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非小细胞肺癌(NSCLC)的化疗宝典

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1827962 315 老马 发表于 2012-5-19 12:38:14 | 置顶 |
老马  博士一年级 发表于 2013-12-1 18:44:31 | 显示全部楼层 来自: 浙江温州
ASCO止吐药临床实践指南
新指南推荐:

  蒽环类联合环磷酰胺应被归为重度致吐性化疗方案。

  对于接受重度致吐性药物化疗的患者,应给予一种5羟色胺3(5-HT3)受体拮抗剂、地塞米松和一种神经激肽1(NK1)受体拮抗剂治疗。

  一项大型研究证明福沙匹坦和阿瑞匹坦有相同止吐效果。

  对于接受中度致吐性药物化疗的患者,应优先给予帕洛诺司琼而非其他药物,并联合地塞米松治疗。

  对于接受轻度致吐性药物化疗的患者,应在化疗开始前给予地塞米松。

  对于接受重度致吐性放疗的患者,应在每次放疗前并在放疗后24小时给予患者5-HT3受体拮抗剂,可在第1~5次放疗期间给予患者1疗程共5日的地塞米松治疗。

  指南更新委员会强调应在治疗过程中持续监测患者症状。医生常低估恶心的发生率,这一症状不如呕吐好控制。
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老马  博士一年级 发表于 2013-12-1 18:48:22 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2013-12-1 18:50 编辑

福沙匹坦是阿瑞匹坦的前体药物,注射后在体内迅速转化成阿瑞吡坦。福沙匹坦和阿瑞匹坦有相同止吐效果。
止吐效果:福沙匹坦=阿瑞匹坦>帕洛诺司琼>格拉司琼>昂丹司琼>胃复安
注:阿瑞匹坦Aprepitant(商品名:止敏吐胶囊、Emend)
帕洛诺司琼,格拉司琼,昂丹司琼,胃复安均有口服和静脉剂型;福沙匹坦只有静脉针剂,阿瑞匹坦只有口服剂型。
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老马  博士一年级 发表于 2013-12-1 19:39:48 | 显示全部楼层 来自: 浙江温州
帕利夫明Palifermin(商品名Kepivance 凯望斯美国Amgen公司)
Amgen公司2004年12月15日宣布FDA已批准了Kepivance(palifermin)用于治疗严重口腔溃疡,而这种口腔溃疡可能会发生在服用过高剂量化疗又接受了骨髓移植的血癌病患者身上。该药用于非血癌患者上的有效性和安全性还正在进行中。
    在双盲临床试验中,血癌患者在接受高剂量化疗加放射治疗前,被随机静注60mμg·kg-1· d-1(n=106)或安慰剂(n=106),共3d。接着患者接受骨髓移植,并被再给予3d的kepivance或安慰剂。最严重的口腔溃疡(4级)发生率在kepivanc组(20%)比安慰机组中(62%)降低了3倍,3~4级溃疡发生率也减少大约1/3(63%比98%)。Kepivanc缩短溃疡疼痛时间(2~4级)达1周之多(8 d比安慰机组的14 d)。研究发现被kepivanc治疗的患者显著减少了口腔和喉头红肿,吃,喝、吞咽和说话能力都有显著改善。此外,接受kepivanc的患者要求吗啡止痛的时间也比安慰机组少(7d比11d)。
kepivanc是一种重组人体角质化细胞生长因子,它通过保护口腔和喉部表皮细胞免遭化疗和放疗的损害而减少溃疡的发生,并可刺激新的表皮细胞在溃疡伤面的生长和发肩。Kepivanc的安全性的耐受性较好。不良反应为皮疹、瘙痒、皮肤红肿、皮肤异常感、口/舌感紊乱,但均为轻微或中度,且短暂。
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老马  博士一年级 发表于 2013-12-1 19:58:05 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2013-12-1 20:11 编辑

