शैडोइंग अभ्यास: PARP Inhibitors: 2023 Updates - वीडियो के साथ अंग्रेजी बोलना सीखें
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1
Thank you for joining us for this session on PARP inhibitors.
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PARP inhibitors have been one of the most exciting advancements in the treatment of ovarian cancer in years,
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but recently have come under increasing scrutiny from the Food and Drug Administration.
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Dr. Ginny Fleming from the University of Chicago will update us on the latest.
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Dr. Fleming is Professor of Medicine and Director of the Medical Gynecologic Oncology program at the University of Chicago,
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and we're thrilled to have her join us for this session.
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Hello, it's a pleasure to be here with you to discuss
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some of the changing indications for PARP inhibitors in the treatment of ovarian cancer.
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Here are the topics I'm going to try to cover.
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First, what is HRD?
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Second, in brief, how do PARP inhibitors work?
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Third, which ones are currently FDA -approved and for what ovarian cancer indications?
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And finally, what has been a whirlwind of changes,
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what are the recent changes in the FDA -approved settings for PARP inhibitor use for women with ovarian cancer?
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And what has motivated these changes.
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First, homologous DNA repair, sometimes abbreviated HR for homologous repair.
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DNA is what carries the messages for all the proteins and enzymes in our body.
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It's the mat for everything.
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DNA is usually wound together in double strands, and there can occur from many various reasons,
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ultraviolet light, many other things, breaks in the DNA.
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And these are primarily repaired by what we call the homologous recombination repair pathway, the HR repair pathway.
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The BRCA gene is involved in homologous repair.
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A mutated BRCA gene does not do its job, So cells with BRCA deficiency lack HR repair,
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and they're referred to as HR deficient or HRD.
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Ovarian cancers may also harbor many other alterations which lead to deficiency in the HR pathway,
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and these tumors are also referred to as HRD.
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About half of ovarian cancers are HRD, including those with germline or tumor BRCA alterations.
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Homologous recombination deficiency leads to increased sensitivity of cancers to both platinum therapy and PARP inhibitor therapy.
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Tests for HRD are generally done on the tumor, and there's a variety of approved companies that do these tests
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and you are probably familiar with their use as physicians consider whether
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or not PARP inhibitor maintenance should be used in a particular situation.
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So PARP inhibitors, as you can see here, are also involved in the repair of DNA breaks.
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That's a double -strand DNA diagram there and the PARP inhibitors help repair a single -strand break.
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Single -strand breaks occur all the time, and PARP helps detect and repair them.
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However, during the replication process, they convert single -strand breaks into double -strand breaks.
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Normal cells then repair these by homologous recombination, but cells that are HRD do not have an effective repair pathway, and this leads to cell death.
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So these are the cells, the HR -deficient cells, that are particularly sensitive to PARP inhibitors.
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PARP inhibitors can clearly shrink ovarian cancer.
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What is not so clear is in what situations they are better than other options
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when they are used in trials of treatment.
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The very first, I'm going to give some examples here of use in what we're calling treatment,
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which is when it's used in the setting of measurable disease, usually not just as maintenance after chemotherapy.
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So Rocaprib, one of the three PARP inhibitors approved for ovarian cancer,
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was initially approved based on two actually quite small studies for
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the total of 106 patients with high -grade ovarian cancer whose disease had progressed after two or more prior therapies.
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All the women in this study had either a germline mutation or their tumor had a somatic mutation.
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So a germline mutation is when the mutation is inherited and can be passed on to your children.
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And it's found in all the cells of your body, blood cells, cells from a cheap swab.
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But ovarian cancers can also have what we call somatic mutations.
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And those are mutations that are only in the tumor and not passed on from, you know, parent to child.
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Either one of these confers sensitivity to platinum or PARP inhibitor therapy.
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The primary endpoint of the study, meaning how was the study designed, what was it designed to find, was response rates or rate of tumor shrinkage.
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And in these two studies, the rate of tumor shrinkage was over 50%,
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and these shrinkages lasted for a median or an average of 9 .2 months.
