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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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1354272 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 C) a) E9 x- o9 f2 l* m! B. a6 v" oNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ' c0 k5 E2 x7 \: `( }
+ Author Affiliations  o9 q3 t9 U  p4 L- J8 z

) W7 D( ?  B8 s3 s3 |0 L" @& q7 k1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
- M8 I# t& \5 n& t% ]2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan - j$ e! ?. C8 ]7 O( V
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 e% {# R# l% v6 @! k4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
1 t: l, X1 T, H9 ~  ?" C% U& J5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan . I8 L; f1 V& p% M! L
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
. g& p; k2 t4 t% E- X7Kinki University School of Medicine, Osaka 589-8511, Japan
3 F0 J, R' N' ~4 O; _% B8Izumi Municipal Hospital, Osaka 594-0071, Japan ( _( X: ^- |; ]- e/ I! G
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan " A1 H+ u: t1 f" U) x7 D
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 9 X% P% P0 c. s. h5 E# N2 ^
AbstractBackground: 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.
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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
2 m: J, x# Y" j/ r8 P  O& f; O# g. \0 ~& R1 I
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ! |; a( x! Z7 z% }9 B
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Published online on: Thursday, December 1, 2011 8 L8 J7 x6 f9 ^9 B; Y
+ e8 ~1 g3 f; j! Y8 h5 |
Doi: 10.3892/ol.2011.507
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9 b% ^& a5 |3 v) |! NPages: 405-410 # ?! _  J. \& f* Q. s. d% C
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Abstract:! f5 t8 C$ a) B: x! f) e- v
S-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.5 k# H, b( @& \" i
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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 population
/ z' K9 {* N" C( F9 ]F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
' M6 e7 S4 M' {" m! _1 O: d* D+ Author Affiliations
2 P* R2 k+ b' T+ |0 a1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu / @8 ~7 X* `4 X  t
2Department of Thoracic Surgery, Kyoto University, Kyoto
5 H. S2 n& O/ R& S% l3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
' J0 V& l7 A3 g- }. q&#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
1 B8 u+ \0 {7 a- D+ R3 S  YReceived September 3, 2010.
- z; z: }6 I7 M! `Revision received November 11, 2010.
/ x1 o9 l/ A! A" V( @8 x+ DAccepted November 17, 2010. 3 p& O" X; a% \& \, P. ]
Abstract* D3 I0 F) E& ^+ I
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.
7 |9 Q1 P! Y  {7 g9 [+ J5 lPatients 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.
' y0 H0 \' u+ q5 u* O, fResults: 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.
0 z7 k& G) |( Y  G2 g1 yConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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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。% A! X, ^6 m6 b3 a# t3 t
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
  X8 N- U. u0 Uhttp://clinicaltrials.gov/ct2/show/NCT01523587
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1 ?/ S" l8 `0 U1 x* o# w+ f5 x9 K9 jBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
1 Z  N. u  [$ c8 {9 X( Qhttp://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   [" m/ t: P$ S! h4 l
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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。
. t; O* D/ X# b, N0 j# U! |- G! M, J4 x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
7 }1 }8 E& ]/ @/ ?* N$ a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。2 ^6 k0 f6 s, r9 k* {- N
至今为止,未出 ...

/ |' ], H* b( H/ C# q没有副作用是第一追求,效果显著是第二追求。" R! m3 W( y8 B/ \9 i1 N% u
不错。

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