口腔炎诊断与处理.pdf (293.31 KB, 下载次数: 385) 口腔炎预防和处理指南.pdf (55.25 KB, 下载次数: 325)
急性放射性口腔和咽喉黏膜炎.pdf (199.39 KB, 下载次数: 213)
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老马  博士一年级 发表于 2013-12-1 20:07:58 | 显示全部楼层 来自: 浙江温州
Use Glutamine To Reduce The Severity Of Mucositis And Neuropathy (During Chemotherapy Or Radiation Therapy)
If you are about to start a course of chemotherapy that can cause mucositis (i.e. of the mouth, throat or esophagus) or peripheral neuropathy (i.e. hands and feet), ask your oncologist if you can use glutamine to help reduce the severity of these common symptoms.
If you are going to receive radiation therapy to the head, neck or chest (specifically, anywhere near the esophagus), Glutamine can be helpful to reduce the development of severe mucositis in these tissues.
**Did you know that honey is also a proven therapy for mucositis? Read my previous blog entry on honey and mucositis.**
HERE ARE THREE COMMONLY USED REGIMENS IN THE PREVENTION OF MUCOSITIS (ORAL, THROAT OR ESOPHAGEAL) AND PERIPHERAL NEUROPATHY:
You can buy glutamine (usually in the form of L-glutamine), in powder, capsule, tablet, or liquid form. However, I recommend using the powder form of L-glutamine, and mixing it in with cold or room temperature liquids (water or juice.) It should not be added to hot beverages because heat destroys glutamine. Glutamine therapy works best if started at the time of beginning radiation therapy or chemotherapy. It will be less effective if you start this after already showing signs or symptoms of mucositis or peripheral neuropathy.
For the prevention of oral mucositis (OM)
Mix 10 grams of powdered glutamine in a small glass (6-8 ounces) of water or juice. Swish and gargle for 30-60 seconds and swallow. You can continue to do this until the 6-8 ounces are gone. Repeat every 8 hours (schedule: morning, mid-day, evening)
Start this regimen on the first day of chemotherapy and continue for 14 days after the last dose of chemotherapy in patients who do not develop OM or until 5 days after resolution of OM for patients who experienced OM.
Other recommendations:
Refrain from eating or drinking for 30 minutes after dosing.
Adhere to good oral hygiene practices and gently brushed their teeth twice daily, 30 minutes or more after using glutamine, using a soft toothbrush and fluoride toothpaste.
Daily flossing and an alcohol-free fluoride rinse is recommended.
This is based on a study that showed a significant reduction in OM among patients using oral glutamine.
These investigators used a proprietary glutamine suspension (Saforis, MGI Pharma, Inc., Bloomington, MN), which was administered at a dose of 2.5 g per 5 mL 3 times per day for a total daily dose of 7.5 g. This product reportedly is able to be better absorbed into the oral mucosa than standard glutamine. (I believe that this can be compensated for by using a higher dose, 10 grams, 3-times per day, of standard glutamine, as recommended above.)
Various chemotherapy regimens used in this study (21-day cycle): cyclophosphamide, doxorubicin, and 5-fluorouracil (CAF); 5-fluorouracil, doxorubicin, and cyclophosphamide (FAC); or doxorubicin and cyclophosphamide (AC).
Compared with placebo, glutamine significantly reduced the incidence of moderate-to-severe OM 39% vs. 50% (placebo.)
For prevention of mucositis of the throat and esophagus (esophagitis) from radiation and chemotherapy:
Mix 10 grams of powdered glutamine in a small glass (6-8 ounces) of water or juice. Drink (swallow). Repeat every 8 hours (schedule: morning, mid-day, evening)
Start this regimen 1 week before radiation therapy and continue for 2 weeks after completion of radiation therapy.
This is based on a study that showed a significant reduction in esophagitis among patients receiving this regimen versus no glutamine:
There was minimal-to-no-esophagitis was seen in 71% of the glutamine supplemented patients versus only 44% without glutamine
By the end of treatment, the glutamine supplemented patients gained 2.6 kg (median), while those without glutamine lost 3.3 kg (median)
There was a significant delay to the time of first noticing esophagitis in the glutamine patients versus the non-glutamine patients: 25 days versus 16 days.
There were also fewer treatment breaks, hospitalizations and late esophageal toxicities among the patients who took glutamine versus those who did not.
Importantly, there were no differences in cancer recurrence rates at 24 months of follow-up (the glutamine did not reduce the effectiveness of treatment.)
For the prevention of chemotherapy-induced peripheral neuropathy (studied with oxaliplatin and paclitaxel)
Mix 15 grams of powdered glutamine in a small glass (6-8 ounces) of water or juice. Drink. Repeat every 12 hours (schedule: morning and evening)
Start this regimen on the day of oxaliplatin infusion and continue for seven days thereafter. Repeat with each infusion.
This is based on a study that showed a significant reduction in chemotherapy-induced peripheral neuropathy among patients receiving this regimen versus no glutamine:
After all 6 cycles of chemotherapy, 48% of patients in the glutamine group had no peripheral neuropathy (PN) versus only 27% in the non-glutamine group.
After all 6 cycles of chemotherapy, 12% of the patients in the glutamine group had moderate-to-severe PN versus 32% in the non-glutamine group.
Glutamine supplementation significantly improved cold intolerance and lessened the interference to activities of daily living.
Chemotherapy dose-reductions were less frequently needed in the glutamine patients (7%) versus those not taking glutamine (27%)
There were no differences found in the response to chemotherapy or survival between the two groups.
HOW DOES GLUTAMINE REDUCE MUCOSITIS AND ESOPHAGITIS?
Glutamine has been shown to reduce the degree of mucositis through:
anti-inflammatory mechanisms (inhibition of one of the main switches that turn on inflammation, NF-kappaB)
inhibition of bacterial toxins
increased tissue healing (increased fibroblast and collagen synthesis.)
HOW DOES GLUTAMINE REDUCE CHEMOTHERAPY-INDUCED PERIPHERAL NEUROPATHY?
We don’t know exactly, however it is believed that glutamine may exert its neuroprotective effects by upregulation of nerve growth factor. In animal studies, supplementation with glutamine appears to increase NGF.

