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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1141767 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
6 j" t% `5 Q. b1 |" U* r% Z# c3 rNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
* g3 `: Z" z* s9 c  I2 |2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
7 p1 f. [8 L! E* A2 d5 G2 |3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * P6 e# u+ T7 p
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. ^0 B  C% g( R  ]! L9 c8 _9 d5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
4 g7 o( \) d# t9 ^" o' X8 D. U6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
6 o- I# Y. v1 H# t) I8 B+ `7Kinki University School of Medicine, Osaka 589-8511, Japan , G1 v" g2 w# ?1 V/ F7 a
8Izumi Municipal Hospital, Osaka 594-0071, Japan
9 S1 h8 m5 a) \$ U. T4 `9 n9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
- n5 [: |2 h- ~  j2 l+ A5 ^Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
1 w1 p! c( |, uAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. ! z0 U4 R( I5 D# D+ w) K& a
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 6 J% E: S  B$ n2 x# t" _
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  3 R9 v8 o1 S3 Y  L
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Published online on: Thursday, December 1, 2011 2 V+ Q8 T9 a( }, z8 E4 z
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Doi: 10.3892/ol.2011.507
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Pages: 405-410
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) O$ f& k9 d+ ?: I) q0 j- j, mAbstract:
! d/ Y+ w+ M, R1 n  X* XS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population3 o- A) K8 n9 j. h
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 % n0 }" n. n+ \7 U. n) g0 R1 s
+ Author Affiliations
# [1 }5 n* E+ h4 L  r$ i; m1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
1 N( L' I$ x- F: e# Q4 v( A8 h5 `2Department of Thoracic Surgery, Kyoto University, Kyoto 7 F$ \! b: V6 [4 q- _
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
; T5 ]1 d# S6 D" b4 [4 L&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
; w* t0 Y$ C, ZReceived September 3, 2010.
; Q( m8 W# B& M* o$ _Revision received November 11, 2010. 0 k. m: P( x/ ]: I5 ]1 d# u
Accepted November 17, 2010. ) g+ k! r( p/ ?. j8 O
Abstract+ N% h# W$ P, \/ {8 j
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. ' j& ^+ D9 z9 M1 @0 ?+ B, f# X# r
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 7 n' O$ ]) K) z) \4 I1 _
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
. d# r1 A" q5 d$ r7 V- [Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ) D. r: W, Z$ L" ?% y0 f. u1 a
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
- c7 L5 \5 @- I1 k* F今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
) O7 S( W2 N/ qhttp://clinicaltrials.gov/ct2/show/NCT01523587
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, k5 I: h: h  _9 W7 gBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC- S4 v! L# S8 m2 X" J
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 % d+ R; m; Z: t, ^/ P3 a0 X

) x" T5 x$ @; w! z) Y从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
2 n0 L" F9 {8 c# A- _3 D至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 ' W5 m- ?! ^- w' |, O. W
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。6 c- X5 O: s( G$ ^( E7 J/ G. X8 \
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。. r, [2 }0 A4 n0 _. k8 A- E- k3 L
不错。

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