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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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1344092 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
; D- V, F8 p( o* L4 a7 B! w( Y( pNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 % k9 q5 l6 J1 O
+ Author Affiliations, l  W4 s5 |9 |9 ]: @# U

2 ?" ^1 }; t- |* B( D* X1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
) F  j& i" X; q% C- h0 b  f2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& P5 e, f4 c! M  V3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 y  [5 Z1 F: h# I, A. t4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan + w* X  }5 n& l- _$ o6 ^
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
8 Z! ~2 s+ e: M" y$ k3 E8 \6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
0 W9 J4 f2 ?0 T: {6 \7Kinki University School of Medicine, Osaka 589-8511, Japan ; P+ }8 v, {/ D4 M+ b
8Izumi Municipal Hospital, Osaka 594-0071, Japan
5 F* U! K( o1 ~# V9 B8 B0 Y9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 f  X' d8 Y$ t# A8 W# P2 C2 KCorrespondence 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
3 ?& f! n2 Q0 ?& DAbstractBackground: 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 6 f4 Y. `2 H, b+ h2 g6 \# k

! u9 S8 G# N& C. Y, dAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 9 z& {7 z# T# a" x# B  }
+ q' Q+ H0 m; C* M1 p% d  B/ B* G8 c
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
6 m# B  p3 _+ Y2 C: ?
& E6 r: J) [3 C4 q5 YPublished online on: Thursday, December 1, 2011
. y& X1 u) {; J+ o# q/ r) ~3 X8 r& W" ]1 r3 K  ^% |. e& k
Doi: 10.3892/ol.2011.507 7 d. u% b! z! R  ^0 M0 ]% l: j
8 ?8 I  t5 q  X  E9 k
Pages: 405-410
# X/ S. E# m3 e0 h$ Q% V; q1 t! b% J3 Q) y9 e( [2 E
Abstract:2 }+ Y; ]/ D' Y: U3 ^  s
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.
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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! t" z( j- p  w; ]5 J+ f/ s
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
1 P; X' n* V4 ]. D1 i6 |+ Author Affiliations# {& O2 Z: b3 B
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
; Y4 ?2 j1 ]9 G% M2Department of Thoracic Surgery, Kyoto University, Kyoto ) s" r) `7 @/ ?3 d; n3 h$ P2 R( o3 K
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
9 N  u6 u9 D  D6 S, v( [/ |# K8 [( d&#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 % X: R2 k2 {( C3 O1 ]8 ^4 \
Received September 3, 2010. & P. r+ y1 g% V7 J
Revision received November 11, 2010. ; J+ j$ ?3 i' [5 u6 t/ Q
Accepted November 17, 2010.
* N9 q) V1 t5 J3 g% B. q2 A3 mAbstract
7 ~/ Y! W4 x9 Q, oBackground: 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.
# M6 }: }' y; u8 Z; O$ uPatients 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. ) z* r" X8 @8 i  l
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. * N( U6 H/ V. i9 j- u+ L
Conclusion: 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。
" @$ i4 {/ Y( @1 _7 G4 N9 x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) g4 }* C0 u, c9 F3 u
http://clinicaltrials.gov/ct2/show/NCT01523587/ s, `5 r4 J' x  S  }
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ b0 D# G: U8 ~% P1 q. x$ H" Vhttp://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 * ^5 ]$ M; Q5 d! Q  m* J, S/ n

  r  y) n* \" ?" r5 E& Y# p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。
- Q3 I1 e+ w$ A# m! 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
- f. }" B2 |$ Q4 K* s  {0 O$ t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。
1 V4 i5 V. U7 w" U( h至今为止,未出 ...

/ _5 l  t2 `+ r8 W没有副作用是第一追求,效果显著是第二追求。
+ z% g1 B$ _# I/ N不错。

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