IS GLUTAMINE SAFE TO GIVE TO PATIENTS WITH CANCER?
This is an area of controversy, as it is well-known that under certain circumstances cancer cells use glutamine for energy even more voraciously than glucose.
However, no human study, have ever shown that glutamine increased tumor growth rates or decreased the efficacy of other cancer therapies.
Over the last 20 years, 36 clinical studies have demonstrated the tolerance, safety and effects of glutamine (oral and IV) in patients undergoing chemotherapy and/or radiation therapy. In each of these studies, researchers have reported that glutamine supplementation in cancer patients improves their metabolism and clinical situation without increasing tumor growth.
Potential Side Effects and Drug Interactions:
Generally, very well-tolerated and is considered safe for use by most people for the duration of cancer care (chemotherapy and/or radiation therapy) in doses up to 40 grams per day (adults.)
Do not use glutamine if you:
Have kidney failure, kidney dysfunction, or if your kidney function is impaired or abnormal.
Have liver failure, liver dysfunction, or if your liver function is impaired or abnormal.
Have ever been diagnosed with or had a period of hepatic encephalopathy (liver function that affects your mental, emotional, or cognitive state).
Have a history of mental illness, especially bipolar depression (manic depression), mania, or hypomania.
Have a history of seizure disorders, such as epilepsy or are taking medications to control a seizure disorder.
Have a history of allergic reaction to monosodium glutamate (MSG), a flavoring agent sometimes used in the preparation of Chinese food in restaurants.
Are taking or have been prescribed to take a medication called lactulose.
Adverse drug-glutamine interactions are not common, but (as with any supplement) always check with your physician before starting glutamine.
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老马  博士一年级 发表于 2013-12-1 20:23:43 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2013-12-1 20:27 编辑

1.不建议使用复方氯己定含漱液(Chlorhexidine)用来预防和治疗口腔炎,临床试验显示无益处。
2.推荐使用0.9%生理盐水,有条件可使用Benzydamine (Difflam)漱口液,用软牙刷刷牙。
3.推荐使用左旋谷酰胺(L-glutamine)粉末,有条件者可使用Aesgen公司的左旋谷酰胺(L-glutamine,Saforis)嗽口液。
剂量:将10-15克左旋谷酰胺溶于180-240ml水或者果汁中,1天分三次服用(三餐前15分钟)。
疗程:放化疗前一周和放化疗周期内。
4.头颈部肿瘤放疗可以使用帕利夫明Palifermin(商品名Kepivance 凯望斯美国Amgen公司),是一种重组人角化细胞生长因子(keratinocytegrowthfactor,KGF),最近被证明可以有效的减少大剂量化疗诱发的口腔黏膜炎的发生。
Difflam.JPG
JRW-15046-3.jpg
Jarrow Formulas, L-Glutamine, 17.6 oz (500 g) Powder $25.97 ¥158.25
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爱笑的天使  小学六年级 发表于 2013-12-31 15:01:59 | 显示全部楼层 来自: 中国
(3)化疗开始前2天,结束后2天内禁用升白针。

马哥,我们主治大夫经常在化疗前一天和后一天立即用升白针,有什么危害吗?