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So that's if it shrank, how long did it stay shrink?
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similarly another one of the PARP inhibitors used for ovarian cancer
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olaparib was in an early study tested again in women all of whom had a germline BRCA1
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or 2 mutation and who had more than three lines of prior chemotherapy
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and was found to have a response rate of 34 percent where these responses lasted an average of eight months.
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However, notice below
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that you can see on this table divides the tumors treated
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on this admittedly small group of patients into tumors in the situation that were expected to be platinum sensitive,
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generally more than six months from prior platinum therapy and shrank with the prior platinum therapy, platinum resistant, so recurrence less than six months,
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and platinum refractory progressed on platinum.
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And you can see that the rate of tumor shrinkage was clearly highest in tumors that were platinum -sensitive,
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and only two patients responded who had platinum refractory disease.
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So clearly there is, as we say, non -cross -resistance between platinum and a PARP inhibitor.
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Tumors that are resistant to platinum are much more likely to be resistant to PARP inhibitors as well.
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And this will become important when we discuss why there have been some changes in indications for PARP inhibitors.
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That is to say, they are no longer indicated.
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The FDA no longer approves them for use as so -called treatment.
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All the current approvals are only as maintenance.
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So one very early trial, again, many years ago, one of the first PARP inhibitor trials, they compared PARP to liposomal doxorubicin in women,
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all of whom had a germline BRCA mutation and had recurrence within 12 months of prior platinum therapy.
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These women were only about 100 in total,
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and they were randomized to one of two different doses of Olaprib versus liposomal doxorubicin,
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and patients were permitted to cross over at the time of progression.
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So a woman who was on doxyl could cross over at the time of progression to a PARP inhibitor and vice versa.
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And here you see the schema of the trial, low -dose olaparib, higher -dose olaparib, and liposomal doxorubicin.
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And here are the response rates and the progression -free survival.
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So the progression -free survival was slightly higher in the high -dose olaparib than it was in liposomal doxorubicin,
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but these results, all of them, were no different than what was expected to be with chance.
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So here was an early trial that began to raise questions about, although PARP inhibitors clearly have activity, are they better than something else?
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And a lot of the trials
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that were used to try to gain FDA approval were trying to show
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that PARP inhibitors were better than something else in some way.
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So again, the terminology I'm using, when I say we're using it as treatment,
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it's used to treat a cancer that would generally have progressed or recurred after some other therapy, although you could use it for first -line treatment.
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But none of the PARP inhibitors are approved as first -line treatment.
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Whereas maintenance, the drug is used to treat a cancer after chemotherapy has already decreased the size of the tumor
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or made it disappear entirely.
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And the idea is to maintain that response, hence maintenance therapy. So back in 2014,
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Olaparib was approved by the FDA for use as treatment in patients who had BRCA -mutated ovarian cancer
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and at least three or more rounds of prior treatment.
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However, and by 2018, Rucaparib and Naraparib were also approved, and in 2022, the FDA began issuing withdrawals.
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Currently, there are no more treatment approvals.
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The approvals are for olaparib for maintenance,
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niraparib as maintenance, and rucaparib as maintenance.
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And the exact indications, whether for BRCA or for any platinum -sensitive disease, have varied by drug.
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probably more due to details of trial design than because the different PARP inhibitors are so different.
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However, we are expecting a withdrawal, the first withdrawal of maintenance of Rucaparib,
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or may have already happened for platinum -sensitive disease.
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What has been withdrawn, which indications are no longer FDA approved?
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All the treatment indications.
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So all the uses of PARP inhibitors other than as maintenance have been withdrawn by the companies in response to FDA communications.
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And niraparib has been withdrawn for maintenance in platinum -sensitive recurrent disease for women and tumors that don't have BRCA mutations. So what happened?
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Why would they approve all these things and then change it?
