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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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1251188 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( x3 y6 |1 T* N! H9 @
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 d9 M3 V) `- U) n/ O% j  h  ]+ Author Affiliations
; H% s. r# w8 y  u: {' Y1 F  p+ \& W. G6 Y9 \% n; H3 T
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 0 Z  r( g! A( ~. J. T2 i) r
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
* k, N0 r- }8 L- O* \3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 4 D8 i- N, b8 j4 o1 a' X
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 9 f" |( f6 L! K' y6 {. g1 ?
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
# Y2 m( M, ~2 Z$ @; _: ~6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
6 N7 ^! e& Y4 b9 J0 w. ~7Kinki University School of Medicine, Osaka 589-8511, Japan
0 W& d) |! C: z% g8Izumi Municipal Hospital, Osaka 594-0071, Japan
& N" |) F1 e9 W+ F$ ~. e9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 3 E  u# }2 Q' J
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
( c; W& b9 g7 O0 b5 KAbstractBackground: 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.
) {- B0 g- t. h4 e$ h* T1 g% H% }: H; R' U; _0 ?5 F# {+ ?
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 ( ]/ X, i/ [! [  l" R

, b5 K. y! O& v1 o: R) i: ZAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
# d) a( @2 }3 _8 ~8 u! N- _+ m# E  Z+ z% p9 A
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
" _' Z7 m8 ?  i  O
  ?/ d! h1 X# a' v# vPublished online on: Thursday, December 1, 2011
. ?* i1 a1 B' @) o8 q- x5 _
) |' K' B' m4 I" x: ZDoi: 10.3892/ol.2011.507 ( X* g# `, Y0 s1 z1 z2 n
/ {+ v2 N# R# K+ M
Pages: 405-410 8 E( R" F! d( q: J2 ~

5 Z6 a$ _4 j  S  j# e6 gAbstract:
# n* e1 |3 Y+ oS-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.: q1 h6 Z2 b6 F) D9 W4 ]. o0 O+ m

5 Y) @# ?2 ?+ U& [% i5 D3 I
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 population5 {0 l0 Z$ W2 o. F
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 % {, y+ I0 }% n. I* K
+ Author Affiliations
$ p! F( I$ W+ Z- V1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
2 ?0 i  y3 x8 t) G* l; f2Department of Thoracic Surgery, Kyoto University, Kyoto ' D5 v: W7 [% K3 |! D: h6 w, s
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
- m4 {9 `1 `# W( y, F0 W&#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
$ y8 ^! J3 D2 Z8 E1 b5 W% w* qReceived September 3, 2010. . p1 \# B* t% X" C! K5 k- j$ h
Revision received November 11, 2010. " z7 P5 J1 z  f9 l, P
Accepted November 17, 2010.
6 A5 e" L! {* F5 p' ~8 d( cAbstract( T( P8 y4 @$ N: R) O
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. ) M, J) T8 B& `* j3 w
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. ( v  i7 x5 `# r8 K
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.
/ }7 i( y# i5 m3 P+ H' lConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.   j" k; S/ j5 X3 r4 R" r
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。
: [0 v! J8 n4 O7 j/ f# u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?+ l3 C9 z( h: D
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
* y) n( l1 A3 E& }+ W0 M5 fhttp://clinicaltrials.gov/ct2/show/NCT01523587
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" B3 C9 s# `9 U" r. X1 RBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
9 F8 p3 o5 p2 X' r( 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 . v0 g8 T/ V. A7 F7 H, ^

, T1 ?& S& H, A# _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。
- N/ e0 u3 L3 X; h6 B. e8 G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
  n, F  ]" c  J1 B& C* I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。
- b3 y7 x3 H. l, P2 `# l+ _( j2 V至今为止,未出 ...

5 w# }! b: R5 o( C  c# }4 F) \' R没有副作用是第一追求,效果显著是第二追求。
5 J' g( \# z* `" M. a, C不错。

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