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同问  发表于 2015-1-15 17:03

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老马  博士一年级 发表于 2014-1-3 11:26:49 | 显示全部楼层 来自: 浙江温州
PLOS ONE: Combination of EGFR-TKIs and Chemotherapy as First-Line Therapy for Advanced NSCLC: A Meta-Analysis
http://www.scoop.it/t/focus-on-lung-cancer
The impact of combining epidermal growth factor receptor tyrosine kinase inhibitors (EGFR–TKIs) and chemotherapy as first-line therapy for patients with advanced non-small-cell lung cancer (NSCLC) remains controversial. Therefore, randomized trials that compared this combined regimen with chemotherapy or EGFR–TKIs monotherapy were included for this meta-analysis. We used published hazard ratios (HRs), if available, or derived treatment estimates from other survival data.  Eight trials eventually entered into this meta-analysis, including 4585 patients. Overall, the combined regimen significantly delayed disease progression (HR = 0.81, 95% CI 0.69–0.95, P = 0.01); subgroup analysis showed significantly higher progression free survival advantages in Asian patients (P<0.001), with sequential combination of TKIs and chemotherapy (P = 0.02). In selected patients by EGFR-mutation, both mutation positive (HR = 0.48, 95% CI 0.28–0.83, P = 0.009) and negative (HR = 0.84, 95% CI 0.72–0.98, P = 0.02) patients gained progression free survival benefit from the combined regimen, albeit the magnitude of benefit was marginally larger in mutation positive patients (P = 0.05). In selected patients by smoking history, never/light smokers achieved a great progression free survival benefit from the combined regimen (HR = 0.51, 95% CI 0.35–0.74, P = 0.0004). Unfortunately, the combined regimen had no significant impact on overall survival, irrespective of ethnicity, dose schedules or EGFR-mutation status.
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老马  博士一年级 发表于 2014-1-5 12:51:06 | 显示全部楼层 来自: 浙江温州
Supplements—for better or worse?
Chemotherapy-induced peripheral neuropathy is a very common and debilitating adverse effect of cancer therapy, which can often lead to treatment discontinuation. There are no good treatments or ways to prevent this adverse effect. However, preclinical studies and a phase&nbsp;II trial showed that the natural compound acetyl-L-carnitine (ALC) has efficacy, with improvements noted in some
patients. This finding prompted Dawn Hershman and colleagues to conduct a prospective, randomized, placebo-controlled trial in women undergoing taxane-based adjuvant therapy for early
stage breast cancer.
In total, 409 patients were randomly assigned to receive ALC or placebo. The primary outcome of the trial was patient-reported symptoms of peripheral neuropathy. Unfortunately, as Hershman
summarizes, the results of the trial were negative. “Not only did we not find a protective effect of ALC at 12 weeks, we found that by 24 weeks there was a statistically significant worsening of
peripheral neuropathy in the patients on trials that were randomized to the ALC&nbsp;supplement.”
To the authors’ knowledge, this is the first study to show a detrimental effect of a supplement on the development of taxane-related peripheral neuropathy. As the use of complementary medicine is widespread, the study researchers caution that patients should be discouraged from using ALC
and other nutritional supplements that do not have proven efficacy. Hershman comments on future plans for this area: “some studies are ongoing to see if ALC is more beneficial for treatment as opposed to prevention. We will investigate other approaches for treating and preventing
this terrible side effect.”
Lisa Hutchinson
Original article Hershman, D. L. et al. Randomized double-
blind placebo-controlled trial of acetyl-l-carnitine for
the prevention of taxane-induced neuropathy in women
undergoing adjuvant breast cancer therapy. J. Clin. Oncol.
doi:10.1200/JCO.2012.44.8738
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小小的解百纳  高中一年级 发表于 2014-2-27 15:47:48 | 显示全部楼层 来自: 山东青岛
高手在民间。虽然害怕化疗,但是还是要学习 再学习。。。。
懂得一切 原谅一切

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