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In general, of PARP inhibitors were initially approved based on information regarding progression -free survival,
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how long the treatment could continue before the cancer grows, or response rate,
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where response rate is generally in trials defined as percentage of subjects whose tumors shrink by 30 % or more.
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But later data began suggesting that overall survival was not as positively affected as progression -free survival.
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And in some trials, it appeared that the subjects getting PARP inhibitor therapy might even have decreased survival compared to controls.
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In many, it wasn't statistically significant, but it was alarming.
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There are a lot of arguments, as you can imagine, that have been flying about the validity of these different endpoints
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that are used to try to justify FDA approval.
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Again, the withdrawals are based on new overall survival information, which as you can imagine takes a lot longer to come by than tumor shrinkage.
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Tumor shrinkage is the first thing that you get out of a clinical trial.
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The time till the cancer grows takes longer and overall survival takes longer yet.
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So it's years before we have an adequate data set to really assess overall survival.
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Many of the trials were designed for progression -free survival, not overall survival.
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So their size and design may not have been adequate for an accurate assessment of overall survival.
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Crossover, as we discussed, is people who were, for example, randomized to placebo,
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but then after progression, maybe broke the blind and then took a PARP inhibitor.
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That's referred to as crossover.
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And that might affect overall survival.
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However, the hypothesis of people who are concerned about the decreased overall survival
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that is numerically shown in some studies is since tumors that are resistant to PARP inhibitors are more resistant to platinum,
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then taking PARP inhibitors may make subsequent treatment work less well.
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As we showed, people with tumors who's resistant to carboplatin will not have as good a response to PARP inhibitors.
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The converse is also true.
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And again, to review the terminology, progression -free survival in a clinical trial is the time from
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when drug therapy is started until the tumor grows or death of disease, if that happens first.
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Overall survival, obviously, is the time from when drug therapy is started on the study until death of the patient from any cause.
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I'm going to review for you one representative example.
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There are too many to go over, but what a specific example of concern that is caused for a withdrawal of indication.
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And I think that you'll find that if you look at all of them in detail, it's similar.
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So the representative example I'm going to use is the trial is called the NOVA trial.
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It was for niraparib, and it's in the setting of recurrent platinum -sensitive maintenance.
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So this is the design of the NOVA trial.
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Women who were on the trial had platinum -sensitive ovarian cancer.
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with at least two prior platinum treatments.
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So typically, they got platinum, maybe the cancer came back a year or two later, they got platinum again, and the tumor shrank.
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And then at that point, they were randomized to either noreparib or to placebo.
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So this was planned to be almost 500 patients participating,
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and all of them had to have high -grade serous tumors.
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And they had to be in complete or partial response to their most recent platinum therapy.
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And then they were randomized to one of these two regimens, placebo or noreparib, to try to maintain that response, hence the term maintenance therapy.
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So initial publication was in the New England Journal in 2016.
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And you can see that if we look at the group of women who had noreparib maintenance compared to those with placebo.
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they did better in all categories.
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Those that got the most benefit were those that had a germline BRCA mutation.
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And here you can see the time to progression was hugely improved, 21 months versus five months.
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In women who are not germline BRCA mutated, the progression was also improved, although it was shorter overall, nine months versus about four months,
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and so on and so forth for each of the subgroups.
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Again, benefits seen in all subgroups and most dramatic for the germline BRCA mutated.
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But when the later results then more recently came out, presented at 2023, again, overall survival takes years until we have the results,
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you can see that there was not any real difference, even in the patients with the germline BRCA mutation,
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that is 40 months, That's 40 .9 versus 38 .1, which, you know, is a little bit better.
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But when these confidence intervals, that's what we call the numbers in the brackets here, 0 .61 to 1 .2.
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When one is included in that, it's generally considered that it could have happened by chance.
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And then numerically, in the patients who did not have a germline BRC mutation,
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there was numerically worse survival in those who got niraparib, 31 months versus almost 35 in placebo.
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Again, you can see that one is included in the confidence interval.
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So none of these differences here are statistically significant.
165
They're all could be the same, and the differences seen between the two groups could be chance.
