolizumab studies.<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
FDA Approves Pembrolizumab for Metastatic Small Cell Lung Cancer | American Pharmaceutical Review – The Review of American Pharmaceutical Business &amp; Technology <a href="https://t.co/oXjjVAGdvQ">https://t.co/oXjjVAGdvQ</a> via <a href="https://twitter.com/American?ref_src=twsrc%5Etfw">@American</a> Pharmaceutical Review
— DR.ARUN ACHUTHAN (@DOCTORHELLOW8YM) <a href="https://twitter.com/DOCTORHELLOW8YM/status/1141558671316590593?ref_src=twsrc%5Etfw">June 20, 2019</a>
</blockquote><script async src="https://platform.twitter.com/widgets.js" charset="utf-8"></script>

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Keytruda® Approved for Small Cell Lung Cancer

Small Cell Lung Cancer

The Food and Drug Administration (FDA) has granted approval for Keytruda® (pembrolizumab) to treat metastatic small cell lung cancer (SCLC).