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But again, there was concern that no survival benefit was seen.
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And even if patients did cross over and take olaparib subsequently, it's hard to understand how that would make them have a shorter survival.
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So the indication, again, for niraparib in the non -germline BRCA mutation was withdrawn as maintenance in the second -line setting.
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Now, in the frontline setting, we don't have overall survival in most of the trials yet.
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The one we do have is the SOLO1 frontline maintenance BRCA mutation carriers.
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And here, there still seems to be an overall survival benefit,
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although for technical reasons, it wasn't quite statistically significant in frontline.
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And I think at this point, the frontline indications are still in place.
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And this is probably where patients are going to get the most benefit.
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And there's also appears to be the lowest risk of secondary myelodysplastic syndrome or leukemia, which is a concern.
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So in conclusion, newer long -term trial results with overall survival continue to gradually come available.
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There is clear benefit for BRCA mutation cares when PARP inhibitors are used in frontline maintenance, and I think focusing on frontline use,
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where the benefit at this point still appears to be very strong is important.
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Thank you.
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इस पाठ की शब्दावली और बोलने के सुझाव
यह स्पीकिंग पाठ वीडियो “PARP Inhibitors: 2023 Updates” पर आधारित है। सबसे ज़्यादा दोहराए गए शब्द ये हैं: Parp, inhibitor, platinum, survival, tumor। इस वीडियो में शैडोइंग के लिए 179 वाक्य और 2557 शब्द हैं। बोला गया हिस्सा 18:18 लंबा है। वक्ता लगभग 140 शब्द प्रति मिनट की स्थिर गति से बोलता है, जो शैडोइंग के लिए आरामदायक है। केवल 78% शब्द अंग्रेज़ी के 3,000 सबसे आम शब्दों में से हैं, इसलिए शब्दावली कठिन है।
इस वीडियो की मुख्य शब्दावली
वीडियो के 15 सीखने लायक शब्द, उच्चारण और अर्थ के साथ:
| शब्द | उच्चारण | अर्थ |
|---|---|---|
| platinum संज्ञा | /ˈplæt.ɪn.əm/ | महातु, प्लैटिनम |
| tumor संज्ञा | /tuː.məɹ/ | फुलाव, नववर्धन |
| approve क्रिया | /əˈpɹuːv/ | अनुमोदन करना |
| strand संज्ञा | /ˈstɹænd/ | तागा, धागा |
| pathway संज्ञा | /ˈpæθˌweɪ/ | पथ, पगडंडी |
| decrease क्रिया | /dɪˈkɹiːs/ | घटना |
| deficiency संज्ञा | /dɪˈfɪʃənsi/ | अभाव, कमी |
| occur क्रिया | /əˈkɜː/ | बीतना |
| gene संज्ञा | /d͡ʒiːn/ | जीन, वंशाणु |
| adequate विशेषण | /ˈæd.ə.kwɪt/ | पर्याप्त |
| sensitivity संज्ञा | /ˌsɛn.səˈtɪv.ə.ti/ | संवेदनशीलता |
| interval संज्ञा | /ˈɪntɚvəl/ | अंतराल |
| terminology संज्ञा | /ˌtɝ.məˈnɑ.lə.d͡ʒi/ | शब्दावली |
| topic संज्ञा | /ˈtɑpɪk/ | प्रसंग, विषय |
| percentage संज्ञा | /pə(ɹ)ˈsɛntɪd͡ʒ/ | प्रतिशतता |
वीडियो में आने वाली फ़्रेज़ल वर्ब
| शब्द | अर्थ |
|---|---|
| come back क्रिया | वापस आना |
इस वीडियो का व्याकरण
वक्ता जिन संरचनाओं का सबसे अधिक प्रयोग करता है, वीडियो के असली शब्दों के साथ:
| संरचना | वीडियो में |
|---|---|
| Present perfect have/has + past participle — बीता हुआ काम जिसका असर अभी भी है | have been · have come · has been |
| Passive voice be + past participle — ज़ोर इस पर कि क्या होता है, न कि कौन करता है | is usually wound · are primarily repaired · is involved |
| Relative clauses who / which + उपवाक्य — व्यक्ति या वस्तु के बारे में अतिरिक्त जानकारी | woman who was · people who were · people who are |
ध्यान देने योग्य उच्चारण
वक्ता 15 बार संक्षिप्त रूपों का प्रयोग करता है, जैसे I'm, we're, don't। इन्हें वैसे ही छोटा बोलें जैसा आप सुनते हैं।
- “th” की ध्वनियाँ: withdrawal /wɪðˈdɹɔ(ə)l/, withdraw /wɪðˈdɹɔ/, pathway /ˈpæθˌweɪ/, chemotherapy /ˌkiːməʊˈθɛɹəpi/, hypothesis /haɪˈpɒθɪsɪs/
- “sh” और “zh” की ध्वनियाँ: mutation /mjuˈteɪʃən/, progression /pɹəˈɡɹɛʃən/, indication /ɪndɪˈkeɪʃən/, deficiency /dɪˈfɪʃənsi/, publication /ˌpʌblɪˈkeɪʃ(ə)n/
- लंबे शब्द — बलाघात सही रखें: indication /ɪndɪˈkeɪʃən/, statistically /stəˈtɪs.tɪ.kə.li/, deficiency /dɪˈfɪʃənsi/, chemotherapy /ˌkiːməʊˈθɛɹəpi/, sensitivity /ˌsɛn.səˈtɪv.ə.ti/
हिंदी भाषियों के लिए मुश्किल ध्वनियाँ:
- /v/ और /w/ का फ़र्क़ — /v/ में ऊपर के दाँत निचले होंठ को छूते हैं, /w/ में होंठ गोल होते हैं: survival /sɚˈvaɪ.vəl/, approve /əˈpɹuːv/, sensitive /ˈsɛn.sɪt.ɪv/, versus /ˈvɝsəs/, withdrawal /wɪðˈdɹɔ(ə)l/
- /z/ — इसे “ज” (/dʒ/) न बनाएँ: resistant /ɹəˈzɪstənt/, whereas /(h)wɛɹˈæz/, physician /fəˈzɪʃən/, positively /ˈpɑ.zɪ.tɪv.li/, enzyme /ˈɛn.zaɪm/
- शब्द की शुरुआत में s + व्यंजन — पहले “इ” न जोड़ें: strand /ˈstɹænd/, statistically /stəˈtɪs.tɪ.kə.li/, scrutiny /ˈskɹuː.tɪ.ni/, schema /ˈskiːmə/, swab /swɒb/
इस वीडियो से अभ्यास कैसे करें
- पहले बिना बोले पूरा वीडियो एक बार सुनें और जो शब्द नहीं आते उन्हें लिख लें।
- सामान्य गति पर एक-एक वाक्य की शैडोइंग करें और हर वाक्य तब तक दोहराएँ जब तक आपकी लय वक्ता से न मिल जाए।
- अपनी आवाज़ रिकॉर्ड करें और मूल से तुलना करें, ख़ासकर platinum, tumor, approve जैसे शब्दों पर ध्यान दें।
शैडोइंग तकनीक क्या है?
शैडोइंग (Shadowing) एक विज्ञान-समर्थित भाषा सीखने की तकनीक है जो मूल रूप से पेशेवर दुभाषिया प्रशिक्षण के लिए विकसित की गई थी। विधि सरल लेकिन शक्तिशाली है: आप मूल अंग्रेज़ी ऑडियो सुनते हैं और तुरंत इसे ज़ोर से दोहराते हैं — जैसे वक्ता की छाया 1-2 सेकंड की देरी से। शोध से पता चलता है कि यह उच्चारण सटीकता, स्वर, लय, जुड़ी हुई ध्वनियाँ, सुनने की समझ और बोलने की प्रवाहशीलता में काफ़ी सुधार करता है।